Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 33 Records) |
Query Trace: STH[original query] |
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Strong association between Saitohin gene polymorphism and tau haplotype in the Polish population. Neuroscience letters 2003 Sep 348 (3): 163-6. Pep?o?ska Beata, Zekanowski Cezary, Religa Dorota, Czyzewski Krzysztof, Styczy?ska Maria, Pfeffer Anna, Gabryelewicz Tomasz, Go?ebiowski Marek, Luczywek Elzbieta, Wasiak Boguslaw, Barczak Anna, Chodakowska Ma?gorzata, Barcikowska Maria, Ku?nicki Jac |
The Saitohin 'Q7R' polymorphism and tau haplotype in multi-ethnic Alzheimer disease and Parkinson's disease cohorts. Neuroscience letters 2003 Aug 347 (1): 17-20. Clark Lorraine N, Levy Gilberto, Tang Ming-Xin, Mejia-Santana Helen, Ciappa Alejandra, Tycko Benjamin, Cote Lucien J, Louis Elan D, Mayeux Richard, Marder Kar |
Evaluation of the Roche LightCycler: a simple and rapid method for direct detection of factor V Leiden and prothrombin G20210A genotypes from blood samples without the need for DNA extraction. Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2003 Jul 14 (5): 499-503. Cooper Peter C, Cooper Susan M, Smith Julie M, Kitchen Steven, Makris Micha |
Age-dependent association between the Q7R polymorphism in the Saitohin gene and sporadic Alzheimer's disease. Dementia and geriatric cognitive disorders 2003 16 (3): 132-5. Combarros Onofre, Rodero Lucía, Infante Jon, Palacio Enrique, Llorca Javier, Fernández-Viadero Carlos, Peña Nicolás, Berciano Jo |
Alzheimer disease risk associated with APOE4 is modified by STH gene polymorphism. Neurology 2004 May 62 (9): 1631-3. Seripa D, Matera M G, D'Andrea R P, Gravina C, Masullo C, Daniele A, Bizzarro A, Rinaldi M, Antuono P, Wekstein D R, Dal Forno G, Fazio V |
Sequence analysis of tau 3'untranslated region and saitohin gene in sporadic progressive supranuclear palsy. Journal of neurology, neurosurgery, and psychiatry 2004 1 75 (1): 155-7. Ezquerra M, Campdelacreu J, Muñoz E, Oliva R, Tolosa |
TAU haplotype and the Saitohin Q7R gene polymorphism do not influence CSF Tau in Alzheimer's disease and are not associated with frontotemporal dementia or Parkinson's disease. Neuro-degenerative diseases 2005 2 (1): 28-35. Johansson Annica, Zetterberg Henrik, Håkansson Anna, Nissbrandt Hans, Blennow K |
Tumour necrosis factor gene complex polymorphisms in chronic obstructive pulmonary disease. Respiratory medicine 2007 Feb 101 (2): 340-4. Ruse Charlotte E, Hill Maureen C, Tobin Martin, Neale Natalie, Connolly Martin J, Parker Stuart G, Wardlaw Andrew |
Variation at APOE and STH loci and Alzheimer's disease. Behavioral and brain functions : BBF 2006 2 (): 13. Zuo Lingjun, van Dyck Christopher H, Luo Xingguang, Kranzler Henry R, Yang Bao-zhu, Gelernter Jo |
Association between glycogen synthase kinase-3beta genetic polymorphism and late-onset Alzheimer's disease. Dementia and geriatric cognitive disorders 2006 21 (4): 228-32. Mateo Ignacio, Infante Jon, Llorca Javier, Rodríguez Eloy, Berciano José, Combarros Onof |
