Literature DB >> 12052772

Disease models for every field: workshop on the molecular basis of human congenital lymphocyte disorders.

C I Edvard Smith1.   

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Year:  2002        PMID: 12052772      PMCID: PMC1084151          DOI: 10.1093/embo-reports/kvf117

Source DB:  PubMed          Journal:  EMBO Rep        ISSN: 1469-221X            Impact factor:   8.807


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  4 in total

1.  Constitutively activating mutation in WASP causes X-linked severe congenital neutropenia.

Authors:  K Devriendt; A S Kim; G Mathijs; S G Frints; M Schwartz; J J Van Den Oord; G E Verhoef; M A Boogaerts; J P Fryns; D You; M K Rosen; P Vandenberghe
Journal:  Nat Genet       Date:  2001-03       Impact factor: 38.330

2.  Mutation of a new gene encoding a putative pyrin-like protein causes familial cold autoinflammatory syndrome and Muckle-Wells syndrome.

Authors:  H M Hoffman; J L Mueller; D H Broide; A A Wanderer; R D Kolodner
Journal:  Nat Genet       Date:  2001-11       Impact factor: 38.330

3.  AID is required to initiate Nbs1/gamma-H2AX focus formation and mutations at sites of class switching.

Authors:  Michel C Nussenzweig; André Nussenzweig; Simone Petersen; Rafael Casellas; Bernardo Reina-San-Martin; Hua Tang Chen; Michael J Difilippantonio; Patrick C Wilson; Leif Hanitsch; Arkady Celeste; Masamichi Muramatsuk; Duane R Pilch; Christophe Redon; Thomas Ried; William M Bonner; Tasuku Honjo
Journal:  Nature       Date:  2001-12-06       Impact factor: 49.962

4.  Expression profiling in transformed human B cells: influence of Btk mutations and comparison to B cell lymphomas using filter and oligonucleotide arrays.

Authors:  Tahmina C Islam; Jessica Lindvall; Anders Wennborg; Lars J Brandén; Hodjatallah Rabbani; C I Edvard Smith
Journal:  Eur J Immunol       Date:  2002-04       Impact factor: 5.532

  4 in total

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