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Human Molecular Genetics|March 31, 2009
A SMN missense mutation complements SMN2 restoring snRNPs and rescuing SMA miceEileen Workman, Luciano Saieva, Tessa L Carrel, et al.
British Journal of Cancer|September 1, 1996
High levels of loss at the 17p telomere suggest the close proximity of a tumour suppressorG R White, M Stack, M Santibáñez-Koref, et al.
Human Molecular Genetics|May 16, 1998
The UTX gene escapes X inactivation in mice and humansA Greenfield, L Carrel, D Pennisi, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 27, 2006
Survival motor neuron function in motor axons is independent of functions required for small nuclear ribonucleoprotein biogenesisTessa L Carrel, Michelle L McWhorter, Eileen Workman, et al.
Clinical Endocrinology|August 20, 2008
Ghrelin concentrations in Prader-Willi syndrome (PWS) infants and children: changes during developmentAndrea M Haqq, Steven C Grambow, Michael Muehlbauer, et al.
American Journal of Human Genetics|April 28, 2001
A recurrent RNA-splicing mutation in the SEDL gene causes X-linked spondyloepiphyseal dysplasia tardaG E Tiller, V L Hannig, D Dozier, et al.
Pediatric Obesity|March 3, 2015
Familial and individual predictors of obesity and insulin resistance in urban Hispanic childrenM Santiago-Torres, Y Cui, A K Adams, et al.
Environmental Health Perspectives|March 10, 2009
Environment and obesity in the National Children's StudyLeonardo Trasande, Chris Cronk, Maureen Durkin, et al.
The American Journal of Clinical Nutrition|March 5, 2010
Effect of conjugated linoleic acid on body fat accretion in overweight or obese childrenNatalie M Racine, Abigail C Watras, Aaron L Carrel, et al.
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