HuGE Literature Finder
Records
1
-
6
A comprehensive analysis of copy number variation in a Turkish dementia cohort. Human genomics 2021 Jul 15 (1): 48. Dehghani Nadia, Guven Gamze, Kun-Rodrigues Celia, Gouveia Catarina, Foster Kalina, Hanagasi Hasmet, Lohmann Ebba, Samanci Bedia, Gurvit Hakan, Bilgic Basar, Bras Jose, Guerreiro Ri |
Association of genetic variants of ABCA1 with susceptibility to dementia: (SADEM study). Metabolic brain disease 2020 May . Teresa Juárez-Cedillo, Fernado Calzada, Nancy Martínez-Rodríguez, Gilberto Vargas-Alarcón, Alberto Cruz-Rocha, Roberto Robles-Ramir |
ABCA1- and ABCG1-mediated cholesterol efflux capacity of cerebrospinal fluid is impaired in Alzheimer's disease. Journal of lipid research 2019 Jun . Marchi Cinzia, Adorni Maria Pia, Caffarra Paolo, Ronda Nicoletta, Spallazzi Marco, Barocco Federica, Galimberti Daniela, Bernini Franco, Zimetti Frances |
Analysis of lipid pathway genes indicates association of sequence variation near SREBF1/TOM1L2/ATPAF2 with dementia risk. Human molecular genetics 2010 May 19 (10): 2068-78. Reynolds Chandra A, Hong Mun-Gwan, Eriksson Ulrika K, Blennow Kaj, Wiklund Fredrik, Johansson Boo, Malmberg Bo, Berg Stig, Alexeyenko Andrey, Grönberg Henrik, Gatz Margaret, Pedersen Nancy L, Prince Jonathan |
A survey of ABCA1 sequence variation confirms association with dementia. Human mutation 2009 Sep 30 (9): 1348-54. Reynolds Chandra A, Hong Mun-Gwan, Eriksson Ulrika K, Blennow Kaj, Bennet Anna M, Johansson Boo, Malmberg Bo, Berg Stig, Wiklund Fredrik, Gatz Margaret, Pedersen Nancy L, Prince Jonathan |
Novel mutation in the ABCA1 gene identified in a chinese patient with dementia and atherothrombotic cerebral infarction. Dementia and geriatric cognitive disorders 2008 26 (3): 234-8. Xue Xie-Hua, Wang Ning, Lin Yi, Zhao Gui-Xian, Fang Ling, Murong Shenxing, Wu Zhi-Yi |
- Page last reviewed:Oct 1, 2021
- Page last updated:May 26, 2022
- Content source: