Human Genome Epidemiology Literature Finder
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Records 1 - 25 (of 25 Records) |
| Query Trace: Disease and PLAU[original query] |
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| Association of late-onset Alzheimer disease with a genotype of PLAU, the gene encoding urokinase-type plasminogen activator on chromosome 10q22.2. Neurogenetics 2003 Aug 4 (4): 213-7. Finckh U, van Hadeln K, Müller-Thomsen T, Alberici A, Binetti G, Hock C, Nitsch R M, Stoppe G, Reiss J, Gal |
| Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004 Jan 124B (1): 29-37. Myers Amanda J, Marshall Helen, Holmans Peter, Compton Danielle, Crook Richard J P, Mander Adrian P, Nowotny Petra, Smemo Scott, Dunstan Melanie, Jehu Luke, Wang Jen C, Hamshere Marian, Morris John C, Norton Joanne, Chakraventy Sumi, Tunstall Nigel, Lovestone Simon, Petersen Ronald, O'Donovan Michael, Jones Lesley, Williams Julie, Owen Michael J, Hardy John, Goate Alis |
| Genetic variants in a haplotype block spanning IDE are significantly associated with plasma Abeta42 levels and risk for Alzheimer disease. Human mutation 2004 Apr 23 (4): 334-42. Ertekin-Taner Nilüfer, Allen Mariet, Fadale Daniel, Scanlin Leah, Younkin Linda, Petersen Ronald C, Graff-Radford Neill, Younkin Steven |
| Elevated amyloid beta protein (Abeta42) and late onset Alzheimer's disease are associated with single nucleotide polymorphisms in the urokinase-type plasminogen activator gene. Human molecular genetics 2005 Feb 14 (3): 447-60. Ertekin-Taner Nilüfer, Ronald James, Feuk Lars, Prince Jonathan, Tucker Michael, Younkin Linda, Hella Maria, Jain Shushant, Hackett Alyssa, Scanlin Leah, Kelly Jason, Kihiko-Ehman Muthoni, Neltner Matthew, Hersh Louis, Kindy Mark, Markesbery William, Hutton Michael, de Andrade Mariza, Petersen Ronald C, Graff-Radford Neill, Estus Steve, Brookes Anthony J, Younkin Steven |
| No association of a non-synonymous PLAU polymorphism with Alzheimer's disease and disease-related traits. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005 Jan 132B (1): 21-3. Papassotiropoulos Andreas, Tsolaki Magdalini, Wollmer M Axel, Molyva Dimitra, Thal Dietmar R, Huynh Kim-Dung, Tracy Jay, Staehelin Hannes B, Monsch Andreas U, Nitsch Roger M, Hock Christo |
| Association of tagSNPs in the urokinase-plasminogen activator (PLAU) gene with Alzheimer's disease and associated quantitative traits. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Jan 144B (1): 79-82. Ozturk Ayla, Minster Ryan L, DeKosky Steven T, Kamboh M Ily |
| A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer's disease. Human molecular genetics 2006 Aug 15 (16): 2446-56. Riemenschneider Matthias, Konta Lidija, Friedrich Patricia, Schwarz Sandra, Taddei Kevin, Neff Frauke, Padovani Alessandro, Kölsch Heike, Laws Simon M, Klopp Norman, Bickeböller Heike, Wagenpfeil Stefan, Mueller Jakob C, Rosenberger Albert, Diehl-Schmid Janine, Archetti Silvana, Lautenschlager Nicola, Borroni Barbara, Müller Ulrich, Illig Thomas, Heun Reinhard, Egensperger Rupert, Schlegel Jürgen, Förstl Hans, Martins Ralph N, Kurz Alexand |
| Association of urokinase-type plasminogen activator with asthma and atopy. American journal of respiratory and critical care medicine 2007 Jun 175 (11): 1109-16. Bégin Philippe, Tremblay Karine, Daley Denise, Lemire Mathieu, Claveau Sébastien, Salesse Charleen, Kacel Sabine, Montpetit Alexandre, Becker Allan, Chan-Yeung Moira, Kozyrskyj Anita L, Hudson Thomas J, Laprise Catheri |
| No replication of genetic association between candidate polymorphisms and Alzheimer's disease. Neurobiology of aging 2011 Aug 32 (8): 1443-51. Cousin Emmanuelle, Macé Sandrine, Rocher Corinne, Dib Colette, Muzard Gaëlle, Hannequin Didier, Pradier Laurent, Deleuze Jean-François, Génin Emmanuelle, Brice Alexis, Campion Dominiq |
