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The Journal of Allergy and Clinical Immunology
|
May 17, 2011
Mold allergen sensitization in adult asthma according to integrin β3 polymorphisms and Toll-like receptor 2/+596 genotype
Lidwien A M Smit, Emmanuelle Bouzigon, Jean Bousquet, et al.
Plos One
|
January 5, 2012
A genome-wide association study of the Protein C anticoagulant pathway
Georgios Athanasiadis, Alfonso Buil, Juan Carlos Souto, et al.
European Journal of Human Genetics : EJHG
|
June 19, 2008
Genome-wide linkage analysis for identifying quantitative trait loci involved in the regulation of lipoprotein a (Lpa) levels
Sonia López, Alfonso Buil, Jordi Ordoñez, et al.
European Journal of Human Genetics : EJHG
|
June 13, 2013
AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome)
Pierre Cacciagli, Jean-Pierre Desvignes, Nadine Girard, et al.
European Journal of Human Genetics : EJHG
|
June 25, 2002
Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations
Myrna Medlej-Hashim, Mirna Mustapha, Eliane Chouery, et al.
Plos One
|
August 24, 2012
Sex-specific regulation of mitochondrial DNA levels: genome-wide linkage analysis to identify quantitative trait loci
Sonia López, Alfonso Buil, Juan Carlos Souto, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
February 11, 2011
KCNJ6 is associated with adult alcohol dependence and involved in gene × early life stress interactions in adolescent alcohol drinking
Toni-Kim Clarke, Manfred Laucht, Monika Ridinger, et al.
The Journal of Infectious Diseases
|
December 21, 2004
Exhaustive genotyping of the CEM15 (APOBEC3G) gene and absence of association with AIDS progression in a French cohort
Hervé Do, Alexandre Vasilescu, Gora Diop, et al.
Plos Genetics
|
July 15, 2006
Lymphotoxin-alpha gene and risk of myocardial infarction in 6,928 cases and 2,712 controls in the ISIS case-control study
Robert Clarke, Peng Xu, Derrick Bennett, et al.
Human Genetics
|
April 10, 2002
A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25
Mirna Mustapha, Eliane Chouery, Delphine Torchard-Pagnez, et al.
Page
of 45
Search research articles
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Showing results (81-90 of 443) with videos related to
Sort By:
Page
of 45
The Journal of Allergy and Clinical Immunology
|
May 17, 2011
Mold allergen sensitization in adult asthma according to integrin β3 polymorphisms and Toll-like receptor 2/+596 genotype
Lidwien A M Smit, Emmanuelle Bouzigon, Jean Bousquet, et al.
Plos One
|
January 5, 2012
A genome-wide association study of the Protein C anticoagulant pathway
Georgios Athanasiadis, Alfonso Buil, Juan Carlos Souto, et al.
European Journal of Human Genetics : EJHG
|
June 19, 2008
Genome-wide linkage analysis for identifying quantitative trait loci involved in the regulation of lipoprotein a (Lpa) levels
Sonia López, Alfonso Buil, Jordi Ordoñez, et al.
European Journal of Human Genetics : EJHG
|
June 13, 2013
AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome)
Pierre Cacciagli, Jean-Pierre Desvignes, Nadine Girard, et al.
European Journal of Human Genetics : EJHG
|
June 25, 2002
Non-syndromic recessive deafness in Jordan: mapping of a new locus to chromosome 9q34.3 and prevalence of DFNB1 mutations
Myrna Medlej-Hashim, Mirna Mustapha, Eliane Chouery, et al.
Plos One
|
August 24, 2012
Sex-specific regulation of mitochondrial DNA levels: genome-wide linkage analysis to identify quantitative trait loci
Sonia López, Alfonso Buil, Juan Carlos Souto, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology
|
February 11, 2011
KCNJ6 is associated with adult alcohol dependence and involved in gene × early life stress interactions in adolescent alcohol drinking
Toni-Kim Clarke, Manfred Laucht, Monika Ridinger, et al.
The Journal of Infectious Diseases
|
December 21, 2004
Exhaustive genotyping of the CEM15 (APOBEC3G) gene and absence of association with AIDS progression in a French cohort
Hervé Do, Alexandre Vasilescu, Gora Diop, et al.
Plos Genetics
|
July 15, 2006
Lymphotoxin-alpha gene and risk of myocardial infarction in 6,928 cases and 2,712 controls in the ISIS case-control study
Robert Clarke, Peng Xu, Derrick Bennett, et al.
Human Genetics
|
April 10, 2002
A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25
Mirna Mustapha, Eliane Chouery, Delphine Torchard-Pagnez, et al.
Page
of 45