Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Gulbenk Anarat-Cappillino"'
Autor:
Rachna Manek, Yao V. Zhang, Patricia Berthelette, Mahmud Hossain, Cathleen S. Cornell, Joseph Gans, Gulbenk Anarat-Cappillino, Sarah Geller, Robert Jackson, Dan Yu, Kuldeep Singh, Sue Ryan, Dinesh S. Bangari, Ethan Y. Xu, Sirkka R. M. Kyostio-Moore
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Abstract Phenylketonuria (PKU) is a genetic deficiency of phenylalanine hydroxylase (PAH) in liver resulting in blood phenylalanine (Phe) elevation and neurotoxicity. A pegylated phenylalanine ammonia lyase (PEG-PAL) metabolizing Phe into cinnamic ac
Externí odkaz:
https://doaj.org/article/f3a454c49a4a458db2c91e87d25ee520
Autor:
Kuldeep Singh, Cathleen S. Cornell, Robert Jackson, Mostafa Kabiri, Michael Phipps, Mitul Desai, Robert Fogle, Xiaoyou Ying, Gulbenk Anarat-Cappillino, Sarah Geller, Jennifer Johnson, Errin Roberts, Katie Malley, Tim Devlin, Matthew DeRiso, Patricia Berthelette, Yao V. Zhang, Susan Ryan, Srinivas Rao, Beth L. Thurberg, Dinesh S. Bangari, Sirkka Kyostio-Moore
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Phenylketonuria (PKU) is an autosomal recessive inborn error of l-phenylalanine (Phe) metabolism. It is caused by a partial or complete deficiency of the enzyme phenylalanine hydroxylase (PAH), which is necessary for conversion of Phe to tyr
Externí odkaz:
https://doaj.org/article/85cf103dd353470493e9b182fec30ee3
Autor:
Kuldeep Singh, Mahmud Hossain, Rachna Manek, Patricia Berthelette, Cathleen S. Cornell, Robert B. Jackson, Dan Yu, Gulbenk Anarat-Cappillino, Ethan Y Xu, Dinesh S. Bangari, Joseph Gans, Yao V. Zhang, Sarah Geller, Sue Ryan, Sirkka Kyostio-Moore
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-13 (2021)
Phenylketonuria (PKU) is a genetic deficiency of phenylalanine hydroxylase (PAH) in liver resulting in blood phenylalanine (Phe) elevation and neurotoxicity. A pegylated phenylalanine ammonia lyase (PEG-PAL) metabolizing Phe into cinnamic acid was re
Autor:
Beth L. Thurberg, Michael Phipps, Gulbenk Anarat-Cappillino, Cathleen S. Cornell, Katie Malley, Jennifer Johnson, Errin Roberts, Tim Devlin, Kuldeep Singh, Xiaoyou Ying, Matthew DeRiso, Srinivas Rao, Susan Ryan, Sirkka Kyostio-Moore, Yao V. Zhang, Sarah Geller, Robert B. Jackson, Dinesh S. Bangari, Mostafa Kabiri, Robert Fogle, Patricia Berthelette, Mitul Desai
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Phenylketonuria (PKU) is an autosomal recessive inborn error of l-phenylalanine (Phe) metabolism. It is caused by a partial or complete deficiency of the enzyme phenylalanine hydroxylase (PAH), which is necessary for conversion of Phe to tyrosine (Ty