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British Journal of Haematology|August 2, 2016
Persistence of DNMT3A R882 mutations during remission does not adversely affect outcomes of patients with acute myeloid leukaemiaBhavana Bhatnagar, Ann-Kathrin Eisfeld, Deedra Nicolet, et al.
Experimental Hematology|February 26, 2005
Failure to define window of time for autologous tumor vaccination in patients with newly diagnosed or relapsed acute lymphoblastic leukemiaW Nicholas Haining, Angelo A Cardoso, Heather L Keczkemethy, et al.
MMWR. Morbidity and Mortality Weekly Report|May 13, 2022
Vital Signs: Changes in Firearm Homicide and Suicide Rates - United States, 2019-2020Scott R Kegler, Thomas R Simon, Marissa L Zwald, et al.
Investigative Ophthalmology & Visual Science|November 24, 2011
Autosomal recessive retinitis pigmentosa caused by mutations in the MAK geneEdwin M Stone, Xunda Luo, Elise Héon, et al.
Journal of Biophotonics|April 15, 2021
Sub millimetre flexible fibre probe for background and fluorescence free Raman spectroscopyStephanos Yerolatsitis, András Kufcsák, Katjana Ehrlich, et al.
Investigative Ophthalmology & Visual Science|June 14, 2000
Disease expression of RP1 mutations causing autosomal dominant retinitis pigmentosaS G Jacobson, A V Cideciyan, A Iannaccone, et al.
Science (New York, N.Y.)|June 6, 1998
Mutations in the SMAD4/DPC4 gene in juvenile polyposisJ R Howe, S Roth, J C Ringold, et al.
Scientific Reports|July 30, 2016
cGMP production of patient-specific iPSCs and photoreceptor precursor cells to treat retinal degenerative blindnessLuke A Wiley, Erin R Burnight, Adam P DeLuca, et al.
Investigative Ophthalmology & Visual Science|May 17, 2017
Outcome Measures for Clinical Trials of Leber Congenital Amaurosis Caused by the Intronic Mutation in the CEP290 GeneSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.
Human Molecular Genetics|December 17, 2008
ABCA4 disease progression and a proposed strategy for gene therapyArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.
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