Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: HTRA2[original query] |
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Genetic variation of Omi/HtrA2 and Parkinson's disease. Parkinsonism & related disorders 2008 Nov 14 (7): 539-43. Ross Owen A, Soto Alexandra I, Vilariño-Güell Carles, Heckman Michael G, Diehl Nancy N, Hulihan Mary M, Aasly Jan O, Sando Sigrid, Gibson J Mark, Lynch Timothy, Krygowska-Wajs Anna, Opala Grzegorz, Barcikowska Maria, Czyzewski Krzysztof, Uitti Ryan J, Wszolek Zbigniew K, Farrer Matthew |
Genetic variability in the mitochondrial serine protease HTRA2 contributes to risk for Parkinson disease. Human mutation 2008 Jun 29 (6): 832-40. Bogaerts Veerle, Nuytemans Karen, Reumers Joke, Pals Philippe, Engelborghs Sebastiaan, Pickut Barbara, Corsmit Ellen, Peeters Karin, Schymkowitz Joost, De Deyn Peter Paul, Cras Patrick, Rousseau Frederic, Theuns Jessie, Van Broeckhoven Christi |
Sequencing analysis of OMI/HTRA2 shows previously reported pathogenic mutations in neurologically normal controls. Human molecular genetics 2008 Jul 17 (13): 1988-93. Simón-Sánchez Javier, Singleton Andrew |
Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease? Movement disorders : official journal of the Movement Disorder Society 2009 Apr 24 (6): 833-8. Sutherland Greg T, Halliday Glenda M, Silburn Peter A, Mastaglia Frank L, Rowe Dominic B, Boyle Richard S, O'Sullivan John D, Ly Tina, Wilton Steve D, Mellick George |
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease. Neurobiology of aging 2009 Dec . Krüger Rejko, Sharma Manu, Riess Olaf, Gasser Thomas, Van Broeckhoven Christine, Theuns Jessie, Aasly Jan, Annesi Grazia, Bentivoglio Anna Rita, Brice Alexis, Djarmati Ana, Elbaz Alexis, Farrer Matthew, Ferrarese Carlo, Gibson J Mark, Hadjigeorgiou Georgios M, Hattori Nobutaka, Ioannidis John P A, Jasinska-Myga Barbara, Klein Christine, Lambert Jean-Charles, Lesage Suzanne, Lin Juei-Jueng, Lynch Timothy, Mellick George D, de Nigris Francesa, Opala Grzegorz, Prigione Alessandro, Quattrone Aldo, Ross Owen A, Satake Wataru, Silburn Peter A, Tan Eng King, Toda Tatsushi, Tomiyama Hiroyuki, Wirdefeldt Karin, Wszolek Zbigniew, Xiromerisiou Georgia, Maraganore Demetrius M, |
Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's disease. The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2010 Dec . Westerlund M, Behbahani H, Gellhaar S, Forsell C, Belin AC, Anvret A, Zettergren A, Nissbrandt H, Lind C, Sydow O, Graff C, Olson L, Ankarcrona M, Galter D |
Novel variant Pro143Ala in HTRA2 contributes to Parkinson's disease by inducing hyperphosphorylation of HTRA2 protein in mitochondria. Human genetics 2011 Dec 130 (6): 817-27. Lin Chin-Hsien, Chen Meng-Ling, Chen Grace Shiahuy, Tai Chun-Hwei, Wu Ruey-Me |
Common variants in PARK loci and related genes and Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2011 Feb 26 (2): 280-8. Chung Sun Ju, Armasu Sebastian M, Biernacka Joanna M, Lesnick Timothy G, Rider David N, Lincoln Sarah J, Ortolaza Alexandra I, Farrer Matthew J, Cunningham Julie M, Rocca Walter A, Maraganore Demetrius |
