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Genome Medicine|October 23, 2025
A quantitative, Bayesian-informed approach to gene-specific variant classification: Updated Expert Panel recommendations improve classification of TP53 germline variants for Li-Fraumeni syndromeCristina Fortuno, Megan N Frone, Jessica Mester, et al.Space Science Reviews|August 23, 2024
Apollo Next Generation Sample Analysis (ANGSA): an Apollo Participating Scientist Program to Prepare the Lunar Sample Community for ArtemisC K Shearer, F M McCubbin, S Eckley, et al.Journal of Bacteriology|April 20, 2006
Pathogenomic sequence analysis of Bacillus cereus and Bacillus thuringiensis isolates closely related to Bacillus anthracisCliff S Han, Gary Xie, Jean F Challacombe, et al.CBE Life Sciences Education|March 3, 2010
The genomics education partnership: successful integration of research into laboratory classes at a diverse group of undergraduate institutionsChristopher D Shaffer, Consuelo Alvarez, Cheryl Bailey, et al.Molecular Genetics and Metabolism|April 16, 2015
How strict is galactose restriction in adults with galactosaemia? International practiceS Adam, R Akroyd, S Bernabei, et al.Journal of Bacteriology|March 6, 2007
The complete genome sequence of Bacillus thuringiensis Al HakamJean F Challacombe, Michael R Altherr, Gary Xie, et al.Frontiers in Veterinary Science|May 9, 2025
Macroepidemiological trends of Influenza A virus detection through reverse transcription real-time polymerase chain reaction (RT-rtPCR) in porcine samples in the United States over the last 20 yearsDaniel C A Moraes, Guilherme A Cezar, Edison S Magalhães, et al.Neuroimage. Clinical|March 21, 2024
COVID-19 Stroke Apical Lung Examination Study 2: a national prospective CTA biomarker study of the lung apices, in patients presenting with suspected acute stroke (COVID SALES 2)T Ratneswaren, N Chan, J Aeron-Thomas, et al.Nature|January 29, 2025
An evaporite sequence from ancient brine recorded in Bennu samplesT J McCoy, S S Russell, T J Zega, et al.Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Loss-of-function variants in CUL3 cause a syndromic neurodevelopmental disorderPatrick R Blackburn, Frédéric Ebstein, Tzung-Chien Hsieh, et al.Pageof 262