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Human Genetics
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December 1, 1994
Determinants of the factor IX mutational spectrum in haemophilia B: an analysis of missense mutations using a multi-domain molecular model of the activated protein
A I Wacey, M Krawczak, V V Kakkar, et al.
Academic Pediatrics
|
November 18, 2020
Differences in Tonsillectomy Utilization by Race/Ethnicity, Type of Health Insurance, and Rurality
Jennifer N Cooper, Swapna Koppera, Emily F Boss, et al.
Plos One
|
July 11, 2015
Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological Sense
Sabine Siegert, Andreas Wolf, David N Cooper, et al.
International Archives of Allergy and Applied Immunology
|
January 1, 1987
Antibody synthesis in the rat liver: an association between antibody-forming cells in the liver and biliary antibodies following intravenous injection of horse erythrocytes
L Carter, P J Barrington, G N Cooper, et al.
Human Genetics
|
January 7, 1998
Homology modelling of the catalytic domain of early mammalian protein C: evolution of structural features
A I Wacey, M Krawczak, G Kemball-Cook, et al.
Human Genetics
|
January 1, 1992
Single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTR gene reliably detects more than one third of non-delta F508 mutations in German cystic fibrosis patients
J Plieth, F Rininsland, M Schlösser, et al.
Journal of Strength and Conditioning Research
|
October 2, 2018
Effects of Lower-Body Muscular Fatigue on Vertical Jump and Balance Performance
Christina N Cooper, Nicole C Dabbs, Judith Davis, et al.
Forensic Science International. Genetics
|
December 20, 2011
How to distinguish genetically between an alleged father and his monozygotic twin: a thought experiment
Michael Krawczak, David N Cooper, Fred Fändrich, et al.
International Journal of Oncology
|
January 26, 1999
Differential expression of endogenous galectin-1 and galectin-3 in human prostate cancer cell lines and effects of overexpressing galectin-1 on cell phenotype
J Ellerhorst, T Nguyen, D N Cooper, et al.
Human Genetics
|
August 1, 1992
A novel homozygous missense mutation in the protein C (PROC) gene causing recurrent venous thrombosis
C B Grundy, M Chisholm, V V Kakkar, et al.
Page
of 144
Search research articles
Search
Showing results (371-380 of 1,438) with videos related to
Sort By:
Page
of 144
Human Genetics
|
December 1, 1994
Determinants of the factor IX mutational spectrum in haemophilia B: an analysis of missense mutations using a multi-domain molecular model of the activated protein
A I Wacey, M Krawczak, V V Kakkar, et al.
Academic Pediatrics
|
November 18, 2020
Differences in Tonsillectomy Utilization by Race/Ethnicity, Type of Health Insurance, and Rurality
Jennifer N Cooper, Swapna Koppera, Emily F Boss, et al.
Plos One
|
July 11, 2015
Mutations Causing Complex Disease May under Certain Circumstances Be Protective in an Epidemiological Sense
Sabine Siegert, Andreas Wolf, David N Cooper, et al.
International Archives of Allergy and Applied Immunology
|
January 1, 1987
Antibody synthesis in the rat liver: an association between antibody-forming cells in the liver and biliary antibodies following intravenous injection of horse erythrocytes
L Carter, P J Barrington, G N Cooper, et al.
Human Genetics
|
January 7, 1998
Homology modelling of the catalytic domain of early mammalian protein C: evolution of structural features
A I Wacey, M Krawczak, G Kemball-Cook, et al.
Human Genetics
|
January 1, 1992
Single-strand conformation polymorphism (SSCP) analysis of exon 11 of the CFTR gene reliably detects more than one third of non-delta F508 mutations in German cystic fibrosis patients
J Plieth, F Rininsland, M Schlösser, et al.
Journal of Strength and Conditioning Research
|
October 2, 2018
Effects of Lower-Body Muscular Fatigue on Vertical Jump and Balance Performance
Christina N Cooper, Nicole C Dabbs, Judith Davis, et al.
Forensic Science International. Genetics
|
December 20, 2011
How to distinguish genetically between an alleged father and his monozygotic twin: a thought experiment
Michael Krawczak, David N Cooper, Fred Fändrich, et al.
International Journal of Oncology
|
January 26, 1999
Differential expression of endogenous galectin-1 and galectin-3 in human prostate cancer cell lines and effects of overexpressing galectin-1 on cell phenotype
J Ellerhorst, T Nguyen, D N Cooper, et al.
Human Genetics
|
August 1, 1992
A novel homozygous missense mutation in the protein C (PROC) gene causing recurrent venous thrombosis
C B Grundy, M Chisholm, V V Kakkar, et al.
Page
of 144