Human Genome Epidemiology Literature Finder
Heart, Lung, Blood and Sleep Disorders
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Records 1 - 13 (of 13 Records) |
| Query Trace: Lung Disorders[original query] |
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| Cytokine polymorphisms in silicosis and other pneumoconioses. Molecular and cellular biochemistry 0 234-235 (1-2): 219-24. Yucesoy Berran, Vallyathan Val, Landsittel Douglas P, Simeonova Petia, Luster Michael |
| Promoter variants in tissue inhibitor of metalloproteinase-3 (TIMP-3) protect against susceptibility in pigeon breeders' disease. Thorax 2004 Jul 59 (7): 586-90. Hill M R, Briggs L, Montaño M M, Estrada A, Laurent G J, Selman M, Pardo |
| Bronchiectasis in adult patients: an expression of heterozygosity for CFTR gene mutations? Clinical genetics 2004 Jun 65 (6): 490-5. Casals T, De-Gracia J, Gallego M, Dorca J, Rodríguez-Sanchón B, Ramos M D, Giménez J, Cisteró-Bahima A, Olveira C, Estivill |
| ATM gene mutations in former uranium miners of SDAG Wismut: a pilot study. Oncology reports 2007 Feb 17 (2): 477-82. Schneider Joachim, Philipp Monika, Yamini Paria, Dörk Thilo, Woitowitz Hans-Joach |
| Peripheral blood gene expression as a novel genomic biomarker in complicated sarcoidosis. PloS one 2012 7 (9): e44818. Zhou Tong, Zhang Wei, Sweiss Nadera J, Chen Edward S, Moller David R, Knox Kenneth S, Ma Shwu-Fan, Wade Michael S, Noth Imre, Machado Roberto F, Garcia Joe G |
| Genetic regulation of expression of leukotriene A4 hydrolase. ERJ open research 2016 Jan 2 (1): . Szul Tomasz, Castaldi Peter, Cho Michael H, Blalock J Edwin, Gaggar Am |
| Liver Fibrosis and Metabolic Alterations in Adults With alpha-1-antitrypsin Deficiency Caused by the Pi*ZZ Mutation. Gastroenterology 2019 5 157 (3): 705-719.e18. Hamesch Karim, Mandorfer Mattias, Pereira Vítor M, Moeller Linda S, Pons Monica, Dolman Grace E, Reichert Matthias C, Schneider Carolin V, Woditsch Vivien, Voss Jessica, Lindhauer Cecilia, Fromme Malin, Spivak Igor, Guldiken Nurdan, Zhou Biaohuan, Arslanow Anita, Schaefer Benedikt, Zoller Heinz, Aigner Elmar, Reiberger Thomas, Wetzel Martin, Siegmund Britta, Simões Carolina, Gaspar Rui, Maia Luís, Costa Dalila, Bento-Miranda Mário, van Helden Josef, Yagmur Eray, Bzdok Danilo, Stolk Jan, Gleiber Wolfgang, Knipel Verena, Windisch Wolfram, Mahadeva Ravi, Bals Robert, Koczulla Rembert, Barrecheguren Miriam, Miravitlles Marc, Janciauskiene Sabina, Stickel Felix, Lammert Frank, Liberal Rodrigo, Genesca Joan, Griffiths William J, Trauner Michael, Krag Aleksander, Trautwein Christian, Strnad Pavel, |
| Cell-specific expression of lung disease risk-related genes in the human small airway epithelium. Respiratory research 2020 7 21 (1): 200. Zuo Wu-Lin, Rostami Mahboubeh R, Shenoy Shushila A, LeBlanc Michelle G, Salit Jacqueline, Strulovici-Barel Yael, O'Beirne Sarah L, Kaner Robert J, Leopold Philip L, Mezey Jason G, Schymeinsky Juergen, Quast Karsten, Visvanathan Sudha, Fine Jay S, Thomas Matthew J, Crystal Ronald |
| A Polymorphism in the Catalase Gene Promoter Confers Protection against Severe RSV Bronchiolitis. Viruses 2020 1 12 (1): . Chambliss Jeffrey M, Ansar Maria, Kelley John P, Spratt Heidi, Garofalo Roberto P, Casola Antonel |
| Correlating SFTPC gene variants to interstitial lung disease in Egyptian children. Journal, genetic engineering & biotechnology 2022 8 20 (1): 117. Abdel Megeid Azza K, Refeat Miral M, Ashaat Engy A, El-Kamah Ghada, El-Saiedi Sonia A, Elfalaki Mona M, El Ruby Mona O, Amr Khalda |
| The FoxP1 gene regulates lung function, production of matrix metalloproteinases and inflammatory mediators, and viability of lung epithelia. Respiratory research 2022 Oct 23 (1): 281. Andreas Alexis, Maloy Abby, Nyunoya Toru, Zhang Yingze, Chandra Div |
| Association of A1AT genetic polymorphism and NSCLC: a case- control study in Egyptian population. BMC medical genomics 2023 7 16 (1): 173. Aliaa N El-Dawa, Afaf M ElSaid, Sherif Refaat, Omali Y El-Khawa |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 05, 2023
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