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Literature DB >> 10541506

Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study.

M Gabolde¹, M Guilloud-Bataille, J Feingold, C Besmond.

Abstract

Entities: Chemical Disease

Mesh：

Substances：

Year: 1999 PMID： 10541506 PMCID： PMC28266 DOI： 10.1136/bmj.319.7218.1166

Source DB: PubMed Journal: BMJ ISSN： 0959-8138

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5 in total

1. Genotyping of the three major allelic variants of the human mannose-binding lectin gene by denaturing gradient gel electrophoresis.

Authors: M Gabolde; S Muralitharan; C Besmond
Journal: Hum Mutat Date: 1999 Impact factor: 4.878

2. Contribution of genetic factors other than CFTR to disease severity in cystic fibrosis.

Authors: J Hull; A H Thomson
Journal: Thorax Date: 1998-12 Impact factor: 9.139

3. Molecular basis of opsonic defect in immunodeficient children.

Authors: M Sumiya; M Super; P Tabona; R J Levinsky; T Arai; M W Turner; J A Summerfield
Journal: Lancet Date: 1991-06-29 Impact factor: 79.321

4. Mannose binding protein gene mutations associated with unusual and severe infections in adults.

Authors: J A Summerfield; S Ryder; M Sumiya; M Thursz; A Gorchein; M A Monteil; M W Turner
Journal: Lancet Date: 1995-04-08 Impact factor: 79.321

5. Increased frequency of homozygosity of abnormal mannan-binding-protein alleles in patients with suspected immunodeficiency.

Authors: P Garred; H O Madsen; B Hofmann; A Svejgaard
Journal: Lancet Date: 1995-10-07 Impact factor: 79.321

5 in total

24 in total

1. The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis.

Authors: M Gabolde; D Hubert; M Guilloud-Bataille; C Lenaerts; J Feingold; C Besmond
Journal: J Med Genet Date: 2001-05 Impact factor: 6.318

Review 2. Cystic fibrosis modifier genes.

Authors: Jane Davies; Eric Alton; Uta Griesenbach
Journal: J R Soc Med Date: 2005 Impact factor: 5.344

3. Association between mannan-binding lectin and impaired lung function in cystic fibrosis may be age-dependent.

Authors: M S Muhlebach; S L MacDonald; B Button; J J Hubbard; M L Turner; R C Boucher; D C Kilpatrick
Journal: Clin Exp Immunol Date: 2006-08 Impact factor: 4.330

4. Common variable immunodeficiency and the complement system; low mannose-binding lectin levels are associated with bronchiectasis.

Authors: B Fevang; T E Mollnes; A M Holm; T Ueland; L Heggelund; J K Damås; P Aukrust; S S Frøland
Journal: Clin Exp Immunol Date: 2005-12 Impact factor: 4.330

Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: cohort study.

1. Genotyping of the three major allelic variants of the human mannose-binding lectin gene by denaturing gradient gel electrophoresis.

2. Contribution of genetic factors other than CFTR to disease severity in cystic fibrosis.

3. Molecular basis of opsonic defect in immunodeficient children.

4. Mannose binding protein gene mutations associated with unusual and severe infections in adults.

5. Increased frequency of homozygosity of abnormal mannan-binding-protein alleles in patients with suspected immunodeficiency.

1. The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis.

Review 2. Cystic fibrosis modifier genes.

3. Association between mannan-binding lectin and impaired lung function in cystic fibrosis may be age-dependent.

4. Common variable immunodeficiency and the complement system; low mannose-binding lectin levels are associated with bronchiectasis.

5. New modifier loci in cystic fibrosis.

6. The influence of genetics on cystic fibrosis phenotypes.

7. Phase I safety, tolerability, and pharmacokinetic study of recombinant human mannan-binding lectin.

8. Elevation of hepatic sulphotransferase activities in mice with resistance to cystic fibrosis.

9. Mannan-binding lectin insufficiency in children with recurrent infections of the respiratory system.

Review 10. Update on gene modifiers in cystic fibrosis.