| Year |
Citation |
Score |
| Low-probability matches (unlikely to be authored by this person) |
| 2024 |
Zhang S, Yun D, Yang H, Eckstein M, Elbait GD, Zhou Y, Lu Y, Yang H, Zhang J, Dörflein I, Britzen-Laurent N, Pfeffer S, Stemmler MP, Dahl A, Mukhopadhyay D, et al. Roflumilast inhibits tumor growth and migration in STK11/LKB1 deficient pancreatic cancer. Cell Death Discovery. 10: 124. PMID 38461159 DOI: 10.1038/s41420-024-01890-y |
0.01 |
|
| 2023 |
Weber S, Sitte S, Voegele AL, Sologub L, Wilfer A, Rath T, Nägel A, Zundler S, Franci L, Opipari AW, Sonnewald S, Reid S, Hartmann A, Eichhorn P, Handtrack C, et al. NLRP3 inhibition leads to impaired mucosal fibroblast function in patients with inflammatory bowel diseases. Journal of Crohn's & Colitis. PMID 37748021 DOI: 10.1093/ecco-jcc/jjad164 |
0.01 |
|
| 2022 |
Hatami N, Büttner C, Bock F, Simfors S, Musial G, Reis A, Cursiefen C, Clahsen T. Cystathionine β-synthase as novel endogenous regulator of lymphangiogenesis via modulating VEGF receptor 2 and 3. Communications Biology. 5: 950. PMID 36088423 DOI: 10.1038/s42003-022-03923-7 |
0.01 |
|
| 2020 |
Clahsen T, Büttner C, Hatami N, Reis A, Cursiefen C. Role of Endogenous Regulators of Hem- And Lymphangiogenesis in Corneal Transplantation. Journal of Clinical Medicine. 9. PMID 32050484 DOI: 10.3390/jcm9020479 |
0.01 |
|
| 2019 |
Heichler C, Scheibe K, Schmied A, Geppert CI, Schmid B, Wirtz S, Thoma OM, Kramer V, Waldner MJ, Büttner C, Farin HF, Pešić M, Knieling F, Merkel S, Grüneboom A, et al. STAT3 activation through IL-6/IL-11 in cancer-associated fibroblasts promotes colorectal tumour development and correlates with poor prognosis. Gut. PMID 31685519 DOI: 10.1136/gutjnl-2019-319200 |
0.01 |
|
| 2019 |
Hauer NN, Popp B, Taher L, Vogl C, Dhandapany PS, Büttner C, Uebe S, Sticht H, Ferrazzi F, Ekici AB, De Luca A, Klinger P, Kraus C, Zweier C, Wiesener A, et al. Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature. European Journal of Human Genetics : Ejhg. PMID 30809043 DOI: 10.1038/S41431-019-0362-0 |
0.01 |
|
| 2019 |
Löhr S, Ekici AB, Uebe S, Büttner C, Köhm M, Behrens F, Böhm B, Sticherling M, Schett G, Simon D, Mössner R, Nimeh A, Oji V, Assmann G, Rech J, et al. Analyses of association of psoriatic arthritis and psoriasis vulgaris with functional NCF1 variants. Rheumatology (Oxford, England). PMID 30753645 DOI: 10.1093/rheumatology/key448 |
0.01 |
|
| 2019 |
Hansen M, Peltier J, Killy B, Amin B, Bodendorfer B, Härtlova A, Uebel S, Bosmann M, Hofmann J, Büttner C, Ekici AB, Kuttke M, Franzyk H, Foged C, Beer-Hammer S, et al. Macrophage phosphoproteome analysis reveals MINCLE-dependent and -independent mycobacterial cord factor signaling. Molecular & Cellular Proteomics : McP. PMID 30635358 DOI: 10.1074/mcp.RA118.000929 |
0.01 |
|
| 2019 |
Büttner C, Clahsen T, Regenfuss B, Dreisow ML, Steiber Z, Bock F, Reis A, Cursiefen C. Tyrosinase Is a Novel Endogenous Regulator of Developmental and Inflammatory Lymphangiogenesis. The American Journal of Pathology. 189: 440-448. PMID 30448402 DOI: 10.1016/j.ajpath.2018.10.014 |
0.01 |
|
| 2018 |
Vasileiou G, Vergarajauregui S, Endele S, Popp B, Büttner C, Ekici AB, Gerard M, Bramswig NC, Albrecht B, Clayton-Smith J, Morton J, Tomkins S, Low K, Weber A, Wenzel M, et al. Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome. American Journal of Human Genetics. PMID 29429572 DOI: 10.1016/j.ajhg.2018.01.014 |
0.01 |
|
| 2017 |
Hauer NN, Popp B, Schoeller E, Schuhmann S, Heath KE, Hisado-Oliva A, Klinger P, Kraus C, Trautmann U, Zenker M, Zweier C, Wiesener A, Abou Jamra R, Kunstmann E, Wieczorek D, et al. Clinical relevance of systematic phenotyping and exome sequencing in patients with short stature. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29758562 DOI: 10.1038/Gim.2017.159 |
0.01 |
|
| 2017 |
