Nuber UA - Search Results

1

Dyschromatosis universalis hereditaria: familial case and ultrastructural skin investigation.

Nuber UA, Tinschert S, Mundlos S, Hauber I. Nuber UA, et al. Am J Med Genet A. 2004 Mar 15;125A(3):261-6. doi: 10.1002/ajmg.a.20519. Am J Med Genet A. 2004. PMID: 14994234

2

Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation.

Kalscheuer VM, Freude K, Musante L, Jensen LR, Yntema HG, Gécz J, Sefiani A, Hoffmann K, Moser B, Haas S, Gurok U, Haesler S, Aranda B, Nshedjan A, Tzschach A, Hartmann N, Roloff TC, Shoichet S, Hagens O, Tao J, Van Bokhoven H, Turner G, Chelly J, Moraine C, Fryns JP, Nuber U, Hoeltzenbein M, Scharff C, Scherthan H, Lenzner S, Hamel BC, Schweiger S, Ropers HH. Kalscheuer VM, et al. Nat Genet. 2003 Dec;35(4):313-5. doi: 10.1038/ng1264. Epub 2003 Nov 23. Nat Genet. 2003. PMID: 14634649

3

Chromatin, epigenetics and stem cells.

Roloff TC, Nuber UA. Roloff TC, et al. Among authors: nuber ua. Eur J Cell Biol. 2005 Mar;84(2-3):123-35. doi: 10.1016/j.ejcb.2004.12.013. Eur J Cell Biol. 2005. PMID: 15819395 Review.

4

Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome.

Nuber UA, Kriaucionis S, Roloff TC, Guy J, Selfridge J, Steinhoff C, Schulz R, Lipkowitz B, Ropers HH, Holmes MC, Bird A. Nuber UA, et al. Hum Mol Genet. 2005 Aug 1;14(15):2247-56. doi: 10.1093/hmg/ddi229. Epub 2005 Jul 7. Hum Mol Genet. 2005. PMID: 16002417

5

X chromosome-specific cDNA arrays: identification of genes that escape from X-inactivation and other applications.

Sudbrak R, Wieczorek G, Nuber UA, Mann W, Kirchner R, Erdogan F, Brown CJ, Wöhrle D, Sterk P, Kalscheuer VM, Berger W, Lehrach H, Ropers HH. Sudbrak R, et al. Among authors: nuber ua. Hum Mol Genet. 2001 Jan 1;10(1):77-83. doi: 10.1093/hmg/10.1.77. Hum Mol Genet. 2001. PMID: 11136717

6

Comparative study of methyl-CpG-binding domain proteins.

Roloff TC, Ropers HH, Nuber UA. Roloff TC, et al. Among authors: nuber ua. BMC Genomics. 2003 Jan 16;4(1):1. doi: 10.1186/1471-2164-4-1. Epub 2003 Jan 16. BMC Genomics. 2003. PMID: 12529184 Free PMC article.

7

Expression of mouse Tbx22 supports its role in palatogenesis and glossogenesis.

Herr A, Meunier D, Müller I, Rump A, Fundele R, Ropers HH, Nuber UA. Herr A, et al. Among authors: nuber ua. Dev Dyn. 2003 Apr;226(4):579-86. doi: 10.1002/dvdy.10260. Dev Dyn. 2003. PMID: 12666195 Free article.

8

Gene expression changes in the course of neural progenitor cell differentiation.

Gurok U, Steinhoff C, Lipkowitz B, Ropers HH, Scharff C, Nuber UA. Gurok U, et al. Among authors: nuber ua. J Neurosci. 2004 Jun 30;24(26):5982-6002. doi: 10.1523/JNEUROSCI.0809-04.2004. J Neurosci. 2004. PMID: 15229246 Free PMC article.

9

Detection of mitochondrial single nucleotide polymorphisms using a primer elongation reaction on oligonucleotide microarrays.

Erdogan F, Kirchner R, Mann W, Ropers HH, Nuber UA. Erdogan F, et al. Among authors: nuber ua. Nucleic Acids Res. 2001 Apr 1;29(7):E36. doi: 10.1093/nar/29.7.e36. Nucleic Acids Res. 2001. PMID: 11266571 Free PMC article.

10

Neural precursor cells induce cell death of high-grade astrocytomas through stimulation of TRPV1.

Stock K, Kumar J, Synowitz M, Petrosino S, Imperatore R, Smith ES, Wend P, Purfürst B, Nuber UA, Gurok U, Matyash V, Wälzlein JH, Chirasani SR, Dittmar G, Cravatt BF, Momma S, Lewin GR, Ligresti A, De Petrocellis L, Cristino L, Di Marzo V, Kettenmann H, Glass R. Stock K, et al. Among authors: nuber ua. Nat Med. 2012 Aug;18(8):1232-8. doi: 10.1038/nm.2827. Epub 2012 Jul 22. Nat Med. 2012. PMID: 22820645 Free PMC article.

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