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The Science of the Total Environment|December 29, 2022
Parallel deployment of passive and composite samplers for surveillance and variant profiling of SARS-CoV-2 in sewageGyuhyon Cha, Katherine E Graham, Kevin J Zhu, et al.
Science Translational Medicine|June 4, 2025
IFN-γ-resistant CD28 CAR T cells demonstrate increased survival, efficacy, and durability in multiple murine tumor modelsStefanie R Bailey, Hana N Takei, Giulia Escobar, et al.
European Journal of Human Genetics : EJHG|September 13, 2023
Börjeson-Forssman-Lehmann syndrome: delineating the clinical and allelic spectrum in 14 new familiesVani Jain, Seow Hoong Foo, Stephen Chooi, et al.
Nature Genetics|June 6, 2006
Mutations in the gene encoding GlyT2 (SLC6A5) define a presynaptic component of human startle diseaseMark I Rees, Kirsten Harvey, Brian R Pearce, et al.
World Journal for Pediatric & Congenital Heart Surgery|March 27, 2014
Linking the congenital heart surgery databases of the Society of Thoracic Surgeons and the Congenital Heart Surgeons' Society: part 2--lessons learned and implicationsJeffrey P Jacobs, Sara K Pasquali, Erle Austin, et al.
Pediatric Research|September 27, 2005
TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndromeDeborah A McDermott, Michael C Bressan, Jie He, et al.
World Journal for Pediatric & Congenital Heart Surgery|March 27, 2014
Linking the congenital heart surgery databases of the Society of Thoracic Surgeons and the Congenital Heart Surgeons' Society: part 1--rationale and methodologyJeffrey P Jacobs, Sara K Pasquali, Erle Austin, et al.
The Journal of Allergy and Clinical Immunology|September 7, 2023
Impact of newborn screening for SCID on the management of congenital athymiaEvey Howley, Zainab Golwala, Matthew Buckland, et al.
Journal of Bacteriology|September 21, 2010
Complete genome sequence of the cellulolytic thermophile Caldicellulosiruptor obsidiansis OB47TJames G Elkins, Adriane Lochner, Scott D Hamilton-Brehm, et al.
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