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Bari J Ballew

Showing results (1-10 of 13) with videos related to

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Aging Cell|May 16, 2013
Multiple genetic pathways regulate replicative senescence in telomerase-deficient yeastBari J Ballew, Victoria Lundblad
Expert Review of Hematology|June 21, 2013
Updates on the biology and management of dyskeratosis congenita and related telomere biology disordersBari J Ballew, Sharon A Savage
Peerj|December 22, 2025
Simpler predictive models provide higher accuracy for ovarian cancer detectionDerrick E Wood, Joseph Roy, Bari J Ballew
Human Genetics|January 19, 2013
Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenitaBari J Ballew, Meredith Yeager, Kevin Jacobs, et al.
American Journal of Medical Genetics. Part A|November 23, 2015
Novel FANCI mutations in Fanconi anemia with VACTERL associationSharon A Savage, Bari J Ballew, Neelam Giri, et al.
Pediatric Neurology|January 27, 2016
Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-UpAshley M Burris, Bari J Ballew, Joshua B Kentosh, et al.
Genes & Development|September 20, 2014
Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1Hande Kocak, Bari J Ballew, Kamlesh Bisht, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|January 27, 2020
Population Frequency of Fanconi Pathway Gene Variants and Their Association with Survival After Hematopoietic Cell Transplantation for Severe Aplastic AnemiaLisa J McReynolds, Youjin Wang, Ashley S Thompson, et al.
Cold Spring Harbor Molecular Case Studies|December 15, 2019
1q21.1 deletion and a rare functional polymorphism in siblings with thrombocytopenia-absent radius-like phenotypesSeth A Brodie, Jean Paul Rodriguez-Aulet, Neelam Giri, et al.
Blood|May 16, 2014
Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia familiesLisa Mirabello, Elizabeth R Macari, Lea Jessop, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Aging Cell|May 16, 2013
Multiple genetic pathways regulate replicative senescence in telomerase-deficient yeastBari J Ballew, Victoria Lundblad
Expert Review of Hematology|June 21, 2013
Updates on the biology and management of dyskeratosis congenita and related telomere biology disordersBari J Ballew, Sharon A Savage
Peerj|December 22, 2025
Simpler predictive models provide higher accuracy for ovarian cancer detectionDerrick E Wood, Joseph Roy, Bari J Ballew
Human Genetics|January 19, 2013
Germline mutations of regulator of telomere elongation helicase 1, RTEL1, in Dyskeratosis congenitaBari J Ballew, Meredith Yeager, Kevin Jacobs, et al.
American Journal of Medical Genetics. Part A|November 23, 2015
Novel FANCI mutations in Fanconi anemia with VACTERL associationSharon A Savage, Bari J Ballew, Neelam Giri, et al.
Pediatric Neurology|January 27, 2016
Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-UpAshley M Burris, Bari J Ballew, Joshua B Kentosh, et al.
Genes & Development|September 20, 2014
Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1Hande Kocak, Bari J Ballew, Kamlesh Bisht, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|January 27, 2020
Population Frequency of Fanconi Pathway Gene Variants and Their Association with Survival After Hematopoietic Cell Transplantation for Severe Aplastic AnemiaLisa J McReynolds, Youjin Wang, Ashley S Thompson, et al.
Cold Spring Harbor Molecular Case Studies|December 15, 2019
1q21.1 deletion and a rare functional polymorphism in siblings with thrombocytopenia-absent radius-like phenotypesSeth A Brodie, Jean Paul Rodriguez-Aulet, Neelam Giri, et al.
Blood|May 16, 2014
Whole-exome sequencing and functional studies identify RPS29 as a novel gene mutated in multicase Diamond-Blackfan anemia familiesLisa Mirabello, Elizabeth R Macari, Lea Jessop, et al.
Pageof 2