Gal A - Search Results

1

Interaction of alphaPIX (ARHGEF6) with beta-parvin (PARVB) suggests an involvement of alphaPIX in integrin-mediated signaling.

Rosenberger G, Jantke I, Gal A, Kutsche K. Rosenberger G, et al. Among authors: gal a. Hum Mol Genet. 2003 Jan 15;12(2):155-67. doi: 10.1093/hmg/ddg019. Hum Mol Genet. 2003. PMID: 12499396

2

AlphaPIX associates with calpain 4, the small subunit of calpain, and has a dual role in integrin-mediated cell spreading.

Rosenberger G, Gal A, Kutsche K. Rosenberger G, et al. Among authors: gal a. J Biol Chem. 2005 Feb 25;280(8):6879-89. doi: 10.1074/jbc.M412119200. Epub 2004 Dec 20. J Biol Chem. 2005. PMID: 15611136 Free article.

3

Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation.

Kutsche K, Yntema H, Brandt A, Jantke I, Nothwang HG, Orth U, Boavida MG, David D, Chelly J, Fryns JP, Moraine C, Ropers HH, Hamel BC, van Bokhoven H, Gal A. Kutsche K, et al. Among authors: gal a. Nat Genet. 2000 Oct;26(2):247-50. doi: 10.1038/80002. Nat Genet. 2000. PMID: 11017088

4

The mouse Arhgef6 gene: cDNA sequence, expression analysis, and chromosome assignment.

Kutsche K, Gal A. Kutsche K, et al. Among authors: gal a. Cytogenet Cell Genet. 2001;95(3-4):196-201. doi: 10.1159/000059346. Cytogenet Cell Genet. 2001. PMID: 12063400

5

Mutations of the mitochondrial holocytochrome c-type synthase in X-linked dominant microphthalmia with linear skin defects syndrome.

Wimplinger I, Morleo M, Rosenberger G, Iaconis D, Orth U, Meinecke P, Lerer I, Ballabio A, Gal A, Franco B, Kutsche K. Wimplinger I, et al. Among authors: gal a. Am J Hum Genet. 2006 Nov;79(5):878-89. doi: 10.1086/508474. Epub 2006 Sep 6. Am J Hum Genet. 2006. PMID: 17033964 Free PMC article.

6

Characterization of breakpoint sequences of five rearrangements in L1CAM and ABCD1 (ALD) genes.

Kutsche K, Ressler B, Katzera HG, Orth U, Gillessen-Kaesbach G, Morlot S, Schwinger E, Gal A. Kutsche K, et al. Among authors: gal a. Hum Mutat. 2002 May;19(5):526-35. doi: 10.1002/humu.10072. Hum Mutat. 2002. PMID: 11968085

7

Disruption of the PDGFB gene in a 1;22 translocation patient does not cause Costello syndrome.

Sutajová M, Neukirchen U, Meinecke P, Czeizel AE, Tímár L, Sólyom E, Gal A, Kutsche K. Sutajová M, et al. Among authors: gal a. Genomics. 2004 May;83(5):883-92. doi: 10.1016/j.ygeno.2003.10.012. Genomics. 2004. PMID: 15081117

8

A new gene family (FAM9) of low-copy repeats in Xp22.3 expressed exclusively in testis: implications for recombinations in this region.

Martinez-Garay I, Jablonka S, Sutajova M, Steuernagel P, Gal A, Kutsche K. Martinez-Garay I, et al. Among authors: gal a. Genomics. 2002 Sep;80(3):259-67. doi: 10.1006/geno.2002.6834. Genomics. 2002. PMID: 12213195

9

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.

Bolz H, von Brederlow B, Ramírez A, Bryda EC, Kutsche K, Nothwang HG, Seeliger M, del C-Salcedó Cabrera M, Vila MC, Molina OP, Gal A, Kubisch C. Bolz H, et al. Among authors: gal a. Nat Genet. 2001 Jan;27(1):108-12. doi: 10.1038/83667. Nat Genet. 2001. PMID: 11138009

10

Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium.

Kutsche K, Glauner E, Knauf S, Pomarino A, Schmidt M, Schröder B, Nothwang H, Schüler H, Goecke T, Kersten A, Althaus C, Gal A. Kutsche K, et al. Among authors: gal a. Cytogenet Cell Genet. 2000;91(1-4):141-7. doi: 10.1159/000056835. Cytogenet Cell Genet. 2000. PMID: 11173847

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