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American Journal of Human Genetics|May 23, 2024
Haploinsufficiency underlies the neurodevelopmental consequences of SLC6A1 variantsDina Buitrago Silva, Marena Trinidad, Alicia Ljungdahl, et al.
Cell Reports|December 21, 2022
Blocking AMPK β1 myristoylation enhances AMPK activity and protects mice from high-fat diet-induced obesity and hepatic steatosisKatyayanee Neopane, Natalie Kozlov, Florentina Negoita, et al.
Nature|December 5, 2003
Oligocene mammals from Ethiopia and faunal exchange between Afro-Arabia and EurasiaJohn Kappelman, D Tab Rasmussen, William J Sanders, et al.
Genome Research|November 12, 2021
Long-read assembly and comparative evidence-based reanalysis of <i>Cryptosporidium</i> genome sequences reveal expanded transporter repertoire and duplication of entire chromosome ends including subtelomeric regionsRodrigo P Baptista, Yiran Li, Adam Sateriale, et al.
Virus Evolution|March 31, 2022
Quantifying rates of HIV-1 flow between risk groups and geographic locations in Kenya: A country-wide phylogenetic studyGeorge M Nduva, Frederick Otieno, Joshua Kimani, et al.
Bioinformatics (Oxford, England)|December 7, 2023
Artificial intelligence-assisted quantification and assessment of whole slide images for pediatric kidney disease diagnosisChunyue Feng, Kokhaur Ong, David M Young, et al.
The Journal of General Virology|November 19, 2013
Characterization of innate responses to influenza virus infection in a novel lung type I epithelial cell modelCarrie M Rosenberger, Rebecca L Podyminogin, Peter S Askovich, et al.
Human Vaccines|April 22, 2011
Prevalence of specific neutralizing antibodies against Sendai virus in populations from different geographic areas: implications for AIDS vaccine development using Sendai virus vectorsHiroto Hara, Hiroto Hara, Takashi Hironaka, et al.
Plos One|May 1, 2008
Baseline morbidity in 2,990 adult African volunteers recruited to characterize laboratory reference intervals for future HIV vaccine clinical trialsWendy Stevens, Anatoli Kamali, Etienne Karita, et al.
Human Molecular Genetics|August 26, 2011
Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHEPatricia B S Celestino-Soper, Chad A Shaw, Stephan J Sanders, et al.
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