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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Dec 1, 2023. (Total: 223516Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Neurodegenerative Diseases and HTT[original query]
Evaluation of polyglutamine repeats in autosomal dominant Parkinson's disease.
Neurobiology of aging 2014 Jul 35 (7): 1779.e17-21.
Yamashita Chikara, Tomiyama Hiroyuki, Funayama Manabu, Inamizu Saeko, Ando Maya, Li Yuanzhe, Yoshino Hiroyo, Araki Takehisa, Ichikawa Tadashi, Ehara Yoshiro, Ishikawa Kinya, Mizusawa Hidehiro, Hattori Nobuta
Searching for Correlations Between the Development of Neurodegenerative Hallmarks: Targeting Huntingtin as a Contributing Factor.
Advances in experimental medicine and biology 2017 10 987 269-281.
Angelova Nelina
HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease.
Neurobiology of aging 2019 04 76 215.e9-215.e14.
Menéndez-González Manuel, Clarimón Jordi, Rosas-Allende Irene, Blázquez Marta, San Martín Esther Suárez, García-Fernández Ciara, Lleó Alberto, Dols-Icardo Oriol, Illán-Gala Ignacio, Morís Germán, Ribacoba Renée, Álvarez Victoria, Martínez Carm
Rare homozygosity in amyotrophic lateral sclerosis suggests the contribution of recessive variants to disease genetics.
Journal of the neurological sciences 2019 May 402 62-68.
Goldstein Orly, Kedmi Merav, Gana-Weisz Mali, Twito Shir, Nefussy Beatrice, Vainer Batel, Fainmesser Yaara, Abraham Alon, Nayshool Omri, Orr-Urtreger Avi, Drory Vivian
Prevalence of Carriers of Intermediate and Pathological Polyglutamine Disease-Associated Alleles Among Large Population-Based Cohorts.
JAMA neurology 2019 Apr .
Gardiner Sarah L, Boogaard Merel W, Trompet Stella, de Mutsert Renée, Rosendaal Frits R, Gussekloo Jacobijn, Jukema J Wouter, Roos Raymund A C, Aziz N Ahm
Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease.
Neurobiology of aging 2019 Nov .
Rosas Irene, Martínez Carmen, Clarimón Jordi, Lleó Alberto, Illán-Gala Ignacio, Dols-Icardo Oriol, Borroni Barbara, Almeida Maria Rosário, van der Zee Julie, Van Broeckhoven Christine, Bruni Amalia C, Anfossi Maria, Bernardi Livia, Maletta Raffaele, Serpente María, Galimberti Daniela, Scarpini Elio, Rossi Giacomina, Caroppo Paola, Benussi Luisa, Ghidoni Roberta, Binetti Giuliano, Nacmias Benedetta, Sorbi Sandro, Piaceri Irene, Bagnoli Silvia, Antonell Anna, Sánchez-Valle Raquel, De la Casa-Fages Beatriz, Grandas Francisco, Diez-Fairen Mónica, Pastor Pau, Ferrari Raffaele, Álvarez Victoria, Menéndez-González Manu
Intermediate and Expanded HTT Alleles and the Risk for ?-Synucleinopathies.
Movement disorders : official journal of the Movement Disorder Society 2022 7 37 (9): 1841-1849.
Pérez-Oliveira Sergio, Álvarez Ignacio, Rosas Irene, Menendez-González Manuel, Blázquez-Estrada Marta, Aguilar Miquel, Corte Daniela, Buongiorno Mariateresa, Molina-Porcel Laura, Aldecoa Iban, Martí María J, Sánchez-Juan Pascual, Infante Jon, González-Aramburu Isabel, García-González Pablo, Rosende-Roca Maitée, Boada Mercè, Ruiz Agustín, Periñán María Teresa, Macías-García Daniel, Muñoz-Delgado Laura, Gómez-Garre Pilar, Mir Pablo, Clarimón Jordi, Lleo Alberto, Alcolea Daniel, De la Casa-Fages Beatriz, Duarte Israel, Álvarez Victoria, Pastor P
DNA methylation age acceleration is associated with age of onset in Chinese spinocerebellar ataxia type 3 patients.
Neurobiology of aging 2022 3 113 1-6.
Li Jiahao, Shu Anli, Sun Yimin, Yang Wanli, Tang Xuelin, Pu Hongjiang, Peng Yun, Hu Xiaowen, Qing Ying, Wang Jian, Wan Chunling, Zhou Mingcheng, Zhang Mi
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