Showing results (71-80 of 86) with videos related to
Sort By:
Pageof 9
American Journal of Medical Genetics. Part A|May 19, 2016
Nephroblastomatosis or Wilms tumor in a fourth patient with a somatic PIK3CA mutationKaren W Gripp, Laura Baker, Vinay Kandula, et al.Hematological Oncology|May 8, 2021
Safety and efficacy of autologous whole cell vaccines in hematologic malignancies: A systematic review and meta-analysisDonald J Bastin, Sarwat T Khan, Joshua Montroy, et al.Sleep|October 10, 2025
Metabolomic biomarkers of rest-activity rhythms in older women: results from the Women's Health Initiative studyLingxiao Zhang, Chris Ho Ching Yeung, Kyoung A Viola Lee, et al.Journal of Toxicology and Environmental Health. Part A|December 3, 2009
Endotoxin exposure and inflammation markers among agricultural workers in Colorado and NebraskaJames B Burch, Erik Svendsen, Paul D Siegel, et al.American Journal of Human Genetics|August 9, 2014
Mutations in LAMA1 cause cerebellar dysplasia and cysts with and without retinal dystrophyKimberly A Aldinger, Stephen J Mosca, Martine Tétreault, et al.Alzheimer'S & Dementia (New York, N. Y.)|April 10, 2024
The AUstralian multidomain Approach to Reduce dementia Risk by prOtecting brain health With lifestyle intervention study (AU-ARROW): A study protocol for a single-blind, multi-site, randomized controlled trialSamantha L Gardener, Stephanie J Fuller, Sharon L Naismith, et al.Nature|July 13, 2022
Structure-function analysis of the SHOC2-MRAS-PP1C holophosphatase complexJason J Kwon, Behnoush Hajian, Yuemin Bian, et al.American Journal of Human Genetics|May 5, 2018
Variants in EXOSC9 Disrupt the RNA Exosome and Result in Cerebellar Atrophy with Spinal Motor NeuronopathyDavid T Burns, Sandra Donkervoort, Juliane S Müller, et al.Brain : a Journal of Neurology|October 4, 2017
Mutations of AKT3 are associated with a wide spectrum of developmental disorders including extreme megalencephalyDiana Alcantara, Andrew E Timms, Karen Gripp, et al.European Journal of Human Genetics : EJHG|November 29, 2017
HUWE1 variants cause dominant X-linked intellectual disability: a clinical study of 21 patientsStéphanie Moortgat, Siren Berland, Ingvild Aukrust, et al.Pageof 9