Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Viviana J. Mancilla"'
Autor:
Viviana J. Mancilla, Paige N. Braden-Kuhle, Kelly N. Brice, Allison E. Mann, Megan T. Williams, Yan Zhang, Michael J. Chumley, Robert C. Barber, Sabrina N. White, Gary W. Boehm, Michael S. Allen
Publikováno v:
Microorganisms, Vol 11, Iss 11, p 2694 (2023)
The effects of synthetic, free-amino acid diets, similar to those prescribed as supplements for (phenylketonuria) PKU patients, on gut microbiota and overall health are not well understood. In the current, multidisciplinary study, we examined the eff
Externí odkaz:
https://doaj.org/article/8f158b55c7bb4b6e81550e121605f381
Autor:
Viviana J. Mancilla, Noah C. Peeri, Talisa Silzer, Riyaz Basha, Martha Felini, Harlan P. Jones, Nicole Phillips, Meng-Hua Tao, Srikantha Thyagarajan, Jamboor K. Vishwanatha
Publikováno v:
Frontiers in Genetics, Vol 11 (2020)
Social epigenomics has emerged as an integrative field of research focused on identification of socio-environmental factors, their influence on human biology through epigenomic modifications, and how they contribute to current health disparities. Sev
Externí odkaz:
https://doaj.org/article/c9571f00d3f143ad952dc6d9a715ee12
Publikováno v:
Microorganisms, Vol 9, Iss 3, p 530 (2021)
Phenylketonuria (PKU) is an inborn error of phenylalanine metabolism primarily treated through a phenylalanine-restrictive diet that is frequently supplemented with an amino acid formula to maintain proper nutrition. Little is known of the effects of
Externí odkaz:
https://doaj.org/article/e1b93cfb25a64b36b9e1b4242567720e
ThePahenu2mutation in C57BL/6J mice is a well characterized model for studying phenylketonuria (PKU), withPahenu2homozygotes displaying heightened blood phenylalanine and other characteristics of PKU.Pahenu2homozygous females do not successfully rear
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::143c8cdc98f8385c3dcebd13f1ebc5f1
https://doi.org/10.1101/2022.12.12.520145
https://doi.org/10.1101/2022.12.12.520145
Publikováno v:
Microorganisms, Vol 9, Iss 530, p 530 (2021)
Microorganisms
Volume 9
Issue 3
Microorganisms
Volume 9
Issue 3
Phenylketonuria (PKU) is an inborn error of phenylalanine metabolism primarily treated through a phenylalanine-restrictive diet that is frequently supplemented with an amino acid formula to maintain proper nutrition. Little is known of the effects of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8ac4185798254ea8050ccd4f4ed139f
https://www.mdpi.com/2076-2607/9/3/530
https://www.mdpi.com/2076-2607/9/3/530