Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Minerva Carrasquillo"'
Autor:
Neha Atulkumar Singh, Peter Martin, Jonathan Graff-Radford, Mary Machulda, Minerva Carrasquillo, Nilufer Taner, Keith Josephs, Jennifer Whitwell
Publikováno v:
Wednesday, April 26.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9b88c8f95d2d98a83603dc3526ac7df
https://doi.org/10.1212/wnl.0000000000202583
https://doi.org/10.1212/wnl.0000000000202583
Autor:
Sarah Lincoln, Mariet Allen, Claire L Cox, Louise P Walker, Kimberly Malphrus, Yushi Qiu, Thuy Nguyen, Christopher Rowley, Naomi Kouri, Julia Crook, V Shane Pankratz, Samuel Younkin, Linda Younkin, Minerva Carrasquillo, Fanggeng Zou, Samer O Abdul-Hay, Wolfdieter Springer, Sigrid B Sando, Jan O Aasly, Maria Barcikowska, Zbigniew K Wszolek, Jada M Lewis, Dennis Dickson, Neill R Graff-Radford, Ronald C Petersen, Elizabeth Eckman, Steven G Younkin, Nilüfer Ertekin-Taner
Publikováno v:
PLoS ONE, Vol 8, Iss 6, p e64164 (2013)
Leucine rich repeat transmembrane protein 3 (LRRTM3) is member of a synaptic protein family. LRRTM3 is a nested gene within α-T catenin (CTNNA3) and resides at the linkage peak for late-onset Alzheimer's disease (LOAD) risk and plasma amyloid β (A
Externí odkaz:
https://doaj.org/article/4b8767a6bff4419787f56889d10ad6f1
Autor:
Hui Shi, Christopher Medway, Kristelle Brown, Noor Kalsheker, Alison Goate, Petroula Proitsi, John Powell, Simon Lovestone, Minerva Carrasquillo, Steven Younkin, null Kevin Morgan (for the ART consortium)
Publikováno v:
Alzheimer's & Dementia. 7
P1-262 GENETIC VARIANTS INFLUENCING HUMAN LONGEVITY FROM LATE-ONSETALZHEIMER’S DISEASE (LOAD) GENOME-WIDE ASSOCIATION STUDIES (GWAS) Hui Shi, Christopher Medway, Kristelle Brown, Noor Kalsheker, Alison Goate, Petroula Proitsi, John Powell, Simon Lo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af9be107d0b53624a675fabd6d580dfb
https://doi.org/10.1016/j.jalz.2011.05.542
https://doi.org/10.1016/j.jalz.2011.05.542
Autor:
Baird, Denis A.1 (AUTHOR) Denis.Baird@bristol.ac.uk, Liu, Jimmy Z.2 (AUTHOR), Zheng, Jie1 (AUTHOR), Sieberts, Solveig K.3 (AUTHOR), Perumal, Thanneer3 (AUTHOR), Elsworth, Benjamin1 (AUTHOR), Richardson, Tom G.1 (AUTHOR), Chen, Chia-Yen2 (AUTHOR), Carrasquillo, Minerva M.4 (AUTHOR), Allen, Mariet4 (AUTHOR), Reddy, Joseph S.5 (AUTHOR), De Jager, Philip L.6,7 (AUTHOR), Ertekin-Taner, Nilufer4,8 (AUTHOR), Mangravite, Lara M.3 (AUTHOR), Logsdon, Ben3 (AUTHOR), Estrada, Karol2,9 (AUTHOR), Haycock, Philip C.1 (AUTHOR), Hemani, Gibran1 (AUTHOR), Runz, Heiko2 (AUTHOR), Smith, George Davey1,10 (AUTHOR)
Publikováno v:
PLoS Genetics. 1/8/2021, Vol. 17 Issue 1, p1-26. 26p.
Autor:
Deming, Yuetiva, Dumitrescu, Logan, Barnes, Lisa L., Thambisetty, Madhav, Kunkle, Brian, Gifford, Katherine A., Bush, William S., Chibnik, Lori B., Mukherjee, Shubhabrata, De Jager, Philip L., Kukull, Walter, Huentelman, Matt, Crane, Paul K., Resnick, Susan M., Keene, C. Dirk, Montine, Thomas J., Schellenberg, Gerard D., Haines, Jonathan L., Zetterberg, Henrik, Blennow, Kaj
Publikováno v:
Acta Neuropathologica; Dec2018, Vol. 136 Issue 6, p857-872, 16p
Publikováno v:
Journal of Alzheimer's Disease; 2018, Vol. 66 Issue 4, p1755-1768, 14p
Publikováno v:
Clinical Trials Week; 4/10/2023, p448-448, 1p
Publikováno v:
Annals of Neurology; Nov2012 Supplement, Vol. 72, pS1-S120, 120p
Autor:
Tokunaga, Katsushi1
Publikováno v:
Journal of Human Genetics. Jan2012, Vol. 57 Issue 1, p1-2. 2p.
Publikováno v:
Ascribe Newswire: Medicine; 10/14/2002, p1-1, 1p