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Tumor suppressor genes in the 9p21 gene cluster are selective targets of inactivation in neuroendocrine gastroenteropancreatic tumors

Cancer research (Chicago, Ill.), 2001-08, Vol.61 (15), p.5905-5910

2001

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Growth factor receptor expression in human gastroenteropancreatic neuroendocrine tumours

European journal of clinical investigation, 1998-12, Vol.28 (12), p.1038-1049

1998

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mRNA expression patterns of insulin-like growth factor system components in human neuroendocrine tumours

European journal of clinical investigation, 2000-08, Vol.30 (8), p.729-739

2000

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Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosis

The Lancet (British edition), 1993-01, Vol.341 (8839), p.189-193

1993

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Treatment of endocrine gastroenteropancreatic tumors with somatostatin analogues

Recent results in cancer research, 2000, Vol.153, p.15

2000

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Micronodular thymoma: an epithelial tumour with abnormal chemokine expression setting the stage for lymphoma development

The Journal of pathology, 2005-09, Vol.207 (1), p.72-82

2005

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Four Novel Cystic Fibrosis Mutations in Splice Junction Sequences Affecting the CFTR Nucleotide Binding Folds

Genomics (San Diego, Calif.), 1993-03, Vol.15 (3), p.688-691

1993

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Role of Connexin32 and β-Catenin in Tumor Promotion in Mouse Liver

Toxicologic pathology, 2003-01, Vol.31 (1), p.99-102

2003

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Correlation between Genotype and Phenotype in Patients with Cystic Fibrosis

The New England journal of medicine, 1993-10, Vol.329 (18), p.1308-1313

1993

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Genetic determinants in cystic fibrosis

The Lancet (British edition), 1991-03, Vol.337 (8741), p.623-623

1991

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Variation of immunocytochemical expression of transforming growth factor (TGF)-β in hepatocytes in culture and liver slices

Cell and tissue research, 1996-12, Vol.287 (1), p.143-152

1996

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Mild course of cystic fibrosis associated with heterozygosity for infrequent mutations in the first nucleotide‐binding fold of CFTR

Acta Paediatrica, 1992-01, Vol.81 (1), p.82-83

1992

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Variation of immunocytochemical expression of transforming growth factor (TGF)-beta in hepatocytes in culture and liver slices

Cell and tissue research, 1997-01, Vol.287 (1), p.143-152

1997

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A novel model for the first nucleotide binding domain of the cystic fibrosis transmembrane conductance regulator

FEBS letters, 1997-05, Vol.407 (3), p.303-308

1997

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Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients

Human genetics, 1994-11, Vol.94 (5), p.533-542

1994

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Growth factor receptor expression in neuroendocrine tumors of the gastroenteropancreatic system

Gastroenterology (New York, N.Y. 1943), 1998-04, Vol.114, p.A1192-A1192

1998

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Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene

Human genetics, 1991-08, Vol.87 (4), p.441-446

1991

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Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus

American journal of human genetics, 1992-08, Vol.51 (2), p.245-250

1992

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Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families

Human genetics, 1992-02, Vol.88 (4), p.417-425

1992

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A Hinfl polymorphism in the cystic fibrosis gene CFTR

Nucleic acids research, 1991-05, Vol.19 (9), p.2517-2517

1991

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A HinfI polymorphism in the cystic fibrosis gene CFTR

Nucleic acids research, 1991-05, Vol.19 (9), p.2517-2517

1991

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Cystic fibrosis: the impact of analytical technology for genotype-phenotype studies

Clinica chimica acta, 1993-07, Vol.217 (1), p.23-28

1993

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Cystic fibrosis patients bearing both the common missense mutation Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk and meconium illeus

American journal of human genetics, 1992, Vol.51 (2), p.245-250

1992

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Liver. Biliary Tract. Portal Circulation. Exocrine Pancreas
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Tumor suppressor genes in the 9p21 gene cluster are selective targets of inactivation in neuroendocrine gastroenteropancreatic tumors

Growth factor receptor expression in human gastroenteropancreatic neuroendocrine tumours

mRNA expression patterns of insulin-like growth factor system components in human neuroendocrine tumours

Genetic determinants of airways' colonisation with Pseudomonas aeruginosa in cystic fibrosis

Treatment of endocrine gastroenteropancreatic tumors with somatostatin analogues

Micronodular thymoma: an epithelial tumour with abnormal chemokine expression setting the stage for lymphoma development

Four Novel Cystic Fibrosis Mutations in Splice Junction Sequences Affecting the CFTR Nucleotide Binding Folds

Role of Connexin32 and β-Catenin in Tumor Promotion in Mouse Liver

Correlation between Genotype and Phenotype in Patients with Cystic Fibrosis

Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) gene

Genetic determinants in cystic fibrosis

Variation of immunocytochemical expression of transforming growth factor (TGF)-β in hepatocytes in culture and liver slices

Mild course of cystic fibrosis associated with heterozygosity for infrequent mutations in the first nucleotide‐binding fold of CFTR

Variation of immunocytochemical expression of transforming growth factor (TGF)-beta in hepatocytes in culture and liver slices

A novel model for the first nucleotide binding domain of the cystic fibrosis transmembrane conductance regulator

Detection of more than 50 different CFTR mutations in a large group of German cystic fibrosis patients

Growth factor receptor expression in neuroendocrine tumors of the gastroenteropancreatic system

Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator gene

Cystic fibrosis patients bearing both the common missense mutation Gly----Asp at codon 551 and the delta F508 mutation are clinically indistinguishable from delta F508 homozygotes, except for decreased risk of meconium ileus

Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families

A Hinfl polymorphism in the cystic fibrosis gene CFTR

A HinfI polymorphism in the cystic fibrosis gene CFTR

Cystic fibrosis: the impact of analytical technology for genotype-phenotype studies

Cystic fibrosis patients bearing both the common missense mutation Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk and meconium illeus

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