| Year |
Citation |
Score |
| 2024 |
Wiedemann A, Oussalah A, Guéant Rodriguez RM, Jeannesson E, Mertens M, Rotaru I, Alberto JM, Baspinar O, Rashka C, Hassan Z, Siblini Y, Matmat K, Jeandel M, Chery C, Robert A, et al. Multiomic analysis in fibroblasts of patients with inborn errors of cobalmin metabolism reveals concordance with clinical and metabolic variability. Ebiomedicine. 99: 104911. PMID 38168585 DOI: 10.1016/j.ebiom.2023.104911 |
0.736 |
|
| 2023 |
Matmat K, Conart JB, Graindorge PH, El Kouche S, Hassan Z, Siblini Y, Umoret R, Safar R, Baspinar O, Robert A, Alberto JM, Oussalah A, Coelho D, Guéant JL, Guéant-Rodriguez RM. A transgenic mice model of retinopathy of cblG-type inherited disorder of one-carbon metabolism highlights epigenome-wide alterations related to cone photoreceptor cells development and retinal metabolism. Clinical Epigenetics. 15: 158. PMID 37798757 DOI: 10.1186/s13148-023-01567-w |
0.754 |
|
| 2023 |
Hergalant S, Casse JM, Oussalah A, Houlgatte R, Helle D, Rech F, Vallar L, Guéant JL, Vignaud JM, Battaglia-Hsu SF, Gauchotte G. MicroRNAs miR-16 and miR-519 control meningioma cell proliferation overlapping transcriptomic programs shared with the RNA-binding protein HuR. Frontiers in Oncology. 13: 1158773. PMID 37601663 DOI: 10.3389/fonc.2023.1158773 |
0.506 |
|
| 2023 |
Michel A, Kokten T, Saber-Cherif L, Umoret R, Alberto JM, Helle D, Julien A, Daval JL, Guéant JL, Bossenmeyer-Pourié C, Pourié G. Folate and Cobalamin Deficiencies during Pregnancy Disrupt the Glucocorticoid Response in Hypothalamus through -Homocysteinilation of the Glucocorticoid Receptor. International Journal of Molecular Sciences. 24. PMID 37372992 DOI: 10.3390/ijms24129847 |
0.679 |
|
| 2023 |
Hassan Z, Coelho D, Bossenmeyer-Pourié C, Matmat K, Arnold C, Savladori A, Alberto JM, Umoret R, Guéant JL, Pourié G. Cognitive Impairment Is Associated with AMPAR Glutamatergic Dysfunction in a Mouse Model of Neuronal Methionine Synthase Deficiency. Cells. 12. PMID 37174668 DOI: 10.3390/cells12091267 |
0.659 |
|
| 2023 |
Safar R, Oussalah A, Mayorga L, Vieths S, Barber D, Torres MJ, Guéant JL. Epigenome alterations in food allergy: A systematic review of candidate gene and epigenome-wide association studies. Clinical and Experimental Allergy : Journal of the British Society For Allergy and Clinical Immunology. PMID 36756739 DOI: 10.1111/cea.14277 |
0.53 |
|
| 2023 |
Alix T, Chéry C, Josse T, Bronowicki JP, Feillet F, Guéant-Rodriguez RM, Namour F, Guéant JL, Oussalah A. Predictors of the utility of clinical exome sequencing as a first-tier genetic test in patients with Mendelian phenotypes: results from a referral center study on 603 consecutive cases. Human Genomics. 17: 5. PMID 36740706 DOI: 10.1186/s40246-023-00455-x |
0.549 |
|
| 2023 |
Oussalah A, Callet J, Manteaux AE, Thilly N, Jay N, Guéant JL, Lozniewski A. Usefulness of procalcitonin at admission as a risk-stratifying biomarker for 50-day in-hospital mortality among patients with community-acquired bloodstream infection: an observational cohort study. Biomarker Research. 11: 4. PMID 36647149 DOI: 10.1186/s40364-023-00450-3 |
0.521 |
|
| 2022 |
Siblini Y, Namour F, Oussalah A, Guéant JL, Chéry C. Stemness of Normal and Cancer Cells: The Influence of Methionine Needs and SIRT1/PGC-1α/PPAR-α Players. Cells. 11. PMID 36429035 DOI: 10.3390/cells11223607 |
0.542 |
|
| 2022 |
Gueant JL, Gueant-Rodriguez RM, Oussalah A, Zuily S, Rosenberg I. Hyperhomocysteinemia in cardiovascular diseases: revisiting observational studies and clinical trials. Thrombosis and Haemostasis. PMID 36170884 DOI: 10.1055/a-1952-1946 |
0.573 |
|
| 2022 |
Wiedemann A, Oussalah A, Lamireau N, Théron M, Julien M, Mergnac JP, Augay B, Deniaud P, Alix T, Frayssinoux M, Feillet F, Guéant JL. Clinical, phenotypic and genetic landscape of case reports with genetically proven inherited disorders of vitamin B metabolism: A meta-analysis. Cell Reports. Medicine. 3: 100670. PMID 35764087 DOI: 10.1016/j.xcrm.2022.100670 |
0.587 |
|
| 2022 |
Quéré M, Alberto JM, Broly F, Hergalant S, Christov C, Gauchotte G, Guéant JL, Namour F, Battaglia-Hsu SF. Knockout in U251 Glioblastoma Cells Reduces Tumor Sphere Formation by Increasing Oxidative Stress and Suppressing Methionine Dependency. Nutrients. 14. PMID 35565854 DOI: 10.3390/nu14091887 |
0.641 |
|
| 2022 |
Oussalah A, Siblini Y, Hergalant S, Chéry C, Rouyer P, Cavicchi C, Guerrini R, Morange PE, Trégouët D, Pupavac M, Watkins D, Pastinen T, Chung WK, Ficicioglu C, Feillet F, et al. Epimutations in both the TESK2 and MMACHC promoters in the Epi-cblC inherited disorder of intracellular metabolism of vitamin B. Clinical Epigenetics. 14: 52. PMID 35440018 DOI: 10.1186/s13148-022-01271-1 |
0.59 |
|
| 2022 |
Guéant JL, Siblini Y, Chéry C, Schmitt G, Guéant-Rodriguez RM, Coelho D, Watkins D, Rosenblatt DS, Oussalah A. Epimutation in inherited metabolic disorders: the influence of aberrant transcription in adjacent genes. Human Genetics. PMID 35190856 DOI: 10.1007/s00439-021-02414-9 |
0.574 |
|
| 2022 |
Wiedemann A, Lin C, Oussalah A, Namour B, Jeannesson É, Guéant JL, Feillet F. [A long non-coding RNA regulates the activity of phenylalanine hydroxylase, the key enzyme of phenylketonuria]. Medecine Sciences : M/S. 38: 12-14. PMID 35060876 DOI: 10.1051/medsci/2021237 |
0.752 |
|
| 2021 |
Trépo E, Caruso S, Yang J, Imbeaud S, Couchy G, Bayard Q, Letouzé E, Ganne-Carrié N, Moreno C, Oussalah A, Féray C, Blanc JF, Clément B, Hillon P, Boursier J, et al. Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association study. The Lancet. Oncology. PMID 34902334 DOI: 10.1016/S1470-2045(21)00603-3 |
0.529 |
|
| 2021 |
Siblini Y, Chéry C, Rouyer P, Raso J, Julien A, Hergalant S, François A, Bezdetnaya L, Vogin G, Guéant JL, Oussalah A. Ionizing radiations induce shared epigenomic signatures unraveling adaptive mechanisms of cancerous cell lines with or without methionine dependency. Clinical Epigenetics. 13: 212. PMID 34852845 DOI: 10.1186/s13148-021-01199-y |
0.528 |
|
| 2021 |
Antoine D, Guéant-Rodriguez RM, Chèvre JC, Hergalant S, Sharma T, Li Z, Rouyer P, Chery C, Halvick S, Bui C, Oussalah A, Ziegler O, Quilliot D, Brunaud L, Guéant JL, et al. Low-frequency coding variants associated with body-mass-index impact the success of bariatric surgery. The Journal of Clinical Endocrinology and Metabolism. PMID 34718599 DOI: 10.1210/clinem/dgab774 |
0.624 |
|
| 2021 |
Romano A, Oussalah A, Chery C, Guéant-Rodriguez RM, Gaeta F, Cornejo-Garcia JA, Rouyer P, Josse T, Mayorga C, Torres MJ, Guéant JL. Next-Generation Sequencing and Genotype Association Studies Reveal the Association of HLA-DRB3*02:02 With Delayed Hypersensitivity to Penicillins. Allergy. PMID 34687232 DOI: 10.1111/all.15147 |
0.539 |
|
| 2021 |
Matmat K, Guéant-Rodriguez RM, Oussalah A, Wiedemann-Fodé A, Dionisi-Vici C, Coelho D, Guéant JL, Conart JB. Ocular manifestations in patients with inborn errors of intracellular cobalamin metabolism: a systematic review. Human Genetics. PMID 34652574 DOI: 10.1007/s00439-021-02350-8 |
0.555 |
|
| 2021 |
Gallet P, Oussalah A, Pouget C, Dittmar G, Chery C, Gauchotte G, Jankowski R, Gueant JL, Houlgatte R. Integrative genomics analysis of nasal intestinal-type adenocarcinomas demonstrates the major role of CACNA1C and paves the way for a simple diagnostic tool in male woodworkers. Clinical Epigenetics. 13: 179. PMID 34563241 DOI: 10.1186/s13148-021-01122-5 |
