| Year |
Citation |
Score |
| 2016 |
Krey JF, Drummond M, Foster S, Porsov E, Vijayakumar S, Choi D, Friderici K, Jones SM, Nuttall AL, Barr-Gillespie PG. Annexin A5 is the Most Abundant Membrane-Associated Protein in Stereocilia but is Dispensable for Hair-Bundle Development and Function. Scientific Reports. 6: 27221. PMID 27251877 DOI: 10.1038/Srep27221 |
0.729 |
|
| 2016 |
Kamradt JM, Nigg JT, Friderici KH, Nikolas MA. Neuropsychological performance measures as intermediate phenotypes for attention-deficit/hyperactivity disorder: A multiple mediation analysis. Development and Psychopathology. 1-14. PMID 27049476 DOI: 10.1017/S0954579416000195 |
0.373 |
|
| 2015 |
Nigg JT, Elmore AL, Natarajan N, Friderici KH, Nikolas MA. Variation in an Iron Metabolism Gene Moderates the Association Between Blood Lead Levels and Attention-Deficit/Hyperactivity Disorder in Children. Psychological Science. PMID 26710823 DOI: 10.1177/0956797615618365 |
0.354 |
|
| 2015 |
Elmore AL, Nigg JT, Friderici KH, Jernigan K, Nikolas MA. Does 5HTTLPR Genotype Moderate the Association of Family Environment With Child Attention-Deficit Hyperactivity Disorder Symptomatology? Journal of Clinical Child and Adolescent Psychology : the Official Journal For the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53. 1-13. PMID 25602736 DOI: 10.1080/15374416.2014.979935 |
0.365 |
|
| 2014 |
Rehman AU, Santos-Cortez RL, Drummond MC, Shahzad M, Lee K, Morell RJ, Ansar M, Jan A, Wang X, Aziz A, Riazuddin S, Smith JD, Wang GT, Ahmed ZM, Gul K, ... ... Friderici KH, et al. Challenges and solutions for gene identification in the presence of familial locus heterogeneity. European Journal of Human Genetics : Ejhg. PMID 25491636 DOI: 10.1038/Ejhg.2014.266 |
0.71 |
|
| 2014 |
Bonner JD, Fisher R, Klein J, Lu Q, Wilch E, Friderici KH, Elfenbein JL, Schutte DL, Schutte BC. Pedigree structure and kinship measurements of a mid-Michigan community: a new North American population isolate identified. Human Biology. 86: 59-68. PMID 25401987 DOI: 10.3378/027.086.0103 |
0.723 |
|
| 2014 |
Lovell KL, Zhu M, Drummond MC, Switzer RC, Friderici KH. Distribution and Severity of Neuropathology in β-Mannosidase-Deficient Mice is Strain Dependent. Jimd Reports. 13: 73-81. PMID 24142277 DOI: 10.1007/8904_2013_258 |
0.718 |
|
| 2013 |
Drummond MC, Friderici KH. A novel actin mRNA splice variant regulates ACTG1 expression. Plos Genetics. 9: e1003743. PMID 24098136 DOI: 10.1371/Journal.Pgen.1003743 |
0.732 |
|
| 2013 |
Dang MT, Gu C, Klavanian JI, Jernigan KA, Friderici KH, Cui Y, Molina-Molina M, Ancochea J, Xaubet A, Uhal BD. Angiotensinogen promoter polymorphisms predict low diffusing capacity in U.S. and Spanish IPF cohorts. Lung. 191: 353-60. PMID 23715995 DOI: 10.1007/S00408-013-9476-2 |
0.309 |
|
| 2012 |
Martel MM, Nikolas M, Jernigan K, Friderici K, Nigg JT. Diversity in pathways to common childhood disruptive behavior disorders. Journal of Abnormal Child Psychology. 40: 1223-36. PMID 22584505 DOI: 10.1007/S10802-012-9646-3 |
0.333 |
|
| 2012 |
