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Cancer Genetics and Cytogenetics
|
January 1, 1987
Sister chromatid exchanges, hyperdiploidy and chromosomal rearrangements studied in cells from melanoma-prone individuals belonging to families with the dysplastic nevus syndrome
N G Jaspers, E J Roza-de Jongh, I G Donselaar, et al.
The EMBO Journal
|
April 1, 1994
Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH)
A J van Vuuren, W Vermeulen, L Ma, et al.
Cell
|
December 28, 1999
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder
G S Stewart, R S Maser, T Stankovic, et al.
Human Genetics
|
March 1, 1992
Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome
Y Ziv, M Frydman, E Lange, et al.
Mutation Research
|
June 23, 1999
Immortalization and characterization of Nijmegen Breakage syndrome fibroblasts
M Kraakman-van der Zwet, W J Overkamp, A A Friedl, et al.
Mutation Research
|
October 18, 1996
The defect in the AT-like hamster cell mutants is complemented by mouse chromosome 9 but not by any of the human chromosomes
W Jongmans, G W Verhaegh, N G Jaspers, et al.
Mutation Research
|
June 24, 1998
Impaired DNA repair capacity in skin fibroblasts from various hereditary cancer-prone syndromes
P J Abrahams, A Houweling, P D Cornelissen-Steijger, et al.
Cell
|
September 6, 1996
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease
A M Sijbers, W L de Laat, R R Ariza, et al.
Biochemical Society Transactions
|
February 1, 1997
Mammalian nucleotide excision repair and syndromes
W Vermeulen, J de Boer, E Citterio, et al.
Human Molecular Genetics
|
April 1, 1996
Predominance of null mutations in ataxia-telangiectasia
S Gilad, R Khosravi, D Shkedy, et al.
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of 8
Search research articles
Search
Showing results (61-70 of 71) with videos related to
Sort By:
Page
of 8
Cancer Genetics and Cytogenetics
|
January 1, 1987
Sister chromatid exchanges, hyperdiploidy and chromosomal rearrangements studied in cells from melanoma-prone individuals belonging to families with the dysplastic nevus syndrome
N G Jaspers, E J Roza-de Jongh, I G Donselaar, et al.
The EMBO Journal
|
April 1, 1994
Correction of xeroderma pigmentosum repair defect by basal transcription factor BTF2 (TFIIH)
A J van Vuuren, W Vermeulen, L Ma, et al.
Cell
|
December 28, 1999
The DNA double-strand break repair gene hMRE11 is mutated in individuals with an ataxia-telangiectasia-like disorder
G S Stewart, R S Maser, T Stankovic, et al.
Human Genetics
|
March 1, 1992
Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome
Y Ziv, M Frydman, E Lange, et al.
Mutation Research
|
June 23, 1999
Immortalization and characterization of Nijmegen Breakage syndrome fibroblasts
M Kraakman-van der Zwet, W J Overkamp, A A Friedl, et al.
Mutation Research
|
October 18, 1996
The defect in the AT-like hamster cell mutants is complemented by mouse chromosome 9 but not by any of the human chromosomes
W Jongmans, G W Verhaegh, N G Jaspers, et al.
Mutation Research
|
June 24, 1998
Impaired DNA repair capacity in skin fibroblasts from various hereditary cancer-prone syndromes
P J Abrahams, A Houweling, P D Cornelissen-Steijger, et al.
Cell
|
September 6, 1996
Xeroderma pigmentosum group F caused by a defect in a structure-specific DNA repair endonuclease
A M Sijbers, W L de Laat, R R Ariza, et al.
Biochemical Society Transactions
|
February 1, 1997
Mammalian nucleotide excision repair and syndromes
W Vermeulen, J de Boer, E Citterio, et al.
Human Molecular Genetics
|
April 1, 1996
Predominance of null mutations in ataxia-telangiectasia
S Gilad, R Khosravi, D Shkedy, et al.
Page
of 8