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Mark Lathrop

Showing results (161-170 of 443) with videos related to

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Cell Reports|February 21, 2020
The Natural Metabolite 4-Cresol Improves Glucose Homeostasis and Enhances β-Cell FunctionFrancois Brial, Fawaz Alzaid, Kazuhiro Sonomura, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 18, 2010
Genetic risk profiles identify different molecular etiologies for gliomaMatthias Simon, Fay J Hosking, Yannick Marie, et al.
American Journal of Human Genetics|September 10, 2013
Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatusPierre Cacciagli, Julie Sutera-Sardo, Ana Borges-Correia, et al.
Plos One|June 16, 2011
Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analysesChikashi Terao, Koichiro Ohmura, Masaki Katayama, et al.
Blood|March 13, 2009
Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approachDavid-Alexandre Trégouët, Simon Heath, Noémie Saut, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 21, 2007
European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategyLise Tarnow, Per-Henrik Groop, Samy Hadjadj, et al.
Diabetes|June 29, 2004
Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndromePamela J Kaisaki, Marc Delépine, Peng Y Woon, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 27, 2013
Using genetic proxies for lifecourse sun exposure to assess the causal relationship of sun exposure with circulating vitamin d and prostate cancer riskCarolina Bonilla, Rebecca Gilbert, John P Kemp, et al.
International Journal of Cancer|June 28, 2016
A comprehensive genome-wide analysis of melanoma Breslow thickness identifies interaction between CDC42 and SCIN genetic variantsAmaury Vaysse, Shenying Fang, Myriam Brossard, et al.
The Journal of Allergy and Clinical Immunology|February 22, 2026
Functional assessment of a convergent gene network underlying allergic diseases and IgEPradeep Eranti, Raphaël Vernet, Christophe Linhard, et al.
Pageof 45

Showing results (161-170 of 443) with videos related to

Sort By:
Pageof 45
Cell Reports|February 21, 2020
The Natural Metabolite 4-Cresol Improves Glucose Homeostasis and Enhances β-Cell FunctionFrancois Brial, Fawaz Alzaid, Kazuhiro Sonomura, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|September 18, 2010
Genetic risk profiles identify different molecular etiologies for gliomaMatthias Simon, Fay J Hosking, Yannick Marie, et al.
American Journal of Human Genetics|September 10, 2013
Mutations in BCAP31 cause a severe X-linked phenotype with deafness, dystonia, and central hypomyelination and disorganize the Golgi apparatusPierre Cacciagli, Julie Sutera-Sardo, Ana Borges-Correia, et al.
Plos One|June 16, 2011
Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analysesChikashi Terao, Koichiro Ohmura, Masaki Katayama, et al.
Blood|March 13, 2009
Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approachDavid-Alexandre Trégouët, Simon Heath, Noémie Saut, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|August 21, 2007
European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategyLise Tarnow, Per-Henrik Groop, Samy Hadjadj, et al.
Diabetes|June 29, 2004
Polymorphisms in type II SH2 domain-containing inositol 5-phosphatase (INPPL1, SHIP2) are associated with physiological abnormalities of the metabolic syndromePamela J Kaisaki, Marc Delépine, Peng Y Woon, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 27, 2013
Using genetic proxies for lifecourse sun exposure to assess the causal relationship of sun exposure with circulating vitamin d and prostate cancer riskCarolina Bonilla, Rebecca Gilbert, John P Kemp, et al.
International Journal of Cancer|June 28, 2016
A comprehensive genome-wide analysis of melanoma Breslow thickness identifies interaction between CDC42 and SCIN genetic variantsAmaury Vaysse, Shenying Fang, Myriam Brossard, et al.
The Journal of Allergy and Clinical Immunology|February 22, 2026
Functional assessment of a convergent gene network underlying allergic diseases and IgEPradeep Eranti, Raphaël Vernet, Christophe Linhard, et al.
Pageof 45