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pro vyhledávání: '"Stephen P. Ray"'
Autor:
Xiying Wu, Stephen P. Ray, James W Wade, Bruce A. Bunnell, Kamran Khoobehi, Lydia Masako Ferreira, Jeffrey M. Gimble, Fabiana Zanata
Publikováno v:
ACS Biomaterials Science & Engineering. 3:1477-1482
Adipose tissue is now recognized as a complex organ serving endocrine, immune, and metabolic functions. Adipose depots are composed of mature adipocytes as well as stromal vascular fraction (SVF) cells, a heterogeneous population of B and T lymphocyt
Autor:
Nathan Duval, Stephen P. Ray, Kingshuk Ghosh, Terry G. Wilkinson, David Patterson, Sean E. Shaheen
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1834:1545-1553
Adenylosuccinate lyase (ADSL) is a homotetrameric enzyme involved in the de novo purine biosynthesis pathway and purine nucleotide cycle. Missense mutations in the protein lead to ADSL deficiency, an inborn error of purine metabolism characterized by
Autor:
Kingshuk Ghosh, Stephen P. Ray, Glenn C. Capodagli, Scott D. Pegan, Lucas Sawle, Lauren A. F. Calkins, David Patterson, Michelle K. Deaton
Publikováno v:
Biochemistry. 51:6701-6713
Adenylosuccinate lyase (ADSL) deficiency is a rare autosomal recessive disorder, which causes a defect in purine metabolism resulting in neurological and physiological symptoms. ADSL executes two nonsequential steps in the de novo synthesis of AMP: t
Publikováno v:
The Journal of pediatrics. 75(2)