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Experimental Cell Research
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April 1, 1987
Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1
W Keijzer, M Stefanini, D Bootsma, et al.
The Journal of Investigative Dermatology
|
November 1, 1974
The genetic defect in the de Sanctis-Cacchione syndrome
V M Der Kaloustian, E A de Weerd-Kastelein EA+DEWEERDAAKATELEIN, W J Kleijer, et al.
Mutation Research
|
December 1, 1973
UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotes
W J Kleijer, E A de Weerd-Kastelein, M L Sluyter, et al.
Cancer Research
|
March 1, 1989
Establishment and characterization of a melanoma cell line from a xeroderma pigmentosum patient: activation of N-ras at a potential pyrimidine dimer site
W Keijzer, M P Mulder, J C Langeveld, et al.
Oncogene
|
November 1, 1989
Activated ras genes in human seminoma: evidence for tumor heterogeneity
M P Mulder, W Keijzer, A Verkerk, 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.
Mutation Research
|
December 1, 1975
Five complementation groups in xeroderma pigmentosum
K H Kraemer, E A De Weerd-Kastelein, J H Robbins, et al.
Cancer Research
|
March 1, 1977
Repair of ultraviolet light damage in a variety of human fibroblast cell strains
A R Lehmann, S Kirk-Bell, C F Arlett, et al.
Mutation Research
|
August 1, 1979
A seventh complementation group in excision-deficient xeroderma pigmentosum
W Keijzer, N G Jaspers, P J Abrahams, et al.
Human Genetics
|
January 1, 1983
Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies
R A Barneveld, W Keijzer, F P Tegelaers, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 33) with videos related to
Sort By:
Page
of 4
Experimental Cell Research
|
April 1, 1987
Localization of a gene involved in complementation of the defect in xeroderma pigmentosum group A cells on human chromosome 1
W Keijzer, M Stefanini, D Bootsma, et al.
The Journal of Investigative Dermatology
|
November 1, 1974
The genetic defect in the de Sanctis-Cacchione syndrome
V M Der Kaloustian, E A de Weerd-Kastelein EA+DEWEERDAAKATELEIN, W J Kleijer, et al.
Mutation Research
|
December 1, 1973
UV-induced DNA repair synthesis in cells of patients with different forms of xeroderma pigmentosum and of heterozygotes
W J Kleijer, E A de Weerd-Kastelein, M L Sluyter, et al.
Cancer Research
|
March 1, 1989
Establishment and characterization of a melanoma cell line from a xeroderma pigmentosum patient: activation of N-ras at a potential pyrimidine dimer site
W Keijzer, M P Mulder, J C Langeveld, et al.
Oncogene
|
November 1, 1989
Activated ras genes in human seminoma: evidence for tumor heterogeneity
M P Mulder, W Keijzer, A Verkerk, 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.
Mutation Research
|
December 1, 1975
Five complementation groups in xeroderma pigmentosum
K H Kraemer, E A De Weerd-Kastelein, J H Robbins, et al.
Cancer Research
|
March 1, 1977
Repair of ultraviolet light damage in a variety of human fibroblast cell strains
A R Lehmann, S Kirk-Bell, C F Arlett, et al.
Mutation Research
|
August 1, 1979
A seventh complementation group in excision-deficient xeroderma pigmentosum
W Keijzer, N G Jaspers, P J Abrahams, et al.
Human Genetics
|
January 1, 1983
Assignment of the gene coding for human beta-glucocerebrosidase to the region q21-q31 of chromosome 1 using monoclonal antibodies
R A Barneveld, W Keijzer, F P Tegelaers, et al.
Page
of 4