Skip to main content

BMJ Journals

  • Subscribe
  • Log In More
    Log in via Institution
    Log in via OpenAthens
    Log in via CCMG

    Log in using your username and password

    For personal accounts OR managers of institutional accounts
    Forgot your log in details?Register a new account?
    Forgot your user name or password?
  • Basket
  • Search More
    Advanced search
Journal of Medical Genetics
  • Latest content
  • Current issue
  • Archive
  • Authors
  • About

Advanced search

  • Close More

    Main menu

    • Latest content
    • Current issue
    • Archive
    • Authors
    • About
  • Subscribe
  • Log in More
    Log in via Institution
    Log in via OpenAthens
    Log in via CCMG

    Log in using your username and password

    For personal accounts OR managers of institutional accounts
    Forgot your log in details?Register a new account?
    Forgot your user name or password?
  • BMJ Journals More

You are here

  • Home
  • topic
  • Journal of Medical Genetics
  • CLINICAL
  • Respiratory medicine
  • Interstitial lung disease
Email alerts

Interstitial lung disease

  • CLINICAL /
  • Respiratory medicine /
  • 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
  • CLINICAL
    • Cardiovascular medicine
      • Arrhythmias (33)
      • Cardiomyopathy (95)
      • Congenital heart disease (93)
      • Hypertension (63)
      • Ischaemic heart disease (48)
      • Valvar diseases (32)
      • Venous thromboembolism (4)
    • Dermatology (272)
    • Diagnostics
      • Clinical diagnostic tests (399)
      • Surgical diagnostic tests (120)
    • Drugs and medicines
    • Endocrinology
      • Adrenal disorders (9)
      • Calcium and bone (344)
      • Diabetes (113)
      • Drugs: endocrine system (125)
      • Lipid disorders (34)
      • Metabolic disorders (386)
      • Pituitary disorders (13)
      • Thyroid disease (24)
    • Evidence based practice
      • Critical appraisal literature
    • Gastroenterology
      • Infection (gastroenterology) (2)
      • Inflammatory bowel disease (17)
      • Liver disease (56)
      • Neurogastroenterology (24)
      • Oesophagus (32)
      • Pancreas and biliary tract (124)
      • Pancreatitis (14)
      • Portal hypertension (2)
      • Small intestine
        • Coeliac disease (15)
      • Stomach and duodenum (16)
    • Genetics
      • Clinical genetics (289)
      • Cytogenetics (26)
      • Genetic screening / counselling (1075)
      • Molecular genetics (1454)
    • Haematology (incl blood transfusion) (8)
    • Immunology (including allergy) (732)
    • Infectious diseases
      • Bone and joint infections (1)
      • Drugs: infectious diseases (45)
      • Emerging infectious diseases
        • Bird flu
      • Foodborne infections (2)
      • Hepatitis and other GI infections (9)
      • Influenza
      • Meningitis (3)
      • Nosocomial infections
      • Otitis (13)
      • Pneumonia (infectious disease) (4)
      • TB and other respiratory infections (25)
      • Travel medicine (4)
      • Tropical medicine (infectious diseases) (7)
      • Urinary tract infections (1)
      • Vaccination / immunisation (4)
    • Neurology
      • Cerebral palsy (5)
      • Cranial nerves
      • Dementia (35)
      • Drugs: CNS (not psychiatric)
      • Epilepsy and seizures (236)
      • Headache (including migraine) (8)
      • Hydrocephalus (19)
      • Infection (neurology)
      • Motor neurone disease (22)
      • Movement disorders (other than Parkinsons) (54)
      • Multiple sclerosis (25)
      • Muscle disease (176)
      • Neuroimaging
      • Neurological injury
      • Neuromuscular disease (301)
      • Neurooncology (89)
      • Pain (neurology)
      • Parkinson's disease (22)
      • Peripheral nerve disease (106)
      • Sleep disorders (neurology)
      • Spinal cord
      • Stroke
      • Trauma CNS / PNS
      • Variant Creutzfeld-Jakob Disease
    • Nutrition and metabolism
      • Obesity (nutrition) (74)
    • Obstetrics and gynaecology
      • Reproductive medicine (586)
    • Oncology
      • Breast cancer (276)
      • Cancer: dermatological (50)
      • CNS cancer (53)
      • Colon cancer (147)
      • Endocrine cancer (65)
      • Gastric cancer
      • Gene therapy (3)
      • Head and neck cancer (7)
      • Hepatic cancer (9)
      • Lung cancer (oncology) (16)
      • Oesophageal cancer (6)
      • Paediatric oncology (140)
      • Prevention (6)
      • Prostate cancer (29)
      • Screening (oncology) (268)
      • Urological cancer (79)
    • Ophthalmology
      • Eye Diseases (351)
      • Glaucoma (22)
      • Hereditary eye disease (103)
      • Neuroophthalmology
      • Visual development (9)
    • Psychiatry
      • Memory disorders (psychiatry) (80)
      • Psychotic disorders (incl schizophrenia) (33)
    • Rehabilitation medicine
      • Disability
      • Other rehabilitative therapies
      • Physiotherapy
    • Respiratory medicine
      • Asthma (25)
      • Cystic fibrosis (44)
      • Interstitial lung disease (11)
      • Pulmonary emphysema (3)
      • Pulmonary hypertension (7)
    • Rheumatology
      • Connective tissue disease (113)
      • Osteoarthritis (13)
      • Osteoporosis (19)
      • Rheumatoid arthritis (18)
      • Systemic lupus erythematosus (8)
      • Vascularitis (3)
    • Surgery (120)
  • NON-CLINICAL
    • Epidemiology (722)
    • Ethics (232)
    • Medical humanities
  • Special collections
    • Editor's choice (125)
    • Guidelines, Recommendations and Consensus Statements
    • JMG Online mutation reports (169)
    • Open access (324)
    • Press releases (5)
  • Content
    • Latest content
    • Current issue
    • Archive
    • Browse by topic
    • Most read articles
    • Responses
  • Journal
    • About
    • Editorial board
    • Sign up for email alerts
    • Thank you to our reviewers
    • Subscribe
  • Authors
    • Instructions for authors
    • Submit an article
    • Editorial policies
    • Open Access at BMJ
    • BMJ Author Hub
  • Help
    • Contact us
    • Reprints
    • Permissions
    • Advertising
    • Feedback form
  • RSS
  • Twitter
  • Facebook
  • Blog
  • Website Terms & Conditions
  • Privacy & Cookies
  • Contact BMJ

Online: ISSN 1468-6244Print: ISSN 0022-2593
Copyright © 2020 BMJ Publishing Group Ltd. All rights reserved.
京ICP备15042040号-3