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International Journal of Biological Macromolecules|January 16, 2025
Identification of novel phenolic inhibitors from traditional Chinese medicine against toxic α-synuclein aggregation via regulating phase separationLinwei Yu, Xi Li, Tianyi Shi, et al.
Human Molecular Genetics|June 13, 1998
Maternal meiosis I non-disjunction of chromosome 15: dependence of the maternal age effect on level of recombinationW P Robinson, B D Kuchinka, F Bernasconi, et al.
Nature Communications|July 17, 2023
A renal YY1-KIM1-DR5 axis regulates the progression of acute kidney injuryChen Yang, Huidie Xu, Dong Yang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|September 25, 2023
Quadruplet pregnancy outcome with and without fetal reduction: Danish national cohort study (2008-2018) and comparison with dichorionic twinsM K Rasmussen, S E Kristensen, C K Ekelund, et al.
Investigative Ophthalmology & Visual Science|January 25, 2006
A large GLC1C Greek family with a myocilin T377M mutation: inheritance and phenotypic variabilityMichael B Petersen, George Kitsos, John R Samples, et al.
Human Mutation|November 20, 2010
Recommendations for genetic variation data capture in developing countries to ensure a comprehensive worldwide data collectionGeorge P Patrinos, Jumana Al Aama, Aida Al Aqeel, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|October 21, 2025
Prenatal detection and outcome of major heart defects in a country with universal screeningC Vedel, J Steensberg, O B Petersen, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|November 11, 2009
Low-dose total body irradiation and fludarabine conditioning for HLA class I-mismatched donor stem cell transplantation and immunologic recovery in patients with hematologic malignancies: a multicenter trialHirohisa Nakamae, Barry E Storer, Rainer Storb, et al.
European Journal of Human Genetics : EJHG|January 11, 2007
A seventh locus for otosclerosis, OTSC7, maps to chromosome 6q13-16.1Melissa Thys, Kris Van Den Bogaert, Vassiliki Iliadou, et al.
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