0.545 |
|
| 2021 |
Berthezène C, Aissa N, Manteaux AE, Guéant JL, Oussalah A, Lozniewski A. Accuracy of procalcitonin for diagnosing peripheral blood culture contamination among patients with positive blood culture for potential contaminants. Infection. 49: 1249-1255. PMID 34524647 DOI: 10.1007/s15010-021-01697-4 |
0.509 |
|
| 2021 |
Mergnac JP, Wiedemann A, Chery C, Ravel JM, Namour F, Guéant JL, Feillet F, Oussalah A. Diagnostic yield of clinical exome sequencing as a first-tier genetic test for the diagnosis of genetic disorders in pediatric patients: results from a referral center study. Human Genetics. PMID 34495415 DOI: 10.1007/s00439-021-02358-0 |
0.549 |
|
| 2021 |
Mosca P, Robert A, Alberto JM, Meyer M, Kundu U, Hergalant S, Umoret R, Coelho D, Guéant JL, Leheup B, Dreumont N. Vitamin B Deficiency Dysregulates m6A mRNA Methylation of Genes Involved in Neurological Functions. Molecular Nutrition & Food Research. e2100206. PMID 34291881 DOI: 10.1002/mnfr.202100206 |
0.677 |
|
| 2021 |
Cavicchi C, Oussalah A, Falliano S, Ferri L, Gozzini A, Gasperini S, Motta S, Rigoldi M, Parenti G, Tummolo A, Meli C, Menni F, Furlan F, Daniotti M, Malvagia S, et al. PRDX1 gene-related epi-cblC disease is a common type of inborn error of cobalamin metabolism with mono- or bi-allelic MMACHC epimutations. Clinical Epigenetics. 13: 137. PMID 34215320 DOI: 10.1186/s13148-021-01117-2 |
0.584 |
|
| 2021 |
Wiedemann A, Jeannesson É, Oussalah A, Guéant JL, Guéant-Rodriguez RM, Feillet F. [Newborn screening of phenylketonuria in France]. Medecine Sciences : M/S. 37: 468-473. PMID 34003092 DOI: 10.1051/medsci/2021061 |
0.516 |
|
| 2021 |
Li Z, Kosgei VJ, Bison A, Alberto JM, Umoret R, Maskali F, Brunaud L, Guéant JL, Guéant-Rodriguez RM. Programming by Methyl Donor Deficiency during Pregnancy and Lactation Produces Cardiomyopathy in Adult Rats Subjected to High Fat Diet. Molecular Nutrition & Food Research. e2100065. PMID 33991387 DOI: 10.1002/mnfr.202100065 |
0.719 |
|
| 2021 |
Levy J, Rodriguez-Guéant RM, Oussalah A, Jeannesson E, Wahl D, Ziuly S, Guéant JL. Cardiovascular manifestations of intermediate and major hyperhomocysteinemia due to vitamin B12 and folate deficiency and/or inherited disorders of one-carbon metabolism: a 3.5-year retrospective cross-sectional study of consecutive patients. The American Journal of Clinical Nutrition. PMID 33693455 DOI: 10.1093/ajcn/nqaa432 |
0.587 |
|
| 2021 |
Guéant JL, Guéant-Rodriguez RM, Fromonot J, Oussalah A, Louis H, Chery C, Gette M, Gleye S, Callet J, Raso J, Blanchecotte F, Lacolley P, Guieu R, Regnault V. Elastase and Exacerbation of Neutrophil Innate Immunity are Involved in Multi-Visceral Manifestations of COVID-19. Allergy. PMID 33484168 DOI: 10.1111/all.14746 |
0.523 |
|
| 2021 |
Ravel JM, Benkirane M, Calmels N, Marelli C, Ory-Magne F, Ewenczyk C, Halleb Y, Tison F, Lecocq C, Pische G, Casenave P, Chaussenot A, Frismand S, Tyvaert L, Larrieu L, et al. Expanding the clinical spectrum of STIP1 homology and U-box containing protein 1-associated ataxia. Journal of Neurology. PMID 33417001 DOI: 10.1007/s00415-020-10348-x |
0.551 |
|
| 2020 |
Pourié G, Martin N, Daval JL, Alberto JM, Umoret R, Guéant JL, Bossenmeyer-Pourié C. The Stimulation of Neurogenesis Improves the Cognitive Status of Aging Rats Subjected to Gestational and Perinatal Deficiency of B9-12 Vitamins. International Journal of Molecular Sciences. 21. PMID 33126444 DOI: 10.3390/ijms21218008 |
0.67 |
|
| 2020 |
Dreumont N, Mimoun K, Pourié C, Quadros EV, Alberto JM, Umoret R, Helle D, Robert A, Daval JL, Guéant JL, Pourié G. Glucocorticoid Receptor Activation Restores Learning Memory by Modulating Hippocampal Plasticity in a Mouse Model of Brain Vitamin B Deficiency. Molecular Neurobiology. PMID 33078371 DOI: 10.1007/s12035-020-02163-2 |
0.651 |
|
| 2020 |
Oussalah A, Gleye S, Urmes IC, Laugel E, Barbé F, Orlowski S, Malaplate C, Aimone-Gastin I, Caillierez BM, Merten M, Jeannesson E, Kormann R, Olivier JL, Rodriguez-Guéant RM, Namour F, et al. The spectrum of biochemical alterations associated with organ dysfunction and inflammatory status and their association with disease outcomes in severe COVID-19: A longitudinal cohort and time-series design study. Eclinicalmedicine. 100554. PMID 32984786 DOI: 10.1016/J.Eclinm.2020.100554 |
0.76 |
|
| 2020 |
Wiedemann A, Oussalah A, Jeannesson É, Guéant JL, François F. [Phenylketonuria, from diet to gene therapy]. Medecine Sciences : M/S. 36: 725-734. PMID 32821049 DOI: 10.1051/Medsci/2020127 |
0.577 |
|
| 2020 |
Kosgei VJ, Coelho D, Guéant-Rodriguez RM, Guéant JL. Sirt1-PPARS Cross-Talk in Complex Metabolic Diseases and Inherited Disorders of the One Carbon Metabolism. Cells. 9. PMID 32796716 DOI: 10.3390/Cells9081882 |
0.362 |
|
| 2020 |
Kormann R, Jacquot A, Alla A, Corbel A, Koszutski M, Voirin P, Garcia Parrilla M, Bevilacqua S, Schvoerer E, Gueant JL, Namour F, Levy B, Frimat L, Oussalah A. Coronavirus disease 2019: acute Fanconi syndrome precedes acute kidney injury. Clinical Kidney Journal. 13: 362-370. PMID 32695327 DOI: 10.1093/Ckj/Sfaa109 |
0.574 |
|
| 2020 |
Harb Z, Deckert V, Bressenot AM, Christov C, Guéant-Rodriguez RM, Raso J, Alberto JM, de Barros JP, Umoret R, Biroulet LP, Lagrost L, Bronowicki JP, Guéant JL. The deficit in folate and vitamin B12 triggers liver macrovesicular steatosis and inflammation in rats with dextran sodium sulfate-induced colitis. The Journal of Nutritional Biochemistry. 84: 108415. PMID 32645655 DOI: 10.1016/J.Jnutbio.2020.108415 |
0.697 |
|
| 2020 |
Oussalah A, Gleye S, Clerc Urmes I, Laugel E, Callet J, Barbé F, Orlowski S, Malaplate C, Aimone-Gastin I, Caillierez BM, Merten M, Jeannesson E, Kormann R, Olivier JL, Rodriguez-Guéant RM, et al. Long-Term ACE Inhibitor/ARB Use Is Associated with Severe Renal Dysfunction and Acute Kidney Injury in Patients with severe COVID-19: Results from a Referral Center Cohort in the North East of France. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. PMID 32623470 DOI: 10.1093/Cid/Ciaa677 |
0.759 |
|
| 2020 |
Antoine D, Li Z, Quilliot D, Sirveaux MA, Meyre D, Mangeon A, Brunaud L, Guéant JL, Guéant-Rodriguez RM. Medium term post-bariatric surgery deficit of vitamin B12 is predicted by deficit at time of surgery. Clinical Nutrition (Edinburgh, Scotland). PMID 32444241 DOI: 10.1016/J.Clnu.2020.04.029 |
0.482 |
|
| 2020 |
Wiedemann A, Renard E, Molin A, Weryha G, Oussalah A, Guéant JL, Feillet F. Prolonged 25-OH Vitamin D Deficiency Does Not Impair Bone Mineral Density in Adult Patients With Vitamin D 25-Hydroxylase Deficiency (CYP2R1). Calcified Tissue International. PMID 32430692 DOI: 10.1007/S00223-020-00704-4 |
0.602 |
|
| 2020 |
Bidla G, Watkins D, Chéry C, Froese DS, Ells C, Kerachian M, Saskin A, Christensen KE, Gilfix BM, Guéant JL, Rosenblatt DS. Biochemical analysis of patients with mutations in MTHFD1 and a diagnosis of methylenetetrahydrofolate dehydrogenase 1 deficiency. Molecular Genetics and Metabolism. PMID 32414565 DOI: 10.1016/J.Ymgme.2020.04.008 |
0.32 |
|
| 2020 |