| Identification of KIF3A as a novel candidate gene for childhood asthma using RNA expression and population allelic frequencies differences. PloS one 2011 6 (8): e23714. Kovacic Melinda Butsch, Myers Jocelyn M Biagini, Wang Ning, Martin Lisa J, Lindsey Mark, Ericksen Mark B, He Hua, Patterson Tia L, Baye Tesfaye M, Torgerson Dara, Roth Lindsey A, Gupta Jayanta, Sivaprasad Umasundari, Gibson Aaron M, Tsoras Anna M, Hu Donglei, Eng Celeste, Chapela Rocío, Rodríguez-Santana José R, Rodríguez-Cintrón William, Avila Pedro C, Beckman Kenneth, Seibold Max A, Gignoux Chris, Musaad Salma M, Chen Weiguo, Burchard Esteban González, Hershey Gurjit K Khura |
| VEGFA gene locus (6p12) amplification identifies a small but highly aggressive subgroup of colorectal cancer [corrected] patients. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2011 Oct 24 (10): 1404-12. Vlajnic Tatjana, Andreozzi Maria Carla, Schneider Sandra, Tornillo Luigi, Karamitopoulou Eva, Lugli Alessandro, Ruiz Christian, Zlobec Inti, Terracciano Lui |
| The role of ECE1 variants in cognitive ability in old age and Alzheimer's disease risk. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Sep 159B (6): 696-709. Hamilton Gillian, Harris Sarah E, Davies Gail, Liewald David C, Tenesa Albert, Payton Antony, Horan Michael A, Ollier William E R, Pendleton Neil, , Starr John M, Porteous David, Deary Ian |
| Meta-analysis of the association between urokinase-plasminogen activator gene rs2227564 polymorphism and Alzheimer's disease. American journal of Alzheimer's disease and other dementias 2013 Aug 28 (5): 517-23. Wu Wenlong, Jiang Hong, Wang Meiyun, Zhang Dongfe |
| The PLAU P141L single nucleotide polymorphism is associated with collateral circulation in patients with coronary artery disease. Revista espan?ola de cardiologi?a (English ed.) 2014 Jul 67 (7): 552-7. Duran Joan, Sánchez-Olavarría Pilar, Mola Marina, Götzens Víctor, Carballo Julio, Martín-Pelegrina Eva, Petit Màrius, García Del Blanco Bruno, García-Dorado David, de Anta Josep |
Meta-analysis of exome array data identifies six novel genetic loci for lung function.
Wellcome open research 2018 9 3 4. Jackson Victoria E, Latourelle Jeanne C, Wain Louise V, Smith Albert V, Grove Megan L, Bartz Traci M, Obeidat Ma'en, Province Michael A, Gao Wei, Qaiser Beenish, Porteous David J, Cassano Patricia A, Ahluwalia Tarunveer S, Grarup Niels, Li Jin, Altmaier Elisabeth, Marten Jonathan, Harris Sarah E, Manichaikul Ani, Pottinger Tess D, Li-Gao Ruifang, Lind-Thomsen Allan, Mahajan Anubha, Lahousse Lies, Imboden Medea, Teumer Alexander, Prins Bram, Lyytikäinen Leo-Pekka, Eiriksdottir Gudny, Franceschini Nora, Sitlani Colleen M, Brody Jennifer A, Bossé Yohan, Timens Wim, Kraja Aldi, Loukola Anu, Tang Wenbo, Liu Yongmei, Bork-Jensen Jette, Justesen Johanne M, Linneberg Allan, Lange Leslie A, Rawal Rajesh, Karrasch Stefan, Huffman Jennifer E, Smith Blair H, Davies Gail, Burkart Kristin M, Mychaleckyj Josyf C, Bonten Tobias N, Enroth Stefan, Lind Lars, Brusselle Guy G, Kumar Ashish, Stubbe Beate, , Kähönen Mika, Wyss Annah B, Psaty Bruce M, Heckbert Susan R, Hao Ke, Rantanen Taina, Kritchevsky Stephen B, Lohman Kurt, Skaaby Tea, Pisinger Charlotta, Hansen Torben, Schulz Holger, Polasek Ozren, Campbell Archie, Starr John M, Rich Stephen S, Mook-Kanamori Dennis O, Johansson Åsa, Ingelsson Erik, Uitterlinden André G, Weiss Stefan, Raitakari Olli T, Gudnason Vilmundur, North Kari E, Gharib Sina A, Sin Don D, Taylor Kent D, O'Connor George T, Kaprio Jaakko, Harris Tamara B, Pederson Oluf, Vestergaard Henrik, Wilson James G, Strauch Konstantin, Hayward Caroline, Kerr Shona, Deary Ian J, Barr R Graham, de Mutsert Renée, Gyllensten Ulf, Morris Andrew P, Ikram M Arfan, Probst-Hensch Nicole, Gläser Sven, Zeggini Eleftheria, Lehtimäki Terho, Strachan David P, Dupuis Josée, Morrison Alanna C, Hall Ian P, Tobin Martin D, London Stephanie |
