Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ashish S. Kaushik"'
Publikováno v:
Pain and Therapy, Vol 9, Iss 2, Pp 487-498 (2020)
Abstract Chronic pain is highly prevalent in the United States, impacting 28.4% of the adult population, or 69.6 million people, as of 2016. Chronic pain is often associated with anxiety, depression, and restrictions in mobility and daily activities,
Externí odkaz:
https://doaj.org/article/de7820bbe0e94cd49e469729914c5cd4
Publikováno v:
Pain and Therapy
Pain and Therapy, Vol 9, Iss 2, Pp 487-498 (2020)
Pain and Therapy, Vol 9, Iss 2, Pp 487-498 (2020)
Chronic pain is highly prevalent in the United States, impacting 28.4% of the adult population, or 69.6 million people, as of 2016. Chronic pain is often associated with anxiety, depression, and restrictions in mobility and daily activities, substant
Autor:
Ashley N, Turner, Reagan S, Andersen, Ivy E, Bookout, Lauren N, Brashear, James C, Davis, David M, Gahan, John P, Gotham, Baraa A, Hijaz, Ashish S, Kaushik, Jordan B, Mcgill, Victoria L, Miller, Zachariah P, Moseley, Cerissa L, Nowell, Riddhi K, Patel, Mia C, Rodgers, Yazen A, Shihab, Austin P, Walker, Sarah R, Glover, Samantha D, Foster, Anil K, Challa
Publikováno v:
Journal of genetics. 97(5)
Nodal-related protein (ndr2) is amember of the transforming growth factor type β superfamily of factors and is required for ventral midline patterning of the embryonic central nervous system in zebrafish. In humans, mutations in the gene encoding no
Autor:
Anil K. Challa, Baraa A. Hijaz, John P. Gotham, Yazen A. Shihab, Riddhi K. Patel, David M. Gahan, Jordan B. Mcgill, Ivy E. Bookout, Mia C. Rodgers, Samantha D. Foster, Cerissa L. Nowell, Ashley N. Turner, Victoria L. Miller, Austin P. Walker, James C. Davis, Sarah R. Glover, Ashish S Kaushik, Zachariah P. Moseley, Lauren N. Brashear, Reagan S Andersen
Nodal-related protein (ndr2) is a member of the transforming growth factor type $$\upbeta $$ superfamily of factors and is required for ventral midline patterning of the embryonic central nervous system in zebrafish. In humans, mutations in the gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a2ba3f6663bd83c0bf48a6fdf1c4b74
https://doi.org/10.1101/277715
https://doi.org/10.1101/277715