Sartorato EL, Friderici K, Del Castillo I. Genetics of deafness. Genetics Research International. 2012: 562848. PMID 22567392 DOI: 10.1155/2012/562848 |
0.359 |
|
| 2012 |
Drummond MC, Belyantseva IA, Friderici KH, Friedman TB. Actin in hair cells and hearing loss. Hearing Research. 288: 89-99. PMID 22200607 DOI: 10.1016/J.Heares.2011.12.003 |
0.749 |
|
| 2012 |
Jones NM, Holzman C, Tian Y, Witkin SS, Genc M, Friderici K, Fisher R, Sezen D, Babula O, Jernigan KA, Chung H, Wirth J. Innate immune system gene polymorphisms in maternal and child genotype and risk of preterm delivery. The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians. 25: 240-7. PMID 21627550 DOI: 10.3109/14767058.2011.569614 |
0.302 |
|
| 2011 |
Schauberger EM, Ewart SL, Arshad SH, Huebner M, Karmaus W, Holloway JW, Friderici KH, Ziegler JT, Zhang H, Rose-Zerilli MJ, Barton SJ, Holgate ST, Kilpatrick JR, Harley JB, Lajoie-Kadoch S, et al. Identification of ATPAF1 as a novel candidate gene for asthma in children. The Journal of Allergy and Clinical Immunology. 128: 753-760.e11. PMID 21696813 DOI: 10.1016/J.Jaci.2011.04.058 |
0.338 |
|
| 2011 |
Martel MM, Nikolas M, Jernigan K, Friderici K, Waldman I, Nigg JT. The dopamine receptor D4 gene (DRD4) moderates family environmental effects on ADHD. Journal of Abnormal Child Psychology. 39: 1-10. PMID 20644990 DOI: 10.1007/S10802-010-9439-5 |
0.357 |
|
| 2010 |
Nikolas M, Friderici K, Waldman I, Jernigan K, Nigg JT. Gene x environment interactions for ADHD: synergistic effect of 5HTTLPR genotype and youth appraisals of inter-parental conflict. Behavioral and Brain Functions : Bbf. 6: 23. PMID 20398347 DOI: 10.1186/1744-9081-6-23 |
0.349 |
|
| 2010 |
Wilch E, Azaiez H, Fisher RA, Elfenbein J, Murgia A, Birkenhäger R, Bolz H, Da Silva-Costa SM, Del Castillo I, Haaf T, Hoefsloot L, Kremer H, Kubisch C, Le Marechal C, Pandya A, ... ... Friderici KH, et al. A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression. Clinical Genetics. 78: 267-74. PMID 20236118 DOI: 10.1111/J.1399-0004.2010.01387.X |
0.758 |
|
| 2010 |
Martel MM, Nikolas M, Jernigan K, Friderici K, Nigg JT. Personality mediation of genetic effects on Attention-Deficit/Hyperactivity Disorder. Journal of Abnormal Child Psychology. 38: 633-43. PMID 20146095 DOI: 10.1007/S10802-010-9392-3 |
0.319 |
|
| 2009 |
Housley DJ, Nikolas M, Venta PJ, Jernigan KA, Waldman ID, Nigg JT, Friderici KH. SNP discovery and haplotype analysis in the segmentally duplicated DRD5 coding region. Annals of Human Genetics. 73: 274-82. PMID 19397556 DOI: 10.1111/J.1469-1809.2009.00513.X |
0.367 |
|
| 2008 |
Molina-Molina M, Xaubet A, Li X, Abdul-Hafez A, Friderici K, Jernigan K, Fu W, Ding Q, Pereda J, Serrano-Mollar A, Casanova A, Rodríguez-Becerra E, Morell F, Ancochea J, Picado C, et al. Angiotensinogen gene G-6A polymorphism influences idiopathic pulmonary fibrosis disease progression European Respiratory Journal. 32: 1004-1008. PMID 18508830 DOI: 10.1183/09031936.00015808 |
0.318 |
|
| 2007 |
