Literature DB >> 8178833

Mutational analysis of the biglycan gene excludes it as a candidate for X-linked dominant chondrodysplasia punctata, dyskeratosis congenita, and incontinentia pigmenti.

S Das, A Metzenberg, G S Pai, J Gitschier.   

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Year:  1994        PMID： 8178833      PMCID： PMC1918258     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  17 in total

1.  Negative regulation of transforming growth factor-beta by the proteoglycan decorin.

Authors:  Y Yamaguchi; D M Mann; E Ruoslahti
Journal:  Nature       Date:  1990-07-19       Impact factor: 49.962

2.  Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.

Authors:  M Orita; H Iwahana; H Kanazawa; K Hayashi; T Sekiya
Journal:  Proc Natl Acad Sci U S A       Date:  1989-04       Impact factor: 11.205

3.  Expression and localization of the two small proteoglycans biglycan and decorin in developing human skeletal and non-skeletal tissues.

Authors:  P Bianco; L W Fisher; M F Young; J D Termine; P G Robey
Journal:  J Histochem Cytochem       Date:  1990-11       Impact factor: 2.479

4.  Assignment of the gene for dyskeratosis congenita to Xq28.

Authors:  J M Connor; D Gatherer; F C Gray; L A Pirrit; N A Affara
Journal:  Hum Genet       Date:  1986-04       Impact factor: 4.132

5.  Latent and replicating forms of Epstein-Barr virus DNA in lymphomas and lymphoproliferative diseases.

Authors:  B Z Katz; N Raab-Traub; G Miller
Journal:  J Infect Dis       Date:  1989-10       Impact factor: 5.226

6.  Etiologic heterogeneity in dyskeratosis congenita.

Authors:  G S Pai; S Morgan; C Whetsell
Journal:  Am J Med Genet       Date:  1989-01

7.  X-linked dominant chondrodysplasia punctata. Review of literature and report of a case.

Authors:  R Happle
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

8.  Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphism.

Authors:  H Traupe; U Vetter; R Happle; L W Fisher; F P Cremers; S J Landy; R Pankau; H H Ropers
Journal:  Hum Genet       Date:  1993-03       Impact factor: 4.132

9.  Deduced protein sequence of bone small proteoglycan I (biglycan) shows homology with proteoglycan II (decorin) and several nonconnective tissue proteins in a variety of species.

Authors:  L W Fisher; J D Termine; M F Young
Journal:  J Biol Chem       Date:  1989-03-15       Impact factor: 5.157

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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  2 in total

1.  Fine mapping of the dyskeratosis congenita locus in Xq28.

Authors:  S W Knight; T Vulliamy; G L Forni; D Oscier; P J Mason; I Dokal
Journal:  J Med Genet       Date:  1996-12       Impact factor: 6.318

2.  The gene for hereditary bullous dystrophy, X-linked macular type, maps to the Xq27.3-qter region.

Authors:  M Wijker; M J Ligtenberg; F Schoute; J C Defesche; G Pals; P A Bolhuis; H H Ropers; T J Hulsebos; F H Menko; B A van Oost
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025
  2 in total

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