Modifier Genes in Cystic Fibrosis

Pediatric Pulmonology

Volumn 37, Issue SUPPL. 26, 2004, Pages 86-87

  Davies, Jane C ^a  

^a ROYAL BROMPTON HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA 1 ANTITRYPSIN; MANNOSE BINDING LECTIN; TRANSMEMBRANE CONDUCTANCE REGULATOR;

CLINICAL FEATURE; CYSTIC FIBROSIS; DISEASE EXACERBATION; DISEASE SEVERITY; GENE MUTATION; GENETIC POLYMORPHISM; GENOTYPE; LUNG FUNCTION; PRIORITY JOURNAL; PSEUDOMONAS AERUGINOSA; SHORT SURVEY; SURVIVAL; ALPHA 1 ANTITRYPSIN DEFICIENCY; GENETICS; HOSPITALIZATION; HUMAN; PHENOTYPE; REVIEW;

ALPHA 1-ANTITRYPSIN DEFICIENCY; CYSTIC FIBROSIS; HUMANS; MANNOSE-BINDING LECTIN; PHENOTYPE; POLYMORPHISM, GENETIC; SEVERITY OF ILLNESS INDEX;

EID: 2342440583     PISSN: 87556863     EISSN: None     Source Type: Journal    
DOI: 10.1002/ppul.70062     Document Type: Short Survey

References (9)

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3. Mahadeva R, et al. Association of alpha(1)-antichymotrypsin deficiency with milder lung disease in patients with cystic fibrosis. Thorax 2001;56:53-8.
4. Grasemann H, et al. Airway nitric oxide levels in cystic fibrosis patients are related to a polymorphism in the neuronal nitric oxide synthase gene. Am J Respir Crit Care Med 2000;162:2172-6.
5. Arkwright PD, et al. TGF-beta(1) genotype and accelerated decline in lung function of patients with cystic fibrosis. Thorax 2000;55:459-62.
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7. Gabolde M, et al. The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis. J Med Genet 2001;38:310-1.
8. Gabolde M, et al. Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study. BMJ 1999;319:1166-7.
9. Zielenski J, et al. Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13. Nat Genet 1999;22:128-9.