Literature DB >> 1863997

Genetics of human X-linked immunodeficiency diseases.

R W Hendriks1, R K Schuurman.   

Abstract

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Year:  1991        PMID： 1863997      PMCID： PMC1535742          DOI： 10.1111/j.1365-2249.1991.tb05702.x

Source DB:  PubMed          Journal:  Clin Exp Immunol        ISSN： 0009-9104            Impact factor:   4.330


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  92 in total

1.  Immunoglobulin heavy chain gene rearrangements in X-linked agammaglobulinemia.

Authors:  E J Mensink; R K Schuurman; J D Schot; A Thompson; F W Alt
Journal:  Eur J Immunol       Date:  1986-08       Impact factor: 5.532

2.  Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.

Authors:  S P Kwan; L Kunkel; G Bruns; R J Wedgwood; S Latt; F S Rosen
Journal:  J Clin Invest       Date:  1986-02       Impact factor: 14.808

3.  Active X chromosome DNA is unmethylated at eight CCGG sites clustered in a guanine-plus-cytosine-rich island at the 5' end of the gene for phosphoglycerate kinase.

Authors:  D H Keith; J Singer-Sam; A D Riggs
Journal:  Mol Cell Biol       Date:  1986-11       Impact factor: 4.272

4.  Close linkage of hypervariable marker DXS255 to disease locus of Wiskott-Aldrich syndrome.

Authors:  G de Saint Basile; B Arveiler; N J Fraser; Y Boyd; I W Graig; G Griscelli; A Fischer
Journal:  Lancet       Date:  1989-12-02       Impact factor: 79.321

5.  Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia.

Authors:  R W Hendriks; E J Mensink; M E Kraakman; A Thompson; R K Schuurman
Journal:  Hum Genet       Date:  1989-10       Impact factor: 4.132

6.  Localization of the properdin structural locus to Xp11.23-Xp21.1.

Authors:  D Goundis; S M Holt; Y Boyd; K B Reid
Journal:  Genomics       Date:  1989-07       Impact factor: 5.736

7.  Evidence for a defect in "switch" T cells in patients with immunodeficiency and hyperimmunoglobulinemia M.

Authors:  L Mayer; S P Kwan; C Thompson; H S Ko; N Chiorazzi; T Waldmann; F Rosen
Journal:  N Engl J Med       Date:  1986-02-13       Impact factor: 91.245

Review 8.  Inherited enzyme deficiencies and immunodeficiency: adenosine deaminase (ADA) and purine nucleoside phosphorylase (PNP) deficiencies.

Authors:  R Hirschhorn
Journal:  Clin Immunol Immunopathol       Date:  1986-07

9.  X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus.

Authors:  E J Mensink; A Thompson; L A Sandkuyl; M E Kraakman; J D Schot; T Espanol; R K Schuurman
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

10.  Epstein-Barr virus infections in males with the X-linked lymphoproliferative syndrome.

Authors:  H Grierson; D T Purtilo
Journal:  Ann Intern Med       Date:  1987-04       Impact factor: 25.391
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  4 in total

1.  Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locus.

Authors:  R W Hendriks; M E Kraakman; R G Mensink; R K Schuurman
Journal:  Hum Genet       Date:  1991-11       Impact factor: 4.132

2.  Bone marrow cells in X-linked agammaglobulinemia express pre-B-specific genes (lambda-like and V pre-B) and present immunoglobulin V-D-J gene usage strongly biased to a fetal-like repertoire.

Authors:  M Milili; F Le Deist; G de Saint-Basile; A Fischer; M Fougereau; C Schiff
Journal:  J Clin Invest       Date:  1993-04       Impact factor: 14.808

3.  Mapping of the X linked form of hyper IgM syndrome (HIGM1)

Authors:  M Padayachee; R J Levinsky; C Kinnon; A Finn; C McKeown; C Feighery; L D Notarangelo; R W Hendriks; A P Read; S Malcolm
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

4.  X chromosome inactivation analysis to distinguish sporadic cases of X-linked agammaglobulinaemia from common variable immunodeficiency.

Authors:  I Tsuge; H Matsuoka; T Abe; Y Kamachi; S Torii
Journal:  Eur J Pediatr       Date:  1993-11       Impact factor: 3.183
  4 in total

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