(Q34202500)

31 July 2017

Increased prevalence of CFTR mutations and variants and decreased chloride secretion in primary sclerosing cholangitis (English)

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primary sclerosing cholangitis

31 July 2017

ascending cholangitis

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Sunil Sheth

1

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31 July 2017

Julie C Shea

2

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31 July 2017

Michele D Bishop

3

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31 July 2017

Sanjiv Chopra

4

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31 July 2017

Meredith M Regan

5

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31 July 2017

Emily Malmberg

6

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31 July 2017

Carolyn Walker

7

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31 July 2017

Ryan Ricci

8

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31 July 2017

Lap-Chee Tsui

9

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31 July 2017

Peter R Durie

10

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31 July 2017

Julian Zielenski

11

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31 July 2017

Steven D Freedman

12

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31 July 2017

3 June 2003

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31 July 2017

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31 July 2017

113

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31 July 2017

3

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31 July 2017

286-292

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https://scigraph.springernature.com/pub.10.1007/s00439-003-0963-z

31 July 2017

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cites work

Cystic Fibrosis Heterozygote Resistance to Cholera Toxin in the Cystic Fibrosis Mouse Model

1 reference

12 December 2020

The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel

1 reference

12 December 2020

Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.

1 reference

12 December 2020

Correction of the cystic fibrosis defect by gene complementation in human intrahepatic biliary epithelial cell lines

1 reference

12 December 2020

Primary sclerosing cholangitis

1 reference

12 December 2020

The spectrum of cystic fibrosis mutations

1 reference

12 December 2020

Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis.

1 reference

12 December 2020

A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilizing pilocarpine by iontophoresis

1 reference

12 December 2020

Liver and biliary problems in cystic fibrosis

1 reference

12 December 2020

Characterization of mutations located in exon 18 of the CFTR gene.

1 reference

12 December 2020

Liver disease and bile duct abnormalities in adults with cystic fibrosis

1 reference

12 December 2020

Primary sclerosing cholangitis: a progressive disease?

1 reference

12 December 2020

Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis

1 reference

12 December 2020

Three novel sequence variations in the 5' upstream region of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: two polymorphisms and one putative molecular defect

1 reference

12 December 2020

Survey of cystic fibrosis transmembrane conductance regulator genotypes in primary sclerosing cholangitis

1 reference

12 December 2020

Congenital bilateral absence of the vas deferens (CBAVD) and cystic fibrosis transmembrane regulator (CFTR): correlation between genotype and phenotype

1 reference

12 December 2020

The relationship between infection and inflammation in the early stages of lung disease from cystic fibrosis

1 reference

12 December 2020

Natural history and prognostic factors in 305 Swedish patients with primary sclerosing cholangitis

1 reference

12 December 2020

Genetic basis of variable exon 9 skipping in cystic fibrosis transmembrane conductance regulator mRNA

1 reference

12 December 2020

Sclerosing cholangitis in adults with cystic fibrosis: a magnetic resonance cholangiographic prospective study.

1 reference

12 December 2020

Pancreatitis and mutations of the cystic fibrosis gene

1 reference

12 December 2020

Polyvariant mutant cystic fibrosis transmembrane conductance regulator genes. The polymorphic (Tg)m locus explains the partial penetrance of the T5 polymorphism as a disease mutation

1 reference

12 December 2020

Characterization of more than 85% of cystic fibrosis alleles in the Greek population, including five novel mutations

1 reference

12 December 2020

A Novel Mutation in the Cystic Fibrosis Gene in Patients with Pulmonary Disease but Normal Sweat Chloride Concentrations

1 reference

12 December 2020

Autonomic and airway reactivity in obligate heterozygotes for cystic fibrosis

1 reference

12 December 2020

CFTR mutation detection by multiplex heteroduplex (mHET) analysis on MDE gel

1 reference

12 December 2020

Biliary complications of cystic fibrosis

1 reference

12 December 2020

Mutation in the gene responsible for cystic fibrosis and predisposition to chronic rhinosinusitis in the general population

1 reference

12 December 2020

Natural history and prognostic variables in primary sclerosing cholangitis

1 reference

12 December 2020

Quantitation of inflammatory responses to bacteria in young cystic fibrosis and control patients

1 reference

12 December 2020

Pancreatic function and extended mutation analysis in DeltaF508 heterozygous infants with an elevated immunoreactive trypsinogen but normal sweat electrolyte levels

1 reference

12 December 2020

Hepatobiliary disease in cystic fibrosis

1 reference

12 December 2020

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

1 reference

12 December 2020

Cystic fibrosis transmembrane conductance regulator (CFTR) gene defects in patients with primary sclerosing cholangitis

1 reference

12 December 2020

Early pulmonary inflammation in infants with cystic fibrosis

1 reference

12 December 2020

Localization of the cystic fibrosis transmembrane conductance regulator in human bile duct epithelial cells

1 reference

12 December 2020

Sweat chloride concentrations in infants homozygous or heterozygous for F508 cystic fibrosis

1 reference

12 December 2020

Mutations of the cystic fibrosis gene in patients with chronic pancreatitis

1 reference

12 December 2020

Genotype and phenotype in cystic fibrosis

1 reference

12 December 2020

10.1007/S00439-003-0963-Z

Identifiers

DOI

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Dimensions Publication ID

31 July 2017

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