Literature DB >> 8535076

Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene.

N G Pasteris1, B de Gouyon, A B Cadle, K Campbell, G E Herman, J L Gorski.   

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Year:  1995        PMID： 8535076     DOI： 10.1007/bf00352375

Source DB:  PubMed          Journal:  Mamm Genome        ISSN： 0938-8990            Impact factor:   2.957


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  14 in total

1.  A radiation hybrid map of the proximal short arm of the human X chromosome spanning incontinentia pigmenti 1 (IP1) translocation breakpoints.

Authors:  J L Gorski; M Boehnke; E L Reyner; E N Burright
Journal:  Genomics       Date:  1992-11       Impact factor: 5.736

2.  Aarskog syndrome.

Authors:  M E Porteous; D R Goudie
Journal:  J Med Genet       Date:  1991-01       Impact factor: 6.318

3.  Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.

Authors:  T A Angel; C J Faust; J C Gonzales; S Kenwrick; R A Lewis; G E Herman
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

Review 4.  Proteins regulating Ras and its relatives.

Authors:  M S Boguski; F McCormick
Journal:  Nature       Date:  1993-12-16       Impact factor: 49.962

5.  Genetic linkage of the erythroid-specific delta-aminolevulinate synthase gene (Alas2) to the distal region of the mouse X chromosome.

Authors:  V M Chapman; B T Keitz; D F Bishop
Journal:  Mamm Genome       Date:  1994-11       Impact factor: 2.957

6.  Aarskog syndrome: full male and female expression associated with an X-autosome translocation.

Authors:  E Bawle; M Tyrkus; S Lipman; D Bozimowski
Journal:  Am J Med Genet       Date:  1984-03

7.  A comprehensive set of sequence analysis programs for the VAX.

Authors:  J Devereux; P Haeberli; O Smithies
Journal:  Nucleic Acids Res       Date:  1984-01-11       Impact factor: 16.971

8.  New insights into the man-mouse comparative map of the X chromosome.

Authors:  H J Blair; V Reed; S H Laval; Y Boyd
Journal:  Genomics       Date:  1994-01-15       Impact factor: 5.736

9.  Isolation and characterization of the faciogenital dysplasia (Aarskog-Scott syndrome) gene: a putative Rho/Rac guanine nucleotide exchange factor.

Authors:  N G Pasteris; A Cadle; L J Logie; M E Porteous; C E Schwartz; R E Stevenson; T W Glover; R S Wilroy; J L Gorski
Journal:  Cell       Date:  1994-11-18       Impact factor: 41.582

10.  Close linkage of the murine locus bare patches to the X-linked visual pigment gene: implications for mapping human X-linked dominant chondrodysplasia punctata.

Authors:  G E Herman; S J Walton
Journal:  Genomics       Date:  1990-07       Impact factor: 5.736
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  3 in total

1.  Comparative genome organization of vertebrates. The First International Workshop on Comparative Genome Organization.

Authors:  L Andersson; A Archibald; M Ashburner; S Audun; W Barendse; J Bitgood; C Bottema; T Broad; S Brown; D Burt; C Charlier; N Copeland; S Davis; M Davisson; J Edwards; A Eggen; G Elgar; J T Eppig; I Franklin; P Grewe; T Gill; J A Graves; R Hawken; J Hetzel; J Womack
Journal:  Mamm Genome       Date:  1996-10       Impact factor: 2.957

2.  The Aarskog-Scott syndrome protein Fgd1 regulates podosome formation and extracellular matrix remodeling in transforming growth factor β-stimulated aortic endothelial cells.

Authors:  Thomas Daubon; Roberto Buccione; Elisabeth Génot
Journal:  Mol Cell Biol       Date:  2011-09-12       Impact factor: 4.272

3.  Smcx lies distal to DXHX674 and DXHX679 on the mouse X chromosome.

Authors:  S H Laval; H J Blair; M J Mitchell; Y Boyd
Journal:  Mamm Genome       Date:  1996-07       Impact factor: 2.957
  3 in total

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