Nigg J, Nikolas M, Friderici K, Park L, Zucker RA. Genotype and neuropsychological response inhibition as resilience promoters for attention-deficit/hyperactivity disorder, oppositional defiant disorder, and conduct disorder under conditions of psychosocial adversity. Development and Psychopathology. 19: 767-86. PMID 17705902 DOI: 10.1017/S0954579407000387 |
0.741 |
|
| 2006 |
Waldman ID, Nigg JT, Gizer IR, Park L, Rappley MD, Friderici K. The adrenergic receptor alpha-2A gene (ADRA2A) and neuropsychological executive functions as putative endophenotypes for childhood ADHD. Cognitive, Affective & Behavioral Neuroscience. 6: 18-30. PMID 16869226 DOI: 10.3758/Cabn.6.1.18 |
0.744 |
|
| 2006 |
Wilch E, Zhu M, Burkhart KB, Regier M, Elfenbein JL, Fisher RA, Friderici KH. Expression of GJB2 and GJB6 is reduced in a novel DFNB1 allele. American Journal of Human Genetics. 79: 174-9. PMID 16773579 DOI: 10.1086/505333 |
0.743 |
|
| 2006 |
Rendtorff ND, Zhu M, Fagerheim T, Antal TL, Jones M, Teslovich TM, Gillanders EM, Barmada M, Teig E, Trent JM, Friderici KH, Stephan DA, Tranebjaerg L. A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment. European Journal of Human Genetics : Ejhg. 14: 1097-105. PMID 16773128 DOI: 10.1038/Sj.Ejhg.5201670 |
0.419 |
|
| 2006 |
Bryan KE, Wen KK, Zhu M, Rendtorff ND, Feldkamp M, Tranebjaerg L, Friderici KH, Rubenstein PA. Effects of human deafness gamma-actin mutations (DFNA20/26) on actin function. The Journal of Biological Chemistry. 281: 20129-39. PMID 16690605 DOI: 10.1074/Jbc.M601514200 |
0.319 |
|
| 2005 |
Park L, Nigg JT, Waldman ID, Nummy KA, Huang-Pollock C, Rappley M, Friderici KH. Association and linkage of alpha-2A adrenergic receptor gene polymorphisms with childhood ADHD. Molecular Psychiatry. 10: 572-80. PMID 15520832 DOI: 10.1038/Sj.Mp.4001605 |
0.761 |
|
| 2003 |
Zhu M, Yang T, Wei S, DeWan AT, Morell RJ, Elfenbein JL, Fisher RA, Leal SM, Smith RJH, Friderici KH. Mutations in the γ-Actin Gene (ACTG1) Are Associated with Dominant Progressive Deafness (DFNA20/26) American Journal of Human Genetics. 73: 1082-1091. PMID 13680526 DOI: 10.1086/379286 |
0.426 |
|
| 2003 |
Rothrock CR, Murgia A, Sartorato EL, Leonardi E, Wei S, Lebeis SL, Yu LE, Elfenbein JL, Fisher RA, Friderici KH. Connexin 26 35delG does not represent a mutational hotspot. Human Genetics. 113: 18-23. PMID 12684873 DOI: 10.1007/S00439-003-0944-2 |
0.399 |
|
| 2002 |
Bedilu R, Nummy KA, Cooper A, Wevers R, Smeitink J, Kleijer WJ, Friderici KH. Variable clinical presentation of lysosomal beta-mannosidosis in patients with null mutations. Molecular Genetics and Metabolism. 77: 282-90. PMID 12468273 DOI: 10.1016/S1096-7192(02)00172-5 |
0.334 |
|
| 2002 |
Elfenbein JL, Fisher RA, Wei S, Morell RJ, Stewart C, Friedman TB, Friderici K. Audiologic aspects of the search for DFNA20: a gene causing late-onset, progressive, sensorineural hearing loss. Ear and Hearing. 22: 279-88. PMID 11527035 DOI: 10.1097/00003446-200108000-00003 |
0.364 |
|
| 2000 |
Morell RJ, Friderici KH, Wei S, Elfenbein JL, Friedman TB, Fisher RA. A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25. Genomics. 63: 1-6. PMID 10662538 DOI: 10.1006/Geno.1999.6058 |
0.368 |
|
| 1998 |
