Niesler B - Search Results

1

Serotonin type 3 receptor genes: HTR3A, B, C, D, E.

Niesler B, Kapeller J, Hammer C, Rappold G. Niesler B, et al. Pharmacogenomics. 2008 May;9(5):501-4. doi: 10.2217/14622416.9.5.501. Pharmacogenomics. 2008. PMID: 18466097 Free article. Review.

2

Expression of TRX1 optimizes the antitumor functions of human CAR T cells and confers resistance to a pro-oxidative tumor microenvironment.

Balta E, Janzen N, Kirchgessner H, Toufaki V, Orlik C, Liang J, Lairikyengbam D, Abken H, Niesler B, Müller-Decker K, Ruppert T, Samstag Y. Balta E, et al. Among authors: niesler b. Front Immunol. 2022 Dec 14;13:1063313. doi: 10.3389/fimmu.2022.1063313. eCollection 2022. Front Immunol. 2022. PMID: 36591284 Free PMC article.

3

Targeted Proteomics Reveals Quantitative Differences in Low-Abundance Glycosyltransferases of Patients with Congenital Disorders of Glycosylation.

Sakson R, Beedgen L, Bernhard P, Alp KM, Lübbehusen N, Röth R, Niesler B, Luzarowski M, Shevchuk O, Mayer MP, Thiel C, Ruppert T. Sakson R, et al. Among authors: niesler b. Int J Mol Sci. 2024 Jan 18;25(2):1191. doi: 10.3390/ijms25021191. Int J Mol Sci. 2024. PMID: 38256263 Free PMC article.

4

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome.

Rao E, Weiss B, Fukami M, Rump A, Niesler B, Mertz A, Muroya K, Binder G, Kirsch S, Winkelmann M, Nordsiek G, Heinrich U, Breuning MH, Ranke MB, Rosenthal A, Ogata T, Rappold GA. Rao E, et al. Among authors: niesler b. Nat Genet. 1997 May;16(1):54-63. doi: 10.1038/ng0597-54. Nat Genet. 1997. PMID: 9140395

5

A member of a gene family on Xp22.3, VCX-A, is deleted in patients with X-linked nonspecific mental retardation.

Fukami M, Kirsch S, Schiller S, Richter A, Benes V, Franco B, Muroya K, Rao E, Merker S, Niesler B, Ballabio A, Ansorge W, Ogata T, Rappold GA. Fukami M, et al. Among authors: niesler b. Am J Hum Genet. 2000 Sep;67(3):563-73. doi: 10.1086/303047. Epub 2000 Jul 20. Am J Hum Genet. 2000. PMID: 10903929 Free PMC article.

6

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

7

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

8

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

9

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

10

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

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