Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Mark D Fleming

Showing results (181-190 of 215) with videos related to

Pageof 22
Sort By:
Science (New York, N.Y.)|August 5, 2017
UBE2O remodels the proteome during terminal erythroid differentiationAnthony T Nguyen, Miguel A Prado, Paul J Schmidt, et al.
Blood|August 5, 2016
A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemiaDaniel A Lichtenstein, Andrew W Crispin, Anoop K Sendamarai, et al.
American Journal of Hematology|October 22, 2021
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6Raffaele Renella, Katelyn Gagne, Ellen Beauchamp, et al.
Blood|April 5, 2013
A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD)Daniel H Wiseman, Alison May, Stephen Jolles, et al.
Blood|April 17, 2014
Pearson marrow pancreas syndrome in patients suspected to have Diamond-Blackfan anemiaKatelyn E Gagne, Roxanne Ghazvinian, Daniel Yuan, et al.
Cancer|July 18, 2013
Impact of hemochromatosis gene mutations on cardiac status in doxorubicin-treated survivors of childhood high-risk leukemiaSteven E Lipshultz, Stuart R Lipsitz, Jeffery L Kutok, et al.
Cancer Cell|September 14, 2016
Physiologic Expression of Sf3b1(K700E) Causes Impaired Erythropoiesis, Aberrant Splicing, and Sensitivity to Therapeutic Spliceosome ModulationEsther A Obeng, Ryan J Chappell, Michael Seiler, et al.
American Journal of Hematology|October 30, 2013
X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutationsDean R Campagna, Charlotte I de Bie, Klaus Schmitz-Abe, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|October 10, 2025
Genomic Profiling of Pediatric Mycosis Fungoides, Lymphomatoid Papulosis, and Primary Cutaneous Anaplastic Large Cell Lymphoma Identifies Recurrent Tyrosine Kinase Gene FusionsGrant M Fischer, Harrison K Tsai, Jennifer Huang, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|May 20, 2026
Recurrent SWI/SNF Deficiency Defines a Subset of Peripheral T-cell Lymphoma With Distinct Clinicopathologic FeaturesJacob R Bledsoe, Judith A Ferry, Jingwei Li, et al.
Pageof 22

Showing results (181-190 of 215) with videos related to

Sort By:
Pageof 22
Science (New York, N.Y.)|August 5, 2017
UBE2O remodels the proteome during terminal erythroid differentiationAnthony T Nguyen, Miguel A Prado, Paul J Schmidt, et al.
Blood|August 5, 2016
A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemiaDaniel A Lichtenstein, Andrew W Crispin, Anoop K Sendamarai, et al.
American Journal of Hematology|October 22, 2021
Congenital X-linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6Raffaele Renella, Katelyn Gagne, Ellen Beauchamp, et al.
Blood|April 5, 2013
A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD)Daniel H Wiseman, Alison May, Stephen Jolles, et al.
Blood|April 17, 2014
Pearson marrow pancreas syndrome in patients suspected to have Diamond-Blackfan anemiaKatelyn E Gagne, Roxanne Ghazvinian, Daniel Yuan, et al.
Cancer|July 18, 2013
Impact of hemochromatosis gene mutations on cardiac status in doxorubicin-treated survivors of childhood high-risk leukemiaSteven E Lipshultz, Stuart R Lipsitz, Jeffery L Kutok, et al.
Cancer Cell|September 14, 2016
Physiologic Expression of Sf3b1(K700E) Causes Impaired Erythropoiesis, Aberrant Splicing, and Sensitivity to Therapeutic Spliceosome ModulationEsther A Obeng, Ryan J Chappell, Michael Seiler, et al.
American Journal of Hematology|October 30, 2013
X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutationsDean R Campagna, Charlotte I de Bie, Klaus Schmitz-Abe, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|October 10, 2025
Genomic Profiling of Pediatric Mycosis Fungoides, Lymphomatoid Papulosis, and Primary Cutaneous Anaplastic Large Cell Lymphoma Identifies Recurrent Tyrosine Kinase Gene FusionsGrant M Fischer, Harrison K Tsai, Jennifer Huang, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|May 20, 2026
Recurrent SWI/SNF Deficiency Defines a Subset of Peripheral T-cell Lymphoma With Distinct Clinicopathologic FeaturesJacob R Bledsoe, Judith A Ferry, Jingwei Li, et al.
Pageof 22