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Mark Lathrop

Showing results (141-150 of 443) with videos related to

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American Journal of Human Genetics|October 3, 2015
Imputation of KIR Types from SNP Variation DataDamjan Vukcevic, James A Traherne, Sigrid Næss, et al.
Nature Medicine|December 21, 2004
The clock gene Per2 influences the glutamatergic system and modulates alcohol consumptionRainer Spanagel, Gurudutt Pendyala, Carolina Abarca, et al.
International Journal of Cancer|April 21, 2015
Integrated pathway and epistasis analysis reveals interactive effect of genetic variants at TERF1 and AFAP1L2 loci on melanoma riskMyriam Brossard, Shenying Fang, Amaury Vaysse, et al.
Thorax|October 5, 2018
Interactive effect between ATPase-related genes and early-life tobacco smoke exposure on bronchial hyper-responsiveness detected in asthma-ascertained familiesMarie-Hélène Dizier, Patricia Margaritte-Jeannin, Lucile Pain, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1Saber Masmoudi, Abdelaziz Tlili, Marja Majava, et al.
Mechanisms of Ageing and Development|July 12, 2011
A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individualsAlmut Nebel, Rabea Kleindorp, Amke Caliebe, et al.
The European Respiratory Journal|January 23, 2016
Interaction between the DNAH9 gene and early smoke exposure in bronchial hyperresponsivenessMarie-Hélène Dizier, Rachel Nadif, Patricia Margaritte-Jeannin, et al.
Oncotarget|June 5, 2018
Aberration hubs in protein interaction networks highlight actionable targets in cancerMehran Karimzadeh, Pouria Jandaghi, Andreas I Papadakis, et al.
Nature Genetics|June 29, 2006
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathySedigheh Delmaghani, Francisco J del Castillo, Vincent Michel, et al.
Plos One|November 10, 2010
Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11Patrice Roll, Damien Sanlaville, Jennifer Cillario, et al.
Pageof 45

Showing results (141-150 of 443) with videos related to

Sort By:
Pageof 45
American Journal of Human Genetics|October 3, 2015
Imputation of KIR Types from SNP Variation DataDamjan Vukcevic, James A Traherne, Sigrid Næss, et al.
Nature Medicine|December 21, 2004
The clock gene Per2 influences the glutamatergic system and modulates alcohol consumptionRainer Spanagel, Gurudutt Pendyala, Carolina Abarca, et al.
International Journal of Cancer|April 21, 2015
Integrated pathway and epistasis analysis reveals interactive effect of genetic variants at TERF1 and AFAP1L2 loci on melanoma riskMyriam Brossard, Shenying Fang, Amaury Vaysse, et al.
Thorax|October 5, 2018
Interactive effect between ATPase-related genes and early-life tobacco smoke exposure on bronchial hyper-responsiveness detected in asthma-ascertained familiesMarie-Hélène Dizier, Patricia Margaritte-Jeannin, Lucile Pain, et al.
European Journal of Human Genetics : EJHG|March 14, 2003
Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1Saber Masmoudi, Abdelaziz Tlili, Marja Majava, et al.
Mechanisms of Ageing and Development|July 12, 2011
A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individualsAlmut Nebel, Rabea Kleindorp, Amke Caliebe, et al.
The European Respiratory Journal|January 23, 2016
Interaction between the DNAH9 gene and early smoke exposure in bronchial hyperresponsivenessMarie-Hélène Dizier, Rachel Nadif, Patricia Margaritte-Jeannin, et al.
Oncotarget|June 5, 2018
Aberration hubs in protein interaction networks highlight actionable targets in cancerMehran Karimzadeh, Pouria Jandaghi, Andreas I Papadakis, et al.
Nature Genetics|June 29, 2006
Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathySedigheh Delmaghani, Francisco J del Castillo, Vincent Michel, et al.
Plos One|November 10, 2010
Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11Patrice Roll, Damien Sanlaville, Jennifer Cillario, et al.
Pageof 45