Renard E, Leheup B, Guéant-Rodriguez RM, Oussalah A, Quadros EV, Guéant JL. Folinic acid improves the score of Autism in the EFFET placebo-controlled randomized trial. Biochimie. 173: 57-61. PMID 32387472 DOI: 10.1016/J.Biochi.2020.04.019 |
0.566 |
|
| 2020 |
Daude S, Remen T, Chateau T, Danese S, Gastin I, Baumann C, Gueant JL, Peyrin-Biroulet L. Comparative accuracy of ferritin, transferrin saturation and soluble transferrin receptor for the diagnosis of iron deficiency in inflammatory bowel disease. Alimentary Pharmacology & Therapeutics. PMID 32323356 DOI: 10.1111/Apt.15739 |
0.313 |
|
| 2020 |
Guéant JL, Oussalah A, Zgheib R, Siblini Y, Hsu SB, Namour B. Genetic, epigenetic and genomic mechanisms of methionine dependency of cancer and tumor-initiating cells: What could we learn from folate and methionine cycles. Biochimie. PMID 32289469 DOI: 10.1016/J.Biochi.2020.03.015 |
0.783 |
|
| 2020 |
Feigerlová E, Oussalah A, Zuily S, Sordet S, Braun M, Guéant JL, Guerci B. E-health education interventions on HbA in patients with type 1 diabetes on intensive insulin therapy: A systematic review and meta-analysis of randomized controlled trials. Diabetes/Metabolism Research and Reviews. PMID 32212412 DOI: 10.1002/Dmrr.3313 |
0.562 |
|
| 2020 |
Oussalah A, Levy J, Berthezène C, Alpers DH, Guéant JL. Health outcomes associated with vegetarian diets: An umbrella review of systematic reviews and meta-analyses. Clinical Nutrition (Edinburgh, Scotland). PMID 32204974 DOI: 10.1016/J.Clnu.2020.02.037 |
0.571 |
|
| 2020 |
Rashka C, Hergalant S, Dreumont N, Oussalah A, Camadro JM, Marchand V, Hassan Z, Baumgartner MR, Rosenblatt DS, Feillet F, Guéant JL, Coelho D. Analysis of fibroblasts from patients with cblC and cblG genetic defects of cobalamin metabolism reveals global dysregulation of alternative splicing. Human Molecular Genetics. PMID 32068834 DOI: 10.1093/Hmg/Ddaa027 |
0.619 |
|
| 2020 |
Oussalah A, Jeannesson-Thivisol E, Chéry C, Perrin P, Rouyer P, Josse T, Cano A, Barth M, Fouilhoux A, Mention K, Labarthe F, Arnoux JB, Maillot F, Lenaerts C, Dumesnil C, et al. Population and evolutionary genetics of the PAH locus to uncover overdominance and adaptive mechanisms in phenylketonuria: Results from a multiethnic study. Ebiomedicine. 51: 102623. PMID 31923802 DOI: 10.1016/J.Ebiom.2019.102623 |
0.589 |
|
| 2020 |
Oussalah A, Yip V, Mayorga C, Blanca M, Barbaud A, Nakonechna A, Cernadas J, Gotua M, Brockow K, Caubet JC, Bircher A, Atanaskovic-Markovic M, Demoly P, Kase-Tanno L, Terreehorst I, et al. Genetic Variants Associated with T-Cell Mediated Cutaneous Adverse Drug Reactions: A Prisma-Compliant Systematic Review - an EAACI Position Paper. Allergy. PMID 31899808 DOI: 10.1111/All.14174 |
0.591 |
|
| 2019 |
Hassan Z, Coelho D, Kokten T, Alberto JM, Umoret R, Daval JL, Guéant JL, Bossenmeyer-Pourié C, Pourié G. Brain Susceptibility to Methyl Donor Deficiency: From Fetal Programming to Aging Outcome in Rats. International Journal of Molecular Sciences. 20. PMID 31739389 DOI: 10.3390/Ijms20225692 |
0.676 |
|
| 2019 |
Blanca M, Oussalah A, Cornejo-García JA, Blanca-López N, Guéant-Rodriguez RM, Doña I, Mayorga C, Chery C, Rouyer P, Carmona FD, Bossini Castillo L, Canto G, Martin J, Torres MJ, Guéant JL. GNAI2 variants predict non-steroidal anti-inflammatory drug hypersensitivity in a genome-wide study. Allergy. PMID 31705548 DOI: 10.1111/All.14100 |
0.562 |
|
| 2019 |
Ghemrawi R, Arnold C, Battaglia-Hsu SF, Pourié G, Trinh I, Bassila C, Rashka C, Wiedemann A, Flayac J, Robert A, Dreumont N, Feillet F, Guéant JL, Coelho D. SIRT1 activation rescues the mislocalization of RNA-binding proteins and cognitive defects induced by inherited cobalamin disorders. Metabolism: Clinical and Experimental. 101: 153992. PMID 31672445 DOI: 10.1016/J.Metabol.2019.153992 |
0.758 |
|
| 2019 |
Wiedemann A, Chery C, Coelho D, Flayac J, Gueguen N, Desquiret-Dumas V, Feillet F, Lavigne C, Neau JP, Fowler B, Baumgartner MR, Reynier P, Guéant JL, Oussalah A. Mutations in MTHFR and POLG impaired activity of the mitochondrial respiratory chain in 46-year-old twins with spastic paraparesis. Journal of Human Genetics. PMID 31645654 DOI: 10.1038/S10038-019-0689-Y |
0.596 |
|
| 2019 |
Saber Cherif L, Pourié G, Geoffroy A, Julien A, Helle D, Robert A, Umoret R, Guéant JL, Bossenmeyer-Pourié C, Daval JL. Methyl Donor Deficiency during Gestation and Lactation in the Rat Affects the Expression of Neuropeptides and Related Receptors in the Hypothalamus. International Journal of Molecular Sciences. 20. PMID 31615150 DOI: 10.3390/Ijms20205097 |
0.34 |
|
| 2019 |
Zgheib R, Battaglia-Hsu SF, Hergalant S, Quéré M, Alberto JM, Chéry C, Rouyer P, Gauchotte G, Guéant JL, Namour F. Folate can promote the methionine-dependent reprogramming of glioblastoma cells towards pluripotency. Cell Death & Disease. 10: 596. PMID 31395852 DOI: 10.1038/S41419-019-1836-2 |
0.67 |
|
| 2019 |
Renard E, Chéry C, Oussalah A, Josse T, Perrin P, Tramoy D, Voirin J, Klein O, Leheup B, Feillet F, Guéant-Rodriguez RM, Guéant JL. Exome sequencing of cases with neural tube defects identifies candidate genes involved in one-carbon/vitamin B12 metabolisms and Sonic Hedgehog pathway. Human Genetics. PMID 31139930 DOI: 10.1007/S00439-019-02015-7 |
0.606 |
|
| 2019 |
Oussalah A, Julien M, Levy J, Hajjar O, Franczak C, Stephan C, Laugel E, Wandzel M, Filhine-Tresarrieu P, Green R, Guéant JL. Global Burden Related to Nitrous Oxide Exposure in Medical and Recreational Settings: A Systematic Review and Individual Patient Data Meta-Analysis. Journal of Clinical Medicine. 8. PMID 31018613 DOI: 10.3390/Jcm8040551 |
0.623 |
|
| 2019 |
Fofou-Caillierez MB, Guéant-Rodriguez RM, Alberto JM, Chéry C, Josse T, Gérard P, Forges T, Foliguet B, Feillet F, Guéant JL. Vitamin B-12 and liver activity and expression of methionine synthase are decreased in fetuses with neural tube defects. The American Journal of Clinical Nutrition. PMID 30848279 DOI: 10.1093/Ajcn/Nqy340 |
0.705 |
|
| 2019 |
Geoffroy A, Saber-Cherif L, Pourié G, Helle D, Umoret R, Guéant JL, Bossenmeyer-Pourié C, Daval JL. Developmental Impairments in a Rat Model of Methyl Donor Deficiency: Effects of a Late Maternal Supplementation with Folic Acid. International Journal of Molecular Sciences. 20. PMID 30813413 DOI: 10.3390/Ijms20040973 |
0.322 |
|
| 2018 |
Battaglia-Hsu SF, Ghemrawi R, Coelho D, Dreumont N, Mosca P, Hergalant S, Gauchotte G, Sequeira JM, Ndiongue M, Houlgatte R, Alberto JM, Umoret R, Robert A, Paoli J, Jung M, et al. Inherited disorders of cobalamin metabolism disrupt nucleocytoplasmic transport of mRNA through impaired methylation/phosphorylation of ELAVL1/HuR. Nucleic Acids Research. PMID 30016500 DOI: 10.1093/Nar/Gky634 |
0.788 |
|
| 2018 |
Fezeu LK, Ducros V, Guéant JL, Guilland JC, Andreeva VA, Hercberg S, Galan P. MTHFR 677C → T genotype modulates the effect of a 5-year supplementation with B-vitamins on homocysteine concentration: The SU.FOL.OM3 randomized controlled trial. Plos One. 13: e0193352. PMID 29813097 DOI: 10.1371/Journal.Pone.0193352 |
0.315 |
|
| 2018 |
Willekens J, Hergalant S, Pourié G, Marin F, Alberto JM, Georges L, Paoli J, Nemos C, Daval JL, Guéant JL, Leininger-Muller B, Dreumont N. Wnt Signaling Pathways Are Dysregulated in Rat Female Cerebellum Following Early Methyl Donor Deficiency. Molecular Neurobiology. PMID 29804229 DOI: 10.1007/S12035-018-1128-3 |
