Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Disease and ADAM17[original query] |
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| Polymorphisms of the tumor necrosis factor-alpha (TNF) and the TNF-alpha converting enzyme (TACE/ADAM17) genes in relation to cardiovascular mortality: the AtheroGene study. Journal of molecular medicine (Berlin, Germany) 2008 Oct 86 (10): 1153-61. Morange P E, Tregouet D A, Godefroy T, Saut N, Bickel C, Rupprecht H J, Lackner K, Barbaux S, Poirier O, Peiretti F, Nalbone G, Juhan-Vague I, Blankenberg S, Tiret |
| The relationship between ADAM17 promoter polymorphisms and sporadic Alzheimer's disease in a Northern Chinese Han population. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2010 Oct 17 (10): 1276-9. Wang Min, Li Yang, Lu Yan, Zuo Xiumei, Wang Fen, Zhang Zhijun, Jia Jianpi |
| Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease. Neurobiology of aging 2012 Feb 33 (2): 416-417.e3. Cai Guiqing, Atzmon Gil, Naj Adam C, Beecham Gary W, Barzilai Nir, Haines Jonathan L, Sano Mary, Pericak-Vance Margaret, Buxbaum Joseph |
| De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects. PLoS genetics 2016 Apr 12 (4): e1005963. Priest James R, Osoegawa Kazutoyo, Mohammed Nebil, Nanda Vivek, Kundu Ramendra, Schultz Kathleen, Lammer Edward J, Girirajan Santhosh, Scheetz Todd, Waggott Daryl, Haddad Francois, Reddy Sushma, Bernstein Daniel, Burns Trudy, Steimle Jeffrey D, Yang Xinan H, Moskowitz Ivan P, Hurles Matthew, Lifton Richard P, Nickerson Debbie, Bamshad Michael, Eichler Evan E, Mital Seema, Sheffield Val, Quertermous Thomas, Gelb Bruce D, Portman Michael, Ashley Euan |
| Genetic variants of ADAM17 are implicated in the pathological process of Kawasaki disease and secondary coronary artery lesions via the TGF-ß/SMAD3 signaling pathway. European journal of pediatrics 2016 Feb . Peng Qian, Deng Yan, Yang Xiling, Leng Xiangyou, Yang Yuan, Liu Hanm |
| A Common Variant of IL-6R is Associated with Elevated IL-6 Pathway Activity in Alzheimer's Disease Brains. Journal of Alzheimer's disease : JAD 2017 Jan . Haddick Patrick C G, Larson Jessica L, Rathore Nisha, Bhangale Tushar R, Phung Qui T, Srinivasan Karpagam, Hansen David V, Lill Jennie R, , Pericak-Vance Margaret A, Haines Jonathan, Farrer Lindsay A, Kauwe John S, Schellenberg Gerard D, Cruchaga Carlos, Goate Alison M, Behrens Timothy W, Watts Ryan J, Graham Robert R, Kaminker Joshua S, van der Brug Marc |
| A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease. Molecular psychiatry 2018 Jul . Hartl Daniela, May Patrick, Gu Wei, Mayhaus Manuel, Pichler Sabrina, Spaniol Christian, Glaab Enrico, Bobbili Dheeraj Reddy, Antony Paul, Koegelsberger Sandra, Kurz Alexander, Grimmer Timo, Morgan Kevin, Vardarajan Badri N, Reitz Christiane, Hardy John, Bras Jose, Guerreiro Rita, Balling Rudi, Schneider Jochen G, Riemenschneider Matthias, |
| Genetic Association Between NGFR, ADAM17 Gene Polymorphism, and Parkinson's Disease in the Chinese Han Population. Neurotoxicity research 2019 Apr . Li Wei-Wei, Shen Ying-Ying, Chen Dong-Wan, Li Hui-Yun, Shi Qian-Qian, Mei Jing, Yang Heng, Zhou Fa-Ying, Shi An-Yu, Zhang Tao, Yao Xiu-Qing, Xu Zhi-Qiang, Zeng Fan, Wang Yan-Jia |
| Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia. Orphanet journal of rare diseases 2020 9 15 (1): 254. Giraud Sophie, Bardel Claire, Dupuis-Girod Sophie, Carette Marie-France, Gilbert-Dussardier Brigitte, Riviere Sophie, Saurin Jean-Christophe, Eyries Mélanie, Patri Sylvie, Decullier Evelyne, Calender Alain, Lesca Gaët |
| Is Polymorphism in the Apoptosis and Inflammatory Pathway Genes Associated With a Primary Response to Anti-TNF Therapy in Crohn's Disease Patients? Frontiers in pharmacology 2020 9 11 1207. Walczak Michal, Lykowska-Szuber Liliana, Plucinska Marianna, Stawczyk-Eder Kamila, Zakerska-Banaszak Oliwia, Eder Piotr, Krela-Kazmierczak Iwona, Michalak Michal, Zywicki Marek, Karlowski Wojciech M, Szalata Marlena, Dobrowolska Agnieszka, Slomski Ryszard, Skrzypczak-Zielinska Marze |
| Whole exome sequencing in unclassified autoinflammatory diseases: more monogenic diseases in the pipeline? Rheumatology (Oxford, England) 2020 5 60 (2): 607-616. Kosukcu Can, Taskiran Ekim Z, Batu Ezgi Deniz, Sag Erdal, Bilginer Yelda, Alikasifoglu Mehmet, Ozen Se |
