Pusch C - Search Results

1

The SOX10/Sox10 gene from human and mouse: sequence, expression, and transactivation by the encoded HMG domain transcription factor.

Pusch C, Hustert E, Pfeifer D, Südbeck P, Kist R, Roe B, Wang Z, Balling R, Blin N, Scherer G. Pusch C, et al. Hum Genet. 1998 Aug;103(2):115-23. doi: 10.1007/s004390050793. Hum Genet. 1998. PMID: 9760192

2

Hirschsprung, RET-SOX and beyond: the challenge of examining non-mendelian traits (Review).

Pusch CM, Sasiadek MM, Blin N. Pusch CM, et al. Int J Mol Med. 2002 Oct;10(4):367-70. Int J Mol Med. 2002. PMID: 12239580 Review.

3

Molecular phylogenetics employing modern and ancient DNA.

Pusch CM, Broghammer M, Blin N. Pusch CM, et al. J Appl Genet. 2003;44(3):269-90. J Appl Genet. 2003. PMID: 12923304

4

Genomic structure of the RNA polymerase II small subunit (hRPB14.4) locus (POLRF) and mapping to 22q13.1 by sequence identity.

Pusch C, Wang Z, Roe B, Blin N. Pusch C, et al. Genomics. 1996 Jun 15;34(3):440-2. doi: 10.1006/geno.1996.0312. Genomics. 1996. PMID: 8786150 No abstract available.

5

Cosmid-derived transcripts and sequence tags mapped to three subregions of human chromosome 22.

Pusch C, Müllenbach R, Gött P, Schmitt H, Wang Z, Roe B, Blin N. Pusch C, et al. Gene. 1996 Dec 12;183(1-2):29-33. doi: 10.1016/s0378-1119(96)00411-8. Gene. 1996. PMID: 8996083

6

Documenting ancient DNA quality via alpha satellite amplification and assessment of clone sequence diversity.

Pusch CM, Kayademir T, Prangenberg K, Conard NJ, Czarnetzki A, Blin N. Pusch CM, et al. J Appl Genet. 2002;43(3):351-64. J Appl Genet. 2002. PMID: 12177525

7

Rab8b GTPase, a protein transport regulator, is an interacting partner of otoferlin, defective in a human autosomal recessive deafness form.

Heidrych P, Zimmermann U, Bress A, Pusch CM, Ruth P, Pfister M, Knipper M, Blin N. Heidrych P, et al. Hum Mol Genet. 2008 Dec 1;17(23):3814-21. doi: 10.1093/hmg/ddn279. Epub 2008 Sep 4. Hum Mol Genet. 2008. PMID: 18772196

8

Expressed sequences within pericentromeric heterochromatin of human chromosome 22.

Blin N, Scholz M, Wissinger B, Müllenbach R, Pusch C. Blin N, et al. Among authors: pusch c. Mamm Genome. 1997;8(11):859-62. doi: 10.1007/s003359900595. Mamm Genome. 1997. PMID: 9337403 No abstract available.

9

The 48 bp centromeric repeat is a functionally conserved motif in great apes and man showing protein-binding properties.

Pusch CM, Wundrack I, Müllenbach R, Schempp W, Blin N. Pusch CM, et al. Electrophoresis. 2002 Jan;23(1):20-6. doi: 10.1002/1522-2683(200201)23:1<20::AID-ELPS20>3.0.CO;2-C. Electrophoresis. 2002. PMID: 11824617

10

Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell.

Heidrych P, Zimmermann U, Kuhn S, Franz C, Engel J, Duncker SV, Hirt B, Pusch CM, Ruth P, Pfister M, Marcotti W, Blin N, Knipper M. Heidrych P, et al. Among authors: pusch cm. Hum Mol Genet. 2009 Aug 1;18(15):2779-90. doi: 10.1093/hmg/ddp213. Epub 2009 May 5. Hum Mol Genet. 2009. PMID: 19417007

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