Genetic variations of Omi/HTRA2 in Chinese patients with Parkinson's disease. Brain research 2011 Apr 1385 293-7. Wang Chun-Yu, Xu Qian, Weng Ling, Zhang Qiang, Zhang Hai-Nan, Guo Ji-Feng, Tan Li-Ming, Tang Jian-Guang, Yan Xin-Xiang, Tang Bei-S |
Mutation analysis of LRRK2, SCNA, UCHL1, HtrA2 and GIGYF2 genes in Chinese patients with autosomal dorminant Parkinson's disease. Neuroscience letters 2012 May 516 (2): 207-11. Tian Jin-yong, Guo Ji-feng, Wang Lei, Sun Qi-ying, Yao Ling-yan, Luo Lin-zi, Shi Chang-he, Hu Ya-cen, Yan Xin-xiang, Tang Bei-s |
Analysis of PRKN Variants and Clinical Features in Polish Patients with Parkinson's Disease. Current genomics 2015 Aug 16 (4): 215-23. Oczkowska Anna, Florczak-Wyspianska Jolanta, Permoda-Osip Agnieszka, Owecki Michal, Lianeri Margarita, Kozubski Wojciech, Dorszewska Jolan |
Parkinson's disease: SNCA-, PARK2-, and LRRK2- targeting microRNAs elevated in cingulate gyrus. Parkinsonism & related disorders 2016 Sep . Tatura Roman, Kraus Theo, Giese Armin, Arzberger Thomas, Buchholz Malte, Höglinger Günter, Müller Ulri |
Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease. Parkinson's disease 2018 7 2018 5651435. Gambardella Stefano, Ferese Rosangela, Scala Simona, Carboni Stefania, Biagioni Francesca, Giardina Emiliano, Zampatti Stefania, Modugno Nicola, Fabbiano Francesco, Fornai Francesco, Centonze Diego, Ruggieri Stefa |
Genetic variants of PARK genes in Korean patients with early-onset Parkinson's disease. Neurobiology of aging 2019 03 75 224.e9-224.e15. Youn Jinyoung, Lee Chung, Oh Eungseok, Park Jinse, Kim Ji Sun, Kim Hee-Tae, Cho Jin Whan, Park Woong-Yang, Jang Wooyoung, Ki Chang-Se |
A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing. Movement disorders : official journal of the Movement Disorder Society 2019 2 34 (4): 506-515. Lin Chin-Hsien, Chen Pei-Lung, Tai Chun-Hwei, Lin Hang-I, Chen Chih-Shan, Chen Meng-Ling, Wu Ruey-Me |
A genetic analysis of a Spanish population with early onset Parkinson's disease. PloS one 2020 15 (9): e0238098. Cristina Tejera-Parrado, Pablo Mir, Teresa Periñán María, Lydia Vela-Desojo, Irene Abreu-Rodríguez, Araceli Alonso-Cánovas, Inmaculada Bernal-Bernal, Marta Bonilla-Toribio, Dolores Buiza-Rueda, José Catalán-Alonso María, Rocío García-Ramos, José García-Ruiz Pedro, Ismael Huertas-Fernández, Silvia Jesús, Labrador Miguel A-Espinosa, Lydia López-Manzanares, Carlos Martínez-Castrillo Juan, Posada Ignacio J, Ana Rojo-Sebastián, Cristina Ruiz-Huete, Javier Del Val, Gómez-Garre Pil |
Analysis of rare variants of autosomal-dominant genes in a Chinese population with sporadic Parkinson's disease. Molecular genetics & genomic medicine 2020 Aug e1449. Zheng Ran, Jin Chong-Yao, Chen Ying, Ruan Yang, Gao Ting, Lin Zhi-Hao, Dong Jia-Xian, Yan Ya-Ping, Tian Jun, Pu Jia-Li, Zhang Bao-Ro |
Mutation Analysis of the Genes Associated with Parkinson's Disease in a Finnish Cohort of Early-Onset Dementia. Journal of Alzheimer's disease : JAD 2020 6 76 (3): 955-965. Luukkainen Laura, Huttula Samuli, Väyrynen Henri, Helisalmi Seppo, Kytövuori Laura, Haapasalo Annakaisa, Hiltunen Mikko, Remes Anne M, Krüger Johan |
