Niesler B - Search Results

1

A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders.

Hammer C, Degenhardt F, Priebe L, Stütz AM, Heilmann S, Waszak SM, Schlattl A, Mangold E, Hoffmann P, Nöthen MM, Rietschel M, Rappold G, Korbel J, Cichon S, Niesler B; MooDS Consortium. Hammer C, et al. Among authors: niesler b. Bipolar Disord. 2014 Nov;16(7):764-8. doi: 10.1111/bdi.12207. Epub 2014 Apr 23. Bipolar Disord. 2014. PMID: 24754353

2

Serotonin receptor gene HTR3A variants in schizophrenic and bipolar affective patients.

Niesler B, Weiss B, Fischer C, Nöthen MM, Propping P, Bondy B, Rietschel M, Maier W, Albus M, Franzek E, Rappold GA. Niesler B, et al. Pharmacogenetics. 2001 Feb;11(1):21-7. doi: 10.1097/00008571-200102000-00003. Pharmacogenetics. 2001. PMID: 11207027

3

Association between the 5' UTR variant C178T of the serotonin receptor gene HTR3A and bipolar affective disorder.

Niesler B, Flohr T, Nöthen MM, Fischer C, Rietschel M, Franzek E, Albus M, Propping P, Rappold GA. Niesler B, et al. Pharmacogenetics. 2001 Aug;11(6):471-5. doi: 10.1097/00008571-200108000-00002. Pharmacogenetics. 2001. PMID: 11505217

4

The Leri-Weill and Turner syndrome homeobox gene SHOX encodes a cell-type specific transcriptional activator.

Rao E, Blaschke RJ, Marchini A, Niesler B, Burnett M, Rappold GA. Rao E, et al. Among authors: niesler b. Hum Mol Genet. 2001 Dec 15;10(26):3083-91. doi: 10.1093/hmg/10.26.3083. Hum Mol Genet. 2001. PMID: 11751690

5

Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short stature.

Rappold GA, Fukami M, Niesler B, Schiller S, Zumkeller W, Bettendorf M, Heinrich U, Vlachopapadoupoulou E, Reinehr T, Onigata K, Ogata T. Rappold GA, et al. Among authors: niesler b. J Clin Endocrinol Metab. 2002 Mar;87(3):1402-6. doi: 10.1210/jcem.87.3.8328. J Clin Endocrinol Metab. 2002. PMID: 11889216

6

The human SHOX mutation database.

Niesler B, Fischer C, Rappold GA. Niesler B, et al. Hum Mutat. 2002 Nov;20(5):338-41. doi: 10.1002/humu.10125. Hum Mutat. 2002. PMID: 12402330

7

Cloning, physical mapping and expression analysis of the human 5-HT3 serotonin receptor-like genes HTR3C, HTR3D and HTR3E.

Niesler B, Frank B, Kapeller J, Rappold GA. Niesler B, et al. Gene. 2003 May 22;310:101-11. doi: 10.1016/s0378-1119(03)00503-1. Gene. 2003. PMID: 12801637

8

Mutational analysis of serotonin receptor genes: HTR3A and HTR3B in fibromyalgia patients.

Frank B, Niesler B, Bondy B, Späth M, Pongratz DE, Ackenheil M, Fischer C, Rappold G. Frank B, et al. Among authors: niesler b. Clin Rheumatol. 2004 Aug;23(4):338-44. doi: 10.1007/s10067-004-0927-2. Epub 2004 May 7. Clin Rheumatol. 2004. PMID: 15293096

9

Investigation of the human serotonin receptor gene HTR3B in bipolar affective and schizophrenic patients.

Frank B, Niesler B, Nöthen MM, Neidt H, Propping P, Bondy B, Rietschel M, Maier W, Albus M, Rappold G. Frank B, et al. Among authors: niesler b. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):1-5. doi: 10.1002/ajmg.b.30070. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389765

10

Mutational analysis of the PITX2 coding region revealed no common cause for transposition of the great arteries (dTGA).

Muncke N, Niesler B, Roeth R, Schön K, Rüdiger HJ, Goldmuntz E, Goodship J, Rappold G. Muncke N, et al. Among authors: niesler b. BMC Med Genet. 2005 May 12;6:20. doi: 10.1186/1471-2350-6-20. BMC Med Genet. 2005. PMID: 15890066 Free PMC article.

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