0.661 |
|
| 2018 |
Romier B, Ivaldi C, Sartelet H, Heinz A, Schmelzer CEH, Garnotel R, Guillot A, Jonquet J, Bertin E, Guéant JL, Alberto JM, Bronowicki JP, Amoyel J, Hocine T, Duca L, et al. Production of Elastin-Derived Peptides Contribute to the Development of Non-Alcoholic Steatohepatitis. Diabetes. PMID 29802129 DOI: 10.2337/Db17-0490 |
0.663 |
|
| 2018 |
Oussalah A, Rischer S, Bensenane M, Conroy G, Filhine-Tresarrieu P, Debard R, Forest-Tramoy D, Josse T, Reinicke D, Garcia M, Luc A, Baumann C, Ayav A, Laurent V, Hollenbach M, et al. Plasma mSEPT9: A Novel Circulating Cell-free DNA-Based Epigenetic Biomarker to Diagnose Hepatocellular Carcinoma. Ebiomedicine. 30: 138-147. PMID 29627389 DOI: 10.1016/S0168-8278(18)30444-6 |
0.703 |
|
| 2018 |
Guéant JL, Chéry C, Oussalah A, Nadaf J, Coelho D, Josse T, Flayac J, Robert A, Koscinski I, Gastin I, Filhine-Tresarrieu P, Pupavac M, Brebner A, Watkins D, Pastinen T, et al. Publisher Correction: A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nature Communications. 9: 554. PMID 29396438 DOI: 10.1038/S41467-018-03054-W |
0.581 |
|
| 2018 |
Guéant JL, Chéry C, Oussalah A, Nadaf J, Coelho D, Josse T, Flayac J, Robert A, Koscinski I, Gastin I, Filhine-Tresarrieu P, Pupavac M, Brebner A, Watkins D, Pastinen T, et al. APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients. Nature Communications. 9: 67. PMID 29302025 DOI: 10.1038/S41467-017-02306-5 |
0.622 |
|
| 2018 |
Guéant J, Chéry C, Oussalah A, Nicolas J, Majewski J, Rosenblatt DS. Une épimutation transgénérationnelle du gène MMACHC produit un nouveau type d’erreur innée du métabolisme dénommée épi-cblC Bulletin De L'AcadéMie Nationale De MéDecine. 202: 1585-1596. DOI: 10.1016/S0001-4079(19)30225-0 |
0.565 |
|
| 2017 |
Oussalah A, Avogbe PH, Guyot E, Chery C, Guéant-Rodriguez RM, Ganne-Carrié N, Cobat A, Moradpour D, Nalpas B, Negro F, Poynard T, Pol S, Bochud PY, Abel L, Jeulin H, et al. BRIP1 coding variants are associated with a high risk of hepatocellular carcinoma occurrence in patients with HCV- or HBV-related liver disease. Oncotarget. 8: 62842-62857. PMID 28968953 DOI: 10.18632/Oncotarget.11327 |
0.767 |
|
| 2017 |
Kökten T, Gibot S, Lepage P, D'Alessio S, Hablot J, Ndiaye NC, Busby-Venner H, Monot C, Garnier B, Moulin D, Jouzeau JY, Hansmannel F, Danese S, Guéant JL, Muller S, et al. TREM-1 inhibition restores impaired autophagy activity and reduces colitis in mice. Journal of Crohn's & Colitis. PMID 28961797 DOI: 10.1093/Ecco-Jcc/Jjx129 |
0.411 |
|
| 2017 |
Maréchal C, Aimone-Gastin I, Baumann C, Dirrenberger B, Guéant JL, Peyrin-Biroulet L. Compliance with the faecal calprotectin test in patients with inflammatory bowel disease. United European Gastroenterology Journal. 5: 702-707. PMID 28815034 DOI: 10.1177/2050640616686517 |
0.705 |
|
| 2017 |
Oussalah A, Levy J, Filhine-Trésarrieu P, Namour F, Guéant JL. Association of TCN2 rs1801198 c.776G>C polymorphism with markers of one-carbon metabolism and related diseases: a systematic review and meta-analysis of genetic association studies. The American Journal of Clinical Nutrition. PMID 28814397 DOI: 10.3945/Ajcn.117.156349 |
0.613 |
|
| 2017 |
Li Z, Gueant-Rodriguez RM, Quilliot D, Sirveaux MA, Meyre D, Gueant JL, Brunaud L. Folate and vitamin B12 status is associated with insulin resistance and metabolic syndrome in morbid obesity. Clinical Nutrition (Edinburgh, Scotland). PMID 28780990 DOI: 10.1016/J.Clnu.2017.07.008 |
0.526 |
|
| 2016 |
Bison A, Marchal-Bressenot A, Li Z, Elamouri I, Feigerlova E, Peng L, Houlgatte R, Beck B, Pourié G, Alberto JM, Umoret R, Conroy G, Bronowicki JP, Guéant JL, Guéant-Rodriguez RM. Foetal programming by methyl donor deficiency produces steato-hepatitis in rats exposed to high fat diet. Scientific Reports. 6: 37207. PMID 27853271 DOI: 10.1038/Srep37207 |
0.689 |
|
| 2016 |
Cornejo-García JA, Oussalah A, Blanca M, Guéant-Rodríguez RM, Mayorga C, Waton J, Barbaud A, Gaeta F, Romano A, Guéant JL. Genetic Predictors of Drug Hypersensitivity. Current Pharmaceutical Design. PMID 27779086 DOI: 10.2174/1381612822666160927114941 |
0.555 |
|
| 2016 |
Bassila C, Ghemrawi R, Flayac J, Froese DS, Baumgartner MR, Guéant JL, Coelho D. Methionine synthase and methionine synthase reductase interact with MMACHC and with MMADHC. Biochimica Et Biophysica Acta. PMID 27771510 DOI: 10.1016/J.Bbadis.2016.10.016 |
0.74 |
|
| 2016 |
Goffinet L, Oussalah A, Guéant-Rodriguez RM, Chery C, Basha M, Avogbe PH, Josse T, Jeannesson E, Rouyer P, Flayac J, Gerard P, Le Touze A, Bonin-Goga B, Goga D, Simon E, et al. Cystathionine β-synthase genetic variant rs2124459 is associated with a reduced risk of cleft palate in French and Belgian populations. Journal of Medical Genetics. PMID 27535090 DOI: 10.1136/Jmedgenet-2016-104111 |
0.79 |
|
| 2016 |
Feigerlova E, Demarquet L, Melhem H, Ghemrawi R, Battaglia-Hsu SF, Ewu E, Alberto JM, Helle D, Weryha G, Guéant JL. Methyl donor deficiency impairs bone development via peroxisome proliferator-activated receptor-γ coactivator-1α-dependent vitamin D receptor pathway. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 30: 3598-3612. PMID 27435264 DOI: 10.1096/Fj.201600332R |
0.778 |
|
| 2016 |
Peng L, Dreumont N, Coelho D, Guéant JL, Arnold C. Genetic animal models to decipher the pathogenic effects of vitamin B12 and folate deficiency. Biochimie. PMID 27178438 DOI: 10.1016/J.Biochi.2016.05.007 |
0.339 |
|
| 2016 |
Feigerlova E, Demarquet L, Guéant JL. One carbon metabolism and bone homeostasis and remodeling: A review of experimental research and population studies. Biochimie. 126: 115-23. PMID 27086080 DOI: 10.1016/J.Biochi.2016.04.009 |
0.323 |
|
| 2016 |
Germain A, Guéant RM, Chamaillard M, Allen PB, Bresler L, Guéant JL, Peyrin-Biroulet L. NOD2 gene variant is a risk factor for postoperative complications in patients with Crohn's disease: A genetic association study. Surgery. PMID 26946932 DOI: 10.1016/J.Surg.2016.01.013 |
0.645 |
|
| 2016 |
Feigerlova E, Oussalah A, Fournier JP, Antonelli A, Hadjadj S, Marechaud R, Guéant JL, Roblot P, Braun M. Predictors of High Motivation Score for Performing Research Initiation Fellowship, Master 1, Research Master 2, and PhD Curricula During Medical Studies: A Strobe-Compliant Article. Medicine. 95: e2633. PMID 26844478 DOI: 10.1097/Md.0000000000002633 |
0.552 |
|
| 2016 |
Melhem H, Hansmannel F, Bressenot A, Battaglia-Hsu SF, Billioud V, Alberto JM, Gueant JL, Peyrin-Biroulet L. Methyl-deficient diet promotes colitis and SIRT1-mediated endoplasmic reticulum stress. Gut. 65: 595-606. PMID 25608526 DOI: 10.1136/Gutjnl-2014-307030 |
0.677 |
|
| 2015 |
Oussalah A, Ferrand J, Filhine-Tresarrieu P, Aissa N, Aimone-Gastin I, Namour F, Garcia M, Lozniewski A, Guéant JL. Diagnostic Accuracy of Procalcitonin for Predicting Blood Culture Results in Patients With Suspected Bloodstream Infection: An Observational Study of 35,343 Consecutive Patients (A STROBE-Compliant Article). Medicine. 94: e1774. PMID 26554775 DOI: 10.1097/Md.0000000000001774 |
0.749 |
|
| 2015 |
Germain A, Guéant RM, Chamaillard M, Bresler L, Guéant JL, Peyrin-Biroulet L. CARD8 gene variant is a risk factor for recurrent surgery in patients with Crohn's disease. Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association For the Study of the Liver. 47: 938-42. PMID 26283210 DOI: 10.1016/J.Dld.2015.07.013 |
