Literature DB >> 7236890

Kx: its relationship to chronic granulomatous disease and genetic linkage with Xg.

P Densen, S Wilkinson-Kroovand, G L Mandell, G Sullivan, R Oyen, W L Marsh.   

Abstract

The relationship between neutrophil function and the neutrophil antigen, Kx, as well as the linkage of the gene, Xk, with Xg was examined in a kindred with X-linked chronic granulomatous disease. Four of the eight male siblings had chronic granulomatous disease by clinical history and tests of neutrophil function, and all four had Kx-negative neutrophils. The remaining four were in good health and had normal nitroblue tetrazolium reduction tests. However, one of these latter four had Kx-negative neutrophils that functioned normally. These data suggest that closely linked but distinct genes on the X chromosome code for chronic granulomatous disease and Kx. In addition, close linkage was demonstrated between Xk and Xg, a gene coding for an erythrocyte surface antigen.

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Year:  1981        PMID: 7236890

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  7 in total

1.  X-Linked chronic granulomatous disease: mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase.

Authors:  J Rae; P E Newburger; M C Dinauer; D Noack; P J Hopkins; R Kuruto; J T Curnutte
Journal:  Am J Hum Genet       Date:  1998-06       Impact factor: 11.025

Review 2.  New perspectives in chronic granulomatous disease.

Authors:  R A Ezekowitz; P E Newburger
Journal:  J Clin Immunol       Date:  1988-11       Impact factor: 8.317

3.  Genetic homology and crossing over in the X and Y chromosomes of Mammals.

Authors:  P S Burgoyne
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

4.  DNA linkage analysis of X chromosome-linked chronic granulomatous disease.

Authors:  R L Baehner; L M Kunkel; A P Monaco; J L Haines; P M Conneally; C Palmer; N Heerema; S H Orkin
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

5.  Xp21 DNA microdeletion in a patient with chronic granulomatous disease, retinitis pigmentosa, and McLeod phenotype.

Authors:  G de Saint-Basile; M C Bohler; A Fischer; J Cartron; J L Dufier; C Griscelli; S H Orkin
Journal:  Hum Genet       Date:  1988-09       Impact factor: 4.132

6.  Minor Xp21 chromosome deletion in a male associated with expression of Duchenne muscular dystrophy, chronic granulomatous disease, retinitis pigmentosa, and McLeod syndrome.

Authors:  U Francke; H D Ochs; B de Martinville; J Giacalone; V Lindgren; C Distèche; R A Pagon; M H Hofker; G J van Ommen; P L Pearson
Journal:  Am J Hum Genet       Date:  1985-03       Impact factor: 11.025

7.  Chronic granulomatous disease, the McLeod phenotype and the contiguous gene deletion syndrome-a review.

Authors:  Casey E Watkins; John Litchfield; Eunkyung Song; Gayatri B Jaishankar; Niva Misra; Nikhil Holla; Michelle Duffourc; Guha Krishnaswamy
Journal:  Clin Mol Allergy       Date:  2011-11-23
  7 in total

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