UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 33

Sortiert nach

Hirschsprung disease, associated syndromes and genetics: a review

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

2008

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Molecular mechanisms of RET-induced Hirschsprung pathogenesis

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

2006

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

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

Link zum Volltext

Verfügbarkeit prüfen

Punishment and Reparation in Philosophy and the Law

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

GRISERI, P

1985

Link zum Volltext

Verfügbarkeit prüfen

CAN A DEAD MAN BE HARMED?

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

Griseri, Paul

1987

Link zum Volltext

Verfügbarkeit prüfen

Punishment and Reparation

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

Griseri, Paul

1985

Link zum Volltext

Verfügbarkeit prüfen

The Molecular Genetics of Hirschsprung’s Disease

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

Link zum Volltext

Verfügbarkeit prüfen

ILC3 GM-CSF production and mobilisation orchestrate acute intestinal inflammation

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

2016

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 33

Suche als RSS-Feed

Aktive Filter

ThemaSurgery

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(29)
Mit Volltextzugriff
(31)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(21)
Science & Technology
(20)
Life Sciences & Biomedicine
(19)
Female
(12)
Male
(12)
Hirschsprung Disease - Genetics
(10)
Biological And Medical Sciences
(9)
Genetics & Heredity
(9)
Medical Sciences
(9)
Mutation
(8)
Receptor Protein-Tyrosine Kinases - Genetics
(8)
Ret Proto-Oncogene
(8)
Hirschsprung Disease
(7)
Proto-Oncogene Proteins C-Ret
(7)
Proto-Oncogene Proteins - Genetics
(6)
Adult
(5)
Alleles
(5)
Drosophila Proteins
(5)
Haplotypes
(5)
Proto-Oncogene Mas
(5)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

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

Aktive Filter

Suchergebnisse filtern