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Basic Life Sciences
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January 1, 1975
Genetic complementation analysis of xeroderma pigmentosum
D Bootsma, E A De Weerd-Kastelein, W J Kleijer, et al.
American Journal of Human Genetics
|
July 1, 1993
Xeroderma pigmentosum complementation group G associated with Cockayne syndrome
W Vermeulen, J Jaeken, N G Jaspers, et al.
Development (Cambridge, England)
|
October 1, 1990
The cellular retinoic-acid-binding protein is expressed in tissues associated with retinoic-acid-induced malformations
M J Vaessen, J H Meijers, D Bootsma, et al.
Mutation Research
|
January 1, 1987
Biological and biochemical consequences of the human ERCC-1 repair gene after transfection into a repair-deficient CHO cell line
M Z Zdzienicka, L Roza, A Westerveld, et al.
Human Heredity
|
January 1, 1974
Genetical studied on the multiple forms of human guanylate kinase in man-chinese hamster somatic cell hybrids
P Meera Khan, W R Los, P L Pearson, et al.
Human Genetics
|
September 10, 1976
Late-replicating ring X-chromosomes identified by R-banding after BrdU pulse. Three new examples of mosaicism 45, XO/46, Xr(X)
A Hagemeijer, J Hoovers, I Hasper-Voogt, et al.
Annals of the New York Academy of Sciences
|
January 1, 1987
The role of the Philadelphia translocation in chronic myelocytic leukemia
G Grosveld, A Hermans, A De Klein, et al.
Cytogenetics and Cell Genetics
|
January 1, 1988
Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients
N G Jaspers, R A Gatti, C Baan, et al.
Mutation Research
|
June 1, 1985
Microinjection of Micrococcus luteus UV-endonuclease restores UV-induced unscheduled DNA synthesis in cells of 9 xeroderma pigmentosum complementation groups
A J de Jonge, W Vermeulen, W Keijzer, et al.
Tsitologiia
|
January 1, 1997
[Decreased survivability and a DNA repair defect in the cells of patients with xeroderma pigmentosum and Cockayne syndrome under the action of radiation and chemical mutagens]
I M Spivak, N M Pleskach, V M Mikhel'son, et al.
Page
of 17
Search research articles
Search
Showing results (71-80 of 165) with videos related to
Sort By:
Page
of 17
Basic Life Sciences
|
January 1, 1975
Genetic complementation analysis of xeroderma pigmentosum
D Bootsma, E A De Weerd-Kastelein, W J Kleijer, et al.
American Journal of Human Genetics
|
July 1, 1993
Xeroderma pigmentosum complementation group G associated with Cockayne syndrome
W Vermeulen, J Jaeken, N G Jaspers, et al.
Development (Cambridge, England)
|
October 1, 1990
The cellular retinoic-acid-binding protein is expressed in tissues associated with retinoic-acid-induced malformations
M J Vaessen, J H Meijers, D Bootsma, et al.
Mutation Research
|
January 1, 1987
Biological and biochemical consequences of the human ERCC-1 repair gene after transfection into a repair-deficient CHO cell line
M Z Zdzienicka, L Roza, A Westerveld, et al.
Human Heredity
|
January 1, 1974
Genetical studied on the multiple forms of human guanylate kinase in man-chinese hamster somatic cell hybrids
P Meera Khan, W R Los, P L Pearson, et al.
Human Genetics
|
September 10, 1976
Late-replicating ring X-chromosomes identified by R-banding after BrdU pulse. Three new examples of mosaicism 45, XO/46, Xr(X)
A Hagemeijer, J Hoovers, I Hasper-Voogt, et al.
Annals of the New York Academy of Sciences
|
January 1, 1987
The role of the Philadelphia translocation in chronic myelocytic leukemia
G Grosveld, A Hermans, A De Klein, et al.
Cytogenetics and Cell Genetics
|
January 1, 1988
Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients
N G Jaspers, R A Gatti, C Baan, et al.
Mutation Research
|
June 1, 1985
Microinjection of Micrococcus luteus UV-endonuclease restores UV-induced unscheduled DNA synthesis in cells of 9 xeroderma pigmentosum complementation groups
A J de Jonge, W Vermeulen, W Keijzer, et al.
Tsitologiia
|
January 1, 1997
[Decreased survivability and a DNA repair defect in the cells of patients with xeroderma pigmentosum and Cockayne syndrome under the action of radiation and chemical mutagens]
I M Spivak, N M Pleskach, V M Mikhel'son, et al.
Page
of 17