Haplotypes and gene expression implicate the MAPT region for Parkinson disease: the GenePD Study. Neurology 2008 May . Tobin JE, Latourelle JC, Lew MF, Klein C, Suchowersky O, Shill HA, Golbe LI, Mark MH, Growdon JH, Wooten GF, Racette BA, Perlmutter JS, Watts R, Guttman M, Baker KB, Goldwurm S, Pezzoli G, Singer C, Saint-Hilaire MH, Hendricks AE, Williamson S, Nagle MW, Wilk JB, Massood T, Laramie JM, Destefano AL, Litvan I, Nicholson G, Corbett A, Isaacson S, Burn DJ, Chinnery PF, Pramstaller PP, Sherman S, Al-Hinti J, Drasby E, Nance M, Moller AT, Ostergaard K, Roxburgh R, Snow B, Slevin JT, Cambi F, Gusella JF, Myers RH |
Genetic analysis of tumor necrosis factor-alpha (TNF-alpha) G-308A and Saitohin Q7R polymorphisms with Alzheimer's disease. Journal of the neurological sciences 2008 Jul 270 (1-2): 148-51. Wang Binbin, Zhou Sirui, Yang Ze, Xie Yan-Chen, Wang Jing, Zhang Peng, Lv Zeping, Zheng Chenguang, Ma |
Cluster analysis of risk factor genetic polymorphisms in Alzheimer's disease. Neurochemical research 2009 Jan 34 (1): 23-8. Randall C N, Strasburger D, Prozonic J, Morris S N, Winkie A D, Parker G R, Cheng D, Fennell E M, Lanham I, Vakil N, Huang J, Cathcart H, Huang R, Poduslo S |
HD phenocopies--possible role of Saitohin gene. The International journal of neuroscience 2008 Mar 118 (3): 391-7. Jankovi? N, Kecmanovi? M, Dimitrijevi? R, Keckarevi? Markovi? M, Dobrici? V, Keckarevi? D, Savi? Pavicevi? D, Romac |
New pedigrees and novel mutation expand the phenotype of REEP1-associated hereditary spastic paraplegia (HSP). Neurogenetics 2009 Apr 10 (2): 105-10. Hewamadduma Channa, McDermott Christopher, Kirby Janine, Grierson Andrew, Panayi Maria, Dalton Ann, Rajabally Yusuuf, Shaw Pame |
The Q7R polymorphism in the saitohin gene is rare in a southern Chinese population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2008 Dec 29 (6): 431-4. Lin Kangguang, Tang Muni, Guo Yangbo, Han Haiying, Lin Yuhua, Ma C |
Saitohin polymorphism and executive dysfunction in schizophrenia. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2011 Dec . Bosia M, Buonocore M, Guglielmino C, Pirovano A, Lorenzi C, Marcone A, Bramanti P, Cappa SF, Aguglia E, Smeraldi E, Cavallaro R |
Association study of candidate gene polymorphisms with amnestic mild cognitive impairment in a Chinese population. PloS one 2012 7 (7): e41198. Liu Xiaoyan, Yue Chunxian, Xu Zhi, Shu Hao, Pu Mengjia, Yu Hui, Shi Yongmei, Zhuang Liying, Xu Xiaohui, Zhang Zhij |
COMT and STH polymorphisms interaction on cognition in schizophrenia. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Feb 36 (2): 215-20. Bosia Marta, Pigoni Alessandro, Pirovano Adele, Lorenzi Cristina, Spangaro Marco, Buonocore Mariachiara, Bechi Margherita, Cocchi Federica, Guglielmino Carmelo, Bramanti Placido, Smeraldi Enrico, Cavallaro Rober |
Association of microtubule associated protein tau/Saitohin (MAPT/STH) MAPT_238bp/STH Q7R polymorphisms and Parkinson's disease: A meta-analysis. Biochemical and biophysical research communications 2014 Oct 453 (3): 653-61. Lu Shan-Shan, Gong Feng-Feng, Feng Fang, Hu Cai-Yun, Qian Zhen-Zhong, Wu Yi-Le, Yang Hui-Yun, Sun Ye-Hu |
17q21.31 duplication causes prominent tau-related dementia with increased MAPT expression. Molecular psychiatry 2016 Dec . Le Guennec K, Quenez O, Nicolas G, Wallon D, Rousseau S, Richard A-C, Alexander J, Paschou P, Charbonnier C, Bellenguez C, Grenier-Boley B, Lechner D, Bihoreau M-T, Olaso R, Boland A, Meyer V, Deleuze J-F, Amouyel P, Munter H M, Bourque G, Lathrop M, Frebourg T, Redon R, Letenneur L, Dartigues J-F, Martinaud O, Kalev O, Mehrabian S, Traykov L, Ströbel T, Le Ber I, Caroppo P, Epelbaum S, Jonveaux T, Pasquier F, Rollin-Sillaire A, Génin E, Guyant-Maréchal L, Kovacs G G, Lambert J-C, Hannequin D, Campion D, Rovelet-Lecrux |
