Human Genome Epidemiology Literature Finder
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Records 1 - 16 (of 16 Records) |
| Query Trace: Cystic Fibrosis and MBL2[original query] |
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| Association of common haplotypes of surfactant protein A1 and A2 (SFTPA1 and SFTPA2) genes with severity of lung disease in cystic fibrosis. Pediatric pulmonology 2006 Mar 41 (3): 255-62. Choi Eun Hwa, Ehrmantraut Mary, Foster Charles B, Moss Joel, Chanock Stephen |
| Mannose-binding lectin gene polymorphic variants predispose to the development of bronchopulmonary complications but have no influence on other clinical and laboratory symptoms or signs of common variable immunodeficiency. Clinical and experimental immunology 2008 Sep 153 (3): 324-30. Litzman J, Freiberger T, Grimbacher B, Gathmann B, Salzer U, Pavlík T, Vlcek J, Postránecká V, Trávnícková Z, Thon |
| Complex two-gene modulation of lung disease severity in children with cystic fibrosis. The Journal of clinical investigation 2008 Mar 118 (3): 1040-9. Dorfman Ruslan, Sandford Andrew, Taylor Chelsea, Huang Baisong, Frangolias Daisy, Wang Yongqian, Sang Richard, Pereira Lilian, Sun Lei, Berthiaume Yves, Tsui Lap-Chee, Paré Peter D, Durie Peter, Corey Mary, Zielenski Juli |
| Genetic modifiers of liver disease in cystic fibrosis. JAMA 2009 Sep 302 (10): 1076-83. Bartlett Jaclyn R, Friedman Kenneth J, Ling Simon C, Pace Rhonda G, Bell Scott C, Bourke Billy, Castaldo Giuseppe, Castellani Carlo, Cipolli Marco, Colombo Carla, Colombo John L, Debray Dominique, Fernandez Adriana, Lacaille Florence, Macek Milan, Rowland Marion, Salvatore Francesco, Taylor Christopher J, Wainwright Claire, Wilschanski Michael, Zemková Dana, Hannah William B, Phillips M James, Corey Mary, Zielenski Julian, Dorfman Ruslan, Wang Yunfei, Zou Fei, Silverman Lawrence M, Drumm Mitchell L, Wright Fred A, Lange Ethan M, Durie Peter R, Knowles Michael R, |
| An MBL2 haplotype and ABCB4 variants modulate the risk of liver disease in cystic fibrosis patients: a multicentre study. Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver 2009 Nov 41 (11): 817-22. Tomaiuolo R, Degiorgio D, Coviello D A, Baccarelli A, Elce A, Raia V, Motta V, Seia M, Castaldo G, Colombo |
| Association of MBL2, TGF-beta1 and CD14 gene polymorphisms with lung disease severity in cystic fibrosis. Jornal brasileiro de pneumologia : publicaça?o oficial da Sociedade Brasileira de Pneumologia e Tisilogia 2009 Apr 35 (4): 334-42. Faria Elisangela Jacinto de, Faria Isabel Cristina Jacinto de, Ribeiro José Dirceu, Ribeiro Antônio Fernando, Hessel Gabriel, Bertuzzo Carmen Sílv |
| Impact of mannose-binding lectin insufficiency on the course of cystic fibrosis: A review and meta-analysis. Glycobiology 2011 Mar 21 (3): 271-82. Chalmers James D, Fleming Gillian B, Hill Adam T, Kilpatrick David |
| Use of a modeling framework to evaluate the effect of a modifier gene (MBL2) on variation in cystic fibrosis. European journal of human genetics : EJHG 2010 Jun 18 (6): 680-4. McDougal Kathryn E, Green Deanna M, Vanscoy Lori L, Fallin M Daniele, Grow Michael, Cheng Suzanne, Blackman Scott M, Collaco J Michael, Henderson Lindsay B, Naughton Kathleen, Cutting Garry |
| Study of the effect of DNA polymorphisms in the mannose-binding lectin gene (MBL2) on disease severity in Slovak cystic fibrosis patients. General physiology and biophysics 2011 Dec 30 (4): 373-8. Tarova Eva Tothova, Polakova Helena, Kayserova Hana, Celec Peter, Zuzulova Maria, Kadasi Ludev |
| Polymorphisms in the lectin pathway genes as a possible cause of early chronic Pseudomonas aeruginosa colonization in cystic fibrosis patients. Human immunology 2012 Nov 73 (11): 1175-83. Haerynck F, Van Steen K, Cattaert T, Loeys B, Van Daele S, Schelstraete P, Claes K, Van Thielen M, De Canck I, Mahachie John J M, De Baets |
| Mannose-binding lectin gene as a modifier of the cystic fibrosis phenotype in Argentinean pediatric patients. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2015 Jan 14 (1): 78-83. Gravina Luis Pablo, Crespo Carolina, Giugno Hilda, Sen Luisa, Chertkoff Lilien, Mangano Andrea, Castaños Claud |
| Mannose-binding lectin 2 gene polymorphism and lung damage in primary ciliary dyskinesia. Pediatric pulmonology 2015 Feb 50 (2): 179-86. Pifferi Massimo, Bush Andrew, Michelucci Angela, Di Cicco Maria, Piras Martina, Caramella Davide, Mazzei Federica, Neri Maria, Pioggia Giovanni, Tartarisco Gennaro, Saggese Giuseppe, Simi Paolo, Boner Attilio |
| The tumor necrosis factor a (-308 A/G) polymorphism is associated with cystic fibrosis in Mexican patients. PloS one 2014 9 (3): e90945. Sanchez-Dominguez Celia N, Reyes-Lopez Miguel A, Bustamante Adriana, Cerda-Flores Ricardo M, Villalobos-Torres Maria Del C, Gallardo-Blanco Hugo L, Rojas-Martinez Augusto, Martinez-Rodriguez Herminia G, Barrera-Saldaña Hugo A, Ortiz-Lopez Roc |
| Influence of SNPs in Genes that Modulate Lung Disease Severity in a Group of Mexican Patients with Cystic Fibrosis. Archives of medical research 2018 Jan 49 (1): 18-26. Yokoyama Emiy, Chávez-Saldaña Margarita, Orozco Lorena, Cuevas Francisco, Lezana José Luis, Vigueras-Villaseñor Rosa María, Rojas-Castañeda Julio Cesar, Landero Daniel Adri |
| The impact of mannose-binding lectin polymorphisms on lung function in primary ciliary dyskinesia. Pediatric pulmonology 2019 4 54 (8): 1182-1189. Videbaek Katja, Buchvald Frederik, Holgersen Mathias Gelderman, Henriksen Alison, Eriksson Frank, Garred Peter, Nielsen Kim Gjer |
| Genetic Association With Pseudomonas aeruginosa Acquisition in Cystic Fibrosis: Influence of Surfactant Protein D and Mannose-Binding Lectin. Frontiers in immunology 2021 587313. Nourkami-Tutdibi Nasenien, Freitag Klemens, Zemlin Michael, Tutdibi Er |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 22, 2023
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