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Showing results (241-250 of 347) with videos related to

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Journal of the International Neuropsychological Society : JINS|February 3, 2016
Decreased Fronto-Limbic Activation and Disrupted Semantic-Cued List Learning in Major Depressive DisorderMichelle T Kassel, Julia A Rao, Sara J Walker, et al.
Plos One|June 1, 2022
COVID-19 vaccines uptake: Public knowledge, awareness, perception and acceptance among adult AfricansJohn K Ahiakpa, Nanma T Cosmas, Felix E Anyiam, et al.
Cell|March 12, 2017
Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO MutationAh Ram Kim, Jacob C Ulirsch, Stephan Wilmes, et al.
Journal of Materials Chemistry. B|April 30, 2025
Antitumor activity and selectivity of a nanostructured peroxo polyoxoniobateLuiz C A Oliveira, Cinthia C Oliveira, Samuel M Breder, et al.
The Journal of Experimental Medicine|March 28, 2019
Impaired human hematopoiesis due to a cryptic intronic <i>GATA1</i> splicing mutationNour J Abdulhay, Claudia Fiorini, Jeffrey M Verboon, et al.
Journal of Clinical Immunology|April 19, 2020
Infantile Myelofibrosis and Myeloproliferation with CDC42 DysfunctionJeffrey M Verboon, Dilnar Mahmut, Ah Ram Kim, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 30, 2016
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanismsMichael H Guo, Satish K Nandakumar, Jacob C Ulirsch, et al.
American Journal of Human Genetics|December 7, 2014
Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disabilityRosalind Law, Tracy Dixon-Salazar, Julie Jerber, et al.
The New England Journal of Medicine|July 31, 2007
Risk alleles for multiple sclerosis identified by a genomewide study, David A Hafler, Alastair Compston, et al.
The New England Journal of Medicine|November 27, 2014
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequenceGiulio Genovese, Anna K Kähler, Robert E Handsaker, et al.
Pageof 35

Showing results (241-250 of 347) with videos related to

Sort By:
Pageof 35
Journal of the International Neuropsychological Society : JINS|February 3, 2016
Decreased Fronto-Limbic Activation and Disrupted Semantic-Cued List Learning in Major Depressive DisorderMichelle T Kassel, Julia A Rao, Sara J Walker, et al.
Plos One|June 1, 2022
COVID-19 vaccines uptake: Public knowledge, awareness, perception and acceptance among adult AfricansJohn K Ahiakpa, Nanma T Cosmas, Felix E Anyiam, et al.
Cell|March 12, 2017
Functional Selectivity in Cytokine Signaling Revealed Through a Pathogenic EPO MutationAh Ram Kim, Jacob C Ulirsch, Stephan Wilmes, et al.
Journal of Materials Chemistry. B|April 30, 2025
Antitumor activity and selectivity of a nanostructured peroxo polyoxoniobateLuiz C A Oliveira, Cinthia C Oliveira, Samuel M Breder, et al.
The Journal of Experimental Medicine|March 28, 2019
Impaired human hematopoiesis due to a cryptic intronic <i>GATA1</i> splicing mutationNour J Abdulhay, Claudia Fiorini, Jeffrey M Verboon, et al.
Journal of Clinical Immunology|April 19, 2020
Infantile Myelofibrosis and Myeloproliferation with CDC42 DysfunctionJeffrey M Verboon, Dilnar Mahmut, Ah Ram Kim, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 30, 2016
Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanismsMichael H Guo, Satish K Nandakumar, Jacob C Ulirsch, et al.
American Journal of Human Genetics|December 7, 2014
Biallelic truncating mutations in FMN2, encoding the actin-regulatory protein Formin 2, cause nonsyndromic autosomal-recessive intellectual disabilityRosalind Law, Tracy Dixon-Salazar, Julie Jerber, et al.
The New England Journal of Medicine|July 31, 2007
Risk alleles for multiple sclerosis identified by a genomewide study, David A Hafler, Alastair Compston, et al.
The New England Journal of Medicine|November 27, 2014
Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequenceGiulio Genovese, Anna K Kähler, Robert E Handsaker, et al.
Pageof 35