Human Genome Epidemiology Literature Finder
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Records 1 - 13 (of 13 Records) |
| Query Trace: Disease and LTBP4[original query] |
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| Genetic association analysis of functional impairment in chronic obstructive pulmonary disease. American journal of respiratory and critical care medicine 2006 May 173 (9): 977-84. Hersh Craig P, Demeo Dawn L, Lazarus Ross, Celedón Juan C, Raby Benjamin A, Benditt Joshua O, Criner Gerard, Make Barry, Martinez Fernando J, Scanlon Paul D, Sciurba Frank C, Utz James P, Reilly John J, Silverman Edwin |
| Assessment of the association between genetic polymorphisms in transforming growth factor beta, and its binding protein (LTBP), and the presence, and expansion, of Abdominal Aortic Aneurysm. Atherosclerosis 2010 Apr 209 (2): 367-73. Thompson Andrew R, Cooper Jackie A, Jones Gregory T, Drenos Fotios, van Bockxmeer Frank M, Biros Erik, Walker Philip J, van Rij Andre M, Golledge Jonathan, Norman Paul E, Hafez Hany, Humphries Stephen |
| Validation of genetic modifiers for Duchenne muscular dystrophy: a multicentre study assessing SPP1 and LTBP4 variants. Journal of neurology, neurosurgery, and psychiatry 2015 Oct 86 (10): 1060-5. van den Bergen Janneke C, Hiller Monika, Böhringer Stefan, Vijfhuizen Linda, Ginjaar Hendrika B, Chaouch Amina, Bushby Kate, Straub Volker, Scoto Mariacristina, Cirak Sebahattin, Humbertclaude Véronique, Claustres Mireille, Scotton Chiara, Passarelli Chiara, Lochmüller Hanns, Muntoni Francesco, Tuffery-Giraud Sylvie, Ferlini Alessandra, Aartsma-Rus Annemieke M, Verschuuren Jan J G M, 't Hoen Peter Ac, Spitali Piet |
Sixteen new lung function signals identified through 1000 Genomes Project reference panel imputation.
Nature communications 2015 6 8658. Artigas María Soler, Wain Louise V, Miller Suzanne, Kheirallah Abdul Kader, Huffman Jennifer E, Ntalla Ioanna, Shrine Nick, Obeidat Ma'en, Trochet Holly, McArdle Wendy L, Alves Alexessander Couto, Hui Jennie, Zhao Jing Hua, Joshi Peter K, Teumer Alexander, Albrecht Eva, Imboden Medea, Rawal Rajesh, Lopez Lorna M, Marten Jonathan, Enroth Stefan, Surakka Ida, Polasek Ozren, Lyytikäinen Leo-Pekka, Granell Raquel, Hysi Pirro G, Flexeder Claudia, Mahajan Anubha, Beilby John, Bossé Yohan, Brandsma Corry-Anke, Campbell Harry, Gieger Christian, Gläser Sven, González Juan R, Grallert Harald, Hammond Chris J, Harris Sarah E, Hartikainen Anna-Liisa, Heliövaara Markku, Henderson John, Hocking Lynne, Horikoshi Momoko, Hutri-Kähönen Nina, Ingelsson Erik, Johansson Åsa, Kemp John P, Kolcic Ivana, Kumar Ashish, Lind Lars, Melén Erik, Musk Arthur W, Navarro Pau, Nickle David C, Padmanabhan Sandosh, Raitakari Olli T, Ried Janina S, Ripatti Samuli, Schulz Holger, Scott Robert A, Sin Don D, Starr John M, , Viñuela Ana, Völzke Henry, Wild Sarah H, Wright Alan F, Zemunik Tatijana, Jarvis Deborah L, Spector Tim D, Evans David M, Lehtimäki Terho, Vitart Veronique, Kähönen Mika, Gyllensten Ulf, Rudan Igor, Deary Ian J, Karrasch Stefan, Probst-Hensch Nicole M, Heinrich Joachim, Stubbe Beate, Wilson James F, Wareham Nicholas J, James Alan L, Morris Andrew P, Jarvelin Marjo-Riitta, Hayward Caroline, Sayers Ian, Strachan David P, Hall Ian P, Tobin Martin |
| Long-range genomic regulators of THBS1 and LTBP4 modify disease severity in duchenne muscular dystrophy.
