Zobrazeno 1 - 5
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pro vyhledávání: '"M K, Shivji"'
Publikováno v:
Methods in molecular biology (Clifton, N.J.). 113
Publikováno v:
The Journal of biological chemistry. 269(36)
A predominant form of the inherited syndrome xeroderma pigmentosum is genetic complementation group C (XP-C). XP-C cells are defective in DNA nucleotide excision repair in the bulk of the genome but can repair transcribed strands of active genes. An
Autor:
C M, Price, F, Rassool, M K, Shivji, J, Gow, C J, Tew, C, Haworth, J M, Goldman, L M, Wiedemann
Publikováno v:
Blood. 72:1829-1832
The Philadelphia (Ph) translocation t(9;22)(q34;q11) occurs frequently in chronic myeloid leukemia (CML) but is less common in acute lymphoblastic leukemia (ALL) and rare in acute myeloid leukemia (AML). In most cases of CML and some cases of Ph+ ALL
Publikováno v:
Oncogene. 3(2)
Approximately 5% of children and 10-20% of adults with acute lymphoblastic leukaemia (ALL) have a chromosome translocation t(9;22) which at the cytogenetic level appears identical to that in chronic myeloid leukaemia (CML). The t(9;22) translocation
Publikováno v:
Haematology and blood transfusion. 32