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Steroids|July 30, 2013
Benzopyran derivative CDRI-85/287 induces G2-M arrest in estrogen receptor-positive breast cancer cells via modulation of estrogen receptors α- and β-mediated signaling, in parallel to EGFR signaling and suppresses the growth of tumor xenograftRuchi Saxena, Iram Fatima, Vishal Chandra, et al.Reproductive Toxicology (Elmsford, N.Y.)|February 15, 2025
The biological effects of bisphenol AF in reproduction and development: What do we know so far?Megan V Alexander, Archana Ayyar, Alexandra W Gannon, et al.Biology of Reproduction|August 9, 2020
In utero low-protein-diet-programmed type 2 diabetes in adult offspring is mediated by sex hormones in rats†Chellakkan S Blesson, Amy K Schutt, Vidyadharan A Vipin, et al.Public Health Action|January 15, 2016
Compliance with infection control practices in sputum microscopy centres: a study from Kerala, IndiaO P Aslesh, N P Ubaid, S B Nagaraja, et al.Antimicrobial Agents and Chemotherapy|January 21, 2016
Validation and Clinical Evaluation of a Novel Method To Measure Miltefosine in Leishmaniasis Patients Using Dried Blood Spot Sample CollectionA E Kip, H Rosing, M J X Hillebrand, et al.American Journal of Obstetrics and Gynecology|February 14, 2016
Novel lean type 2 diabetic rat model using gestational low-protein programmingChellakkan S Blesson, Amy K Schutt, Meena P Balakrishnan, et al.Clinical Genetics|January 7, 2011
Twenty-five novel mutations including duplications in the ATP7A geneM-P Moizard, N Ronce, S Blesson, et al.Molecular Psychiatry|February 25, 2009
Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autismF Laumonnier, C Shoubridge, C Antar, et al.American Journal of Medical Genetics. Part A|November 13, 2025
Variant Update on ASCC1: Characterization of the First Homozygous Missense Variant Involved in Prenatal-Onset Spinal Muscular Atrophy With Congenital Bone Fractures 2A Civit, L Kerbellec, D Laurenceau, et al.Clinical Genetics|September 26, 2015
Fetal phenotypes in otopalatodigital spectrum disordersS Naudion, S Moutton, I Coupry, et al.Pageof 5