Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

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Genetics and pulmonary medicine 8: asthma.Genetic exceptionalism vs. paradigm shift: lessons from HIV.Bone Mineral Density in Cystic Fibrosis Patients with the CFTR I1234V Mutation in a Large Kindred Family Is Associated with Pancreatic Sufficiency.

P2860

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P2860

Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

Item

http://www.wikidata.org/entity/Q43061141

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1998 nî lūn-bûn

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1998年の論文

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1998年学术文章

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1998年学术文章

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1998年学术文章

@zh-cn

1998年学术文章

@zh-hans

1998年学术文章

@zh-my

1998年学术文章

@zh-sg

1998年學術文章

@yue

1998年學術文章

@zh-hant

name

Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

@en

Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

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type

Item

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Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

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Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

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prefLabel

Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

@en

Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

@nl

P1476

Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

@en

P2093

Davidson DJ

http://www.w3.org/2001/XMLSchema#string

Porteous DJ

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P2860

A peptide antibiotic from human skin

Human beta-defensin-1 is a salt-sensitive antibiotic in lung that is inactivated in cystic fibrosis

Microbial pathogenesis in cystic fibrosis: mucoid Pseudomonas aeruginosa and Burkholderia cepacia

Pseudomonas aeruginosa pili bind to asialoGM1 which is increased on the surface of cystic fibrosis epithelial cells

Pathology of cystic fibrosis review of the literature and comparison with 146 autopsied cases.

Role of mutant CFTR in hypersusceptibility of cystic fibrosis patients to lung infections.

Cystic fibrosis airway epithelia fail to kill bacteria because of abnormal airway surface fluid.

Asialo GM1 is a receptor for Pseudomonas aeruginosa adherence to regenerating respiratory epithelial cells

Cystic fibrosis transmembrane conductance regulator is an epithelial cell receptor for clearance of Pseudomonas aeruginosa from the lung.

Mucociliary transport in trachea of patients with cystic fibrosis.

P304

389-397

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scholarly article

P356

10.1136/THX.53.5.389

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English

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P478

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1998-05-01T00:00:00Z

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9708232

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P921

cystic fibrosis

P932

1745224

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Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

about

P2860

P2860

Genetics and pulmonary medicine. 1. The genetics of cystic fibrosis lung disease.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P921

P932