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Mark D Fleming

Showing results (171-180 of 215) with videos related to

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Blood|June 4, 2010
Recurrent BRAF mutations in Langerhans cell histiocytosisGayane Badalian-Very, Jo-Anne Vergilio, Barbara A Degar, et al.
Cancer Cell|June 11, 2024
T-Lymphoblastic Lymphoma Cells Express High Levels of BCL2, S1P1, and ICAM1, Leading to a Blockade of Tumor Cell IntravasationHui Feng, David L Stachura, Richard M White, et al.
The Journal of Clinical Investigation|July 8, 2020
Mutations in the iron-sulfur cluster biogenesis protein HSCB cause congenital sideroblastic anemiaAndrew Crispin, Chaoshe Guo, Caiyong Chen, et al.
Blood|October 29, 2008
Identification of a Steap3 endosomal targeting motif essential for normal iron metabolismTeresa Lambe, Robert J Simpson, Sara Dawson, et al.
Scientific Reports|May 21, 2016
Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterationsJoshua E Mangum, Justin P Hardee, Dennis K Fix, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2020
Evidence in the UK Biobank for the underdiagnosis of erythropoietic protoporphyriaAmy K Dickey, Corbin Quick, Sarah Ducamp, et al.
Nature Genetics|May 5, 2009
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemiaDuane L Guernsey, Haiyan Jiang, Dean R Campagna, et al.
Blood|June 14, 2018
Normalizing hepcidin predicts <i>TMPRSS6</i> mutation status in patients with chronic iron deficiencyMatthew M Heeney, Dongjing Guo, Luigia De Falco, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 21, 2006
Immunosurveillance and survivin-specific T-cell immunity in children with high-risk neuroblastomaChristina M Coughlin, Mark D Fleming, Richard G Carroll, et al.
American Journal of Human Genetics|November 1, 2019
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism IndividualsGiuliana Giannuzzi, Paul J Schmidt, Eleonora Porcu, et al.
Pageof 22

Showing results (171-180 of 215) with videos related to

Sort By:
Pageof 22
Blood|June 4, 2010
Recurrent BRAF mutations in Langerhans cell histiocytosisGayane Badalian-Very, Jo-Anne Vergilio, Barbara A Degar, et al.
Cancer Cell|June 11, 2024
T-Lymphoblastic Lymphoma Cells Express High Levels of BCL2, S1P1, and ICAM1, Leading to a Blockade of Tumor Cell IntravasationHui Feng, David L Stachura, Richard M White, et al.
The Journal of Clinical Investigation|July 8, 2020
Mutations in the iron-sulfur cluster biogenesis protein HSCB cause congenital sideroblastic anemiaAndrew Crispin, Chaoshe Guo, Caiyong Chen, et al.
Blood|October 29, 2008
Identification of a Steap3 endosomal targeting motif essential for normal iron metabolismTeresa Lambe, Robert J Simpson, Sara Dawson, et al.
Scientific Reports|May 21, 2016
Pseudouridine synthase 1 deficient mice, a model for Mitochondrial Myopathy with Sideroblastic Anemia, exhibit muscle morphology and physiology alterationsJoshua E Mangum, Justin P Hardee, Dennis K Fix, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 3, 2020
Evidence in the UK Biobank for the underdiagnosis of erythropoietic protoporphyriaAmy K Dickey, Corbin Quick, Sarah Ducamp, et al.
Nature Genetics|May 5, 2009
Mutations in mitochondrial carrier family gene SLC25A38 cause nonsyndromic autosomal recessive congenital sideroblastic anemiaDuane L Guernsey, Haiyan Jiang, Dean R Campagna, et al.
Blood|June 14, 2018
Normalizing hepcidin predicts <i>TMPRSS6</i> mutation status in patients with chronic iron deficiencyMatthew M Heeney, Dongjing Guo, Luigia De Falco, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|December 21, 2006
Immunosurveillance and survivin-specific T-cell immunity in children with high-risk neuroblastomaChristina M Coughlin, Mark D Fleming, Richard G Carroll, et al.
American Journal of Human Genetics|November 1, 2019
The Human-Specific BOLA2 Duplication Modifies Iron Homeostasis and Anemia Predisposition in Chromosome 16p11.2 Autism IndividualsGiuliana Giannuzzi, Paul J Schmidt, Eleonora Porcu, et al.
Pageof 22