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Cell Reports|December 29, 2014
An estrogen-responsive module in the ventromedial hypothalamus selectively drives sex-specific activity in femalesStephanie M Correa, David W Newstrom, James P Warne, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 18, 2010
Effect of complete remission and responses less than complete remission on survival in acute myeloid leukemia: a combined Eastern Cooperative Oncology Group, Southwest Oncology Group, and M. D. Anderson Cancer Center StudyRoland B Walter, Hagop M Kantarjian, Xuelin Huang, et al.
The Journal of Clinical Investigation|August 23, 2000
Retinal expression, regulation, and functional bioactivity of prostacyclin-stimulating factorY Hata, A Clermont, T Yamauchi, et al.
Investigative Ophthalmology & Visual Science|January 8, 2011
Generation of Cre transgenic mice with postnatal RPE-specific ocular expressionJared Iacovelli, Chen Zhao, Natalie Wolkow, et al.
Cytometry. Part B, Clinical Cytometry|December 29, 2021
Comprehensive immunophenotypic study of acute myeloid leukemia with KMT2A (MLL) rearrangement in adults: A single-institution experienceSergej Konoplev, Xiaoqiong Wang, Guilin Tang, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 18, 2002
Progressive photoreceptor degeneration, outer segment dysplasia, and rhodopsin mislocalization in mice with targeted disruption of the retinitis pigmentosa-1 (Rp1) geneJiangang Gao, Kyeongmi Cheon, Steven Nusinowitz, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|November 11, 2025
Oxidative stress and fetal weight: observational findings from a pregnancy cohort in New York CityCarol Duh-Leong, Akhgar Ghassabian, Whitney Cowell, et al.
Biorxiv : the Preprint Server for Biology|July 10, 2023
Multi-omics characterization of partial chemical reprogramming reveals evidence of cell rejuvenationWayne Mitchell, Ludger J E Goeminne, Alexander Tyshkovskiy, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 11, 2020
Copy-number variation contributes 9% of pathogenicity in the inherited retinal degenerationsErin Zampaglione, Benyam Kinde, Emily M Place, et al.
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