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Stem Cell Research|January 13, 2026
Generation of iPSC and isogenic gene-corrected lines from a patient with RPS7 (c.277_279delGTC)-mutated Diamond-Blackfan anemia syndromeShruthi Suryaprakash, Yan Ju, James P Papizan, et al.The Journal of Biological Chemistry|January 31, 2012
Insights into hemoglobin assembly through in vivo mutagenesis of α-hemoglobin stabilizing proteinEugene Khandros, Todd L Mollan, Xiang Yu, et al.American Journal of Hematology|March 23, 2026
The Longitudinal Effect of APOL1 Risk Alleles on Sickle Cell Anemia-Associated Kidney FunctionSara R Rashkin, Guolian Kang, Clifford M Takemoto, et al.Molecular Therapy. Methods & Clinical Development|December 15, 2015
Amelioration of murine sickle cell disease by nonablative conditioning and γ-globin gene-corrected bone marrow cellsTamara I Pestina, Phillip W Hargrove, Huifen Zhao, et al.Cardiovascular Research|February 23, 2012
Loss of the miR-144/451 cluster impairs ischaemic preconditioning-mediated cardioprotection by targeting Rac-1Xiaohong Wang, Hongyan Zhu, Xiaowei Zhang, et al.Molecular Cell|February 8, 2005
Proximity among distant regulatory elements at the beta-globin locus requires GATA-1 and FOG-1Christopher R Vakoc, Danielle L Letting, Nele Gheldof, et al.Nature|June 18, 2002
An abundant erythroid protein that stabilizes free alpha-haemoglobinAnthony J Kihm, Yi Kong, Wei Hong, et al.Blood Advances|March 24, 2024
Machine learning to optimize automated RH genotyping using whole-exome sequencing dataTi-Cheng Chang, Jing Yu, Zhaoming Wang, et al.Molecular and Cellular Biology|July 2, 2003
GATA-1-mediated proliferation arrest during erythroid maturationMarcin Rylski, John J Welch, Ying-Yu Chen, et al.Nature Genetics|April 13, 2021
Chromothripsis as an on-target consequence of CRISPR-Cas9 genome editingMitchell L Leibowitz, Stamatis Papathanasiou, Phillip A Doerfler, et al.Pageof 22