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Nijmegen breakage syndrome

Tauchi H, Matsuura S, Kobayashi J, Sakamoto S, Komatsu K (2002) Nijmegen breakage syndrome gene, NBSl, molecular links to factors for genome stability. Oncogene 21(58) 8967—8980 Taylor SS (1982) The in vitro phosphorylation of chromatin by die catalytic subunit of cAMP-dependent... [Pg.335]

Nlbrln, a novel DNA double-strand break repair protein, Is mutated In Nijmegen breakage syndrome... [Pg.19]

NBS1 Nijmegen breakage syndrome Processing of dsDNA breaks Lymphomas, brain... [Pg.583]

Nijmegen breakage syndrome (NBS) is associated with defects in NBSl involved in homologous recombination. The patients display an excessively high risk for the development of lymphatic tumors, immunodeficiency, and chromosomal instabihty as well as microcephaly and growth retardation [77]. [Pg.163]

See other pages where Nijmegen breakage syndrome is mentioned: [Pg.320]    [Pg.328]    [Pg.329]    [Pg.215]    [Pg.472]    [Pg.320]    [Pg.154]    [Pg.172]    [Pg.92]    [Pg.122]    [Pg.134]    [Pg.344]    [Pg.260]    [Pg.320]    [Pg.328]    [Pg.329]    [Pg.215]    [Pg.472]    [Pg.320]    [Pg.154]    [Pg.172]    [Pg.92]    [Pg.122]    [Pg.134]    [Pg.344]    [Pg.260]   
See also in sourсe #XX -- [ Pg.472 ]

See also in sourсe #XX -- [ Pg.163 ]

See also in sourсe #XX -- [ Pg.92 ]



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Nijmegen

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