Hoard HM, Leipprandt JR, Cavanagh KT, Truscott NK, Levene BA, Friderici KH, Jones MZ. Determination of genotypic frequency of caprine mucopolysaccharidosis IIID. Journal of Veterinary Diagnostic Investigation : Official Publication of the American Association of Veterinary Laboratory Diagnosticians, Inc. 10: 181-3. PMID 9576348 DOI: 10.1177/104063879801000212 |
0.318 |
|
| 1998 |
Alkhayat AH, Kraemer SA, Leipprandt JR, Macek M, Kleijer WJ, Friderici KH. Human beta-mannosidase cDNA characterization and first identification of a mutation associated with human beta-mannosidosis. Human Molecular Genetics. 7: 75-83. PMID 9384606 DOI: 10.1093/Hmg/7.1.75 |
0.342 |
|
| 1997 |
Litjens T, Bielicki J, Anson DS, Friderici K, Jones MZ, Hopwood JJ. Expression, purification and characterization of recombinant caprine N-acetylglucosamine-6-sulphatase. The Biochemical Journal. 327: 89-94. PMID 9355739 DOI: 10.1042/Bj3270089 |
0.305 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 1999 |
Leipprandt JR, Chen H, Horvath JE, Qiao XT, Jones MZ, Friderici KH. Identification of a bovine beta-mannosidosis mutation and detection of two beta-mannosidase pseudogenes. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 10: 1137-41. PMID 10594236 DOI: 10.1007/S003359901179 |
0.3 |
|
| 2006 |
Sedel F, Friderici K, Nummy K, Caillaud C, Chabli A, Dürr A, Lubetzki C, Agid Y. Atypical Gilles de la Tourette Syndrome with beta-mannosidase deficiency. Archives of Neurology. 63: 129-31. PMID 16401745 DOI: 10.1001/Archneur.63.1.129 |
0.297 |
|
| 1996 |
Leipprandt JR, Kraemer SA, Haithcock BE, Chen H, Dyme JL, Cavanagh KT, Friderici KH, Jones MZ. Caprine beta-mannosidase: sequencing and characterization of the cDNA and identification of the molecular defect of caprine beta-mannosidosis. Genomics. 37: 51-6. PMID 8921369 DOI: 10.1006/Geno.1996.0519 |
0.296 |
|
| 2010 |
Nigg JT, Nikolas M, Mark Knottnerus G, Cavanagh K, Friderici K. Confirmation and extension of association of blood lead with attention-deficit/hyperactivity disorder (ADHD) and ADHD symptom domains at population-typical exposure levels. Journal of Child Psychology and Psychiatry, and Allied Disciplines. 51: 58-65. PMID 19941632 DOI: 10.1111/J.1469-7610.2009.02135.X |
0.293 |
|
| 1997 |
Friderici KH. Molecular Diagnostics for Cystic Fibrosis Clinics in Laboratory Medicine. 17: 59-72. DOI: 10.1016/S0272-2712(18)30231-2 |
0.288 |
|
| 2009 |
Messaros BM, Rossano MG, Liu G, Diamond MP, Friderici K, Nummy-Jernigan K, Daly D, Puscheck E, Paneth N, Wirth JJ. Negative effects of serum p,p'-DDE on sperm parameters and modification by genetic polymorphisms. Environmental Research. 109: 457-64. PMID 19303595 DOI: 10.1016/J.Envres.2009.02.009 |
0.284 |
|
| 2010 |
Jones NM, Holzman C, Friderici KH, Jernigan K, Chung H, Wirth J, Fisher R. Interplay of cytokine polymorphisms and bacterial vaginosis in the etiology of preterm delivery. Journal of Reproductive Immunology. 87: 82-9. PMID 20965572 DOI: 10.1016/J.Jri.2010.06.158 |
0.283 |
|
| 2009 |
