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N M Day

Showing results (91-100 of 126) with videos related to

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Human Molecular Genetics|April 7, 2007
Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patientsTheodosios Kyriakou, David E Pontefract, Enrique Viturro, et al.
European Journal of Human Genetics : EJHG|February 12, 2009
Two British women studies replicated the association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) and BMIYin Yao Shugart, Lina Chen, Ian N M Day, et al.
Lancet (London, England)|December 6, 2005
C-reactive protein and its role in metabolic syndrome: mendelian randomisation studyNicholas J Timpson, Debbie A Lawlor, Roger M Harbord, et al.
Plos One|March 24, 2015
Proxy molecular diagnosis from whole-exome sequencing reveals Papillon-Lefevre syndrome caused by a missense mutation in CTSCA Mesut Erzurumluoglu, Muslim M Alsaadi, Santiago Rodriguez, et al.
Bone|October 18, 2012
Genetic markers of bone and joint health and physical capability in older adults: the HALCyon programmeTamuno Alfred, Yoav Ben-Shlomo, Rachel Cooper, et al.
Laterality|June 23, 2012
Non-replication of an association of Apolipoprotein E2 with sinistralityBrian J Piper, Alia L Yasen, Amy E Taylor, et al.
The Journal of Nutrition|March 8, 2013
Genetic variants influencing biomarkers of nutrition are not associated with cognitive capability in middle-aged and older adultsTamuno Alfred, Yoav Ben-Shlomo, Rachel Cooper, et al.
Clinical Chemistry|November 22, 2012
Very low PSA concentrations and deletions of the KLK3 geneSantiago Rodriguez, Osama A Al-Ghamdi, Kimberley Burrows, et al.
Journal of Medical Genetics|February 3, 2016
A study of common Mendelian disease carriers across ageing British cohorts: meta-analyses reveal heterozygosity for alpha 1-antitrypsin deficiency increases respiratory capacity and heightTeri-Louise North, Yoav Ben-Shlomo, Cyrus Cooper, et al.
Plos One|January 19, 2012
A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: the HALCyon programmeTamuno Alfred, Yoav Ben-Shlomo, Rachel Cooper, et al.
Pageof 13

Showing results (91-100 of 126) with videos related to

Sort By:
Pageof 13
Human Molecular Genetics|April 7, 2007
Functional polymorphism in ABCA1 influences age of symptom onset in coronary artery disease patientsTheodosios Kyriakou, David E Pontefract, Enrique Viturro, et al.
European Journal of Human Genetics : EJHG|February 12, 2009
Two British women studies replicated the association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) and BMIYin Yao Shugart, Lina Chen, Ian N M Day, et al.
Lancet (London, England)|December 6, 2005
C-reactive protein and its role in metabolic syndrome: mendelian randomisation studyNicholas J Timpson, Debbie A Lawlor, Roger M Harbord, et al.
Plos One|March 24, 2015
Proxy molecular diagnosis from whole-exome sequencing reveals Papillon-Lefevre syndrome caused by a missense mutation in CTSCA Mesut Erzurumluoglu, Muslim M Alsaadi, Santiago Rodriguez, et al.
Bone|October 18, 2012
Genetic markers of bone and joint health and physical capability in older adults: the HALCyon programmeTamuno Alfred, Yoav Ben-Shlomo, Rachel Cooper, et al.
Laterality|June 23, 2012
Non-replication of an association of Apolipoprotein E2 with sinistralityBrian J Piper, Alia L Yasen, Amy E Taylor, et al.
The Journal of Nutrition|March 8, 2013
Genetic variants influencing biomarkers of nutrition are not associated with cognitive capability in middle-aged and older adultsTamuno Alfred, Yoav Ben-Shlomo, Rachel Cooper, et al.
Clinical Chemistry|November 22, 2012
Very low PSA concentrations and deletions of the KLK3 geneSantiago Rodriguez, Osama A Al-Ghamdi, Kimberley Burrows, et al.
Journal of Medical Genetics|February 3, 2016
A study of common Mendelian disease carriers across ageing British cohorts: meta-analyses reveal heterozygosity for alpha 1-antitrypsin deficiency increases respiratory capacity and heightTeri-Louise North, Yoav Ben-Shlomo, Cyrus Cooper, et al.
Plos One|January 19, 2012
A multi-cohort study of polymorphisms in the GH/IGF axis and physical capability: the HALCyon programmeTamuno Alfred, Yoav Ben-Shlomo, Rachel Cooper, et al.
Pageof 13