Hetzner K, Garcia-Cuellar MP, Büttner C, Slany RK. The interaction of ENL with PAF1 mitigates polycomb silencing and facilitates murine leukemogenesis. Blood. 131: 662-673. PMID 29217648 DOI: 10.1182/blood-2017-11-815035 |
0.01 |
|
| 2017 |
Hauer NN, Sticht H, Boppudi S, Büttner C, Kraus C, Trautmann U, Zenker M, Zweier C, Wiesener A, Jamra RA, Wieczorek D, Kelkel J, Jung AM, Uebe S, Ekici AB, et al. Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature. Scientific Reports. 7: 12225. PMID 28939912 DOI: 10.1038/s41598-017-12465-6 |
0.01 |
|
| 2017 |
Huber SE, Zoicas I, Reichel M, Mühle C, Büttner C, Ekici AB, Eulenburg V, Lenz B, Kornhuber J, Müller CP. Prenatal androgen receptor activation determines adult alcohol and water drinking in a sex-specific way. Addiction Biology. PMID 28776866 DOI: 10.1111/Adb.12540 |
0.01 |
|
| 2017 |
Chiriac MT, Buchen B, Wandersee A, Hundorfean G, Günther C, Bourjau Y, Doyle SE, Frey B, Ekici AB, Büttner C, Weigmann B, Atreya R, Wirtz S, Becker C, Siebler J, et al. Activation of Epithelial STAT1 by Interleukin 28 Controls Mucosal Healing in Mice with Colitis and is Increased in Mucosa of Patients With Inflammatory Bowel Disease. Gastroenterology. PMID 28342759 DOI: 10.1053/j.gastro.2017.03.015 |
0.01 |
|
| 2017 |
Oppelt PG, Mueller A, Stephan L, Dittrich R, Lermann J, Büttner C, Ekici AB, Conzelmann G, Seeger H, Schöller D, Rall K, Beckmann MW, Strissel PL, Brucker S, Strick R. Hyperandrogenemia and high prolactin in congenital utero-vaginal aplasia patients. Reproduction (Cambridge, England). PMID 28246310 DOI: 10.1530/REP-16-0408 |
0.01 |
|
| 2016 |
Müller CP, Kalinichenko LS, Tiesel J, Witt M, Stöckl T, Sprenger E, Fuchser J, Beckmann J, Praetner M, Huber SE, Amato D, Mühle C, Büttner C, Ekici AB, Smaga I, et al. Paradoxical antidepressant effects of alcohol are related to acid sphingomyelinase and its control of sphingolipid homeostasis. Acta Neuropathologica. PMID 28000031 DOI: 10.1007/S00401-016-1658-6 |
0.01 |
|
| 2016 |
Popp B, Trollmann R, Büttner C, Caliebe A, Thiel CT, Hüffmeier U, Reis A, Zweier C. Do the exome: A case of Williams-Beuren syndrome with severe epilepsy due to a truncating de novo variant in GABRA1. European Journal of Medical Genetics. 59: 549-53. PMID 27613244 DOI: 10.1016/j.ejmg.2016.09.002 |
0.01 |
|
| 2016 |
Ettle B, Kerman BE, Valera E, Gillmann C, Schlachetzki JC, Reiprich S, Büttner C, Ekici AB, Reis A, Wegner M, Bäuerle T, Riemenschneider MJ, Masliah E, Gage FH, Winkler J. α-Synuclein-induced myelination deficit defines a novel interventional target for multiple system atrophy. Acta Neuropathologica. PMID 27059609 DOI: 10.1007/S00401-016-1572-Y |
0.01 |
|
| 2016 |
Garcia-Cuellar MP, Büttner C, Bartenhagen C, Dugas M, Slany RK. Leukemogenic MLL-ENL Fusions Induce Alternative Chromatin States to Drive a Functionally Dichotomous Group of Target Genes. Cell Reports. 15: 310-22. PMID 27050521 DOI: 10.1016/j.celrep.2016.03.018 |
0.01 |
|
| 2015 |
Kuechler A, Willemsen MH, Albrecht B, Bacino CA, Bartholomew DW, van Bokhoven H, van den Boogaard MJ, Bramswig N, Büttner C, Cremer K, Czeschik JC, Engels H, van Gassen K, Graf E, van Haelst M, et al. De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum. Human Genetics. 134: 97-109. PMID 25326669 DOI: 10.1007/S00439-014-1498-1 |
0.01 |
|
| 2014 |
Murakami Y, Tawamie H, Maeda Y, Büttner C, Buchert R, Radwan F, Schaffer S, Sticht H, Aigner M, Reis A, Kinoshita T, Jamra RA. Null mutation in PGAP1 impairing Gpi-anchor maturation in patients with intellectual disability and encephalopathy. Plos Genetics. 10: e1004320. PMID 24784135 DOI: 10.1371/journal.pgen.1004320 |
0.01 |
|
| 2005 |
Perl M, Gebhard F, Brückner UB, Ayala A, Braumüller S, Büttner C, Kinzl L, Knöferl MW. Pulmonary contusion causes impairment of macrophage and lymphocyte immune functions and increases mortality associated with a subsequent septic challenge. Critical Care Medicine. 33: 1351-8. PMID 15942355 DOI: 10.1097/01.CCM.0000166352.28018.A9 |
0.01 |
|
| Hide low-probability matches. |
