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Clinical Genetics
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June 2, 2007
Constitutive deficiency in DNA mismatch repair: is it time for Lynch III?
K E A Felton, D M Gilchrist, S E Andrew
Oncogene
|
December 7, 2005
Msh2 deficiency leads to chromosomal abnormalities, centrosome amplification, and telomere capping defect
M R Campbell, Y Wang, S E Andrew, et al.
Clinical Genetics
|
June 2, 2007
Constitutive deficiency in DNA mismatch repair
K E A Felton, D M Gilchrist, S E Andrew
Mutation Research
|
July 7, 1999
Comparison of selectable and plaque assay systems to detect menadione- and UV-induced lacI mutations in mammalian cells
S E Andrew, L Hsiao, K Milhausen, et al.
Veterinary Ophthalmology
|
December 3, 2003
Effect of topical tropicamide on tear production as measured by Schirmer's tear test in normal dogs and cats
D L Margadant, K Kirkby, S E Andrew, et al.
Clinical Genetics
|
March 22, 2001
The "flap" endonuclease gene FEN1 is excluded as a candidate gene implicated in the CAG repeat expansion underlying Huntington disease
C J Otto, E Almqvist, M R Hayden, et al.
Carcinogenesis
|
January 3, 2001
Candidate mutator genes in mismatch repair-deficient thymic lymphomas: no evidence of mutations in the DNA polymerase delta gene
M R Campbell, T Y Thang, F R Jirik, et al.
American Journal of Veterinary Research
|
May 1, 2001
Density of corneal endothelial cells and corneal thickness in eyes of euthanatized horses
S E Andrew, D T Ramsey, J G Hauptman, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 22, 1998
Tumors of DNA mismatch repair-deficient hosts exhibit dramatic increases in genomic instability
A Baross-Francis, S E Andrew, J E Penney, et al.
Human Molecular Genetics
|
June 1, 1993
A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease
Y P Goldberg, S E Andrew, L A Clarke, et al.
Page
of 6
Search research articles
Search
Showing results (11-20 of 53) with videos related to
Sort By:
Page
of 6
Clinical Genetics
|
June 2, 2007
Constitutive deficiency in DNA mismatch repair: is it time for Lynch III?
K E A Felton, D M Gilchrist, S E Andrew
Oncogene
|
December 7, 2005
Msh2 deficiency leads to chromosomal abnormalities, centrosome amplification, and telomere capping defect
M R Campbell, Y Wang, S E Andrew, et al.
Clinical Genetics
|
June 2, 2007
Constitutive deficiency in DNA mismatch repair
K E A Felton, D M Gilchrist, S E Andrew
Mutation Research
|
July 7, 1999
Comparison of selectable and plaque assay systems to detect menadione- and UV-induced lacI mutations in mammalian cells
S E Andrew, L Hsiao, K Milhausen, et al.
Veterinary Ophthalmology
|
December 3, 2003
Effect of topical tropicamide on tear production as measured by Schirmer's tear test in normal dogs and cats
D L Margadant, K Kirkby, S E Andrew, et al.
Clinical Genetics
|
March 22, 2001
The "flap" endonuclease gene FEN1 is excluded as a candidate gene implicated in the CAG repeat expansion underlying Huntington disease
C J Otto, E Almqvist, M R Hayden, et al.
Carcinogenesis
|
January 3, 2001
Candidate mutator genes in mismatch repair-deficient thymic lymphomas: no evidence of mutations in the DNA polymerase delta gene
M R Campbell, T Y Thang, F R Jirik, et al.
American Journal of Veterinary Research
|
May 1, 2001
Density of corneal endothelial cells and corneal thickness in eyes of euthanatized horses
S E Andrew, D T Ramsey, J G Hauptman, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 22, 1998
Tumors of DNA mismatch repair-deficient hosts exhibit dramatic increases in genomic instability
A Baross-Francis, S E Andrew, J E Penney, et al.
Human Molecular Genetics
|
June 1, 1993
A PCR method for accurate assessment of trinucleotide repeat expansion in Huntington disease
Y P Goldberg, S E Andrew, L A Clarke, et al.
Page
of 6