Gessler M - Search Results

1

Placental alpha(2)-adrenoceptors control vascular development at the interface between mother and embryo.

Philipp M, Brede ME, Hadamek K, Gessler M, Lohse MJ, Hein L. Philipp M, et al. Among authors: gessler m. Nat Genet. 2002 Jul;31(3):311-5. doi: 10.1038/ng919. Epub 2002 Jun 17. Nat Genet. 2002. PMID: 12068299

2

The Notch target genes Hey1 and Hey2 are required for embryonic vascular development.

Fischer A, Schumacher N, Maier M, Sendtner M, Gessler M. Fischer A, et al. Among authors: gessler m. Genes Dev. 2004 Apr 15;18(8):901-11. doi: 10.1101/gad.291004. Genes Dev. 2004. PMID: 15107403 Free PMC article.

3

Upregulation of soluble vascular endothelial growth factor receptor 1 contributes to angiogenesis defects in the placenta of alpha 2B-adrenoceptor deficient mice.

Muthig V, Gilsbach R, Haubold M, Philipp M, Ivacevic T, Gessler M, Hein L. Muthig V, et al. Among authors: gessler m. Circ Res. 2007 Sep 28;101(7):682-91. doi: 10.1161/CIRCRESAHA.107.151563. Epub 2007 Aug 2. Circ Res. 2007. PMID: 17673674

4

An essential developmental function for murine phosphoglycolate phosphatase in safeguarding cell proliferation.

Segerer G, Hadamek K, Zundler M, Fekete A, Seifried A, Mueller MJ, Koentgen F, Gessler M, Jeanclos E, Gohla A. Segerer G, et al. Among authors: gessler m. Sci Rep. 2016 Oct 12;6:35160. doi: 10.1038/srep35160. Sci Rep. 2016. PMID: 27731369 Free PMC article.

5

GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families.

Vortkamp A, Gessler M, Grzeschik KH. Vortkamp A, et al. Among authors: gessler m. Nature. 1991 Aug 8;352(6335):539-40. doi: 10.1038/352539a0. Nature. 1991. PMID: 1650914

6

Mosaic variegated aneuploidy in mouse BubR1 deficient embryos and pregnancy loss in human.

Schmid M, Steinlein C, Tian Q, Hanlon Newell AE, Gessler M, Olson SB, Rosenwald A, Kneitz B, Fedorov LM. Schmid M, et al. Among authors: gessler m. Chromosome Res. 2014 Sep;22(3):375-92. doi: 10.1007/s10577-014-9432-x. Epub 2014 Jul 1. Chromosome Res. 2014. PMID: 24981203

7

Frasier syndrome is caused by defective alternative splicing of WT1 leading to an altered ratio of WT1 +/-KTS splice isoforms.

Klamt B, Koziell A, Poulat F, Wieacker P, Scambler P, Berta P, Gessler M. Klamt B, et al. Among authors: gessler m. Hum Mol Genet. 1998 Apr;7(4):709-14. doi: 10.1093/hmg/7.4.709. Hum Mol Genet. 1998. PMID: 9499425

8

Very-KIND is a novel nervous system specific guanine nucleotide exchange factor for Ras GTPases.

Mees A, Rock R, Ciccarelli FD, Leberfinger CB, Borawski JM, Bork P, Wiese S, Gessler M, Kerkhoff E. Mees A, et al. Among authors: gessler m. Gene Expr Patterns. 2005 Dec;6(1):79-85. doi: 10.1016/j.modgep.2005.04.015. Epub 2005 Aug 15. Gene Expr Patterns. 2005. PMID: 16099729

9

Loss of Fat4 disrupts PCP signaling and oriented cell division and leads to cystic kidney disease.

Saburi S, Hester I, Fischer E, Pontoglio M, Eremina V, Gessler M, Quaggin SE, Harrison R, Mount R, McNeill H. Saburi S, et al. Among authors: gessler m. Nat Genet. 2008 Aug;40(8):1010-5. doi: 10.1038/ng.179. Epub 2008 Jul 6. Nat Genet. 2008. PMID: 18604206

10

The potassium channel gene HK1 maps to human chromosome 11p14.1, close to the FSHB gene.

Gessler M, Grupe A, Grzeschik KH, Pongs O. Gessler M, et al. Hum Genet. 1992 Nov;90(3):319-21. doi: 10.1007/BF00220091. Hum Genet. 1992. PMID: 1487251

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