Literature DB >> 2883112

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

E J Mensink, A Thompson, L A Sandkuyl, M E Kraakman, J D Schot, T Espanol, R K Schuurman.   

Abstract

The gene involved in X-linked immunodeficiency with hyperimmunoglobulinemia M (XHM) was localized by the use of nine restriction fragment length polymorphic (RFLP) markers covering the entire X chromosome. Multipoint linkage analysis of RFLP data obtained in a three generation XHM pedigree indicates the Xq24-q27 area around the DXS42 RFLP locus as the most likely localization of the XHM locus.

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Year:  1987        PMID： 2883112     DOI： 10.1007/bf00283057

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  17 in total

1.  Expression of the gene defect in X-linked agammaglobulinemia.

Authors:  M E Conley; P Brown; A R Pickard; R H Buckley; D S Miller; W H Raskind; J W Singer; P J Fialkow
Journal:  N Engl J Med       Date:  1986-08-28       Impact factor: 91.245

Review 2.  The gamma globulins. 3. The antibody deficiency syndromes.

Authors:  F S Rosen; C A Janeway
Journal:  N Engl J Med       Date:  1966-09-29       Impact factor: 91.245

3.  Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP loci.

Authors:  J Ott; E J Mensink; A Thompson; J D Schot; R K Schuurman
Journal:  Hum Genet       Date:  1986-11       Impact factor: 4.132

4.  A strategy to reveal high-frequency RFLPs along the human X chromosome.

Authors:  J Aldridge; L Kunkel; G Bruns; U Tantravahi; M Lalande; T Brewster; E Moreau; M Wilson; W Bromley; T Roderick
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

5.  Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

Authors:  D Drayna; K Davies; D Hartley; J L Mandel; G Camerino; R Williamson; R White
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

6.  The genetic linkage map of the human X chromosome.

Authors:  D Drayna; R White
Journal:  Science       Date:  1985-11-15       Impact factor: 47.728

7.  Dysgammaglobulinemic antibody deficiency syndrome.

Authors:  A S Goldman; S E Ritzmann; E W Houston; S Sidwell; R Bratcher; W C Levin
Journal:  J Pediatr       Date:  1967-01       Impact factor: 4.406

8.  Strategies for multilocus linkage analysis in humans.

Authors:  G M Lathrop; J M Lalouel; C Julier; J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1984-06       Impact factor: 11.205

9.  Genetic heterogeneity in X-linked agammaglobulinemia complicates carrier detection and prenatal diagnosis.

Authors:  E J Mensink; A Thompson; J D Schot; M E Kraakman; L A Sandkuyl; R K Schuurman
Journal:  Clin Genet       Date:  1987-02       Impact factor: 4.438

10.  The site of synthesis of the 19S gamma-globulins in dysgammaglobulinemia.

Authors:  A CRUCHAUD; F S ROSEN; J M CRAIG; C A JANEWAY; D GITLIN
Journal:  J Exp Med       Date:  1962-06-01       Impact factor: 14.307
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  12 in total

1.  Analysis of X-chromosome inactivation in X-linked immunodeficiency with hyper-IgM (HIGM1): evidence for involvement of different hematopoietic cell lineages.

Authors:  L D Notarangelo; O Parolini; A Albertini; M Duse; E Mazzolari; A Plebani; G Camerino; A G Ugazio
Journal:  Hum Genet       Date:  1991-12       Impact factor: 4.132

Review 2.  Genetics of human X-linked immunodeficiency diseases.

Authors:  R W Hendriks; R K Schuurman
Journal:  Clin Exp Immunol       Date:  1991-08       Impact factor: 4.330

Review 3.  The biology of the human ligand for CD40.

Authors:  M K Spriggs; W C Fanslow; R J Armitage; J Belmont
Journal:  J Clin Immunol       Date:  1993-11       Impact factor: 8.317

Review 4.  The hyper-IgM (HIM) syndrome.

Authors:  N Ramesh; M Seki; L D Notarangelo; R S Geha
Journal:  Springer Semin Immunopathol       Date:  1998

Review 5.  Prenatal diagnosis and carrier detection in primary immunodeficiency disorders.

Authors:  Y L Lau; R J Levinsky
Journal:  Arch Dis Child       Date:  1988-07       Impact factor: 3.791

6.  X-linked cleft palate: the gene is localized between polymorphic DNA markers DXYS12 and DXS17.

Authors:  A Ivens; G E Moore; J Chambers; A Arnason; O Jensson; A Bjornsson; R Williamson
Journal:  Hum Genet       Date:  1988-04       Impact factor: 4.132

7.  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

8.  A novel X-linked combined immunodeficiency disease.

Authors:  E G Brooks; F C Schmalstieg; D P Wirt; H M Rosenblatt; L T Adkins; D P Lookingbill; H E Rudloff; T A Rakusan; A S Goldman
Journal:  J Clin Invest       Date:  1990-11       Impact factor: 14.808

9.  Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation.

Authors:  M Teresa de la Morena; David Leonard; Troy R Torgerson; Otavio Cabral-Marques; Mary Slatter; Asghar Aghamohammadi; Sharat Chandra; Luis Murguia-Favela; Francisco A Bonilla; Maria Kanariou; Rongras Damrongwatanasuk; Caroline Y Kuo; Christopher C Dvorak; Isabelle Meyts; Karin Chen; Lisa Kobrynski; Neena Kapoor; Darko Richter; Daniela DiGiovanni; Fatima Dhalla; Evangelia Farmaki; Carsten Speckmann; Teresa Español; Anna Shcherbina; Imelda Celine Hanson; Jiri Litzman; John M Routes; Melanie Wong; Ramsay Fuleihan; Suranjith L Seneviratne; Trudy N Small; Ales Janda; Liliana Bezrodnik; Reinhard Seger; Andrea Gomez Raccio; J David M Edgar; Janet Chou; Jordan K Abbott; Joris van Montfrans; Luis Ignacio González-Granado; Nancy Bunin; Necil Kutukculer; Paul Gray; Gisela Seminario; Srdjan Pasic; Victor Aquino; Christian Wysocki; Hassan Abolhassani; Morna Dorsey; Charlotte Cunningham-Rundles; Alan P Knutsen; John Sleasman; Beatriz Tavares Costa Carvalho; Antonio Condino-Neto; Eyal Grunebaum; Helen Chapel; Hans D Ochs; Alexandra Filipovich; Mort Cowan; Andrew Gennery; Andrew Cant; Luigi D Notarangelo; Chaim M Roifman
Journal:  J Allergy Clin Immunol       Date:  2016-09-30       Impact factor: 10.793

Review 10.  The molecular basis of X-linked immunodeficiency disease.

Authors:  C Kinnon; R Levinsky
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982
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