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Nature Communications|September 23, 2023
An inverse agonist of orphan receptor GPR61 acts by a G protein-competitive allosteric mechanismJoshua A Lees, João M Dias, Francis Rajamohan, et al.
American Journal of Medical Genetics. Part A|June 18, 2019
Perinatal distress in 1p36 deletion syndrome can mimic hypoxic ischemic encephalopathyLauren B Carter, Agatino Battaglia, Athena Cherry, et al.
Alzheimer'S Research & Therapy|February 18, 2021
CERTL reduces C16 ceramide, amyloid-β levels, and inflammation in a model of Alzheimer's diseaseSimone M Crivelli, Qian Luo, Jo A A Stevens, et al.
Journal of the Academy of Consultation-Liaison Psychiatry|May 26, 2022
Behavioral and Emotional Dyscontrol Following Traumatic Brain Injury: A Systematic Review of Neuroimaging and Electrophysiological CorrelatesBarry R Bryant, Lisa N Richey, Sahar Jahed, et al.
Plos Genetics|September 18, 2018
Disrupted structure and aberrant function of CHIP mediates the loss of motor and cognitive function in preclinical models of SCAR16Chang-He Shi, Carrie Rubel, Sarah E Soss, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical regionEugen-Matthias Strehle, Linbo Yu, Jill A Rosenfeld, et al.
British Journal of Haematology|April 10, 2024
Outcome and feasibility of radiotherapy bridging in large B-cell lymphoma patients receiving CD19 CAR T in the UKA Kuhnl, C Roddie, A A Kirkwood, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|June 5, 2001
Need for alternative trial designs and evaluation strategies for therapeutic studies of invasive mycosesJ H Rex, T J Walsh, M Nettleman, et al.
The Plant Journal : for Cell and Molecular Biology|May 5, 2016
The walnut (Juglans regia) genome sequence reveals diversity in genes coding for the biosynthesis of non-structural polyphenolsPedro J Martínez-García, Marc W Crepeau, Daniela Puiu, et al.
American Journal of Medical Genetics. Part A|October 13, 2006
Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformationNathaniel H Robin, Clare J Taylor, Donna M McDonald-McGinn, et al.
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