Literature DB >> 3879134

The coexistence of IgA deficiency and 21-hydroxylase deficiency marked by specific MHC supratypes.

T J Cobain, M S Stuckey, J McCluskey, A N Wilton, A Gedeon, M J Garlepp, F T Christiansen, R L Dawkins.   

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Year:  1985        PMID: 3879134     DOI: 10.1111/j.1749-6632.1985.tb14593.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


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  5 in total

1.  Rearrangement of 21-hydroxylase genes in disease-associated MHC supratypes.

Authors:  M J Garlepp; A N Wilton; R L Dawkins; P C White
Journal:  Immunogenetics       Date:  1986       Impact factor: 2.846

2.  Class III gene rearrangements in Thai/Chinese supratypes containing null or defective C4 alleles.

Authors:  P H Kay; E Martin; R L Dawkins; P Charoenwong
Journal:  Immunogenetics       Date:  1988       Impact factor: 2.846

Review 3.  Physiology of IgA and IgA deficiency.

Authors:  C Cunningham-Rundles
Journal:  J Clin Immunol       Date:  2001-09       Impact factor: 8.317

4.  The immunological detection of a 21-OH deficiency mutation HLA supratype.

Authors:  M S Pollack; B Keenan; F T Christiansen; T J Cobain; R L Dawkins; G Clayton
Journal:  Am J Hum Genet       Date:  1986-05       Impact factor: 11.025

5.  Family studies of IgA deficiency.

Authors:  A N Wilton; T J Cobain; R L Dawkins
Journal:  Immunogenetics       Date:  1985       Impact factor: 2.846

  5 in total

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