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Nucleic Acids Research|November 25, 2010
ModBase, a database of annotated comparative protein structure models, and associated resourcesUrsula Pieper, Benjamin M Webb, David T Barkan, et al.Journal of Medicinal Chemistry|July 27, 2018
Reevaluating the Substrate Specificity of the L-Type Amino Acid Transporter (LAT1)Huan-Chieh Chien, Claire Colas, Karissa Finke, et al.Plos Computational Biology|September 14, 2021
Crowdsourced identification of multi-target kinase inhibitors for RET- and TAU- based disease: The Multi-Targeting Drug DREAM ChallengeZhaoping Xiong, Minji Jeon, Robert J Allaway, et al.Annals of Neurology|January 13, 2019
SLC13A3 variants cause acute reversible leukoencephalopathy and α-ketoglutarate accumulationJoseph P Dewulf, Elsa Wiame, Imen Dorboz, et al.American Journal of Human Genetics|May 23, 2024
Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variantsDina Buitrago Silva, Marena Trinidad, Alicia Ljungdahl, et al.Science Translational Medicine|February 11, 2021
Human neurons from Christianson syndrome iPSCs reveal mutation-specific responses to rescue strategiesSofia B Lizarraga, Li Ma, Abbie M Maguire, et al.Nucleic Acids Research|May 17, 2021
PredictProtein - Predicting Protein Structure and Function for 29 YearsMichael Bernhofer, Christian Dallago, Tim Karl, et al.Cell|December 3, 2016
Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum DisorderDora C Tărlungeanu, Elena Deliu, Christoph P Dotter, et al.Nature Communications|June 4, 2021
Crowdsourced mapping of unexplored target space of kinase inhibitorsAnna Cichońska, Balaguru Ravikumar, Robert J Allaway, et al.European Journal of Human Genetics : EJHG|August 21, 2014
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndromeAlma Kuechler, Alexander M Zink, Thomas Wieland, et al.Pageof 12