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D PATERSON

Showing results (461-470 of 540) with videos related to

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Journal of the American Society of Nephrology : JASN|May 20, 2017
Polycystic Kidney Disease without an Apparent Family HistoryIoan-Andrei Iliuta, Vinusha Kalatharan, Kairong Wang, et al.
The Canadian Journal of Cardiology|October 13, 2024
Challenges in the Evaluation of Aortic Stenosis: A Guide to Multimodal ImagingMichael-Roy Durr, Ian G Burwash, Anahita Tavoosi, et al.
Science (New York, N.Y.)|January 8, 2005
Expanded repeat in canine epilepsyHannes Lohi, Edwin J Young, Susan N Fitzmaurice, et al.
Gene|September 20, 2022
Role of 19 SNPs in 10 genes with type 2 diabetes in the Pakistani populationNetasha Khan, Andrew D Paterson, Delnaz Roshandel, et al.
The Journal of Clinical Endocrinology and Metabolism|September 16, 2020
Genome-Wide Association for HbA1c in Malay Identified Deletion on SLC4A1 that Influences HbA1c Independent of GlycemiaJin-Fang Chai, Shih-Ling Kao, Chaolong Wang, et al.
Arthritis Research & Therapy|September 12, 2008
Reduced proportions of natural killer T cells are present in the relatives of lupus patients and are associated with autoimmunityJoan Wither, Yong-chun Cai, Sooyeol Lim, et al.
Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
BMJ Open Diabetes Research & Care|January 16, 2026
Association of genetic variation with age at diagnosis in type 1 diabetesCharlotte E Vollenbrock, Delnaz Roshandel, Kristine E Lee, et al.
American Journal of Medical Genetics|December 20, 2000
Long repeat tracts at SCA8 in major psychosisJ B Vincent, Q P Yuan, M Schalling, et al.
Diabetologia|February 7, 2018
Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetesDelnaz Roshandel, Rose Gubitosi-Klug, Shelley B Bull, et al.
Pageof 54

Showing results (461-470 of 540) with videos related to

Sort By:
Pageof 54
Journal of the American Society of Nephrology : JASN|May 20, 2017
Polycystic Kidney Disease without an Apparent Family HistoryIoan-Andrei Iliuta, Vinusha Kalatharan, Kairong Wang, et al.
The Canadian Journal of Cardiology|October 13, 2024
Challenges in the Evaluation of Aortic Stenosis: A Guide to Multimodal ImagingMichael-Roy Durr, Ian G Burwash, Anahita Tavoosi, et al.
Science (New York, N.Y.)|January 8, 2005
Expanded repeat in canine epilepsyHannes Lohi, Edwin J Young, Susan N Fitzmaurice, et al.
Gene|September 20, 2022
Role of 19 SNPs in 10 genes with type 2 diabetes in the Pakistani populationNetasha Khan, Andrew D Paterson, Delnaz Roshandel, et al.
The Journal of Clinical Endocrinology and Metabolism|September 16, 2020
Genome-Wide Association for HbA1c in Malay Identified Deletion on SLC4A1 that Influences HbA1c Independent of GlycemiaJin-Fang Chai, Shih-Ling Kao, Chaolong Wang, et al.
Arthritis Research & Therapy|September 12, 2008
Reduced proportions of natural killer T cells are present in the relatives of lupus patients and are associated with autoimmunityJoan Wither, Yong-chun Cai, Sooyeol Lim, et al.
Journal of Medical Genetics|October 26, 2010
Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disabilityAlistair T Pagnamenta, Hameed Khan, Susan Walker, et al.
BMJ Open Diabetes Research & Care|January 16, 2026
Association of genetic variation with age at diagnosis in type 1 diabetesCharlotte E Vollenbrock, Delnaz Roshandel, Kristine E Lee, et al.
American Journal of Medical Genetics|December 20, 2000
Long repeat tracts at SCA8 in major psychosisJ B Vincent, Q P Yuan, M Schalling, et al.
Diabetologia|February 7, 2018
Meta-genome-wide association studies identify a locus on chromosome 1 and multiple variants in the MHC region for serum C-peptide in type 1 diabetesDelnaz Roshandel, Rose Gubitosi-Klug, Shelley B Bull, et al.
Pageof 54