Beate Niesler
Beate Niesler
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Zitiert von
Zitiert von
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
E Rao, B Weiss, M Fukami, A Rump, B Niesler, A Mertz, K Muroya, ...
Nature genetics 16 (1), 54-63, 1997
Genotypes and phenotypes in children with short stature: clinical indicators of SHOX haploinsufficiency
G Rappold, WF Blum, EP Shavrikova, BJ Crowe, R Roeth, CA Quigley, ...
Journal of medical genetics 44 (5), 306-313, 2007
Deletions of the Homeobox Gene SHOX (Short Stature Homeobox) Are an Important Cause of Growth Failure in Children with Short Stature
GA Rappold, M Fukami, B Niesler, S Schiller, W Zumkeller, M Bettendorf, ...
The Journal of Clinical Endocrinology & Metabolism 87 (3), 1402-1406, 2002
Cloning, physical mapping and expression analysis of the human 5-HT3 serotonin receptor-like genes HTR3C, HTR3D and HTR3E
B Niesler, B Frank, J Kapeller, GA Rappold
Gene 310, 101-111, 2003
First evidence for an association of a functional variant in the microRNA-510 target site of the serotonin receptor-type 3E gene with diarrhea predominant irritable bowel syndrome
J Kapeller, LA Houghton, H Mönnikes, J Walstab, D Möller, H Bönisch, ...
Human molecular genetics 17 (19), 2967-2977, 2008
5-HT3 receptors: role in disease and target of drugs
J Walstab, G Rappold, B Niesler
Pharmacology & therapeutics 128 (1), 146-169, 2010
Characterization of the novel human serotonin receptor subunits 5-HT3C, 5-HT3D, and 5-HT3E
B Niesler, J Walstab, S Combrink, D Moeller, J Kapeller, J Rietdorf, ...
Molecular pharmacology 72 (1), 8-17, 2007
Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS)
Retinoschisis Consortium
Human Molecular Genetics 7 (7), 1185-1192, 1998
Association between the 5′ UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder
B Niesler, T Flohr, MM Nöthen, C Fischer, M Rietschel, E Franzek, ...
Pharmacogenetics and Genomics 11 (6), 471-475, 2001
The Leri–Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator
E Rao, RJ Blaschke, A Marchini, B Niesler, M Burnett, GA Rappold
Human Molecular Genetics 10 (26), 3083-3091, 2001
A member of a gene family on Xp22. 3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation
M Fukami, S Kirsch, S Schiller, A Richter, V Benes, B Franco, K Muroya, ...
The American Journal of Human Genetics 67 (3), 563-573, 2000
Serotonin type 3 receptor genes: HTR3A, B, C, D, E
B Niesler, J Kapeller, C Hammer, G Rappold
Future Medicine Ltd 9 (5), 501-504, 2008
Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts
WE Ek, A Reznichenko, S Ripke, B Niesler, M Zucchelli, NV Rivera, ...
Gut 64 (11), 1774-1782, 2015
The HTR3A polymorphism c.-42C> T is associated with amygdala responsiveness in patients with irritable bowel syndrome
LA Kilpatrick, JS Labus, K Coveleskie, C Hammer, G Rappold, K Tillisch, ...
Gastroenterology 140 (7), 1943-1951, 2011
Mutational analysis of serotonin receptor genes: HTR3A and HTR3B in fibromyalgia patients
B Frank, B Niesler, B Bondy, M Späth, DE Pongratz, M Ackenheil, ...
Clinical rheumatology 23 (4), 338-344, 2004
Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients
B Niesler, B Weiss, C Fischer, MM Nöthen, P Propping, B Bondy, ...
Pharmacogenetics and Genomics 11 (1), 21-27, 2001
Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients
B Frank, B Niesler, MM Nöthen, H Neidt, P Propping, B Bondy, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 131 …, 2004
Polymorphisms in the novel serotonin receptor subunit gene HTR3C show different risks for acute chemotherapy-induced vomiting after anthracycline chemotherapy
PA Fasching, B Kollmannsberger, PL Strissel, B Niesler, J Engel, H Kreis, ...
Journal of cancer research and clinical oncology 134 (10), 1079-1086, 2008
5-HTTLPR and STin2 polymorphisms in the serotonin transporter gene and irritable bowel syndrome: effect of bowel habit and sex
B Niesler, J Kapeller, C Fell, W Atkinson, D Möller, C Fischer, P Whorwell, ...
European journal of gastroenterology & hepatology 22 (7), 856-861, 2010
Lessons learned—resolving the enigma of genetic factors in IBS
M Gazouli, MM Wouters, L Kapur-Pojskić, MB Bengtson, E Friedman, ...
Nature Reviews Gastroenterology & Hepatology 13 (2), 77-87, 2016
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