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Plos One|August 6, 2011

Hypertension is associated with marked alterations in sphingolipid biology: a potential role for ceramideLéon J A Spijkers, Rob F P van den Akker, Ben J A Janssen, et al.

Journal of the American Heart Association|May 22, 2016

Sphingosine-1-Phosphate Receptor 1 Regulates Cardiac Function by Modulating Ca2+ Sensitivity and Na+/H+ Exchange and Mediates Protection by Ischemic PreconditioningPetra Keul, Marcel M G J van Borren, Alexander Ghanem, et al.

American Journal of Human Genetics|November 25, 2000

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.

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Showing results (61-70 of 63) with videos related to

Sort By:

Pageof 7

You have reached the last page of results.This site can display upto 63 results.

Plos One|August 6, 2011

Hypertension is associated with marked alterations in sphingolipid biology: a potential role for ceramideLéon J A Spijkers, Rob F P van den Akker, Ben J A Janssen, et al.

Journal of the American Heart Association|May 22, 2016

Sphingosine-1-Phosphate Receptor 1 Regulates Cardiac Function by Modulating Ca2+ Sensitivity and Na+/H+ Exchange and Mediates Protection by Ischemic PreconditioningPetra Keul, Marcel M G J van Borren, Alexander Ghanem, et al.

American Journal of Human Genetics|November 25, 2000

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.

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