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- 2007
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Mark
Phenotype and genotype of a cohort of families historically diagnosed with type 1 von Willebrand disease in the European study, Molecular and Clinical Markers for the Diagnosis and Management of Type 1 von Willebrand Disease (MCMDM-1VWD)
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- Contribution to journal › Article
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Mark
Ectopic expression of PAX5 promotes self renewal of bi-phenotypic myeloid progenitors co-expressing myeloid and B-cell lineage associated genes.
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- Contribution to journal › Article
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Mark
RhoH is important for positive thymocyte selection and T-cell receptor signaling
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- Contribution to journal › Article
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Mark
Hematopoietic stem cell targeted neonatal gene therapy reverses lethally progressive osteopetrosis in oc/oc mice.
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- Contribution to journal › Article
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Mark
Connecting ribosomes with bone marrow failure
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- Contribution to journal › Debate/Note/Editorial
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Mark
A randomized comparison of bypassing agents in hemophilia complicated by an inhibitor.
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- Contribution to journal › Article
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Mark
Human RPS19, the gene mutated in Diamond Blackfan anemia, encodes a ribosomal protein required for the maturation of 40S ribosomal subunits.
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- Contribution to journal › Article
- 2006
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Mark
Human short-term repopulating cells have enhanced telomerase reverse transcriptase expression.
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- Contribution to journal › Article
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Mark
Gut associated lymphoid tissue primed CD4+ T cells display CCR9 dependent and independent homing to the small intestine.
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- Contribution to journal › Article
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Mark
Identification of Y589 and Y599 in the juxamembrane domain of Flt3 as ligand-induced autophosphorylation sites involved in binding of Src family kinases and the protein tyrosine phosphatase SHP2
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- Contribution to journal › Article