Literature DB >> 19731800

V(D)J recombination deficiencies.

Jean-Pierre de Villartay1.   

Abstract

V(D)J recombination not only comprises the molecular mechanism that insures diversity of the immune system but also constitutes a critical checkpoint in the developmental program of B- and T-lymphocytes. The analysis of human patients with Severe Combined Immune Deficiency (SCID) has contributed to the understanding of the biochemistry of the V(D)J recombination reaction. The molecular study V(D)J recombination settings in humans, mice and in cellular mutants has allowed to unravel the process of Non Homologous End Joining (NHEJ), one of the key pathway that insure proper repair of DNA double strand breaks (dsb), whether they occur during V(D)J recombination or secondary to other DNA injuries. Two NHEJ factors, Artemis and Cernunnos, were indeed discovered through the study of human V(D)J recombination defective human SCID patients.

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Year:  2009        PMID: 19731800     DOI: 10.1007/978-1-4419-0296-2_4

Source DB:  PubMed          Journal:  Adv Exp Med Biol        ISSN: 0065-2598            Impact factor:   2.622


  30 in total

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7.  Severe combined immunodeficiency in Greek children over a 20-year period: rarity of γc-chain deficiency (X-linked) type.

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Review 8.  Stem cell transplantation for primary immunodeficiency diseases: the North American experience.

Authors:  Sung-Yun Pai; Morton J Cowan
Journal:  Curr Opin Allergy Clin Immunol       Date:  2014-12

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Journal:  J Immunol       Date:  2015-08-28       Impact factor: 5.422

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