0.641 |
|
| 2015 |
Fréling E, Peyrin-Biroulet L, Poreaux C, Morali A, Waton J, Schmutz JL, Guéant JL, Barbaud A. IgE antibodies and skin tests in immediate hypersensitivity reactions to infliximab in inflammatory bowel disease: impact on infliximab retreatment. European Journal of Gastroenterology & Hepatology. 27: 1200-8. PMID 26181108 DOI: 10.1097/Meg.0000000000000436 |
0.375 |
|
| 2015 |
Belle A, Baumann C, Bigard MA, Zallot C, Gizard E, Guéant JL, Bronowicki JP, Peyrin-Biroulet L. Impact of immunosuppressive therapy on hepatitis B vaccination in inflammatory bowel diseases. European Journal of Gastroenterology & Hepatology. 27: 877-81. PMID 26121376 DOI: 10.1097/Meg.0000000000000370 |
0.384 |
|
| 2015 |
Oussalah A, Bosco P, Anello G, Spada R, Guéant-Rodriguez RM, Chery C, Rouyer P, Josse T, Romano A, Elia M, Bronowicki JP, Guéant JL. Exome-Wide Association Study Identifies New Low-Frequency and Rare UGT1A1 Coding Variants and UGT1A6 Coding Variants Influencing Serum Bilirubin in Elderly Subjects: A Strobe Compliant Article. Medicine. 94: e925. PMID 26039129 DOI: 10.1097/Md.0000000000000925 |
0.548 |
|
| 2015 |
Pourié G, Martin N, Bossenmeyer-Pourié C, Akchiche N, Guéant-Rodriguez RM, Geoffroy A, Jeannesson E, Chehadeh SE, Mimoun K, Brachet P, Koziel V, Alberto JM, Helle D, Debard R, Leininger B, et al. Folate- and vitamin B12-deficient diet during gestation and lactation alters cerebellar synapsin expression via impaired influence of estrogen nuclear receptor α. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. PMID 26018677 DOI: 10.1096/Fj.14-264267 |
0.659 |
|
| 2015 |
Cornejo-García JA, Romano A, Guéant-Rodríguez RM, Oussalah A, Blanca-López N, Gaeta F, Tramoy D, Josse T, Doña I, Torres MJ, Canto G, Blanca M, Guéant JL. A non-synonymous polymorphism in galectin-3 lectin domain is associated with allergic reactions to beta-lactam antibiotics. The Pharmacogenomics Journal. PMID 25869013 DOI: 10.1038/Tpj.2015.24 |
0.592 |
|
| 2015 |
Oussalah A, Fournier JP, Guéant JL, Braun M. Information-seeking behavior during residency is associated with quality of theoretical learning, academic career achievements, and evidence-based medical practice : A strobe-compliant article Medicine (United States). 94. PMID 25674756 DOI: 10.1097/Md.0000000000000535 |
0.509 |
|
| 2015 |
Mignot C, Lambert L, Pasquier L, Bienvenu T, Delahaye-Duriez A, Keren B, Lefranc J, Saunier A, Allou L, Roth V, Valduga M, Moustaïne A, Auvin S, Barrey C, Chantot-Bastaraud S, et al. WWOX-related encephalopathies: delineation of the phenotypical spectrum and emerging genotype-phenotype correlation. Journal of Medical Genetics. 52: 61-70. PMID 25411445 DOI: 10.1136/Jmedgenet-2014-102748 |
0.773 |
|
| 2014 |
El Hajj Chehadeh S, Dreumont N, Willekens J, Canabady-Rochelle L, Jeannesson E, Alberto JM, Daval JL, Guéant JL, Leininger-Muller B. Early methyl donor deficiency alters cAMP signaling pathway and neurosteroidogenesis in the cerebellum of female rat pups. American Journal of Physiology. Endocrinology and Metabolism. 307: E1009-19. PMID 25294213 DOI: 10.1152/Ajpendo.00364.2014 |
0.702 |
|
| 2014 |
Cornejo-García JA, Flores C, Plaza-Serón MC, Acosta-Herrera M, Blanca-López N, Doña I, Torres MJ, Mayorga C, Guéant-Rodríguez RM, Ayuso P, Fernández J, Laguna JJ, Agúndez JA, García-Martín E, Guéant JL, et al. Variants of CEP68 gene are associated with acute urticaria/angioedema induced by multiple non-steroidal anti-inflammatory drugs. Plos One. 9: e90966. PMID 24618698 DOI: 10.1371/Journal.Pone.0090966 |
0.302 |
|
| 2014 |
El Hajj Chehadeh S, Pourié G, Martin N, Alberto JM, Daval JL, Guéant JL, Leininger-Muller B. Gestational methyl donor deficiency alters key proteins involved in neurosteroidogenesis in the olfactory bulbs of newborn female rats and is associated with impaired olfactory performance. The British Journal of Nutrition. 111: 1021-31. PMID 24229781 DOI: 10.1017/S0007114513003553 |
0.676 |
|
| 2014 |
Elakoum R, Gauchotte G, Oussalah A, Wissler MP, Clément-Duchêne C, Vignaud JM, Guéant JL, Namour F. CARM1 and PRMT1 are dysregulated in lung cancer without hierarchical features. Biochimie. 97: 210-8. PMID 24211191 DOI: 10.1016/J.Biochi.2013.10.021 |
0.595 |
|
| 2014 |
Gueant J, Romano A, Cornejo-Garcia JA, Guéant-Rodriguez R, Gaeta F, Blanca M. Genetic associations in beta-lactam allergy Clinical and Translational Allergy. 4: 68. DOI: 10.1186/2045-7022-4-S3-P68 |
0.302 |
|
| 2013 |
Fofou-Caillierez MB, Mrabet NT, Chéry C, Dreumont N, Flayac J, Pupavac M, Paoli J, Alberto JM, Coelho D, Camadro JM, Feillet F, Watkins D, Fowler B, Rosenblatt DS, Guéant JL. Interaction between methionine synthase isoforms and MMACHC: characterization in cblG-variant, cblG and cblC inherited causes of megaloblastic anaemia. Human Molecular Genetics. 22: 4591-601. PMID 23825108 DOI: 10.1093/Hmg/Ddt308 |
0.669 |
|
| 2013 |
Bressenot A, Chevaux JB, Williet N, Oussalah A, Germain A, Gauchotte G, Wissler MP, Vignaud JM, Bresler L, Bigard MA, Plénat F, Guéant JL, Peyrin-Biroulet L. Submucosal plexitis as a predictor of postoperative surgical recurrence in Crohn's disease. Inflammatory Bowel Diseases. 19: 1654-61. PMID 23751396 DOI: 10.1097/Mib.0B013E318281F336 |
0.702 |
|
| 2013 |
Guéant JL, Namour F, Guéant-Rodriguez RM, Daval JL. Folate and fetal programming: a play in epigenomics? Trends in Endocrinology and Metabolism: Tem. 24: 279-89. PMID 23474063 DOI: 10.1016/J.Tem.2013.01.010 |
0.306 |
|
| 2013 |
Chery C, Hehn A, Mrabet N, Oussalah A, Jeannesson E, Besseau C, Alberto JM, Gross I, Josse T, Gérard P, Guéant-Rodriguez RM, Freund JN, Devignes J, Bourgaud F, Peyrin-Biroulet L, et al. Gastric intrinsic factor deficiency with combined GIF heterozygous mutations and FUT2 secretor variant. Biochimie. 95: 995-1001. PMID 23402911 DOI: 10.1016/J.Biochi.2013.01.022 |
0.786 |
|
| 2013 |
Bossenmeyer-Pourié C, Pourié G, Koziel V, Helle D, Jeannesson E, Guéant JL, Beck B. Early methyl donor deficiency produces severe gastritis in mothers and offspring through N-homocysteinylation of cytoskeleton proteins, cellular stress, and inflammation. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 27: 2185-97. PMID 23401564 DOI: 10.1096/Fj.12-224642 |
0.304 |
|
| 2013 |
Martinez E, Gérard N, Garcia MM, Mazur A, Guéant-Rodriguez RM, Comte B, Guéant JL, Brachet P. Myocardium proteome remodelling after nutritional deprivation of methyl donors. The Journal of Nutritional Biochemistry. 24: 1241-50. PMID 23318136 DOI: 10.1016/J.Jnutbio.2012.09.008 |
0.375 |
|
| 2013 |
Marguerite V, Gkikopoulou E, Alberto JM, Guéant JL, Merten M. Phospholipase D activation mediates cobalamin-induced downregulation of Multidrug Resistance-1 gene and increase in sensitivity to vinblastine in HepG2 cells. The International Journal of Biochemistry & Cell Biology. 45: 213-20. PMID 23032700 DOI: 10.1016/J.Biocel.2012.09.018 |
0.666 |
|
| 2013 |
Bressenot A, Pooya S, Bossenmeyer-Pourie C, Gauchotte G, Germain A, Chevaux JB, Coste F, Vignaud JM, Guéant JL, Peyrin-Biroulet L. Methyl donor deficiency affects small-intestinal differentiation and barrier function in rats. The British Journal of Nutrition. 109: 667-77. PMID 22794784 DOI: 10.1017/S0007114512001869 |
