Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Sneha Mokashi"'
Autor:
Jessica Cooley Coleman, Sneha Mokashi, Adithya Kandhadai, Aubrey Rose, Richard Steet, Raymond Louie, Michael Lyons, Fatima Abidi
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101569- (2024)
Externí odkaz:
https://doaj.org/article/54c619472c384253bb957d216e8642ed
Autor:
Maxwell B Colonna, Tonya Moss, Sneha Mokashi, Sujata Srikanth, Julie R Jones, Jackson R Foley, Cindy Skinner, Angie Lichty, Anthony Kocur, Tim Wood, Tracy Murray Stewart, Robert A Casero Jr., Heather Flanagan-Steet, Arthur S Edison, Michael J Lyons, Richard Steet
Publikováno v:
Human Molecular Genetics. 32:732-744
Mono- and bi-allelic variants in ALDH18A1 cause a spectrum of human disorders associated with cutaneous and neurological findings that overlap with both cutis laxa and spastic paraplegia. ALDH18A1 encodes the bifunctional enzyme pyrroline-5-carboxyla
Autor:
MacPherson, Rebecca A.1 (AUTHOR), Shankar, Vijay1 (AUTHOR), Sunkara, Lakshmi T.2 (AUTHOR), Hannah, Rachel C.1 (AUTHOR), Campbell III, Marion R.1 (AUTHOR), Anholt, Robert R. H.1 (AUTHOR) ranholt@clemson.edu, Mackay, Trudy F. C.1 (AUTHOR) tmackay@clemson.edu
Publikováno v:
BMC Genomics. 11/30/2022, Vol. 23 Issue 1, p1-16. 16p.
Autor:
Colonna, Maxwell B, Moss, Tonya, Mokashi, Sneha, Srikanth, Sujata, Jones, Julie R, Foley, Jackson R, Skinner, Cindy, Lichty, Angie, Kocur, Anthony, Wood, Tim, Stewart, Tracy Murray, Casero Jr., Robert A, Flanagan-Steet, Heather, Edison, Arthur S, Lyons, Michael J, Steet, Richard
Publikováno v:
Human Molecular Genetics; Mar2023, Vol. 32 Issue 5, p732-744, 13p
Publikováno v:
Chemical Senses; Sep2016, Vol. 41 Issue 7, pe1-e110, 110p
Autor:
Rajalakshmi Sriram
This book covers the underexplored subject of ‘fathering'in India. It delves into the shared aspirations of men in India to nurture their children in sensitively attuned ways within the culturally prescriptive context that governs men's roles as pr