| Common and Rare Variant Prediction and Penetrance of IBD in a Large, Multi-ethnic, Health System-based Biobank Cohort. Gastroenterology 2020 Dec . Gettler Kyle, Levantovsky Rachel, Moscati Arden, Giri Mamta, Wu Yiming, Hsu Nai-Yun, Chuang Ling-Shiang, Sazonovs Aleksejs, Venkateswaran Suresh, Korie Ujunwa, Chasteau Colleen, , Duerr Richard H, Silverberg Mark S, Snapper Scott B, Daly Mark J, McGovern Dermot P, Brant Steven R, Kugathasan Subra, Anderson Carl A, Itan Yuval, Cho Judy |
| Severe COVID-19 Patients Show an Increase in Soluble TNFR1 and ADAM17, with a Relationship to Mortality. International journal of molecular sciences 2021 8 22 (16): . Palacios Yadira, Ruiz Andy, Ramón-Luing Lucero A, Ocaña-Guzman Ranferi, Barreto-Rodriguez Omar, Sánchez-Monciváis Anahí, Tecuatzi-Cadena Brenda, Regalado-García Ana G, Pineda-Gudiño Rey David, García-Martínez Alicia, Juárez-Hernández Fortunato, Farias-Contreras Juan Pablo, Fricke-Galindo Ingrid, Pérez-Rubio Gloria, Falfán-Valencia Ramcés, Buendia-Roldan Ivette, Medina-Quero Karen, Chavez-Galan Lesl |
| Polymorphisms in some proinflammatory genes (TNF? and ?, IL-1?, IL-6, ADAM17) in severe chronic venous disease. Journal of the European Academy of Dermatology and Venereology : JEADV 2022 11 37 (3): 590-597. Slonková Veronika, Vašk? Anna, Vašk? Vladim |
| [Effect of components of the renin-angiotensin system, rs2106809 polymorphism of the ACE2 gene, and therapy with RAS blockers on the severity of COVID-19]. Problemy endokrinologii 2023 9 69 (4): 21-31. Z T Zuraeva, O K Vikulova, N M Malysheva, L V Nikankina, N V Zaytceva, O Y Sukhareva, M S Shamhalova, M V Shestakova, N G Mokryshe |
| Ectodomain Shedding by ADAM17 Increases the Release of Soluble CD40 from Human Endothelial Cells under Pro-Inflammatory Conditions. Cells 2023 8 12 (15): . Anton Klersy, Sören Meyer, Florian Leuschner, Thorsten Kessler, Markus Hecker, Andreas H Wagn |
| Association of the ILR1 and FAS genes variants with a primary non-response to Anti-TNF therapy in Crohn's disease patients. Polish archives of internal medicine 2023 3 . Lykowska-Szuber Liliana, Skrzypczak-Zielinska Marzena, Zuraszek Joanna, Walczak Michal, Stawczyk-Eder Kamila, Krela-Kazmierczak Iwona, Michalak Michal, Slomski Ryszard, Dobrowolska Agniesz |
| The first genome-wide association study in the Argentinian and Chilean populations identifies shared genetics with Europeans in Alzheimer's disease. Alzheimer's & dementia : the journal of the Alzheimer's Association 2023 11 . Maria Carolina Dalmasso, Itziar de Rojas, Natividad Olivar, Carolina Muchnik, Bárbara Angel, Sergio Gloger, Mariana Soledad Sanchez Abalos, María Victoria Chacón, Rafael Aránguiz, Paulina Orellana, Carolina Cuesta, Pablo Galeano, Lorenzo Campanelli, Gisela Vanina Novack, Luis Eduardo Martinez, Nancy Medel, Julieta Lisso, Zulma Sevillano, Nicolás Irureta, Eduardo Miguel Castaño, Laura Montrreal, Michaela Thoenes, Claudia Hanses, Stefanie Heilmann-Heimbach, Claudia Kairiyama, Inés Mintz, Ivana Villella, Fabiana Rueda, Amanda Romero, Nancy Wukitsevits, Ivana Quiroga, Cristian Gona, Jean-Charles Lambert, Patricia Solis, Daniel Gustavo Politis, Carlos Alberto Mangone, Christian Gonzalez-Billault, Mercè Boada, Lluís Tàrraga, Andrea Slachevsky, Cecilia Albala, Patricio Fuentes, Silvia Kochen, Luis Ignacio Brusco, Agustín Ruiz, Laura Morelli, Alfredo Ramír |
| Single nucleotide polymorphisms in ADAM17, IL23R and SLCO1C1 genes protect against infliximab failure in adults with Crohn's disease. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie 2023 1 159 114225. Laserna-Mendieta E J, Salvador-Martín S, Arias A, López-Cauce B, Marín-Jiménez I, Menchén L A, Marín-Rubio L, Ontañón Rodríguez J, López-Fernández L A, Lucendo A |
| The Role of NOTCH Pathway Genes in the Inherited Susceptibility to Aortic Stenosis. Journal of cardiovascular development and disease 2024 7 11 (7): . Olga Irtyuga, Rostislav Skitchenko, Mary Babakekhyan, Dmitrii Usoltsev, Svetlana Tarnovskaya, Anna Malashicheva, Yulya Fomicheva, Oksana Rotar, Olga Moiseeva, Ulyana Shadrina, Mykyta Artomov, Anna Kostareva, Evgeny Shlyakh |
- Page last reviewed:Feb 1, 2024
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