0.617 |
|
| 2013 |
Zallot C, Quilliot D, Chevaux JB, Peyrin-Biroulet C, Guéant-Rodriguez RM, Freling E, Collet-Fenetrier B, Williet N, Ziegler O, Bigard MA, Guéant JL, Peyrin-Biroulet L. Dietary beliefs and behavior among inflammatory bowel disease patients. Inflammatory Bowel Diseases. 19: 66-72. PMID 22467242 DOI: 10.1002/Ibd.22965 |
0.397 |
|
| 2012 |
Akchiche N, Bossenmeyer-Pourié C, Kerek R, Martin N, Pourié G, Koziel V, Helle D, Alberto JM, Ortiou S, Camadro JM, Léger T, Guéant JL, Daval JL. Homocysteinylation of neuronal proteins contributes to folate deficiency-associated alterations of differentiation, vesicular transport, and plasticity in hippocampal neuronal cells. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 26: 3980-92. PMID 22713523 DOI: 10.1096/Fj.12-205757 |
0.658 |
|
| 2012 |
Pooya S, Blaise S, Moreno Garcia M, Giudicelli J, Alberto JM, Guéant-Rodriguez RM, Jeannesson E, Gueguen N, Bressenot A, Nicolas B, Malthiery Y, Daval JL, Peyrin-Biroulet L, Bronowicki JP, Guéant JL. Methyl donor deficiency impairs fatty acid oxidation through PGC-1α hypomethylation and decreased ER-α, ERR-α, and HNF-4α in the rat liver. Journal of Hepatology. 57: 344-51. PMID 22521344 DOI: 10.1016/J.Jhep.2012.03.028 |
0.702 |
|
| 2012 |
Billioud V, Gibot S, Massin F, Oussalah A, Chevaux JB, Williet N, Bronowicki JP, Bigard MA, Guéant JL, Peyrin-Biroulet L. Plasma soluble triggering receptor expressed on myeloid cells-1 in Crohn's disease. Digestive and Liver Disease : Official Journal of the Italian Society of Gastroenterology and the Italian Association For the Study of the Liver. 44: 466-70. PMID 22341488 DOI: 10.1016/J.Dld.2012.01.005 |
0.633 |
|
| 2012 |
Williet N, Pillot C, Oussalah A, Billioud V, Chevaux JB, Bresler L, Bigard MA, Gueant JL, Peyrin-Biroulet L. Incidence of and impact of medications on colectomy in newly diagnosed ulcerative colitis in the era of biologics. Inflammatory Bowel Diseases. 18: 1641-6. PMID 22139830 DOI: 10.1002/Ibd.21932 |
0.581 |
|
| 2012 |
Pellanda H, Namour F, Fofou-Caillierez M, Bressenot A, Alberto JM, Chéry C, Ayav A, Bronowicki JP, Guéant JL, Forges T. A splicing variant leads to complete loss of function of betaine-homocysteine methyltransferase (BHMT) gene in hepatocellular carcinoma. The International Journal of Biochemistry & Cell Biology. 44: 385-92. PMID 22138536 DOI: 10.1016/J.Biocel.2011.11.014 |
0.74 |
|
| 2012 |
Peyrin-Biroulet L, Pillot C, Oussalah A, Billioud V, Aissa N, Balde M, Williet N, Germain A, Lozniewski A, Bresler L, Guéant JL, Bigard MA. Urinary tract infections in hospitalized inflammatory bowel disease patients: a 10-year experience. Inflammatory Bowel Diseases. 18: 697-702. PMID 21739531 DOI: 10.1002/Ibd.21777 |
0.732 |
|
| 2012 |
Pellanda H, Namour B, Fofou-Caillierez M, Bressenot A, Alberto J, Chéry C, Ayav A, Bronowicki J, Guéant J, Forges T. Methionine regeneration by homocysteine remethylation in healthy and tumoral liver tissues F1000research. 3. DOI: 10.7490/F1000Research.1089984.1 |
0.643 |
|
| 2012 |
Bressenot A, Pooya S, Bossenmeyer-Pourie C, Gauchotte G, Germain A, Chevaux JB, Coste F, Vignaud J, Gueant J, Biroulet LP. Mo1800 Methyl Donor Deficiency Affects Small Intestinal Differentiation and Barrier Function in Rats Gastroenterology. 142: S-688. DOI: 10.1016/S0016-5085(12)62653-5 |
0.596 |
|
| 2012 |
Oussalah A, Aimone-Gastin I, Salignac S, Bigard M, Gueant J, Biroulet LP. Mo1677 Predictors of Clinical Remission in Ulcerative Colitis Patients Treated With Anti-TNF: Results From a Prospective Study Gastroenterology. 142: S-656-S-657. DOI: 10.1016/S0016-5085(12)62532-3 |
0.753 |
|
| 2012 |
Oussalah A, Aimone-Gastin I, Salignac S, Bigard M, Gueant J, Biroulet LP. 163 Comparison of the Diagnostic Performance of the “Ferritin/CRP” and the “Soluble Transferrin Receptor (sTfR)” Strategies for Diagnosing Iron Deficiency in Patients With Inflammatory Bowel Diseases: Results From a Prospective Study Gastroenterology. 142: S-40. DOI: 10.1016/S0016-5085(12)60152-8 |
0.759 |
|
| 2011 |
Chen M, Peyrin-Biroulet L, George A, Coste F, Bressenot A, Bossenmeyer-Pourie C, Alberto JM, Xia B, Namour B, Guéant JL. Methyl deficient diet aggravates experimental colitis in rats. Journal of Cellular and Molecular Medicine. 15: 2486-97. PMID 21199330 DOI: 10.1111/J.1582-4934.2010.01252.X |
0.797 |
|
| 2010 |
Forges T, Chery C, Audonnet S, Feillet F, Gueant JL. Life-threatening methylenetetrahydrofolate reductase (MTHFR) deficiency with extremely early onset: characterization of two novel mutations in compound heterozygous patients. Molecular Genetics and Metabolism. 100: 143-8. PMID 20356773 DOI: 10.1016/J.Ymgme.2010.03.002 |
0.306 |
|
| 2010 |
Bossenmeyer-Pourié C, Blaise S, Pourié G, Tomasetto C, Audonnet S, Ortiou S, Koziel V, Rio MC, Daval JL, Guéant JL, Beck B. Methyl donor deficiency affects fetal programming of gastric ghrelin cell organization and function in the rat. The American Journal of Pathology. 176: 270-7. PMID 19948829 DOI: 10.2353/Ajpath.2010.090153 |
0.303 |
|
| 2010 |
Chevaux JB, Nani A, Oussalah A, Venard V, Bensenane M, Belle A, Gueant JL, Bigard MA, Bronowicki JP, Peyrin-Biroulet L. Prevalence of hepatitis B and C and risk factors for nonvaccination in inflammatory bowel disease patients in Northeast France. Inflammatory Bowel Diseases. 16: 916-24. PMID 19885908 DOI: 10.1002/Ibd.21147 |
0.641 |
|
| 2010 |
Pourie C, Pourie G, Daval J, Tomasetto C, Koziel V, Biroulet LP, Rio MC, Gueant J, Beck B. M1710 Vitamins B Deficiency During Gestation and Suckling Periods Induces Growth Retardation Related With Atrophic Gatritis and Altered Ghrelin Expression in the Rat Pup Gastroenterology. 138. DOI: 10.1016/S0016-5085(10)61853-7 |
0.302 |
|
| 2009 |
Orozco-Barrios CE, Battaglia-Hsu SF, Arango-Rodriguez ML, Ayala-Davila J, Chery C, Alberto JM, Schroeder H, Daval JL, Martinez-Fong D, Gueant JL. Vitamin B12-impaired metabolism produces apoptosis and Parkinson phenotype in rats expressing the transcobalamin-oleosin chimera in substantia nigra. Plos One. 4: e8268. PMID 20027219 DOI: 10.1371/Journal.Pone.0008268 |
0.677 |
|
| 2009 |
Battaglia-Hsu SF, Akchiche N, Noel N, Alberto JM, Jeannesson E, Orozco-Barrios CE, Martinez-Fong D, Daval JL, Guéant JL. Vitamin B12 deficiency reduces proliferation and promotes differentiation of neuroblastoma cells and up-regulates PP2A, proNGF, and TACE Proceedings of the National Academy of Sciences of the United States of America. 106: 21930-21935. PMID 19959661 DOI: 10.1073/Pnas.0811794106 |
0.705 |
|
| 2009 |
Pons L, Battaglia-Hsu SF, Orozco-Barrios CE, Ortiou S, Chery C, Alberto JM, Arango-Rodriguez ML, Dumas D, Martinez-Fong D, Freund JN, Gueant JL. Anchoring secreted proteins in endoplasmic reticulum by plant oleosin: The example of vitamin B12 cellular sequestration by transcobalamin Plos One. 4. PMID 19623264 DOI: 10.1371/Journal.Pone.0006325 |
0.667 |
|
| 2009 |
Blaise SA, Nédélec E, Alberto JM, Schroeder H, Audonnet S, Bossenmeyer-Pourié C, Guéant JL, Daval JL. Short hypoxia could attenuate the adverse effects of hyperhomocysteinemia on the developing rat brain by inducing neurogenesis. Experimental Neurology. 216: 231-8. PMID 19124018 DOI: 10.1016/J.Expneurol.2008.11.020 |
