Finckh U - Search Results

1

Plexin B3 is genetically associated with verbal performance and white matter volume in human brain.

Rujescu D, Meisenzahl EM, Krejcova S, Giegling I, Zetzsche T, Reiser M, Born CM, Möller HJ, Veske A, Gal A, Finckh U. Rujescu D, et al. Among authors: finckh u. Mol Psychiatry. 2007 Feb;12(2):190-4, 115. doi: 10.1038/sj.mp.4001903. Epub 2006 Oct 10. Mol Psychiatry. 2007. PMID: 17033634

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: finckh u. 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. 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

Prenatal molecular diagnosis of L1-spectrum disorders.

Finckh U, Gal A. Finckh U, et al. Prenat Diagn. 2000 Sep;20(9):744-5. Prenat Diagn. 2000. PMID: 11015704 Review. No abstract available.

5

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: finckh u. Hum Mutat. 2002 Dec;20(6):481-2. doi: 10.1002/humu.9096. Hum Mutat. 2002. PMID: 12442287

6

Elevated phenylalanine levels interfere with neurite outgrowth stimulated by the neuronal cell adhesion molecule L1 in vitro.

Hartwig C, Gal A, Santer R, Ullrich K, Finckh U, Kreienkamp HJ. Hartwig C, et al. Among authors: finckh u. FEBS Lett. 2006 Jun 12;580(14):3489-92. doi: 10.1016/j.febslet.2006.05.026. Epub 2006 May 15. FEBS Lett. 2006. PMID: 16716305 Free article.

7

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. Among authors: finckh u. Curr Eye Res. 1997 Mar;16(3):270-4. doi: 10.1076/ceyr.16.3.270.15413. Curr Eye Res. 1997. PMID: 9088745

8

Variable expression of familial Alzheimer disease associated with presenilin 2 mutation M239I.

Finckh U, Alberici A, Antoniazzi M, Benussi L, Fedi V, Giannini C, Gal A, Nitsch RM, Binetti G. Finckh U, et al. Neurology. 2000 May 23;54(10):2006-8. doi: 10.1212/wnl.54.10.2006. Neurology. 2000. PMID: 10822446

9

Prenatal diagnosis of carbamoyl phosphate synthetase I deficiency by identification of a missense mutation in CPS1.

Finckh U, Kohlschütter A, Schäfer H, Sperhake K, Colombo JP, Gal A. Finckh U, et al. Hum Mutat. 1998;12(3):206-11. doi: 10.1002/(SICI)1098-1004(1998)12:3<206::AID-HUMU8>3.0.CO;2-E. Hum Mutat. 1998. PMID: 9711878

10

Possible association of mitochondrial transcription factor A (TFAM) genotype with sporadic Alzheimer disease.

Günther C, von Hadeln K, Müller-Thomsen T, Alberici A, Binetti G, Hock C, Nitsch RM, Stoppe G, Reiss J, Gal A, Finckh U. Günther C, et al. Among authors: finckh u. Neurosci Lett. 2004 Oct 21;369(3):219-23. doi: 10.1016/j.neulet.2004.07.070. Neurosci Lett. 2004. PMID: 15464268

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