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Showing results (861-870 of 959) with videos related to

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Blood|October 29, 2020
The impact of MYC and BCL2 structural variants in tumors of DLBCL morphology and mechanisms of false-negative MYC IHCBrett Collinge, Susana Ben-Neriah, Lauren Chong, et al.
American Journal of Human Genetics|June 18, 2022
Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traitsRoshni A Patel, Shaila A Musharoff, Jeffrey P Spence, et al.
Scientific Reports|October 17, 2023
Multi-ancestry epigenome-wide analyses identify methylated sites associated with aortic augmentation index in TOPMed MESAXiaowei Hu, Jeongok G Logan, Younghoon Kwon, et al.
Oncogene|August 26, 2021
Comprehensive molecular profiling of UV-induced metastatic melanoma in Nme1/Nme2-deficient mice reveals novel markers of survival in human patientsM Kathryn Leonard, Gemma S Puts, Nidhi Pamidimukkala, et al.
Cancer Discovery|May 2, 2019
Mechanisms of Lymphoma Clearance Induced by High-Dose Alkylating AgentsChen Lossos, Yunpeng Liu, Kellie E Kolb, et al.
The New England Journal of Medicine|January 13, 2012
Germline mutations in HOXB13 and prostate-cancer riskCharles M Ewing, Anna M Ray, Ethan M Lange, et al.
Journal of Affective Disorders|November 13, 2013
Investigating the genetic variation underlying episodicity in major depressive disorder: suggestive evidence for a bipolar contributionPanagiotis Ferentinos, Margarita Rivera, Marcus Ising, et al.
BMC Medicine|April 24, 2015
A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorderChi-Fa Hung, Gerome Breen, Darina Czamara, et al.
American Journal of Human Genetics|April 14, 2009
Genetic control of human brain transcript expression in Alzheimer diseaseJennifer A Webster, J Raphael Gibbs, Jennifer Clarke, et al.
Molecular Psychiatry|November 2, 2011
Genome-wide association analysis of copy number variation in recurrent depressive disorderJ J H Rucker, G Breen, D Pinto, et al.
Pageof 96

Showing results (861-870 of 959) with videos related to

Sort By:
Pageof 96
Blood|October 29, 2020
The impact of MYC and BCL2 structural variants in tumors of DLBCL morphology and mechanisms of false-negative MYC IHCBrett Collinge, Susana Ben-Neriah, Lauren Chong, et al.
American Journal of Human Genetics|June 18, 2022
Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traitsRoshni A Patel, Shaila A Musharoff, Jeffrey P Spence, et al.
Scientific Reports|October 17, 2023
Multi-ancestry epigenome-wide analyses identify methylated sites associated with aortic augmentation index in TOPMed MESAXiaowei Hu, Jeongok G Logan, Younghoon Kwon, et al.
Oncogene|August 26, 2021
Comprehensive molecular profiling of UV-induced metastatic melanoma in Nme1/Nme2-deficient mice reveals novel markers of survival in human patientsM Kathryn Leonard, Gemma S Puts, Nidhi Pamidimukkala, et al.
Cancer Discovery|May 2, 2019
Mechanisms of Lymphoma Clearance Induced by High-Dose Alkylating AgentsChen Lossos, Yunpeng Liu, Kellie E Kolb, et al.
The New England Journal of Medicine|January 13, 2012
Germline mutations in HOXB13 and prostate-cancer riskCharles M Ewing, Anna M Ray, Ethan M Lange, et al.
Journal of Affective Disorders|November 13, 2013
Investigating the genetic variation underlying episodicity in major depressive disorder: suggestive evidence for a bipolar contributionPanagiotis Ferentinos, Margarita Rivera, Marcus Ising, et al.
BMC Medicine|April 24, 2015
A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorderChi-Fa Hung, Gerome Breen, Darina Czamara, et al.
American Journal of Human Genetics|April 14, 2009
Genetic control of human brain transcript expression in Alzheimer diseaseJennifer A Webster, J Raphael Gibbs, Jennifer Clarke, et al.
Molecular Psychiatry|November 2, 2011
Genome-wide association analysis of copy number variation in recurrent depressive disorderJ J H Rucker, G Breen, D Pinto, et al.
Pageof 96