Annals of neurology 2018 Jul . Weiss Robert B, Vieland Veronica J, Dunn Diane M, Kaminoh Yuuki, Flanigan Kevin M, |
| Regulatory variants in cancer-related pathway genes predict survival of patients with surgically resected non-small cell lung cancer. Gene 2017 Dec . Shin Kyung Min, Hong Mi Jeong, Lee Shin Yup, Jin Cheng Cheng, Baek Sun Ah, Lee Jang Hyuck, Choi Jin Eun, Kang Hyo-Gyoung, Lee Won Kee, Seok Yangki, Lee Eung Bae, Jeong Ji Yun, Yoo Seung Soo, Lee Jaehee, Cha Seung Ick, Kim Chang Ho, Kim Young Chul, Oh In Jae, Na Kook Joo, Cho Sukki, Jheon Sanghoon, Park Jae Yo |
| Aberrant interaction between mutated ADAMTSL2 and LTBP4 is associated with adolescent idiopathic scoliosis. Gene 2021 12 814 146126. Liu Bowen, Zhao Sen, Liu Lian, Du Huakang, Zhao Hengqiang, Wang Shengru, Niu Yuchen, Li Xiaoxin, Qiu Guixing, , Wu Zhihong, Zhang Terry Jianguo, Wu N |
| Genetic modifiers of upper limb function in Duchenne muscular dystrophy. Journal of neurology 2022 5 269 (9): 4884-4894. Sabbatini Daniele, Fusto Aurora, Vianello Sara, Villa Matteo, Janik Joanna, D'Angelo Grazia, Diella Eleonora, Magri Francesca, Comi Giacomo P, Panicucci Chiara, Bruno Claudio, D'Amico Adele, Bertini Enrico, Astrea Guja, Battini Roberta, Politano Luisa, Masson Riccardo, Baranello Giovanni, Previtali Stefano C, Messina Sonia, Vita Gianluca, Berardinelli Angela, Mongini Tiziana, Pini Antonella, Pane Marika, Mercuri Eugenio, Hoffman Eric P, Morgenroth Lauren, Gordish-Dressman Heather, Duong Tina, McDonald Craig M, Bello Luca, Pegoraro Ele |
| Cytokines in Abdominal Aortic Aneurysm: Master Regulators With Clinical Application. Biomarker insights 2022 5 17 11772719221095676. Puchenkova Olesya A, Soldatov Vladislav O, Belykh Andrei E, Bushueva OlgaYu, Piavchenko Gennadii A, Venediktov Artem A, Shakhpazyan Nikolay K, Deykin Alexey V, Korokin Mikhail V, Pokrovskiy Mikhail |
| Evaluating Genetic Modifiers of Duchenne Muscular Dystrophy Disease Progression Using Modeling and MRI. Neurology 2022 10 99 (21): e2406-e2416. Barnard Alison M, Hammers David W, Triplett William T, Kim Sarah, Forbes Sean C, Willcocks Rebecca J, Daniels Michael J, Senesac Claudia R, Lott Donovan J, Arpan Ishu, Rooney William D, Wang Richard T, Nelson Stanley F, Sweeney H Lee, Vandenborne Krista, Walter Glenn |
| Predictors of Loss of Ambulation in Duchenne Muscular Dystrophy: A Systematic Review and Meta-Analysis. Journal of neuromuscular diseases 2024 4 . E Landfeldt, A Alemán, S Abner, R Zhang, C Werner, I Tomazos, N Ferizovic, H Lochmüller, J Kirschn |
| Prognostic significance of ACTN3 genotype in Duchenne muscular dystrophy: Findings from an Argentine patient cohort. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2024 12 54 32-41. Leonela Luce, Chiara Mazzanti, Micaela Carcione, Carmen Llames Massini, Paula Inés Buonfiglio, Viviana Dalamón, Carla Bolaño Díaz, Lilia Mesa, Alberto Dubrovsky, Javier Cotignola, Florencia Giliber |
| Matrisome and Immune Pathways Contribute to Extreme Vascular Outcomes in Williams-Beuren Syndrome. Journal of the American Heart Association 2024 1 13 (3): e031377. Delong Liu, Charles J Billington, Neelam Raja, Zoe C Wong, Mark D Levin, Wulfgang Resch, Camille Alba, Daniel N Hupalo, Elisa Biamino, Maria Francesca Bedeschi, Maria Cristina Digilio, Gabriella Maria Squeo, Roberta Villa, Pheobe C R Parrish, Russell H Knutsen, Sharon Osgood, Joy A Freeman, Clifton L Dalgard, Giuseppe Merla, Barbara R Pober, Carolyn B Mervis, Amy E Roberts, Colleen A Morris, Lucy R Osborne, Beth A Koz |
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