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Blood
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January 9, 2017
Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia
Suthesh Sivapalaratnam, Sarah K Westbury, Jonathan C Stephens, et al.
Nature Genetics
|
August 15, 2017
Transcriptional risk scores link GWAS to eQTLs and predict complications in Crohn's disease
Urko M Marigorta, Lee A Denson, Jeffrey S Hyams, et al.
Current Protocols
|
February 5, 2025
Optimizing In Situ Proximity Ligation Assays for Mitochondria, ER, or MERC Markers in Skeletal Muscle Tissue and Cells
Amber Crabtree, Han Le, Chanel Harris, et al.
Nature Medicine
|
September 1, 1996
Retrovirus-mediated wild-type p53 gene transfer to tumors of patients with lung cancer
J A Roth, D Nguyen, D D Lawrence, et al.
Mayo Clinic Proceedings
|
March 6, 2016
Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience
Konstantinos N Lazaridis, Kimberly A Schahl, Margot A Cousin, et al.
Current Protocols
|
February 5, 2025
Creating Optimal Western Blot Conditions for OPA1 Isoforms in Skeletal Muscle Cells and Tissue
Margaret Mungai, Amber Crabtree, Han Le, et al.
Blood
|
June 21, 2019
Germline mutations in the transcription factor IKZF5 cause thrombocytopenia
Claire Lentaigne, Daniel Greene, Suthesh Sivapalaratnam, et al.
Science (New York, N.Y.)
|
July 14, 2001
Haplotype variation and linkage disequilibrium in 313 human genes
J C Stephens, J A Schneider, D A Tanguay, et al.
Iscience
|
September 22, 2023
Project Strengthen: An STEMM-focused career development workshop to prepare underrepresented minority students for graduate school
Taylor Barongan, Kit Neikirk, Bryanna Shao, et al.
American Journal of Industrial Medicine
|
October 25, 2001
Development of a life events/icon calendar questionnaire to ascertain occupational histories and other characteristics of migrant farmworkers
S H Zahm, J S Colt, L S Engel, et al.
Page
of 74
Search research articles
Search
Showing results (691-700 of 739) with videos related to
Sort By:
Page
of 74
Blood
|
January 9, 2017
Rare variants in GP1BB are responsible for autosomal dominant macrothrombocytopenia
Suthesh Sivapalaratnam, Sarah K Westbury, Jonathan C Stephens, et al.
Nature Genetics
|
August 15, 2017
Transcriptional risk scores link GWAS to eQTLs and predict complications in Crohn's disease
Urko M Marigorta, Lee A Denson, Jeffrey S Hyams, et al.
Current Protocols
|
February 5, 2025
Optimizing In Situ Proximity Ligation Assays for Mitochondria, ER, or MERC Markers in Skeletal Muscle Tissue and Cells
Amber Crabtree, Han Le, Chanel Harris, et al.
Nature Medicine
|
September 1, 1996
Retrovirus-mediated wild-type p53 gene transfer to tumors of patients with lung cancer
J A Roth, D Nguyen, D D Lawrence, et al.
Mayo Clinic Proceedings
|
March 6, 2016
Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience
Konstantinos N Lazaridis, Kimberly A Schahl, Margot A Cousin, et al.
Current Protocols
|
February 5, 2025
Creating Optimal Western Blot Conditions for OPA1 Isoforms in Skeletal Muscle Cells and Tissue
Margaret Mungai, Amber Crabtree, Han Le, et al.
Blood
|
June 21, 2019
Germline mutations in the transcription factor IKZF5 cause thrombocytopenia
Claire Lentaigne, Daniel Greene, Suthesh Sivapalaratnam, et al.
Science (New York, N.Y.)
|
July 14, 2001
Haplotype variation and linkage disequilibrium in 313 human genes
J C Stephens, J A Schneider, D A Tanguay, et al.
Iscience
|
September 22, 2023
Project Strengthen: An STEMM-focused career development workshop to prepare underrepresented minority students for graduate school
Taylor Barongan, Kit Neikirk, Bryanna Shao, et al.
American Journal of Industrial Medicine
|
October 25, 2001
Development of a life events/icon calendar questionnaire to ascertain occupational histories and other characteristics of migrant farmworkers
S H Zahm, J S Colt, L S Engel, et al.
Page
of 74