The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis (Q28364166)

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English	The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis	scientific article

Statements

instance of

scholarly article

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title

The mannose binding lectin gene influences the severity of chronic liver disease in cystic fibrosis (English)

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main subject

cystic fibrosis

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liver disease

1 reference

based on heuristic

inferred from title

chronic liver disease

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author name string

M Gabolde

series ordinal

1

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D Hubert

series ordinal

2

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M Guilloud-Bataille

series ordinal

3

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C Lenaerts

series ordinal

4

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J Feingold

series ordinal

5

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C Besmond

series ordinal

6

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language of work or name

English

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publication date

May 2001

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published in

Journal of Medical Genetics

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volume

38

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issue

5

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page(s)

310-1

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cites work

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734861

retrieved

29 September 2017

Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734861

retrieved

29 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734861

retrieved

29 September 2017

Association of mutations in mannose binding protein gene with childhood infection in consecutive hospital series

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734861

retrieved

29 September 2017

The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734861

retrieved

29 September 2017

Mannose binding lectin gene mutations are associated with progression of liver disease in chronic hepatitis B infection

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734861

retrieved

27 November 2018

Association of mannose-binding lectin gene haplotype LXPA and LYPB with interferon-resistant hepatitis C virus infection in Japanese patients

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1734861

retrieved

27 November 2018

Natural history of liver disease in cystic fibrosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11333866

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular basis of opsonic defect in immunodeficient children

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11333866

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The major histocompatibility complex influences the development of chronic liver disease in male children and young adults with cystic fibrosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11333866

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Liver and biliary problems in cystic fibrosis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11333866

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/11333866

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1136/JMG.38.5.310

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PMC publication ID

1734861

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PubMed publication ID

11333866

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