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Beate Niesler
Beate Niesler
Verifisert e-postadresse på med.uni-heidelberg.de - Startside
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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
12031997
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
3502007
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
2992003
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
2982002
5-HT3 receptors: role in disease and target of drugs
J Walstab, G Rappold, B Niesler
Pharmacology & therapeutics 128 (1), 146-169, 2010
2552010
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
2472008
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
2032007
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
C Eijsbouts, T Zheng, NA Kennedy, F Bonfiglio, CA Anderson, ...
Nature genetics 53 (11), 1543-1552, 2021
1772021
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
1771998
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
1572001
Disorders of the enteric nervous system—a holistic view
B Niesler, S Kuerten, IE Demir, KH Schäfer
Nature reviews Gastroenterology & hepatology 18 (6), 393-410, 2021
1492021
Heterogeneity of response to immune checkpoint blockade in hypermutated experimental gliomas
K Aslan, V Turco, J Blobner, JK Sonner, AR Liuzzi, NG Núñez, D De Feo, ...
Nature communications 11 (1), 931, 2020
1462020
miR-16 and miR-125b are involved in barrier function dysregulation through the modulation of claudin-2 and cingulin expression in the jejunum in IBS with diarrhoea
C Martínez, BK Rodiño-Janeiro, B Lobo, ML Stanifer, B Klaus, M Granzow, ...
Gut 66 (9), 1537-1538, 2017
1382017
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
1362015
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
1352001
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
1182000
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
1132016
Ginger and its pungent constituents non‐competitively inhibit activation of human recombinant and native 5‐HT3 receptors of enteric neurons
J Walstab, D Krüger, T Stark, T Hofmann, IE Demir, GO Ceyhan, B Feistel, ...
Neurogastroenterology & Motility 25 (5), 439-e302, 2013
1102013
Serotonin Type 3 Receptor Genes: HTR3A, B, C, D, E
B Niesler, J Kapeller, C Hammer, G Rappold
Pharmacogenomics 9 (5), 501-504, 2008
1092008
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
932011
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