Gargano JW, Holzman CB, Senagore PK, Reuss ML, Pathak DR, Friderici KH, Jernigan K, Fisher R. Polymorphisms in thrombophilia and renin-angiotensin system pathways, preterm delivery, and evidence of placental hemorrhage. American Journal of Obstetrics and Gynecology. 201: 317.e1-9. PMID 19733287 DOI: 10.1016/J.Ajog.2009.05.060 |
0.282 |
|
| 1995 |
Chen H, Leipprandt JR, Traviss CE, Sopher BL, Jones MZ, Cavanagh KT, Friderici KH. Molecular cloning and characterization of bovine beta-mannosidase. The Journal of Biological Chemistry. 270: 3841-8. PMID 7876128 DOI: 10.1074/Jbc.270.8.3841 |
0.276 |
|
| 2009 |
Belyantseva IA, Perrin BJ, Sonnemann KJ, Zhu M, Stepanyan R, McGee J, Frolenkov GI, Walsh EJ, Friderici KH, Friedman TB, Ervasti JM. Gamma-actin is required for cytoskeletal maintenance but not development. Proceedings of the National Academy of Sciences of the United States of America. 106: 9703-8. PMID 19497859 DOI: 10.1073/Pnas.0900221106 |
0.275 |
|
| 1989 |
Hacker DL, Friderici K, Fluck MM. A nonlethal mutation in large T antigen of polyomavirus which affects viral DNA synthesis Journal of Virology. 63: 776-781. PMID 2536103 DOI: 10.1128/Jvi.63.2.776-781.1989 |
0.266 |
|
| 2006 |
Zhu M, Lovell KL, Patterson JS, Saunders TL, Hughes ED, Friderici KH. Beta-mannosidosis mice: a model for the human lysosomal storage disease. Human Molecular Genetics. 15: 493-500. PMID 16377659 DOI: 10.1093/Hmg/Ddi465 |
0.262 |
|
| 1998 |
Morell RJ, Kim HJ, Hood LJ, Goforth L, Friderici K, Fisher R, Van Camp G, Berlin CI, Oddoux C, Ostrer H, Keats B, Friedman TB. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness. The New England Journal of Medicine. 339: 1500-5. PMID 9819448 DOI: 10.1056/NEJM199811193392103 |
0.255 |
|
| 1985 |
Winberry L, Priehs C, Friderici K, Thompson M, Fluck M. Expression of proto-oncogenes in normal and papovavirus-transformed or -infected rat fibroblasts Virology. 147: 154-168. PMID 2414921 DOI: 10.1016/0042-6822(85)90235-1 |
0.254 |
|
| 1995 |
Friderici K, Cavanagh KT, Leipprandt JR, Traviss CE, Anson DS, Hopwood JJ, Jones MZ. Cloning and sequence analysis of caprine N-acetylglucosamine 6-sulfatase cDNA. Biochimica Et Biophysica Acta. 1271: 369-73. PMID 7605804 DOI: 10.1016/0925-4439(95)00054-8 |
0.253 |
|
| 1995 |
Cavanagh KT, Leipprandt JR, Jones MZ, Friderici K. Molecular defect of caprine N-acetylglucosamine-6-sulphatase deficiency. A single base substitution creates a stop codon in the 5'-region of the coding sequence. Journal of Inherited Metabolic Disease. 18: 96. PMID 7623459 DOI: 10.1007/Bf00711390 |
0.252 |
|
| 2003 |
Nagelkirk PR, Coughlin AM, Cooper JA, Paton CM, Friderici KH, Wingerd BA, Womack CJ. THE INFLUENCE OF THE 4G/5G POLYMORPHISM OF THE PAI-1 GENE ON PLASMA PAI-1 CONCENTRATIONS DURING EXERCISE Medicine & Science in Sports & Exercise. 35: S127. DOI: 10.1097/00005768-200305001-00699 |
0.252 |
|
| 1975 |
Perry RP, Kelley DE, Friderici KH, Rottman FM. Methylated constituents of heterogeneous nuclear RNA: Presence in blocked 5′ terminal structures Cell. 6: 13-19. PMID 1164731 DOI: 10.1016/0092-8674(75)90068-9 |
0.248 |
|
| 2010 |
