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Hirschsprung disease, associated syndromes and genetics: a review

Journal of Medical Genetics, 2008-01, Vol.45 (1), p.1-14

2008

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210 Genetic and epigenetic factors affect RET gene expression in breast cancer cell lines and influence survival in patients

European journal of cancer (1990), 2015-09, Vol.51, p.S30-S30

2015

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Haplotypes of the Human RET Proto‐oncogene Associated with Hirschsprung Disease in the Italian Population Derive from a Single Ancestral Combination of Alleles

Annals of human genetics, 2006-01, Vol.70 (1), p.12-26

2006

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Single nucleotide polymorphic alleles in the 5′ region of the RET proto-oncogene define a risk haplotype in Hirschsprung’s disease

Journal of medical genetics, 2003-09, Vol.40 (9), p.714-718

2003

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Double Heterozygosity for a RET Substitution Interfering with Splicing and an EDNRB Missense Mutation in Hirschsprung Disease

American journal of human genetics, 1999-04, Vol.64 (4), p.1216-1221

1999

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A Rare Haplotype of the RET Proto-Oncogene Is a Risk-Modifying Allele in Hirschsprung Disease

American journal of human genetics, 2002-10, Vol.71 (4), p.969-974

2002

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Rescue of human RET gene expression by sodium butyrate: a novel powerful tool for molecular studies in Hirschsprung disease

Gut, 2003-08, Vol.52 (8), p.1154-1158

2003

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Specific haplotypes of the RET proto-oncogene are over-represented in patients with sporadic papillary thyroid carcinoma

Journal of medical genetics, 2002-04, Vol.39 (4), p.260-265

2002

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Genetic and epigenetic factors affect RET gene expression in breast cancer cell lines and influence survival in patients

Annals of oncology, 2015-10, Vol.26, p.vi12

2015

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Genetic analysis of lung tumours of non-smoking subjects: p53 gene mutations are constantly associated with loss of heterozygosity in the FHIT locus

British journal of cancer, 1998-07, Vol.78 (1), p.73-78

1998

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Early Life Socioeconomic Indicators and Risk of Type 1 Diabetes in Children and Young Adults

The Journal of pediatrics, 2013-03, Vol.162 (3), p.600-605.e1

2013

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Molecular mechanisms of RET-induced Hirschsprung pathogenesis

Annals of medicine (Helsinki), 2006-01, Vol.38 (1), p.11-19

2006

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A common haplotype at the 5′ end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expression

Human mutation, 2005-02, Vol.25 (2), p.189-195

2005

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incidence of type 1 diabetes is increasing in both children and young adults in Northern Italy: 1984-2004 temporal trends

Diabetologia, 2009-12, Vol.52 (12), p.2531-2535

2009

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Diabetes-specific variables associated with quality of life changes in young diabetic people: The type 1 diabetes Registry of Turin (Italy)

Nutrition, metabolism, and cardiovascular diseases, 2013-10, Vol.23 (10), p.1031-1036

2013

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Short-term mortality risk in children and young adults with type 1 diabetes: The population-based Registry of the Province of Turin, Italy

Nutrition, metabolism, and cardiovascular diseases, 2009-06, Vol.19 (5), p.340-344

2009

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A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease

European journal of human genetics : EJHG, 2000-09, Vol.8 (9), p.721-724

2000

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Cell-line specific chromatin acetylation at the Sox10–Pax3 enhancer site modulates the RET proto-oncogene expression

FEBS letters, 2002-07, Vol.523 (1), p.123-127

2002

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Comparative genomic sequence analysis coupled to chromatin immunoprecipitation: a screening procedure applied to search for regulatory elements at the RET locus

Physiological genomics, 2005-11, Vol.23 (3), p.269-274

2005

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FHIT and p53 gene abnormalities in bronchioloalveolar carcinomas. Correlations with clinicopathological data and K-ras mutations

The Journal of pathology, 1998-03, Vol.184 (3), p.240-246

1998

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Punishment and Reparation in Philosophy and the Law

The Philosophical quarterly, 1985, Vol.35 (141), p.394-413

GRISERI, P

1985

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CAN A DEAD MAN BE HARMED?

Philosophical investigations, 1987-10, Vol.10 (4), p.317-329

Griseri, Paul

1987

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Punishment and Reparation

The Philosophical quarterly, 1985-10, Vol.35 (141), p.394-413

Griseri, Paul

1985

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The Molecular Genetics of Hirschsprung’s Disease

Hirschsprung's Disease and Allied Disorders, p.63-78

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ILC3 GM-CSF production and mobilisation orchestrate acute intestinal inflammation

eLife, 2016-01, Vol.5, p.e10066-e10066

2016

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Hirschsprung disease, associated syndromes and genetics: a review

210 Genetic and epigenetic factors affect RET gene expression in breast cancer cell lines and influence survival in patients

Haplotypes of the Human RET Proto‐oncogene Associated with Hirschsprung Disease in the Italian Population Derive from a Single Ancestral Combination of Alleles

Single nucleotide polymorphic alleles in the 5′ region of the RET proto-oncogene define a risk haplotype in Hirschsprung’s disease

Double Heterozygosity for a RET Substitution Interfering with Splicing and an EDNRB Missense Mutation in Hirschsprung Disease

A Rare Haplotype of the RET Proto-Oncogene Is a Risk-Modifying Allele in Hirschsprung Disease

Rescue of human RET gene expression by sodium butyrate: a novel powerful tool for molecular studies in Hirschsprung disease

Specific haplotypes of the RET proto-oncogene are over-represented in patients with sporadic papillary thyroid carcinoma

Genetic and epigenetic factors affect RET gene expression in breast cancer cell lines and influence survival in patients

Genetic analysis of lung tumours of non-smoking subjects: p53 gene mutations are constantly associated with loss of heterozygosity in the FHIT locus

Early Life Socioeconomic Indicators and Risk of Type 1 Diabetes in Children and Young Adults

Molecular mechanisms of RET-induced Hirschsprung pathogenesis

A common haplotype at the 5′ end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expression

incidence of type 1 diabetes is increasing in both children and young adults in Northern Italy: 1984-2004 temporal trends

Diabetes-specific variables associated with quality of life changes in young diabetic people: The type 1 diabetes Registry of Turin (Italy)

Short-term mortality risk in children and young adults with type 1 diabetes: The population-based Registry of the Province of Turin, Italy

A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease

Cell-line specific chromatin acetylation at the Sox10–Pax3 enhancer site modulates the RET proto-oncogene expression

Comparative genomic sequence analysis coupled to chromatin immunoprecipitation: a screening procedure applied to search for regulatory elements at the RET locus

FHIT and p53 gene abnormalities in bronchioloalveolar carcinomas. Correlations with clinicopathological data and K-ras mutations

Punishment and Reparation in Philosophy and the Law

CAN A DEAD MAN BE HARMED?

Punishment and Reparation

The Molecular Genetics of Hirschsprung’s Disease

ILC3 GM-CSF production and mobilisation orchestrate acute intestinal inflammation

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