Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Bronchiectasis and CFTR[original query] |
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| CFTR gene mutations--including three novel nucleotide substitutions--and haplotype background in patients with asthma, disseminated bronchiectasis and chronic obstructive pulmonary disease. Human genetics 2001 Mar 108 (3): 216-21. Tzetis M, Efthymiadou A, Strofalis S, Psychou P, Dimakou A, Pouliou E, Doudounakis S, Kanavakis |
| 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 |
| Indirect CFTR mutation identification by PCR/OLA anomalous electropherograms. Genetic testing 2005 9 (4): 285-91. Stanziale Pietro, Savino Maria, De Bonis Patrizia, Granatiero Matteo, Zelante Leopoldo, Bisceglia Lui |
| Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Asians with chronic pulmonary disease: a pilot study. Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2006 Aug 5 (3): 159-64. Ngiam Nicola S P, Chong Samuel S, Shek Lynette P C, Goh Denise L M, Ong K C, Chng S Y, Yeo G H, Goh Daniel Y |
| Non-classic cystic fibrosis associated with D1152H CFTR mutation. Clinical genetics 2010 Apr 77 (4): 355-64. Burgel P-R, Fajac I, Hubert D, Grenet D, Stremler N, Roussey M, Siret D, Languepin J, Mely L, Fanton A, Labbé A, Domblides P, Vic P, Dagorne M, Reynaud-Gaubert M, Counil F, Varaigne F, Bienvenu T, Bellis G, Dusser |
| Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis. American journal of respiratory and critical care medicine 2010 May 181 (10): 1078-84. Bienvenu Thierry, Sermet-Gaudelus Isabelle, Burgel Pierre-Regis, Hubert Dominique, Crestani Bruno, Bassinet Laurence, Dusser Daniel, Fajac Isabel |
| Mutations of the cystic fibrosis gene in patients with bronchiectasis associated with rheumatoid arthritis. Annals of the rheumatic diseases 2011 Apr 70 (4): 653-9. Puéchal Xavier, Bienvenu Thierry, Génin Emmanuelle, Berthelot Jean-Marie, Sibilia Jean, Gaudin Philippe, Marcelli Christian, Lasbleiz Sandra, Michou Laëtitia, Cornélis François, Kahan André, Dusser Daniel |
| Analysis of CFTR Gene Variants in Idiopathic Bronchiectasis in Serbian Children. Pediatric allergy, immunology, and pulmonology 2013 Jun 26 (2): 93-98. Milosevic Katarina, Nikolic Aleksandra, Divac Rankov Aleksandra, Ljujic Mila, Nestorovic Branimir, Radojkovic Dragi |
| Phenotypic expression of the p.Leu1077Pro CFTR mutation in Sicilian cystic fibrosis patients. BMC research notes 2013 6 (1): 461. Parisi Giuseppe Fabio, Cutello Silvia, Di Dio Giovanna, Rotolo Novella, La Rosa Mario, Leonardi Salvato |
| Poor survival in rheumatoid arthritis associated with bronchiectasis: a family-based cohort study. PloS one 2014 9 (10): e110066. Puéchal Xavier, Génin Emmanuelle, Bienvenu Thierry, Le Jeunne Claire, Dusser Daniel |
| p.Arg75Gln, a CFTR variant involved in the risk of CFTR-related disorders? Journal of human genetics 2014 Apr 59 (4): 206-10. Martinez Brigitte, Heller Marion, Gaitch Natacha, Hubert Dominique, Burgel Pierre-Regis, Levy Philippe, Girodon Emmanuelle, Bienvenu Thier |
| Frequency of Genotype With ?F508 Mutation in CFTR Gene Among Iranian Cystic Fibrosis Patients With Pancreatic Insufficiency. Iranian journal of pediatrics 2015 Dec 25 (6): e3419. Khodadad Ahmad, Elahi Elaheh, Bani Hassani Setareh Sadat, Rouhani Pejman, Sadeghi Bamdad, Rezaei Ni |
| F508del CFTR gene mutation in patients with allergic bronchopulmonary aspergillosis. The Journal of asthma : official journal of the Association for the Care of Asthma 2017 Oct 1-7. Gamaletsou Maria N, Hayes Gemma, Harris Chris, Brock Joanna, Muldoon Eavan G, Denning David |
| Next-generation sequencing for identifying genetic mutations in adults with bronchiectasis. Journal of thoracic disease 2018 May 10 (5): 2618-2630. Guan Wei-Jie, Li Jia-Cheng, Liu Fang, Zhou Jian, Liu Ya-Ping, Ling Chao, Gao Yong-Hua, Li Hui-Min, Yuan Jing-Jing, Huang Yan, Chen Chun-Lan, Chen Rong-Chang, Zhang Xue, Zhong Nan-Sh |
| Characterization of clinical and genetic spectrum of Chinese patients with cystic fibrosis. Orphanet journal of rare diseases 2020 6 15 (1): 150. Liu Keqiang, Xu Wenshuai, Xiao Meng, Zhao Xinyue, Bian Chun, Zhang Qianli, Song Jiaxing, Chen Keqi, Tian Xinlun, Liu Yaping, Xu Kai-Feng, Zhang X |
| Morbidity and mortality in carriers of the cystic fibrosis mutation CFTR Phe508del in the general population. The European respiratory journal 2020 5 56 (3): . Çolak Yunus, Nordestgaard Børge G, Afzal Shoa |
| Occurrence of Cystic Fibrosis Transmembrane Conductance Regulator Gene Mutations in Patients with Allergic Bronchopulmonary Aspergillosis Complicating Asthma. Mycopathologia 2022 4 187 (2-3): 147-155. Kanaujia Rimjhim, Arora Amit, Chakrabarti Arunaloke, Rudramurthy Shivaprakash M, Agarwal Rite |
| Prevalence of CFTR variants in PID patients with bronchiectasis - an important modifying co-factor. The Journal of allergy and clinical immunology 2023 2 . Lawless Dylan, Allen Hana Lango, Thaventhiran James E D, Goddard Sarah, Burren Oliver S, Robson Evie, , Peckham Daniel, Smith Kenneth G C, Savic Sini |
| Diagnosis of cystic fibrosis: a high heterogeneity of symptoms and genotypes in a Brazil population. BMC pediatrics 2024 7 24 (1): 422. Daniela Gois Meneses, Fábia Regina Dos Santos, Anne Jardim Botelho, Luciana Mota Bispo, Camilla Guerra Matos, Vynicius Goltran Sobral Propheta, Alexia Ferreira Rodrigues, Géssica Uruga Oliveira, Angela Maria da Silva, Ricardo Queiroz Gurg |
| Increased prevalence of CFTR variants and susceptibility to CRS: A real-world study based on Chinese children. Heliyon 2024 4 10 (7): e27681. Yang Han, Jinhao Zhao, Wenjing Liu, Xiaojian Yang, Wei Zhang, Xiao Xiao, Xiaoge Liu, Xiaoxu Chen, Lixing Tang, Pengpeng Wang, Wentong |
- Page last reviewed:Feb 1, 2024
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