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Mutation Research
|
March 27, 2001
Complementation of chromosomal aberrations in AT/NBS hybrids: inadequacy of RDS as an endpoint in complementation studies with immortal NBS cells
M Kraakman-van der Zwet, W J Overkamp, N G Jaspers, et al.
Cancer Research
|
March 15, 1990
Effects of microinjected photoreactivating enzyme on thymine dimer removal and DNA repair synthesis in normal human and xeroderma pigmentosum fibroblasts
L Roza, W Vermeulen, J B Bergen Henegouwen, et al.
Clinical Genetics
|
September 1, 1979
Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair
D J Halley, W Keijzer, N G Jaspers, et al.
Journal of Medical Genetics
|
July 1, 1996
Xeroderma pigmentosum--Cockayne syndrome complex: a further case
B C Hamel, A Raams, A R Schuitema-Dijkstra, et al.
Human Mutation
|
October 29, 1998
ATM germline mutations in classical ataxia-telangiectasia patients in the Dutch population
A Broeks, A de Klein, A N Floore, et al.
American Journal of Human Genetics
|
August 1, 1989
ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome
C J Curry, P O'Lague, J Tsai, et al.
Mutation Research
|
September 1, 1995
A novel type of X-ray-sensitive Chinese hamster cell mutant with radioresistant DNA synthesis and hampered DNA double-strand break repair
G W Verhaegh, W Jongmans, B Morolli, et al.
Nature
|
December 8, 1988
Localization of an ataxia-telangiectasia gene to chromosome 11q22-23
R A Gatti, I Berkel, E Boder, et al.
Nature Genetics
|
March 10, 2001
A temperature-sensitive disorder in basal transcription and DNA repair in humans
W Vermeulen, S Rademakers, N G Jaspers, et al.
The British Journal of Dermatology
|
December 15, 2010
Narrowband ultraviolet B inhibits innate cytosolic double-stranded RNA receptors in psoriatic skin and keratinocytes
E Rácz, E P Prens, M Kant, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 71) with videos related to
Sort By:
Page
of 8
Mutation Research
|
March 27, 2001
Complementation of chromosomal aberrations in AT/NBS hybrids: inadequacy of RDS as an endpoint in complementation studies with immortal NBS cells
M Kraakman-van der Zwet, W J Overkamp, N G Jaspers, et al.
Cancer Research
|
March 15, 1990
Effects of microinjected photoreactivating enzyme on thymine dimer removal and DNA repair synthesis in normal human and xeroderma pigmentosum fibroblasts
L Roza, W Vermeulen, J B Bergen Henegouwen, et al.
Clinical Genetics
|
September 1, 1979
Prenatal diagnosis of xeroderma pigmentosum (group C) using assays of unscheduled DNA synthesis and postreplication repair
D J Halley, W Keijzer, N G Jaspers, et al.
Journal of Medical Genetics
|
July 1, 1996
Xeroderma pigmentosum--Cockayne syndrome complex: a further case
B C Hamel, A Raams, A R Schuitema-Dijkstra, et al.
Human Mutation
|
October 29, 1998
ATM germline mutations in classical ataxia-telangiectasia patients in the Dutch population
A Broeks, A de Klein, A N Floore, et al.
American Journal of Human Genetics
|
August 1, 1989
ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome
C J Curry, P O'Lague, J Tsai, et al.
Mutation Research
|
September 1, 1995
A novel type of X-ray-sensitive Chinese hamster cell mutant with radioresistant DNA synthesis and hampered DNA double-strand break repair
G W Verhaegh, W Jongmans, B Morolli, et al.
Nature
|
December 8, 1988
Localization of an ataxia-telangiectasia gene to chromosome 11q22-23
R A Gatti, I Berkel, E Boder, et al.
Nature Genetics
|
March 10, 2001
A temperature-sensitive disorder in basal transcription and DNA repair in humans
W Vermeulen, S Rademakers, N G Jaspers, et al.
The British Journal of Dermatology
|
December 15, 2010
Narrowband ultraviolet B inhibits innate cytosolic double-stranded RNA receptors in psoriatic skin and keratinocytes
E Rácz, E P Prens, M Kant, et al.
Page
of 8