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Human Molecular Genetics|September 6, 2013
Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemiaYoung H Lim, Diana Ovejero, Jeffrey S Sugarman, et al.
Scientific Reports|September 14, 2022
Novel tricyclic small molecule inhibitors of Nicotinamide N-methyltransferase for the treatment of metabolic disordersSven Ruf, Sridharan Rajagopal, Sanjay Venkatachalapathi Kadnur, et al.
Bioorganic & Medicinal Chemistry Letters|May 22, 2019
Design, synthesis and biological evaluation of indane derived GPR40 agoPAMsBarbara Pio, Harry R Chobanian, Yan Guo, et al.
American Journal of Medical Genetics. Part A|August 2, 2021
Exome survey of individuals affected by VATER/VACTERL with renal phenotypes identifies phenocopies and novel candidate genesCaroline M Kolvenbach, Amelie T van der Ven, Franziska Kause, et al.
Scientific Reports|February 28, 2018
A small molecule inhibitor of Nicotinamide N-methyltransferase for the treatment of metabolic disordersAimo Kannt, Sridharan Rajagopal, Sanjay Venkatachalapathi Kadnur, et al.
Infection and Immunity|September 8, 2011
PATRIC: the comprehensive bacterial bioinformatics resource with a focus on human pathogenic speciesJoseph J Gillespie, Alice R Wattam, Stephen A Cammer, et al.
Biological Psychiatry|December 16, 2011
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autismThomas V Fernandez, Stephan J Sanders, Ilana R Yurkiewicz, et al.
Bjpsych Open|November 6, 2025
Characterising negative symptoms in schizophrenia: CHANSS study protocolNoham Wolpe, Clàudia Aymerich, Ying Jin, et al.
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