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Journal of Human Evolution|July 31, 2019
A multiscale stratigraphic investigation of the context of StW 573 'Little Foot' and Member 2, Sterkfontein Caves, South AfricaLaurent Bruxelles, Dominic J Stratford, Richard Maire, et al.
Endocrinology|May 12, 2018
Thyroid Hormone Receptor β Suppression of RUNX2 Is Mediated by Brahma-Related Gene 1-Dependent Chromatin RemodelingNoelle E Gillis, Thomas H Taber, Eric L Bolf, et al.
BMJ Open|April 6, 2021
Digital health interventions for the management of mental health in people with chronic diseases: a rapid reviewMaxime Sasseville, Annie LeBlanc, Mylène Boucher, et al.
Nature Biotechnology|March 27, 2012
A proteomics approach for the identification and cloning of monoclonal antibodies from serumWan Cheung Cheung, Sean A Beausoleil, Xiaowu Zhang, et al.
Nature Genetics|October 1, 2013
Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autismChristian P Schaaf, Manuel L Gonzalez-Garay, Fan Xia, et al.
Scientific Reports|March 18, 2020
The atlas of StW 573 and the late emergence of human-like head mobility and brain metabolismAmélie Beaudet, Ronald J Clarke, Jason L Heaton, et al.
Journal of Human Evolution|February 20, 2019
The bony labyrinth of StW 573 ("Little Foot"): Implications for early hominin evolution and paleobiologyAmélie Beaudet, Ronald J Clarke, Laurent Bruxelles, et al.
Folia Primatologica; International Journal of Primatology|September 28, 2021
StW 573 Australopithecus prometheus: Its Significance for an Australopith BauplanRobin Huw Crompton, Juliet McClymont, Sarah Elton, et al.
The Journal of Experimental Medicine|July 7, 1998
Spontaneous skin ulceration and defective T cell function in CD18 null miceK Scharffetter-Kochanek, H Lu, K Norman, et al.
Data in Brief|July 9, 2020
Data set describing the <i>in vitro</i> biological activity of JMV2009, a novel silylated neurotensin(8-13) analogÉlie Besserer-Offroy, Pascal Tétreault, Rebecca L Brouillette, et al.
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