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The Journal of Biological Chemistry|August 31, 2016
Rational Design of a Parthenolide-based Drug Regimen That Selectively Eradicates Acute Myelogenous Leukemia Stem CellsShanshan Pei, Mohammad Minhajuddin, Angelo D'Alessandro, et al.
Frontiers in Oncology|November 30, 2020
Management of Isolated Local Failures Following Stereotactic Body Radiation Therapy for Low to Intermediate Risk Prostate CancerNima Aghdam, Abigail N Pepin, Michael Creswell, et al.
Genes, Chromosomes & Cancer|January 13, 2005
A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutationsStefan Meyer, William D Fergusson, Anneke B Oostra, et al.
Scientific Reports|November 14, 2019
Clinical and genetic variability in children with partial albinismPatrick Campbell, Jamie M Ellingford, Neil R A Parry, et al.
American Journal of Human Genetics|May 14, 2004
Delineation of Cohen syndrome following a large-scale genotype-phenotype screenJuha Kolehmainen, Robert Wilkinson, Anna-Elina Lehesjoki, et al.
American Journal of Human Genetics|January 15, 2013
ALDH1A3 mutations cause recessive anophthalmia and microphthalmiaLucas Fares-Taie, Sylvie Gerber, Nicolas Chassaing, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|November 23, 2019
Unlicensed Umbilical Cord Blood Units Provide a Safe and Effective Graft Source for a Diverse Population: A Study of 2456 Umbilical Cord Blood RecipientsKaren Ballen, Brent R Logan, Pintip Chitphakdithai, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 2, 2016
Microduplication of the ARID1A gene causes intellectual disability with recognizable syndromic featuresMarie Bidart, Michèle El Atifi, Sarra Miladi, et al.
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