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Human Genomics
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December 13, 2012
A new era in the discovery of de novo mutations underlying human genetic disease
Chee-Seng Ku, Vasilis Vasiliou, David N Cooper
Human Mutation
|
April 23, 2013
Patterns and mutational signatures of tandem base substitutions causing human inherited disease
Jian-Min Chen, Claude Férec, David N Cooper
Physiological and Biochemical Zoology : PBZ
|
December 6, 2018
Short-Term Sleep Loss Alters Cytokine Gene Expression in Brain and Peripheral Tissues and Increases Plasma Corticosterone of Zebra Finch (Taeniopygia guttata)
Laken N Cooper, Ila Mishra, Noah T Ashley
Human Genetics
|
June 30, 2006
A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes II: the importance of mRNA secondary structure in assessing the functionality of 3' UTR variants
Jian-Min Chen, Claude Férec, David N Cooper
Psychiatric Medicine
|
January 1, 1986
Sleep disorders in medical illness
B S Dicicco, J N Cooper, R Waldhorn
Human Mutation
|
July 15, 2015
Complex Multiple-Nucleotide Substitution Mutations Causing Human Inherited Disease Reveal Novel Insights into the Action of Translesion Synthesis DNA Polymerases
Jian-Min Chen, Claude Férec, David N Cooper
Journal of Biomedicine & Biotechnology
|
August 1, 2006
LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease: mutation detection bias and multiple mechanisms of target gene disruption
Jian-Min Chen, Claude Férec, David N Cooper
The British Journal of Dermatology
|
June 24, 2006
Utilization of a cryptic noncanonical donor splice site in the KRT14 gene causes a mild form of epidermolysis bullosa simplex
S Han, D N Cooper, P E Bowden
Nucleic Acids Research
|
February 21, 1998
The human gene mutation database
D N Cooper, E V Ball, M Krawczak
Newsweek
|
November 4, 1983
The case of Baby Jane Doe
A Press, N Cooper, M Hager, et al.
Page
of 144
Search research articles
Search
Showing results (201-210 of 1,438) with videos related to
Sort By:
Page
of 144
Human Genomics
|
December 13, 2012
A new era in the discovery of de novo mutations underlying human genetic disease
Chee-Seng Ku, Vasilis Vasiliou, David N Cooper
Human Mutation
|
April 23, 2013
Patterns and mutational signatures of tandem base substitutions causing human inherited disease
Jian-Min Chen, Claude Férec, David N Cooper
Physiological and Biochemical Zoology : PBZ
|
December 6, 2018
Short-Term Sleep Loss Alters Cytokine Gene Expression in Brain and Peripheral Tissues and Increases Plasma Corticosterone of Zebra Finch (Taeniopygia guttata)
Laken N Cooper, Ila Mishra, Noah T Ashley
Human Genetics
|
June 30, 2006
A systematic analysis of disease-associated variants in the 3' regulatory regions of human protein-coding genes II: the importance of mRNA secondary structure in assessing the functionality of 3' UTR variants
Jian-Min Chen, Claude Férec, David N Cooper
Psychiatric Medicine
|
January 1, 1986
Sleep disorders in medical illness
B S Dicicco, J N Cooper, R Waldhorn
Human Mutation
|
July 15, 2015
Complex Multiple-Nucleotide Substitution Mutations Causing Human Inherited Disease Reveal Novel Insights into the Action of Translesion Synthesis DNA Polymerases
Jian-Min Chen, Claude Férec, David N Cooper
Journal of Biomedicine & Biotechnology
|
August 1, 2006
LINE-1 endonuclease-dependent retrotranspositional events causing human genetic disease: mutation detection bias and multiple mechanisms of target gene disruption
Jian-Min Chen, Claude Férec, David N Cooper
The British Journal of Dermatology
|
June 24, 2006
Utilization of a cryptic noncanonical donor splice site in the KRT14 gene causes a mild form of epidermolysis bullosa simplex
S Han, D N Cooper, P E Bowden
Nucleic Acids Research
|
February 21, 1998
The human gene mutation database
D N Cooper, E V Ball, M Krawczak
Newsweek
|
November 4, 1983
The case of Baby Jane Doe
A Press, N Cooper, M Hager, et al.
Page
of 144