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

J T Prchal

Showing results (121-130 of 133) with videos related to

Pageof 14
Sort By:
Blood|December 1, 1995
Plasma/serum levels of flt3 ligand are low in normal individuals and highly elevated in patients with Fanconi anemia and acquired aplastic anemiaS D Lyman, M Seaberg, R Hanna, et al.
Blood|June 1, 1990
Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosisT Coetzer, J Palek, J Lawler, et al.
Blood|February 9, 2000
Effect of recombinant human erythropoietin combined with granulocyte/ macrophage colony-stimulating factor in the treatment of patients with myelodysplastic syndrome. GM/EPO MDS Study GroupJ A Thompson, D G Gilliland, J T Prchal, et al.
Hemoglobin|May 1, 1995
Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from AlabamaJ T Prchal, B Adler, J B Wilson, et al.
Journal of Clinical Immunology|December 19, 1998
Leukocyte transfusion-associated granulocyte responses in a patient with X-linked hyper-IgM syndromeT P Atkinson, C A Smith, Y M Hsu, et al.
Blood|June 1, 1992
Familial and congenital polycythemia in three unrelated familiesP D Emanuel, C J Eaves, V C Broudy, et al.
Blood|May 1, 1990
Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertionsJ B Wilson, B B Webber, H Hu, et al.
Blood|January 1, 1995
Clonality in juvenile chronic myelogenous leukemiaL Busque, D G Gilliland, J T Prchal, et al.
Leukemia|January 14, 2014
Whole-exome sequencing of polycythemia vera revealed novel driver genes and somatic mutation shared by T cells and granulocytesL Wang, S I Swierczek, J Drummond, et al.
Blood|December 1, 1996
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiencyP Jarolim, J L Murray, H L Rubin, et al.
Pageof 14

Showing results (121-130 of 133) with videos related to

Sort By:
Pageof 14
Blood|December 1, 1995
Plasma/serum levels of flt3 ligand are low in normal individuals and highly elevated in patients with Fanconi anemia and acquired aplastic anemiaS D Lyman, M Seaberg, R Hanna, et al.
Blood|June 1, 1990
Structural and functional heterogeneity of alpha spectrin mutations involving the spectrin heterodimer self-association site: relationships to hematologic expression of homozygous hereditary elliptocytosis and hereditary pyropoikilocytosisT Coetzer, J Palek, J Lawler, et al.
Blood|February 9, 2000
Effect of recombinant human erythropoietin combined with granulocyte/ macrophage colony-stimulating factor in the treatment of patients with myelodysplastic syndrome. GM/EPO MDS Study GroupJ A Thompson, D G Gilliland, J T Prchal, et al.
Hemoglobin|May 1, 1995
Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from AlabamaJ T Prchal, B Adler, J B Wilson, et al.
Journal of Clinical Immunology|December 19, 1998
Leukocyte transfusion-associated granulocyte responses in a patient with X-linked hyper-IgM syndromeT P Atkinson, C A Smith, Y M Hsu, et al.
Blood|June 1, 1992
Familial and congenital polycythemia in three unrelated familiesP D Emanuel, C J Eaves, V C Broudy, et al.
Blood|May 1, 1990
Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertionsJ B Wilson, B B Webber, H Hu, et al.
Blood|January 1, 1995
Clonality in juvenile chronic myelogenous leukemiaL Busque, D G Gilliland, J T Prchal, et al.
Leukemia|January 14, 2014
Whole-exome sequencing of polycythemia vera revealed novel driver genes and somatic mutation shared by T cells and granulocytesL Wang, S I Swierczek, J Drummond, et al.
Blood|December 1, 1996
Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiencyP Jarolim, J L Murray, H L Rubin, et al.
Pageof 14