Bergeron SE, Zhu M, Thiem SM, Friderici KH, Rubenstein PA. Ion-dependent polymerization differences between mammalian beta- and gamma-nonmuscle actin isoforms. The Journal of Biological Chemistry. 285: 16087-95. PMID 20308063 DOI: 10.1074/Jbc.M110.110130 |
0.243 |
|
| 2008 |
Gargano J, Holzman C, Senagore P, Friderici K, Fisher R. 20: Polymorphisms in thrombophilia and renin-angiotensin system pathways in relation to preterm delivery, placental abruption and histologic evidence of disrupted vascular integrity American Journal of Obstetrics and Gynecology. 199: S10. DOI: 10.1016/J.Ajog.2008.09.048 |
0.242 |
|
| 1975 |
Perry RP, Kelley DE, Friderici K, Rottman F. The methylated constituents of L cell messenger RNA: Evidence for an unusual cluster at the 5′ terminus Cell. 4: 387-394. PMID 1168101 DOI: 10.1016/0092-8674(75)90159-2 |
0.239 |
|
| 2007 |
Scheid JM, Holzman CB, Jones N, Friderici KH, Nummy KA, Symonds LL, Sikorskii A, Regier MK, Fisher R. Depressive symptoms in mid-pregnancy, lifetime stressors and the 5-HTTLPR genotype Genes, Brain and Behavior. 6: 453-464. PMID 16965382 DOI: 10.1111/J.1601-183X.2006.00272.X |
0.236 |
|
| 1975 |
Desrosiers RC, Friderici KH, Rottman FM. Characterization of novikoff hepatoma mRNA methylation and heterogeneity in the methylated 5′ terminus Biochemistry. 14: 4367-4374. PMID 169893 DOI: 10.1021/Bi00691A004 |
0.236 |
|
| 1986 |
Friderici K, Priehs C, Fluck MM. Superinfection rescue of an integrated defective polyomavirus genome Journal of Virology. 57: 205-210. PMID 3001345 DOI: 10.1128/Jvi.57.1.205-210.1986 |
0.235 |
|
| 1977 |
Rottman FM, Desrosiers RC, Friderici K. Nucleotide Methylation Patterns in Eukaryotic mRNA Progress in Nucleic Acid Research and Molecular Biology. 19: 21-38. PMID 190642 DOI: 10.1016/S0079-6603(08)60906-X |
0.232 |
|
| 1979 |
Sasavage NL, Friderici K, Rottman FM. Specific inhibition of capped mRNA translation in vitro by m7G5′ pppp5′G and m7G5′pppp5′- m7G Nucleic Acids Research. 6: 3613-3624. PMID 493116 DOI: 10.1093/Nar/6.11.3613 |
0.229 |
|
| 1986 |
Priehs C, Friderici K, Winberry L, Fluck MM. Properties of cells transformed by the middle T-antigen-coding region of polyomavirus Journal of Virology. 57: 211-218. PMID 3001346 DOI: 10.1128/Jvi.57.1.211-218.1986 |
0.229 |
|
| 1990 |
Oh SY, Amalfitano A, Friderici K, Chen MC, Fluck MM. Low probability of double integration in transformation of nonpermissive cells by polyomavirus Journal of Virology. 64: 1304-1313. PMID 2154610 DOI: 10.1128/Jvi.64.3.1304-1313.1990 |
0.228 |
|
| 1984 |
Friderici K, Yin Oh S, Ellis R, Guacci V, Fluck MM. Recombination induces tandem repeats of integrated viral sequences in polyoma-transformed cells Virology. 137: 67-73. PMID 6089421 DOI: 10.1016/0042-6822(84)90009-6 |
0.228 |
|
| 2003 |
Coughlin AM, Nagelkirk PR, Cooper JA, Paton CM, Friderici KH, Wingerd B, Pivarnik JM, Womack CJ. THE INFLUENCE OF TISSUE PLASMINOGEN ACTIVATOR POLYMORPHISMS ON THE FIBRINOLYTIC RESPONSE TO EXERCISE Medicine & Science in Sports & Exercise. 35: S127. DOI: 10.1097/00005768-200305001-00697 |
0.222 |
|
| 2011 |
