Showing results (141-150 of 149) with videos related to
Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 149 results.
Nature Immunology|July 13, 2010
Deletion of the RNA-binding proteins ZFP36L1 and ZFP36L2 leads to perturbed thymic development and T lymphoblastic leukemiaDaniel J Hodson, Michelle L Janas, Alison Galloway, et al.Journal of Immunology (Baltimore, Md. : 1950)|April 4, 2009
Enrichment of human CD4+ V(alpha)24/Vbeta11 invariant NKT cells in intrahepatic malignant tumorsGabriel Bricard, Valerie Cesson, Estelle Devevre, et al.Blood|January 29, 2011
Global gene expression analysis of human erythroid progenitorsAlison T Merryweather-Clarke, Ann Atzberger, Shamit Soneji, et al.Human Molecular Genetics|August 14, 2003
Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosisAlison T Merryweather-Clarke, Estelle Cadet, Adrian Bomford, et al.Journal of Medical Genetics|January 20, 2004
The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loadingK J Livesey, V L C Wimhurst, K Carter, et al.The Journal of Clinical Investigation|February 7, 2018
Ribonuclease inhibitor 1 regulates erythropoiesis by controlling GATA1 translationVijaykumar Chennupati, Diogo Ft Veiga, Kendle M Maslowski, et al.Journal of Internal Medicine|January 25, 2003
A targeted approach significantly increases the identification rate of patients with undiagnosed haemochromatosisE Cadet, D Capron, A S Perez, et al.Blood|April 4, 2009
Iron overload in the Asian communityChun Yu Lok, Alison T Merryweather-Clarke, Vip Viprakasit, et al.Cell Reports|December 19, 2012
Mutations in the β-tubulin gene TUBB5 cause microcephaly with structural brain abnormalitiesMartin Breuss, Julian Ik-Tsen Heng, Karine Poirier, et al.Pageof 15