Veske A - Search Results

1

Missense mutations in the extracellular domain of the human neural cell adhesion molecule L1 reduce neurite outgrowth of murine cerebellar neurons.

Michelson P, Hartwig C, Schachner M, Gal A, Veske A, Finckh U. Michelson P, et al. Among authors: veske a. Hum Mutat. 2002 Dec;20(6):481-2. doi: 10.1002/humu.9096. Hum Mutat. 2002. PMID: 12442287

2

Plexin B3 promotes neurite outgrowth, interacts homophilically, and interacts with Rin.

Hartwig C, Veske A, Krejcova S, Rosenberger G, Finckh U. Hartwig C, et al. Among authors: veske a. BMC Neurosci. 2005 Aug 25;6:53. doi: 10.1186/1471-2202-6-53. BMC Neurosci. 2005. PMID: 16122393 Free PMC article.

3

Spectrum and detection rate of L1CAM mutations in isolated and familial cases with clinically suspected L1-disease.

Finckh U, Schröder J, Ressler B, Veske A, Gal A. Finckh U, et al. Among authors: veske a. Am J Med Genet. 2000 May 1;92(1):40-6. doi: 10.1002/(sici)1096-8628(20000501)92:1<40::aid-ajmg7>3.0.co;2-r. Am J Med Genet. 2000. PMID: 10797421

4

Isolation of canine retinal arrestin cDNA and exclusion of three candidate genes for Swedish Briard retinal dystrophy.

Veske A, Narfström K, Finckh U, Sargan DR, Nilsson SE, Gal A. Veske A, et al. Curr Eye Res. 1997 Mar;16(3):270-4. doi: 10.1076/ceyr.16.3.270.15413. Curr Eye Res. 1997. PMID: 9088745

5

Microsatellite (TTCC)n polymorphism in intron 6 of the canine rod photoreceptor cGMP-gated cation channel alpha-subunit gene.

Veske A, Nilsson SE, Gal A. Veske A, et al. Anim Genet. 1997 Oct;28(5):374-5. Anim Genet. 1997. PMID: 9363608 No abstract available.

6

Characterization of canine rod photoreceptor cGMP-gated cation channel alpha-subunit gene and exclusion of its involvement in the hereditary retinal dystrophy of Swedish Briards.

Veske A, Nilsson SE, Gal A. Veske A, et al. Gene. 1997 Nov 20;202(1-2):115-9. doi: 10.1016/s0378-1119(97)00461-7. Gene. 1997. PMID: 9427553

7

Organization of the canine gene encoding the E isoform of retinal guanylate cyclase (cGC-E) and exclusion of its involvement in the inherited retinal dystrophy of the Swedish Briard and Briard-beagle dogs.

Veske A, Nilsson SE, Gal A. Veske A, et al. Biochim Biophys Acta. 1998 Jun 24;1372(1):69-77. doi: 10.1016/s0005-2736(98)00047-9. Biochim Biophys Acta. 1998. PMID: 9651484 Free article.

8

Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan.

Veske A, Oehlmann R, Younus F, Mohyuddin A, Müller-Myhsok B, Mehdi SQ, Gal A. Veske A, et al. Hum Mol Genet. 1996 Jan;5(1):165-8. doi: 10.1093/hmg/5.1.165. Hum Mol Genet. 1996. PMID: 8789456

9

Microsatellite (CA)n polymorphism in intron 2 of the canine rod photoreceptor cGMP-phosphodiesterase alpha-subunit gene.

Veske A, Nilsson SE, Gal A. Veske A, et al. Anim Genet. 1997 Oct;28(5):380. doi: 10.1111/j.1365-2052.1997.tb03284.x. Anim Genet. 1997. PMID: 9363616 No abstract available.

10

Retinal dystrophy of Swedish briard/briard-beagle dogs is due to a 4-bp deletion in RPE65.

Veske A, Nilsson SE, Narfström K, Gal A. Veske A, et al. Genomics. 1999 Apr 1;57(1):57-61. doi: 10.1006/geno.1999.5754. Genomics. 1999. PMID: 10191083

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