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American Journal of Human Genetics|March 3, 1999
Location score and haplotype analyses of the locus for autosomal recessive spastic ataxia of Charlevoix-Saguenay, in chromosome region 13q11A Richter, J D Rioux, J P Bouchard, et al.Nature Genetics|February 2, 2000
ARSACS, a spastic ataxia common in northeastern Québec, is caused by mutations in a new gene encoding an 11.5-kb ORFJ C Engert, P Bérubé, J Mercier, et al.Frontiers in Tuberculosis|June 3, 2026
Dose optimization of inhaled tigecycline in humans to overcome inherent adverse events and maximize bacterial clearance using a physiologically-based pharmacokinetic modeling approachHyunseo Park, Amarinder Singh, Ashish Srivastava, et al.Bioorganic & Medicinal Chemistry|May 20, 2018
BET bromodomain ligands: Probing the WPF shelf to improve BRD4 bromodomain affinity and metabolic stabilityLaura E Jennings, Matthias Schiedel, David S Hewings, et al.Nature Communications|February 9, 2019
Folliculin regulates mTORC1/2 and WNT pathways in early human pluripotencyJ Mathieu, D Detraux, D Kuppers, et al.Nature Genetics|February 14, 1998
Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophyB Brais, J P Bouchard, Y G Xie, et al.Journal of Medicinal Chemistry|July 13, 2021
Controlling Intramolecular Interactions in the Design of Selective, High-Affinity Ligands for the CREBBP BromodomainMichael Brand, James Clayton, Mustafa Moroglu, et al.The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 20, 2012
Diversity of ARSACS mutations in French-CanadiansI Thiffault, M J Dicaire, M Tetreault, et al.Annals of Neurology|May 1, 1997
Phenotypic variability in Friedreich ataxia: role of the associated GAA triplet repeat expansionL Montermini, A Richter, K Morgan, et al.Pageof 16