Saitohin Q7R polymorphism is associated with late-onset Alzheimer's disease susceptibility among caucasian populations: a meta-analysis. Journal of cellular and molecular medicine 2017 Feb . Huang Rong, Tian Sai, Cai Rongrong, Sun Jie, Xia Wenqing, Dong Xue, Shen Yanjue, Wang Shaoh |
Development and application of a rapid and sensitive genotyping method for pharmacogene variants using the single-stranded tag hybridization chromatographic printed-array strip (STH-PAS). Drug metabolism and pharmacokinetics 2018 10 33 (6): 258-263. Kumondai Masaki, Ito Akio, Hishinuma Eiji, Kikuchi Aoi, Saito Takahiro, Takahashi Masamitsu, Tsukada Chiharu, Saito Sakae, Yasuda Jun, Nagasaki Masao, Minegishi Naoko, Yamamoto Masayuki, Kaneko Akira, Teramoto Isao, Kimura Masatsugu, Hirasawa Noriyasu, Hiratsuka Masahi |
Association of Saitohin gene rs62063857 polymorphism with dry type age-related macular degeneration. Ophthalmic genetics 2020 Jul 1-2. Bonyadi Mortaza, Ahmadieh Hamid, Jabbarpoor Bonyadi Mohammad Hossein, Shahpasand Koorosh, Suri Fatemeh, Nasrabadi Niyousha, Yaseri Mehdi, Kheiri Bahare, Soheilian Maso |
Expression analysis and single-nucleotide polymorphisms of SYNDIG1L and UNC13C genes associated with thoracic vertebral numbers in sheep (Ovis aries). Archives animal breeding 2021 64 (1): 131-138. Zhong Ying-Jie, Yang Yang, Wang Xiang-Yu, Di Ran, Chu Ming-Xing, Liu Qiu-Y |
Associations of IL13 gene polymorphisms and immune factors with Schistosoma haematobium infection in schoolchildren in four schistosomiasis-endemic communities in Ghana. PLoS neglected tropical diseases 2021 Jun 15 (6): e0009455. Sarpong-Baidoo Margaret, Ofori Michael F, Asuming-Brempong Elias Kwesi, Kyei-Baafour Eric, Idun Bright K, Owusu-Frimpong Isaac, Amonoo Nana A, Quarshie Queenstar D, Tettevi Edward J, Osei-Atweneboana Mike |
Polymorphism of neurodegeneration-related genes associated with Parkinson's disease risk. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 6 43 (9): 5301-5312. Li Jiaxin, Yi Minhan, Li Binbin, Yin Shujuan, Zhang Ying, Huang Zini, Shu Li, Zhang Yu |
Rapid Genetic Diagnosis for Okinawan Patients with Enlarged Vestibular Aqueduct Using Single-Stranded Tag Hybridization Chromatographic Printed-Array Strip. Journal of clinical medicine 2022 2 11 (4): . Ganaha Akira, Hishinuma Eiji, Kaname Tadashi, Hiratsuka Masahiro, Kondo Shunsuke, Tono Tetsu |
Effects of New Mutations in BMPRIB, GDF9, BMP15, LEPR, and B4GALNT2 Genes on Litter Size in Sheep. Veterinary sciences 2023 4 10 (4): . Xuewen Ji, Ziwei Cao, Qi Hao, Mei He, Ming Cang, Haiquan Yu, Qing Ma, Xihe Li, Siqin Bao, Jianguo Wang, Bin To |
Validation of a genotyping technique for a surrogate marker of HLA-B58:01 for allopurinol-induced Stevens-Johnson syndrome and toxic epidermal necrolysis in the Japanese population. Drug metabolism and pharmacokinetics 2023 3 49 100495. Tsukagoshi Eri, Nakamura Ryosuke, Tanaka Yoichi, Maekawa Keiko, Hiratsuka Masahiro, Asada Hideo, Saito Yoshi |
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- Page last updated:Apr 16, 2024
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