| Clinical correlation of opposing molecular signatures in head and neck squamous cell carcinoma. BMC cancer 2019 8 19 (1): 830. Qadir Fatima, Lalli Anand, Dar Huma Habib, Hwang Sungjae, Aldehlawi Hebah, Ma Hong, Dai Haiyan, Waseem Ahmad, Teh Muy-Te |
| Reactive stroma and trastuzumab resistance in HER2-positive early breast cancer. International journal of cancer 2020 1 147 (1): 266-276. Sonnenblick Amir, Salmon-Divon Mali, Salgado Roberto, Dvash Efrat, Pondé Noam, Zahavi Tamar, Salmon Asher, Loibl Sibylle, Denkert Carsten, Joensuu Heikki, Ameye Lieveke, Van den Eynden Gert, Kellokumpu-Lehtinen Pirkko-Liisa, Azaria Amos, Loi Sherene, Michiels Stefan, Richard François, Sotiriou Christ |
| Association of CASR, CALCR, and ORAI1 Genes Polymorphisms With the Calcium Urolithiasis Development in Russian Population. Frontiers in genetics 2021 12 621049. Litvinova Maria M, Khafizov Kamil, Korchagin Vitaly I, Speranskaya Anna S, Asanov Aliy Yu, Matsvay Alina D, Kiselev Daniil A, Svetlichnaya Diana V, Nuralieva Sevda Z, Moskalev Alexey A, Filippova Tamara |
| Two Rare Variants in PLAU and BACE1 Genes-Do They Contribute to Semantic Dementia Clinical Phenotype? Genes 2021 11 12 (11): . Gaweda-Walerych Katarzyna, Sitek Emilia J, Borczyk Ma?gorzata, Berdy?ski Mariusz, Naro?a?ska Ewa, Brockhuis Bogna, Korosty?ski Micha?, S?awek Jaros?aw, Zekanowski Ceza |
| Predictive value of common genetic variants in idiopathic pulmonary fibrosis survival. Journal of molecular medicine (Berlin, Germany) 2022 Sep 100 (9): 1341-1353. Mota Patrícia Caetano, Soares Miguel Luz, Vasconcelos Carlos Daniel, Ferreira António Carlos, Lima Bruno A, Manduchi Elisabetta, Moore Jason H, Melo Natália, Novais-Bastos Hélder, Pereira José Miguel, Guimarães Susana, Moura Conceição Souto, Marques José Agostinho, Morais Antón |
| Genetic insights into therapeutic targets for aortic aneurysms: A Mendelian randomization study. EBioMedicine 2022 8 83 104199. Chen Yanghui, Xu Xin, Wang Linlin, Li Ke, Sun Yang, Xiao Lei, Dai Jiaqi, Huang Man, Wang Yan, Wang Dao W |
| Searching for Genetic Biomarkers for Hereditary Angioedema Due to C1-Inhibitor Deficiency (C1-INH-HAE). Frontiers in allergy 2022 7 3 868185. Parsopoulou Faidra, Loules Gedeon, Zamanakou Maria, Csuka Dorottya, Szilagyi Agnes, Kompoti Maria, Porebski Grzegorz, Psarros Fotis, Magerl Markus, Valerieva Anna, Staevska Maria, Obtulowicz Krystyna, Maurer Marcus, Speletas Matthaios, Farkas Henriette, Germenis Anastasios |
| The Association of PLAUR Genotype and Soluble suPAR Serum Level with COVID-19-Related Lung Damage Severity. International journal of molecular sciences 2022 12 23 (24): . Nekrasova Ludmila A, Shmakova Anna A, Samokhodskaya Larisa M, Kirillova Karina I, Stoyanova Simona S, Mershina Elena A, Nazarova Galina B, Rubina Kseniya A, Semina Ekaterina V, Kamalov Armais |
| Effects of copy number variations on longevity in late-onset Alzheimer's disease patients: insights from a causality network analysis. Frontiers in aging neuroscience 2023 11 15 1241412. Yanan Hao, Chuhao Li, He Wang, Chen Mi |
| Gene Association Study of the Urokinase Plasminogen Activator and Its Receptor Gene in Alzheimer's Disease. Journal of Alzheimer's disease : JAD 2024 4 . Ozde Cetinsoy, Ijeoma Anyanwu, Harikrishnan Krishnanand, Gokulakrishnan Natarajan, Naveen Ramachandran, Alan Thomas, Keeley J Brook |
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