Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Christie Sapp"'
Autor:
Blaine R. Roberts, Roman S. Polishchuk, Vladimir Lupashin, Victor Faundez, Daniel N. Cox, Alysia D. Vrailas-Mortimer, Gretchen Macias Mendez, Stephanie A. Zlatic, Cortnie Hartwig, Avanti Gokhale, Mafalda Concilli, Laura Palmer, Nicole Shearing, Jacob McArthy, Savanah Taylor, Lindsey Margewich, Samantha Rudin-Rush, Ramon A. Jorquera, Christie Sapp Savas, Shatabdi Bhattacharjee, Amanda A. H. Freeman, Erica Werner
Publikováno v:
J Neurosci
Rare genetic diseases preponderantly affect the nervous system causing neurodegeneration to neurodevelopmental disorders. This is the case for both Menkes and Wilson disease, arising from mutations in ATP7A and ATP7B, respectively. The ATP7A and ATP7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::383c44d1ac297837410e83e4223bfea3
https://doi.org/10.1523/jneurosci.1284-20.2020
https://doi.org/10.1523/jneurosci.1284-20.2020
Autor:
Roman R Polishchuk, Lindsey Margewich, Blaine R. Roberts, Samantha Rudin-Rush, Vladimir Lupashin, Cortnie Hartwig, Stephanie A. Zlatic, Daniel N. Cox, Gretchen Macias Mendez, Christie Sapp Savas, Ramon A. Jorquera, Victor Faundez, Alysia D. Vrailas-Mortimer, Laura Palmer, Avanti Gokhale, Mafalda Concilli, Jacob McArthy, Nicole Shearing, Shatabdi Bhattacharjee, Amanda A. H. Freeman, Savanah Taylor
Rare genetic diseases preponderantly affect the nervous system with phenotypes spanning from neurodegeneration to neurodevelopmental disorders. This is the case for both Menkes and Wilson disease, arising from mutations in ATP7A and ATP7B, respective
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f49910bc38f32f43f814ea47192cc4c
https://doi.org/10.1101/2020.05.22.110627
https://doi.org/10.1101/2020.05.22.110627
Akademický článek
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Autor:
Zhexing Wen, Farida Abudulai, Amanda A. H. Freeman, Jennifer K. Forsyth, Carrie E. Bearden, Christie Sapp, Stephanie A. Zlatic, Nicholas T. Seyfried, Cortnie Hartwig, David A. Lewis, Amanda Crocker, Erica Werner, Gabriela M. Repetto, Jill Gausier, Avanti Gokhale, Trishna Vadlamudi, Julia L. Bassell, Joseph A. Gogos, Victor Faundez, Steven M. Claypool
Neurodevelopmental disorders offer insight into synaptic mechanisms. To unbiasedly uncover these mechanisms, we studied the 22q11.2 syndrome, a recurrent copy number variant, which is the highest schizophrenia genetic risk factor. We quantified the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f25090286e38515ad3d68f0da2c4d82
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Trishna Vadlamudi, Nicholas T. Seyfried, Victor Faundez, Farida Abudulai, David A. Lewis, Jill Gausier, Joseph A. Gogos, Steven M. Claypool, Carrie E. Bearden, Jennifer K. Forsyth, Gabriela M. Repetto, Christie Sapp, Amanda Crocker, Julia L. Bassell, Cortnie Hartwig, Stephanie A. Zlatic, Zhexing Wen, Amanda A. H. Freeman, Erica Werner, Avanti Gokhale
Publikováno v:
The Journal of neuroscience : the official journal of the Society for Neuroscience, vol 39, iss 18
Neurodevelopmental disorders offer insight into synaptic mechanisms. To unbiasedly uncover these mechanisms, we studied the 22q11.2 syndrome, a recurrent copy number variant, which is the highest schizophrenia genetic risk factor. We quantified the p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58d3d7ffe0ca92e202a9040389d33244
https://doi.org/10.1523/jneurosci.1983-18.2019
https://doi.org/10.1523/jneurosci.1983-18.2019