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pro vyhledávání: '"Ned Porter"'
Autor:
Babunageswararao Kanuri, Vincent Fong, Sithara Raju Ponny, Keri A. Tallman, Sriganesh Ramachandra Rao, Ned Porter, Steven J. Fliesler, Shailendra B. Patel
Publikováno v:
Journal of Lipid Research, Vol 62, Iss , Pp 100002- (2021)
Smith-Lemli-Opitz Syndrome (SLOS) is a developmental disorder (OMIM #270400) caused by autosomal recessive mutations in the Dhcr7 gene, which encodes the enzyme 3β-hydroxysterol-Δ7 reductase. SLOS patients present clinically with dysmorphology and
Externí odkaz:
https://doaj.org/article/fffd503a6747449ba298d727bfc30580
Autor:
Rodney D. Britt, Ned Porter, Mitchell H. Grayson, Kymberly M. Gowdy, Megan Ballinger, Kara Wada, Hye-Young Kim, Mireia Guerau-de-Arellano
Publikováno v:
Journal of Allergy and Clinical Immunology. 151:47-59
Autor:
Ned Porter, Paul Koenigs, Dagmar Ringe, Gregory A. Petsko, Barry L. Stoddard, Kyriacos Petratos
Publikováno v:
Scopus-Elsevier
Crystals of gamma-chymotrypsin inhibited with the photodissociable group trans-p-diethylamino-o-hydroxy-alpha-methylcinnamate were irradiated with a 1-msec flash from a high-energy xenon flashlamp in the presence of the mechanism-based inhibitor 3-be