0.684 |
|
| 2009 |
Daval JL, Blaise S, Guéant JL. Vitamin B deficiency causes neural cell loss and cognitive impairment in the developing rat. Proceedings of the National Academy of Sciences of the United States of America. 106: E1; author reply E2. PMID 19106288 DOI: 10.1073/Pnas.0809217106 |
0.306 |
|
| 2008 |
Chen M, Peyrin-Biroulet L, Xia B, Guéant-Rodriguez RM, Bronowicki JP, Bigard MA, Guéant JL. Methionine synthase A2756G polymorphism may predict ulcerative colitis and methylenetetrahydrofolate reductase C677T pancolitis, in Central China. Bmc Medical Genetics. 9: 78. PMID 18700049 DOI: 10.1186/1471-2350-9-78 |
0.343 |
|
| 2008 |
Bronowicki JP, Abdelmouttaleb I, Peyrin-Biroulet L, Venard V, Khiri H, Chabi N, Amouzou EK, Barraud H, Halfon P, Sanni A, Bigard MA, Le Faou A, Guéant JL. Methylenetetrahydrofolate reductase 677 T allele protects against persistent HBV infection in West Africa. Journal of Hepatology. 48: 532-9. PMID 18222012 DOI: 10.1016/J.Jhep.2007.11.017 |
0.767 |
|
| 2008 |
Feillet F, Merten M, Battaglia-Hsu SF, Rabier D, Kobayashi K, Straczek J, Brivet M, Favre E, Guéant JL. Evidence of cataplerosis in a patient with neonatal classical galactosemia presenting as citrin deficiency. Journal of Hepatology. 48: 517-22. PMID 18207281 DOI: 10.1016/J.Jhep.2007.11.016 |
0.305 |
|
| 2008 |
Peyrin-Biroulet L, Guéant-Rodriguez RM, Chen M, Bronowicki JP, Bigard MA, Guéant JL. Association of MTRR 66A>G polymorphism with superoxide dismutase and disease activity in patients with Crohn's disease. The American Journal of Gastroenterology. 103: 399-406. PMID 17925002 DOI: 10.1111/J.1572-0241.2007.01573.X |
0.458 |
|
| 2007 |
Blaise SA, Alberto JM, Audonnet-Blaise S, Guéant JL, Daval JL. Influence of preconditioning-like hypoxia on the liver of developing methyl-deficient rats. American Journal of Physiology. Endocrinology and Metabolism. 293: E1492-502. PMID 17726145 DOI: 10.1152/Ajpendo.00255.2007 |
0.707 |
|
| 2007 |
Abdel Nour AM, Ringot D, Guéant JL, Chango A. Folate receptor and human reduced folate carrier expression in HepG2 cell line exposed to fumonisin B1 and folate deficiency. Carcinogenesis. 28: 2291-7. PMID 17615259 DOI: 10.1093/Carcin/Bgm149 |
0.302 |
|
| 2007 |
Alberto JM, Hamelet J, Noll C, Blaise S, Bronowicki JP, Guéant JL, Delabar JM, Janel N. Mice deficient in cystathionine beta synthase display altered homocysteine remethylation pathway. Molecular Genetics and Metabolism. 91: 396-8. PMID 17562377 DOI: 10.1016/J.Ymgme.2007.05.002 |
0.675 |
|
| 2007 |
Peyrin-Biroulet L, Rodriguez-Guéant RM, Chamaillard M, Desreumaux P, Xia B, Bronowicki JP, Bigard MA, Guéant JL. Vascular and cellular stress in inflammatory bowel disease: revisiting the role of homocysteine. The American Journal of Gastroenterology. 102: 1108-15. PMID 17355415 DOI: 10.1111/J.1572-0241.2007.01170.X |
0.484 |
|
| 2007 |
Blaise SA, Nédélec E, Schroeder H, Alberto JM, Bossenmeyer-Pourié C, Guéant JL, Daval JL. Gestational vitamin B deficiency leads to homocysteine-associated brain apoptosis and alters neurobehavioral development in rats. The American Journal of Pathology. 170: 667-79. PMID 17255334 DOI: 10.2353/Ajpath.2007.060339 |
0.695 |
|
| 2007 |
Peyrin-Biroulet L, Guéant JL, Roblin X. Coffee and diabetes: is homocysteine the missing link? Archives of Internal Medicine. 167: 204; author reply 20. PMID 17242324 DOI: 10.1001/Archinte.167.2.204-A |
0.338 |
|
| 2006 |
Peyrin-Biroulet L, Barraud H, Darfeuil F, Lefebvre M, Bigard MA, Gueant JL, Bronowicki JP. [Epigenetic changes and liver carcinogenesis]. Gastroenterologie Clinique Et Biologique. 30: 1354-9. PMID 17211332 DOI: 10.1016/S0399-8320(06)73554-0 |
0.426 |
|
| 2006 |
Namour F, Ayav A, Lu X, Klein M, Muresan M, Bresler L, Tramoy D, Guéant JL, Brunaud L. Lack of association between microsatellite instability and benign adrenal tumors. World Journal of Surgery. 30: 1240-6. PMID 16715450 DOI: 10.1007/S00268-005-0471-5 |
0.647 |
|
| 2006 |
Candito M, Guéant JL, Naimi M, Bongain A, Van Obberghen E. Antiepileptic drugs: a case report in a pregnancy with a neural tube defect. Pediatric Neurology. 34: 323-4. PMID 16638512 DOI: 10.1016/J.Pediatrneurol.2005.08.023 |
0.334 |
|
| 2006 |
Guéant-Rodriguez RM, Guéant JL, Debard R, Thirion S, Lu XH, Bronowicki JP, Namour F, Chabi NW, Sanni A, Anello G, Bosco P, Romano C, Amouzou E, Arrieta HR, Sánchez BE, et al. Prevalence of methylenetetrahydrofolate reductase 677T and 1298C alleles and folate status: A comparative study in Mexican, West African, and European populations American Journal of Clinical Nutrition. 83: 701-707. PMID 16522920 DOI: 10.1093/Ajcn.83.3.701 |
0.749 |
|
| 2005 |
Guéant-Rodriguez RM, Juilliére Y, Candito M, Adjalla CE, Gibelin P, Herbeth B, Van Obberghen E, Gueánt JL. Association of MTRRA66G polymorphism (but not of MTHFR C677T and A1298C, MTRA2756G, TCN C776G) with homocysteine and coronary artery disease in the French population. Thrombosis and Haemostasis. 94: 510-5. PMID 16268464 DOI: 10.1160/Th05-04-0262 |
0.301 |
|
| 2005 |
Pons L, Chéry C, Mrabet N, Schohn H, Lapicque F, Guéant JL. Purification and cloning of two high molecular mass isoforms of peanut seed oleosin encoded by cDNAs of equal sizes. Plant Physiology and Biochemistry : Ppb. 43: 659-68. PMID 16095908 DOI: 10.1016/J.Plaphy.2005.06.002 |
0.66 |
|
| 2005 |
Blaise S, Alberto JM, Nédélec E, Ayav A, Pourié G, Bronowicki JP, Guéant JL, Daval JL. Mild neonatal hypoxia exacerbates the effects of vitamin-deficient diet on homocysteine metabolism in rats. Pediatric Research. 57: 777-82. PMID 15845641 DOI: 10.1203/01.Pdr.0000161406.19231.98 |
0.774 |
|
| 2005 |
Marrion O, Fleurence J, Schwertz A, Guéant J, Mamelouk L, Ksouri J, Villaume C. Evaluation of protein in vitro digestibility of Palmaria palmata and Gracilaria verrucosa Journal of Applied Phycology. 17: 99-102. DOI: 10.1007/S10811-005-5154-Y |
0.616 |
|
| 2004 |
Ortiou S, Alberto JM, Guéant JL, Merten M. Homocysteine increases methionine synthase mRNA level in Caco-2 cells. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 14: 407-14. PMID 15319544 DOI: 10.1159/000080350 |
0.661 |
|
| 2004 |
Peyrin-Biroulet L, Barraud H, Ancel D, Petit-Laurent F, Bigard MA, Gueant JL, Bronowicki JP. [Folate metabolism and colorectal carcinogenesis]. Gastroenterologie Clinique Et Biologique. 28: 582-92. PMID 15243392 DOI: 10.1016/S0399-8320(04)95015-4 |
0.395 |
|
| 2004 |
Anello G, Guéant-Rodríguez RM, Bosco P, Guéant JL, Romano A, Namour B, Spada R, Caraci F, Pourié G, Daval JL, Ferri R. Homocysteine and methylenetetrahydrofolate reductase polymorphism in Alzheimer's disease. Neuroreport. 15: 859-61. PMID 15073531 |
0.774 |
|
| 2004 |
Amouzou EK, Chabi NW, Adjalla CE, Rodriguez-Guéant RM, Feillet F, Villaume C, Sanni A, Guéant JL. High prevalence of hyperhomocysteinemia related to folate deficiency and the 677C-->T mutation of the gene encoding methylenetetrahydrofolate reductase in coastal West Africa. The American Journal of Clinical Nutrition. 79: 619-24. PMID 15051606 DOI: 10.1093/Ajcn/79.4.619 |
0.746 |
|
| 2004 |
Guéant J, Candito M, Andres E, Obberghen EV, Nicolas J. Familial pernicious anaemia with hyperhomocysteinaemia in recurrent early pregnancy loss Thrombosis and Haemostasis. 92: 1147-1149. DOI: 10.1055/S-0037-1614292 |
