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Genes and Function|June 1, 1997
Mutation analysis of the mouse myosin VIIA deafness geneP Mburu, X Z Liu, J Walsh, et al.
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|September 16, 2000
Expression of the type I diabetes-associated gene LRP5 in macrophages, vitamin A system cells, and the Islets of Langerhans suggests multiple potential roles in diabetesD J Figueroa, J F Hess, B Ky, et al.
Human Molecular Genetics|February 1, 1993
Human olfactory marker protein maps close to tyrosinase and is a candidate gene for Usher syndrome type IK L Evans, J Fantes, C Simpson, et al.
Annals of the New York Academy of Sciences|June 8, 2000
A missense mutation in myosin VIIA prevents aminoglycoside accumulation in early postnatal cochlear hair cellsG P Richardson, A Forge, C J Kros, et al.
Human Molecular Genetics|December 10, 1999
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing lossX Z Liu, X J Xia, L R Xu, et al.
Physical Review Letters|October 6, 2000
Surface-enhanced and normal stokes and anti-stokes Raman spectroscopy of single-walled carbon nanotubesK Kneipp, H Kneipp, P Corio, et al.
Diabetes & Metabolism|February 28, 2017
Moderate intensity sports and exercise is associated with glycaemic control in women with gestational diabetesS F Ehrlich, M M Hedderson, S D Brown, et al.
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