Genetic testing of FUS, HTRA2, and TENM4 genes in Chinese patients with essential tremor. CNS neuroscience & therapeutics 2020 Mar . Yan Ya-Ping, Xu Cong-Ying, Gu Lu-Yan, Zhang Bo, Shen Ting, Gao Ting, Tian Jun, Pu Jia-Li, Yin Xin-Zhen, Zhang Bao-Rong, Zhao Guo-H |
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease. Neurobiology of aging 2020 Oct . Saini Prabhjyot, Rudakou Uladzislau, Yu Eric, Ruskey Jennifer A, Asayesh Farnaz, Laurent Sandra B, Spiegelman Dan, Fahn Stanley, Waters Cheryl, Monchi Oury, Dauvilliers Yves, Dupré Nicolas, Greenbaum Lior, Hassin-Baer Sharon, Espay Alberto J, Rouleau Guy A, Alcalay Roy N, Fon Edward A, Postuma Ronald B, Gan-Or Z |
Identification of sixteen novel candidate genes for late onset Parkinson's disease. Molecular neurodegeneration 2021 6 16 (1): 35. Gialluisi Alessandro, Reccia Mafalda Giovanna, Modugno Nicola, Nutile Teresa, Lombardi Alessia, Di Giovannantonio Luca Giovanni, Pietracupa Sara, Ruggiero Daniela, Scala Simona, Gambardella Stefano, , Iacoviello Licia, Gianfrancesco Fernando, Acampora Dario, D'Esposito Maurizio, Simeone Antonio, Ciullo Marina, Esposito Tere |
Genomic Markers for Essential Tremor. Pharmaceuticals (Basel, Switzerland) 2021 6 14 (6): . Jiménez-Jiménez Félix Javier, Alonso-Navarro Hortensia, García-Martín Elena, Álvarez Ignacio, Pastor Pau, Agúndez José A |
Loss of GSK-3? mediated phosphorylation in HtrA2 contributes to uncontrolled cell death with Parkinsonian phenotype. International journal of biological macromolecules 2021 3 180 97-111. Bose Kakoli, Wagh Ajay, Mishra Vasudha, Dutta Shubhankar, Parui Aasna L, Puja Rashmi, Mudrale Snehal Pandav, Kulkarni Suyamindra S, Gai Pramod B, Sarin Raj |
GAS6/Axl Signaling Modulates Blood-Brain Barrier Function Following Intravenous Thrombolysis in Acute Ischemic Stroke. Frontiers in immunology 2021 11 12 742359. Guo Zhen-Ni, Liu Jie, Chang Junlei, Zhang Peng, Jin Hang, Sun Xin, Yang |
High-Throughput Sequencing Haplotype Analysis Indicates in LRRK2 Gene a Potential Risk Factor for Endemic Parkinsonism in Southeastern Moravia, Czech Republic. Life (Basel, Switzerland) 2022 1 12 (1): . Kolarikova Kristyna, Vodicka Radek, Vrtel Radek, Stellmachova Julia, Prochazka Martin, Mensikova Katerina, Bartonikova Tereza, Furst Tomas, Kanovsky Petr, Geryk J |
The genetic spectrum of a cohort of patients clinically diagnosed as Parkinson's disease in mainland China. NPJ Parkinson's disease 2023 5 9 (1): 76. Yi-Min Sun, Xin-Yue Zhou, Xiao-Niu Liang, Jin-Ran Lin, Yi-Dan Xu, Chen Chen, Si-Di Wei, Qi-Si Chen, Feng-Tao Liu, Jue Zhao, Yi-Lin Tang, Bo Shen, Lin-Hua Gan, Boxun Lu, Zheng-Tong Ding, Yu An, Jian-Jun Wu, Jian Wa |
Genetic screening of Filipinos suspected with familial Parkinson's disease: A pilot study. Parkinsonism & related disorders 2023 2 108 105319. Caritativo Erin Camille A, Yu Jeryl Ritzi T, Bautista Juan Miguel P, Nishioka Kenya, Jamora Roland Dominic G, Yalung Patrick M, Ng Arlene R, Hattori Nobuta |
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- Page last updated:Apr 16, 2024
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