Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Adina Schonbrun"'
Autor:
Adina Schonbrun, Marilyn Resh
Publikováno v:
Bio-Protocol, Vol 12, Iss 24 (2022)
Several assays have been developed to monitor the in vitro catalytic activity of Hedgehog acyltransferase (Hhat), an enzyme critical to the Hedgehog signaling pathway in cells. However, the majority of these previously reported assays involve radioac
Externí odkaz:
https://doaj.org/article/dd51a5129f6849eba17ba6a51a36431c
Autor:
Surya Jyoti Banerjee, Adina Schonbrun, Sogol Eizadshenass, Shimshon Benji, Yaakov Tzvi Cantor, Liam Eliach, Matthew Lubin, Zev Narrowe, Jeremy Purow, Benjamin Shulman, Leib Wiener, Josefa Steinhauer
Publikováno v:
PLoS ONE, Vol 16, Iss 9, p e0256738 (2021)
Neurodegenerative disease (ND) is a growing health burden worldwide, but its causes and treatments remain elusive. Although most cases of ND are sporadic, rare familial cases have been attributed to single genes, which can be investigated in animal m
Externí odkaz:
https://doaj.org/article/fe9e763e7e17403fbc75272083127bfc
Autor:
Matthew Lubin, Josefa Steinhauer, Surya Banerjee, Yaakov Tzvi Cantor, Shimshon Benji, Benjamin Shulman, Leib Wiener, Jeremy Purow, Liam Eliach, Adina Schonbrun, Sogol Eizadshenass, Zev Narrowe
Neurodegenerative disease (ND) is a growing health burden worldwide, but its causes and treatments remain elusive. Although most cases of ND are sporadic, rare familial cases have been attributed to single genes, which can be investigated in animal m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::306741d6c922343350b7e2f0c6810a20
https://doi.org/10.1101/2021.04.25.441319
https://doi.org/10.1101/2021.04.25.441319
Autor:
Zev Narrowe, Jeremy Purow, Yaakov Tzvi Cantor, Shimshon Benji, Adina Schonbrun, Leib Wiener, Sogol Eizadshenass, Surya Banerjee, Benjamin Shulman, Liam Eliach, Josefa Steinhauer, Matthew Lubin
Publikováno v:
PLoS ONE
PLoS ONE, Vol 16, Iss 9, p e0256738 (2021)
PLoS ONE, Vol 16, Iss 9, p e0256738 (2021)
Neurodegenerative disease (ND) is a growing health burden worldwide, but its causes and treatments remain elusive. Although most cases of ND are sporadic, rare familial cases have been attributed to single genes, which can be investigated in animal m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fae0c0dcf5f4b8ef718b931a796fc9fa
https://doi.org/10.1371/journal.pone.0256738
https://doi.org/10.1371/journal.pone.0256738