Gal A - Search Results

1

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.

2

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

3

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

4

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.

5

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

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

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

8

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

9

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

10

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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

890 results

Search Page

Filters