Showing results (111-120 of 327) with videos related to

Sort By:
Pageof 33
Blood Cells, Molecules & Diseases|February 25, 2005
Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical featuresRonald L Sham, Pradyumna D Phatak, Carol West, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Polymorphisms in iron-responsive binding protein 2 and lack of association with sporadic Parkinson's diseasePauline L Lee, Terri Gelbart, Carol West, et al.
Blood|May 10, 2011
Disruption of MyD88 signaling suppresses hemophagocytic lymphohistiocytosis in micePhilippe Krebs, Karine Crozat, Daniel Popkin, et al.
The Journal of Investigative Dermatology|August 26, 2019
Research Techniques Made Simple: Forward Genetic Screening to Uncover Genes Involved in Skin BiologyWilliam McAlpine, Jamie Russell, Anne R Murray, et al.
American Journal of Hematology|April 1, 2004
Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose-6-phosphate dehydrogenase (G-6-PD) deficiencyJames D Hoyer, Steven L Allen, Ernest Beutler, et al.
Journal of Virology|September 5, 2002
Asian genotypes of JC virus in Japanese-Americans suggest familial transmissionMakoto Suzuki, Huai-Ying Zheng, Tomokazu Takasaka, et al.
Scandinavian Journal of Infectious Diseases|November 19, 2003
Lps2 and signal transduction in sepsis: at the intersection of host responses to bacteria and virusesBruce Beutler, Kasper Hoebe, Xin Du, et al.
European Journal of Immunology|November 1, 2005
An essential role for Rxr alpha in the development of Th2 responsesXin Du, Koichi Tabeta, Navjiwan Mann, et al.
Pageof 33