Scheid JM, Holzman CB, Jones N, Friderici KH, Jernigan KA, Symonds LL, Sikorskii A, Fisher R. Life stressors and 5-HTTLPR interaction in relation to midpregnancy depressive symptoms among African-American women. Psychiatric Genetics. 21: 271-80. PMID 22030619 DOI: 10.1097/Ypg.0B013E32834603E8 |
0.22 |
|
| 1976 |
Friderici K, Kaehler M, Rottman F. Kinetics of Novikoff cytoplasmic messenger RNA methylation Biochemistry. 15: 5234-5241. PMID 187213 DOI: 10.1021/Bi00669A006 |
0.22 |
|
| 1974 |
Desrosiers R, Friderici K, Rottman F. Identification of methylated nucleosides in messenger RNA from Novikoff hepatoma cells Proceedings of the National Academy of Sciences of the United States of America. 71: 3971-3975. PMID 4372599 DOI: 10.1073/Pnas.71.10.3971 |
0.215 |
|
| 2004 |
Nagelkirk PR, Coughlin AM, Paton JC, Paton CM, Friderici KH, Wingerd BA, Womack CJ. The Influence of the ACE I/D Polymorphism on Plasma PAI-1 Concentrations During Exercise Medicine & Science in Sports & Exercise. 36: S259. DOI: 10.1097/00005768-200405001-01239 |
0.214 |
|
| 1993 |
Sopher BL, Traviss CE, Cavanagh KT, Jones MZ, Friderici KH. Bovine kidney beta-mannosidase: purification and characterization. The Biochemical Journal. 289: 343-7. PMID 8424779 DOI: 10.1042/Bj2890343 |
0.21 |
|
| 1995 |
Leipprandt JR, Friderici K, Sprecher DJ, Jones MZ. Prenatal testing for caprine N-acetylglucosamine-6-sulphatase deficiency and sex identification. Journal of Inherited Metabolic Disease. 18: 647-8. PMID 8598652 DOI: 10.1007/Bf02436016 |
0.2 |
|
| 1983 |
Goodman GT, Akers RM, Friderici KH, Tucker HA. Hormonal regulation of alpha-lactalbumin secretion from bovine mammary tissue cultured in vitro. Endocrinology. 112: 1324-30. PMID 6832048 DOI: 10.1210/Endo-112-4-1324 |
0.194 |
|
| 2010 |
Ajibola AJ, Omar SA, Friderici KH. Genetic mutation in pontocerebellar hypoplasia. Clinical Genetics. 77: 197-9. PMID 19807738 DOI: 10.1111/j.1399-0004.2009.01283.x |
0.183 |
|
| 2018 |
Coughlin AM, Nagelkirk PR, Cooper JA, Paton CM, Friderici KH, Wingerd BA, Pivarnik JM, Womack CJ. The Influence of Tissue Plasminogen Activator I/D Polymorphism on the tPA Response to Exercise. International Journal of Exercise Science. 11: 1136-1144. PMID 30338017 |
0.08 |
|
| 1978 |
Thomason AR, Friderici KH, Velicer LF, Rottman F. Presence of 5'-terminal cap structures in virus-specific RNA from feline leukemia virus-infected cells Journal of Virology. 26: 226-235. PMID 207884 |
0.055 |
|
| 1974 |
Rottman F, Friderici K, Comstock P, Khan MK. Influence of 2′-O-alkylation on the structure of single-stranded polynucleotides and the stability of 2′-O-alkylated polynucleotide complexes Biochemistry. 13: 2762-2771. PMID 4847544 DOI: 10.1021/bi00710a016 |
0.043 |
|
| 1982 |
Padmanabhan V, Friderici KH, Convey EM, Rottman FM. D-valine medium maintains prolactin production in primary culture. Molecular and Cellular Endocrinology. 28: 613-26. PMID 6818057 DOI: 10.1016/0303-7207(82)90150-2 |
0.037 |
|
| 1971 |
Dunlap BE, Friderici KH, Rottman F. 2′-O-methyl polynucleotides as templates for cell-free amino acid incorporation Biochemistry. 10: 2581-2587. PMID 4934115 |
0.036 |
|
| Hide low-probability matches. |