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Immunity, Inflammation and Disease|November 18, 2014
Human pre-B cell receptor signal transduction: evidence for distinct roles of PI3kinase and MAP-kinase signalling pathwaysKolandaswamy Anbazhagan, Amrathlal Rabbind Singh, Piec Isabelle, et al.Journal of Medicinal Chemistry|April 2, 2004
Synthesis, antimalarial activity, and molecular modeling of new pyrrolo[1,2-a]quinoxalines, bispyrrolo[1,2-a]quinoxalines, bispyrido[3,2-e]pyrrolo[1,2-a]pyrazines, and bispyrrolo[1,2-a]thieno[3,2-e]pyrazinesJean Guillon, Philippe Grellier, Mehdi Labaied, et al.The Journal of Clinical Investigation|October 22, 2005
PPAR alpha inhibits vascular smooth muscle cell proliferation underlying intimal hyperplasia by inducing the tumor suppressor p16INK4aFlorence Gizard, Carole Amant, Olivier Barbier, et al.Journal of Cellular and Molecular Medicine|December 29, 2022
HDAC6 regulates human erythroid differentiation through modulation of JAK2 signallingPascal Vong, Kahia Messaoudi, Nicolas Jankovsky, et al.Epileptic Disorders : International Epilepsy Journal with Videotape|August 19, 2010
Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndromeJacques Rochette, Patrice Roll, Ying-Hui Fu, et al.Journal of Hepatology|July 23, 2003
Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overloadAnne-Marie Jouanolle, Véronique Douabin-Gicquel, Chantal Halimi, et al.Plos One|November 10, 2010
Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11Patrice Roll, Damien Sanlaville, Jennifer Cillario, et al.Blood Advances|November 19, 2020
A new role of glutathione peroxidase 4 during human erythroblast enucleationHakim Ouled-Haddou, Kahia Messaoudi, Yohann Demont, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 18, 2015
Severe phenotypic spectrum of biallelic mutations in PRRT2 geneMarion Delcourt, Florence Riant, Josette Mancini, et al.Human Molecular Genetics|April 10, 2014
Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patientsIsabelle Callebaut, Rozenn Joubrel, Serge Pissard, et al.Pageof 5