Zobrazeno 1 - 4
of 4
pro vyhledávání: '"David M, Gahan"'
Autor:
Aundrea F. Bartley, Kavitha Abiraman, Luke T. Stewart, Mohammed Iqbal Hossain, David M. Gahan, Abhishek V. Kamath, Mary K. Burdette, Shaida Andrabe, Stephen H. Foulger, Lori L. McMahon, Lynn E. Dobrunz
Publikováno v:
Frontiers in Synaptic Neuroscience, Vol 11 (2019)
Optogenetics is widely used in neuroscience to control neural circuits. However, non-invasive methods for light delivery in brain are needed to avoid physical damage caused by current methods. One potential strategy could employ x-ray activation of r
Externí odkaz:
https://doaj.org/article/0a82dd247d5944328a160740c46979f0
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9bf5e2a2369f51902d41d48e350d19ee
https://pubmed.ncbi.nlm.nih.gov/30555080
https://pubmed.ncbi.nlm.nih.gov/30555080
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
Autor:
Turner, Ashley N.1,2, Andersen, Reagan S.3, Bookout, Ivy E.3, Brashear, Lauren N.3, Davis, James C.3, Gahan, David M.3, Gotham, John P.3, Hijaz, Baraa A.3, Kaushik, Ashish S.3, Mcgill, Jordan B.3, Miller, Victoria L.3, Moseley, Zachariah P.3, Nowell, Cerissa L.3, Patel, Riddhi K.3, Rodgers, MIA C.3, Shihab, Yazen A.3, Walker, Austin P.3, Glover, Sarah R.3, Foster, Samantha D.3, Challa, Anil K.1 challa.anilkumar@gmail.com
Publikováno v:
Journal of Genetics. Dec2018, Vol. 97 Issue 5, p1315-1325. 11p.