Search research articles
Contact Us
Filters
Showing results (141-150 of 443) with videos related to
Page
of 45
Sort By:
American Journal of Human Genetics
|
October 3, 2015
Imputation of KIR Types from SNP Variation Data
Damjan Vukcevic, James A Traherne, Sigrid Næss, et al.
Nature Medicine
|
December 21, 2004
The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption
Rainer 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 risk
Myriam 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 families
Marie-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 1p13.3-22.1
Saber 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 individuals
Almut 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 hyperresponsiveness
Marie-Hélène Dizier, Rachel Nadif, Patricia Margaritte-Jeannin, et al.
Oncotarget
|
June 5, 2018
Aberration hubs in protein interaction networks highlight actionable targets in cancer
Mehran 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 neuropathy
Sedigheh 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 16p11
Patrice Roll, Damien Sanlaville, Jennifer Cillario, et al.
Page
of 45
Search research articles
Search
Showing results (141-150 of 443) with videos related to
Sort By:
Page
of 45
American Journal of Human Genetics
|
October 3, 2015
Imputation of KIR Types from SNP Variation Data
Damjan Vukcevic, James A Traherne, Sigrid Næss, et al.
Nature Medicine
|
December 21, 2004
The clock gene Per2 influences the glutamatergic system and modulates alcohol consumption
Rainer 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 risk
Myriam 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 families
Marie-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 1p13.3-22.1
Saber 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 individuals
Almut 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 hyperresponsiveness
Marie-Hélène Dizier, Rachel Nadif, Patricia Margaritte-Jeannin, et al.
Oncotarget
|
June 5, 2018
Aberration hubs in protein interaction networks highlight actionable targets in cancer
Mehran 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 neuropathy
Sedigheh 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 16p11
Patrice Roll, Damien Sanlaville, Jennifer Cillario, et al.
Page
of 45