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Cardiovascular Research|April 6, 2017
Early sensitization of myofilaments to Ca2+ prevents genetically linked dilated cardiomyopathy in miceMarco L Alves, Chad M Warren, Jillian N Simon, et al.
American Journal of Human Genetics|September 12, 2007
The variant inv(2)(p11.2q13) is a genuinely recurrent rearrangement but displays some breakpoint heterogeneityIna Fickelscher, Thomas Liehr, Kathryn Watts, et al.
Cell Host & Microbe|December 10, 2008
Three-dimensional analysis of budding sites and released virus suggests a revised model for HIV-1 morphogenesisLars-Anders Carlson, John A G Briggs, Bärbel Glass, et al.
Brain : a Journal of Neurology|September 6, 2003
Dosage-sensitive X-linked locus influences the development of amygdala and orbitofrontal cortex, and fear recognition in humansCatriona D Good, Kate Lawrence, N Simon Thomas, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2023
A gene pathogenicity tool 'GenePy' identifies missed biallelic diagnoses in the 100,000 Genomes ProjectEleanor G Seaby, Gary Leggatt, Guo Cheng, et al.
L'Encephale|February 27, 2017
[How may practitioners interpret the results of clinical trials?]J-M Azorin, M Adida, O Blin, et al.
American Journal of Physiology. Heart and Circulatory Physiology|February 3, 2023
Endothelial cell-specific roles for tetrahydrobiopterin in myocardial function, cardiac hypertrophy, and response to myocardial ischemia-reperfusion injurySurawee Chuaiphichai, Sandy M Chu, Ricardo Carnicer, et al.
Genome Medicine|September 9, 2024
Identification of diagnostic candidates in Mendelian disorders using an RNA sequencing-centric approachCarolina Jaramillo Oquendo, Htoo A Wai, Wil I Rich, et al.
British Journal of Clinical Pharmacology|May 21, 2004
Population pharmacokinetics of pyrimethamine and sulfadoxine in children with congenital toxoplasmosisT Trenque, N Simon, I Villena, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 21, 2024
A gene pathogenicity tool "GenePy" identifies missed biallelic diagnoses in the 100,000 Genomes ProjectEleanor G Seaby, Gary Leggatt, Guo Cheng, et al.
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