Zobrazeno 1 - 10 of 10 pro vyhledávání: '"Pasteris, N G"'
1
Periodical
Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene
Autor: Pasteris, N. G., Gouyon, B., Cadle, A. B., Campbell, K., Herman, G. E., Gorski, J. L.
Publikováno v: Mammalian Genome; September 1995, Vol. 6 Issue: 9 p658-661, 4p
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2
Periodical
The faciogenital dysplasia gene product FGD1 functions as a Cdc42Hs-specific guanine-nucleotide exchange factor.
Autor: Zheng, Y, Fischer, D J, Santos, M F, Tigyi, G, Pasteris, N G, Gorski, J L, Xu, Y
Publikováno v: Journal of Biological Chemistry; December 1996, Vol. 271 Issue: 52 p33169-72, 4p
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3
Akademický článek
Isolation, characterization, and mapping of the mouse Fgd3 gene, a new Faciogenital Dysplasia (FGD1; Aarskog Syndrome) gene homologue.
Autor: Pasteris NG; Department of Pediatrics, University of Michigan Medical School, Ann Arbor 48109-0688, USA., Nagata K, Hall A, Gorski JL
Publikováno v: Gene [Gene] 2000 Jan 25; Vol. 242 (1-2), pp. 237-47.
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4
Akademický článek
Isolation, characterization, and mapping of the mouse and human Fgd2 genes, faciogenital dysplasia (FGD1; Aarskog syndrome) gene homologues.
Autor: Pasteris NG; Department of Human Genetics, University of Michigan Medical Center, Ann Arbor, Michigan, 48109-0688, USA., Gorski JL
Publikováno v: Genomics [Genomics] 1999 Aug 15; Vol. 60 (1), pp. 57-66.
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5
Akademický článek
Genomic organization of the faciogenital dysplasia (FGD1; Aarskog syndrome) gene.
Autor: Pasteris NG; Department of Human Genetics, University of Michigan Medical Center, Ann Arbor 48109-0688, USA., Buckler J, Cadle AB, Gorski JL
Publikováno v: Genomics [Genomics] 1997 Aug 01; Vol. 43 (3), pp. 390-4.
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6
Akademický článek
Faciogenital dysplasia protein (FGD1) and Vav, two related proteins required for normal embryonic development, are upstream regulators of Rho GTPases.
Autor: Olson MF; CRC Oncogene and Signal Transduction Group, MRC Laboratory for Molecular Cell Biology, London, UK., Pasteris NG, Gorski JL, Hall A
Publikováno v: Current biology : CB [Curr Biol] 1996 Dec 01; Vol. 6 (12), pp. 1628-33.
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7
Akademický článek
An intragenic TaqI polymorphism in the faciogenital dysplasia (FGD1) locus, the gene responsible for Aarskog syndrome.
Autor: Pasteris NG; Department of Human Genetics and Pediatrics and Communicable Diseases, University of Michigan Medical Center, Ann Arbor 48109-0688, USA., Gorski JL
Publikováno v: Human genetics [Hum Genet] 1995 Oct; Vol. 96 (4), pp. 494.
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8
Akademický článek
Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor.
Autor: Pasteris NG; Department of Human Genetics, University of Michigan, Ann Arbor 48109-0688., Cadle A, Logie LJ, Porteous ME, Schwartz CE, Stevenson RE, Glover TW, Wilroy RS, Gorski JL
Publikováno v: Cell [Cell] 1994 Nov 18; Vol. 79 (4), pp. 669-78.
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9
Akademický článek
YAC subclone contig assembly by serial interspersed repetitive sequence (IRS)-PCR product hybridizations.
Autor: Pasteris NG; Department of Human Genetics, School of Medicine, University of Michigan, Ann Arbor 48109., Bialecki MD, Gorski JL
Publikováno v: Nucleic acids research [Nucleic Acids Res] 1993 Nov 11; Vol. 21 (22), pp. 5275-6.
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10
Akademický článek
Discordant phenotype of two overlapping deletions involving the PAX3 gene in chromosome 2q35.
Autor: Pasteris NG; Department of Human Genetics, University of Michigan Medical Center, Ann Arbor 48109-0688., Trask BJ, Sheldon S, Gorski JL
Publikováno v: Human molecular genetics [Hum Mol Genet] 1993 Jul; Vol. 2 (7), pp. 953-9.
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