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Human Pathology|April 1, 1992
Immunohistochemical localization of human immunodeficiency virus p24 antigen in placental tissueA W Martin, K Brady, S I Smith, et al.Archives of Orthopaedic and Trauma Surgery|November 14, 2009
Expression of TRAIL and death receptor DR4 in Palmer type 2 TFCC lesionsFrank Unglaub, Susanne B Thomas, Markus W Kroeber, et al.The Journal of Pharmacology and Experimental Therapeutics|March 1, 1990
Low-dose caffeine discrimination in humansR R Griffiths, S M Evans, S J Heishman, et al.Molecular Biology and Evolution|April 19, 2021
Inferring Adaptive Codon Preference to Understand Sources of Selection Shaping Codon Usage BiasJanaina Lima de Oliveira, Atahualpa Castillo Morales, Laurence D Hurst, et al.Leukemia Research|February 1, 1993
Intervention treatment of established neutropenia with human recombinant granulocyte-macrophage colony-stimulating factor (rhGM-CSF) in patients undergoing cancer chemotherapyH H Gerhartz, A C Stern, B Wolf-Hornung, et al.Journal of Inherited Metabolic Disease|January 7, 2004
Neonatal screening for biotinidase deficiency in Hungary: clinical, biochemical and molecular studiesA László, E A Schuler, E Sallay, et al.Journal of Breath Research|March 10, 2015
Influence of the respirator on volatile organic compounds: an animal study in rats over 24 hoursF W Albrecht, T Hüppe, T Fink, et al.American Journal of Hematology|September 20, 2014
Factors associated with growth and blood pressure patterns in children with sickle cell anemia: Silent Cerebral Infarct Multi-Center Clinical Trial cohortRachel B Wolf, Benjamin R Saville, Dionna O Roberts, et al.Human Genetics|April 1, 1997
Arg538 to Cys mutation in a CpG dinucleotide of the human biotinidase gene is the second most common cause of profound biotinidase deficiency in symptomatic childrenR J Pomponio, K J Norrgard, J Hymes, et al.The Journal of Biological Chemistry|March 4, 1994
Human serum biotinidase. cDNA cloning, sequence, and characterizationH Cole, T R Reynolds, J M Lockyer, et al.Pageof 69