Interstitial lung disease

Epigenetic inheritance of telomere length obscures identification of causative PARN locus
Chao Xing, Christine Kim Garcia

Journal of Medical Genetics May 2016, 53 (5) 356-358; DOI: 10.1136/jmedgenet-2015-103685
Moving beyond genetics: is FAM13A a major biological contributor in lung physiology and chronic lung diseases?
Harriet Corvol, Craig A Hodges, Mitchell L Drumm, Loïc Guillot

Journal of Medical Genetics Oct 2014, 51 (10) 646-649; DOI: 10.1136/jmedgenet-2014-102525
Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenita
Erin M Parry, Jonathan K Alder, Stella S Lee, John A Phillips, James E Loyd, Priya Duggal, Mary Armanios

Journal of Medical Genetics May 2011, 48 (5) 327-333; DOI: 10.1136/jmg.2010.085100
Clinical and cellular characterisation of Hermansky–Pudlak syndrome type 6
M Huizing, B Pederson, R A Hess, A Griffin, A Helip-Wooley, W Westbroek, H Dorward, K J O’Brien, G Golas, E Tsilou, J G White, W A Gahl

Journal of Medical Genetics Dec 2009, 46 (12) 803-810; DOI: 10.1136/jmg.2008.065961
New surfactant protein C gene mutations associated with diffuse lung disease
L Guillot, R Epaud, G Thouvenin, L Jonard, A Mohsni, R Couderc, F Counil, J de Blic, R A Taam, M Le Bourgeois, P Reix, F Flamein, A Clement, D Feldmann

Journal of Medical Genetics Jul 2009, 46 (7) 490-494; DOI: 10.1136/jmg.2009.066829
A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis
T Mushiroda, S Wattanapokayakit, A Takahashi, T Nukiwa, S Kudoh, T Ogura, H Taniguchi, M Kubo, N Kamatani, Y Nakamura, the Pirfenidone Clinical Study Group

Journal of Medical Genetics Oct 2008, 45 (10) 654-656; DOI: 10.1136/jmg.2008.057356
Murine candidate bleomycin induced pulmonary fibrosis susceptibility genes identified by gene expression and sequence analysis of linkage regions
C K Haston, T G Tomko, N Godin, L Kerckhoff, M T Hallett

Journal of Medical Genetics Jun 2005, 42 (6) 464-473; DOI: 10.1136/jmg.2004.027938
P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome
N A Garrison, Z Yi, O Cohen-Barak, M Huizing, L M Hartnell, W A Gahl, M H Brilliant

Journal of Medical Genetics Jun 2004, 41 (6) e86; DOI: 10.1136/jmg.2003.014902
Effect of TNF and LTA polymorphisms on biological markers of response to oxidative stimuli in coal miners: a model of gene-environment interaction
R Nadif, A Jedlicka, M Mintz, J-P Bertrand, S Kleeberger, F Kauffmann

Journal of Medical Genetics Feb 2003, 40 (2) 96-103; DOI: 10.1136/jmg.40.2.96
Atypical haemochromatosis: phenotypic spectrum and β₂-microglobulin candidate gene analysis
Ann P Walker, Daniel F Wallace, Jason Partridge, Adrian B Bomford, James S Dooley

Journal of Medical Genetics Jul 1999, 36 (7) 537-541; DOI: 10.1136/jmg.36.7.537

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Interstitial lung disease