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Mark D Fleming

Showing results (191-200 of 215) with videos related to

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Blood Advances|November 10, 2021
Hematologic complications with age in Shwachman-Diamond syndromeElissa Furutani, Shanshan Liu, Ashley Galvin, et al.
Blood|June 15, 2018
Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized miceInga Hofmann, Mitchell J Geer, Timo Vögtle, et al.
Molecular and Cellular Biology|August 26, 2009
Emi1 maintains genomic integrity during zebrafish embryogenesis and cooperates with p53 in tumor suppressionJennifer Rhodes, Adam Amsterdam, Takaomi Sanda, et al.
Human Mutation|July 23, 2021
SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literatureMatthew M Heeney, Simon Berhe, Dean R Campagna, et al.
Nature Genetics|June 29, 2023
Single-cell multi-omics of mitochondrial DNA disorders reveals dynamics of purifying selection across human immune cellsCaleb A Lareau, Sonia M Dubois, Frank A Buquicchio, et al.
Science Immunology|September 16, 2022
DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signalingCassandra R Harapas, Kim S Robinson, Kenneth Lay, et al.
Nature Genetics|December 8, 2015
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiencyHaifa H Jabara, Steven E Boyden, Janet Chou, et al.
Nature|November 9, 2012
Mitochondrial Atpif1 regulates haem synthesis in developing erythroblastsDhvanit I Shah, Naoko Takahashi-Makise, Jeffrey D Cooney, et al.
Cancer Cell|February 5, 2019
A Murine Model of Chronic Lymphocytic Leukemia Based on B Cell-Restricted Expression of Sf3b1 Mutation and Atm DeletionShanye Yin, Rutendo G Gambe, Jing Sun, et al.
The Lancet. Haematology|December 28, 2019
Clinical features and outcomes of patients with Shwachman-Diamond syndrome and myelodysplastic syndrome or acute myeloid leukaemia: a multicentre, retrospective, cohort studyKasiani C Myers, Elissa Furutani, Edie Weller, et al.
Pageof 22

Showing results (191-200 of 215) with videos related to

Sort By:
Pageof 22
Blood Advances|November 10, 2021
Hematologic complications with age in Shwachman-Diamond syndromeElissa Furutani, Shanshan Liu, Ashley Galvin, et al.
Blood|June 15, 2018
Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized miceInga Hofmann, Mitchell J Geer, Timo Vögtle, et al.
Molecular and Cellular Biology|August 26, 2009
Emi1 maintains genomic integrity during zebrafish embryogenesis and cooperates with p53 in tumor suppressionJennifer Rhodes, Adam Amsterdam, Takaomi Sanda, et al.
Human Mutation|July 23, 2021
SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literatureMatthew M Heeney, Simon Berhe, Dean R Campagna, et al.
Nature Genetics|June 29, 2023
Single-cell multi-omics of mitochondrial DNA disorders reveals dynamics of purifying selection across human immune cellsCaleb A Lareau, Sonia M Dubois, Frank A Buquicchio, et al.
Science Immunology|September 16, 2022
DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signalingCassandra R Harapas, Kim S Robinson, Kenneth Lay, et al.
Nature Genetics|December 8, 2015
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiencyHaifa H Jabara, Steven E Boyden, Janet Chou, et al.
Nature|November 9, 2012
Mitochondrial Atpif1 regulates haem synthesis in developing erythroblastsDhvanit I Shah, Naoko Takahashi-Makise, Jeffrey D Cooney, et al.
Cancer Cell|February 5, 2019
A Murine Model of Chronic Lymphocytic Leukemia Based on B Cell-Restricted Expression of Sf3b1 Mutation and Atm DeletionShanye Yin, Rutendo G Gambe, Jing Sun, et al.
The Lancet. Haematology|December 28, 2019
Clinical features and outcomes of patients with Shwachman-Diamond syndrome and myelodysplastic syndrome or acute myeloid leukaemia: a multicentre, retrospective, cohort studyKasiani C Myers, Elissa Furutani, Edie Weller, et al.
Pageof 22