Gal A - Search Results

1

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

2

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

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

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

5

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

6

Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with Costello syndrome.

Maróti Z, Kutsche K, Sutajova M, Gal A, Nothwang HG, Czeizel AE, Tímár L, Sólyom E. Maróti Z, et al. Among authors: gal a. Am J Med Genet. 2002 May 1;109(3):234-7. doi: 10.1002/ajmg.10314. Am J Med Genet. 2002. PMID: 11977185 No abstract available.

7

Microphthalmia with linear skin defects syndrome (MLS): a male with a mosaic paracentric inversion of Xp.

Kutsche K, Werner W, Bartsch O, von der Wense A, Meinecke P, Gal A. Kutsche K, et al. Among authors: gal a. Cytogenet Genome Res. 2002;99(1-4):297-302. doi: 10.1159/000071607. Cytogenet Genome Res. 2002. PMID: 12900578

8

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

9

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

10

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

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