0.348 |
|
| 2003 |
Guéant JL, Guéant-Rodriguez RM, Anello G, Bosco P, Brunaud L, Romano C, Ferri R, Romano A, Candito M, Namour B. Genetic determinants of folate and vitamin B12 metabolism: a common pathway in neural tube defect and Down syndrome? Clinical Chemistry and Laboratory Medicine. 41: 1473-7. PMID 14656028 DOI: 10.1515/CCLM.2003.226 |
0.789 |
|
| 2003 |
Brunaud L, Alberto JM, Ayav A, Gérard P, Namour F, Antunes L, Braun M, Bronowicki JP, Bresler L, Guéant JL. Vitamin B12 is a strong determinant of low methionine synthase activity and DNA hypomethylation in gastrectomized rats. Digestion. 68: 133-40. PMID 14646334 DOI: 10.1159/000075307 |
0.788 |
|
| 2003 |
Marrion O, Schwertz A, Fleurence J, Guéant JL, Villaume C. Improvement of the digestibility of the proteins of the red alga Palmaria palmata by physical processes and fermentation. Die Nahrung. 47: 339-44. PMID 14609091 DOI: 10.1002/Food.200390078 |
0.572 |
|
| 2003 |
Adjalla CE, Amouzou EK, Sanni A, Abdelmouttaleb I, Chabi NW, Namour F, Soussou B, Guéant JL. Low frequency of mutated methylenetetrahydrofolate reductase 677C-->T and 1298A-->C genetics single nucleotide polymorphisms (SNPs) in Sub-Saharan populations. Clinical Chemistry and Laboratory Medicine. 41: 1028-32. PMID 12964809 DOI: 10.1515/Cclm.2003.158 |
0.769 |
|
| 2003 |
Brunaud L, Alberto JM, Ayav A, Gérard P, Namour F, Antunes L, Braun M, Bronowicki JP, Bresler L, Guéant JL. Effects of vitamin B12 and folate deficiencies on DNA methylation and carcinogenesis in rat liver. Clinical Chemistry and Laboratory Medicine. 41: 1012-9. PMID 12964806 DOI: 10.1515/Cclm.2003.155 |
0.788 |
|
| 2002 |
Chéry C, Barbé F, Lequere C, Abdelmouttaleb I, Gérard P, Barbarino P, Boutroy JL, Guéant JL. Hyperhomocysteinemia is related to a decreased blood level of vitamin B12 in the second and third trimester of normal pregnancy. Clinical Chemistry and Laboratory Medicine. 40: 1105-8. PMID 12521226 DOI: 10.1515/Cclm.2002.193 |
0.778 |
|
| 2002 |
Pascal N, Amouzou EK, Sanni A, Namour F, Abdelmouttaleb I, Vidailhet M, Guéant JL. Serum concentrations of sex hormone binding globulin are elevated in kwashiorkor and anorexia nervosa but not in marasmus. The American Journal of Clinical Nutrition. 76: 239-44. PMID 12081841 DOI: 10.1093/Ajcn/76.1.239 |
0.753 |
|
| 2002 |
Blain H, Abdelmouttaleb I, Belmin J, Blain A, Floquet J, Guéant JL, Jeandel C. Arterial wall production of cytokines in giant cell arteritis: results of a pilot study using human temporal artery cultures. The Journals of Gerontology. Series a, Biological Sciences and Medical Sciences. 57: M241-5. PMID 11909890 DOI: 10.1093/Gerona/57.4.M241 |
0.753 |
|
| 2001 |
Anwar W, Guéant JL, Abdelmouttaleb I, Adjalla C, Gérard P, Lemoel G, Erraess N, Moutabarrek A, Namour F. Hyperhomocysteinemia is related to residual glomerular filtration and folate, but not to methylenetetrahydrofolate-reductase and methionine synthase polymorphisms, in supplemented end-stage renal disease patients undergoing hemodialysis Clinical Chemistry and Laboratory Medicine. 39: 747-752. PMID 11592445 DOI: 10.1515/Cclm.2001.124 |
0.784 |
|
| 2001 |
Angioi M, Abdelmouttaleb I, Rodriguez RM, Aimone-Gastin I, Adjalla C, Guéant JL, Danchin N. Increased C-reactive protein levels in patients with in-stent restenosis and its implications. The American Journal of Cardiology. 87: 1189-93; A4. PMID 11356396 DOI: 10.1016/S0002-9149(01)01492-8 |
0.764 |
|
| 2001 |
Barbé F, Klein M, Chango A, Frémont S, Gérard P, Weryha G, Guéant JL, Nicolas JP. Homocysteine, folate, vitamin B12, and transcobalamins in patients undergoing successive hypo- and hyperthyroid states. The Journal of Clinical Endocrinology and Metabolism. 86: 1845-6. PMID 11297639 DOI: 10.1210/Jcem.86.4.7436-14 |
0.304 |
|
| 2001 |
Namour F, Olivier JL, Abdelmouttaleb I, Adjalla C, Debard R, Salvat C, Guéant JL. Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: Relation to transcobalamin and homocysteine concentration in blood Blood. 97: 1092-1098. PMID 11159542 DOI: 10.1182/Blood.V97.4.1092 |
0.763 |
|
| 1999 |
Galland-Irmouli AV, Fleurence J, Lamghari R, Luçon M, Rouxel C, Barbaroux O, Bronowicki JP, Villaume C, Guéant JL. Nutritional value of proteins from edible seaweed Palmaria palmata (dulse). The Journal of Nutritional Biochemistry. 10: 353-9. PMID 15539310 DOI: 10.1016/S0955-2863(99)00014-5 |
0.758 |
|
| 1999 |
Guéant J, Chery C, Namour F, Aimone-Gastin I, Wustinger M. Decreased affinity of urinary intrinsic factor–cobalamin receptor in a case of Gräsbeck–Imerslund syndrome Gastroenterology. 116: 1274-1275. PMID 10220529 DOI: 10.1016/S0016-5085(99)70041-7 |
0.662 |
|
| 1999 |
Abdelmouttaleb I, Danchin N, Ilardo C, Aimone-Gastin I, Angioï M, Lozniewski A, Loubinoux J, Le Faou A, Guéant JL. C-Reactive protein and coronary artery disease: additional evidence of the implication of an inflammatory process in acute coronary syndromes. American Heart Journal. 137: 346-51. PMID 9924170 DOI: 10.1053/Hj.1999.V137.92052 |
0.761 |
|
| 1998 |
Namour F, Guy M, Aimone-Gastin I, de Nonancourt M, Mrabet N, Guéant JL. Isoelectrofocusing phenotype and relative concentration of transcobalamin II isoproteins related to the codon 259 Arg/Pro polymorphism. Biochemical and Biophysical Research Communications. 251: 769-74. PMID 9790985 DOI: 10.1006/Bbrc.1998.9463 |
0.697 |
|
| 1998 |
Dugué B, Aminoff M, Aimone-Gastin I, Leppänen E, Gräsbeck R, Guéant J. A urinary radioisotope-binding assay to diagnose Gräsbeck-Imerslund disease Journal of Pediatric Gastroenterology and Nutrition. 26: 21-25. PMID 9443115 DOI: 10.1097/00005176-199801000-00004 |
0.696 |
|
| 1997 |
Lambert D, Messing B, Benhayoun S, Thuillier F, Adjalla C, Beliah M, Gélot M, Nicolas JP, Guéant J. Home Parenteral Nutrition and Vitamin B12 Status Nutrition. 13: 313-318. DOI: 10.1016/S0899-9007(97)00081-6 |
0.323 |
|
| 1996 |
Lambert D, Benhayoun S, Adjalla C, Gelot MA, Renkes P, Felden F, Gerard P, Belleville F, Gaucher P, Guéant JL, Nicolas JP. Crohn's disease and vitamin B12 metabolism. Digestive Diseases and Sciences. 41: 1417-22. PMID 8689919 DOI: 10.1007/Bf02088567 |
0.349 |
|
| 1996 |
Bougrine R, Masson C, Hatier R, Nexø E, Nicolas J, Gueant J. Receptor binding of transcobalamin II-cobalamin in human colon adenocarcinoma HT 29 cell line Journal of Nutritional Biochemistry. 7: 397-402. DOI: 10.1016/S0955-2863(96)00062-9 |
0.591 |
|
| 1990 |
Guéant J, Champigneulle B, Gaucher P, Nicolas J. Malabsorption of vitamin B12 in pancreatic insufficiency of the adult and of the child. Pancreas. 5: 559-567. PMID 2235967 DOI: 10.1097/00006676-199009000-00011 |
0.302 |
|
| 1990 |
Djalali M, Gueant J, Lambert D, Kholty SE, Saunier M, Nicolas J. High-performance liquid chromatographic separation and dual competitive binding assay of corrinoids in biological material. Journal of Chromatography B: Biomedical Sciences and Applications. 529: 81-91. PMID 2211943 DOI: 10.1016/S0378-4347(00)83809-8 |
0.738 |
|
| 1985 |
Gueant J, Kouvonen I, Michalski J, Masson C, Gräsbeck R, Nicolas J. Purification of human intrinsic factor using high-performance ion-exchange chromatography as the final step Febs Letters. 184: 14-19. PMID 3987902 DOI: 10.1016/0014-5793(85)80643-8 |
0.595 |
|
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