UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

The E180splice mutation in the GHR gene causing Laron syndrome: Witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?

American journal of medical genetics. Part A, 2014-05, Vol.164A (5), p.1204-1208

2014

Volltextzugriff (PDF)

Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility

HGG advances, 2024-01, Vol.5 (1), p.100244-100244, Article 100244

2024

Volltextzugriff (PDF)

An update on the central nervous system manifestations of Li–Fraumeni syndrome

Acta neuropathologica, 2020-04, Vol.139 (4), p.669-687

2020

Volltextzugriff (PDF)

Pathological and Genetic Stratification for Management of Adrenocortical Carcinoma

The journal of clinical endocrinology and metabolism, 2022-03, Vol.107 (4), p.1159-1169

2022

Volltextzugriff (PDF)

Acromegaly: correlation between expression of somatostatin receptor subtypes and response to octreotide-lar treatment

Pituitary, 2009, Vol.12 (4), p.297-303

2009

Volltextzugriff (PDF)

Treatment of Pediatric Adrenocortical Carcinoma With Surgery, Retroperitoneal Lymph Node Dissection, and Chemotherapy: The Children's Oncology Group ARAR0332 Protocol

Journal of clinical oncology, 2021-08, Vol.39 (22), p.2463-2473

2021

Volltextzugriff (PDF)

Familial predisposition to adrenocortical tumors: Clinical and biological features and management strategies

Baillière's best practice & research. Clinical endocrinology & metabolism, 2010-06, Vol.24 (3), p.477-490

2010

Volltextzugriff (PDF)

Genomic landscape of paediatric adrenocortical tumours

Nature communications, 2015-03, Vol.6 (1), p.6302-6302, Article 6302

2015

Volltextzugriff (PDF)

The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene

Clinical endocrinology (Oxford), 2008-02, Vol.68 (2), p.226-232

2008

Volltextzugriff (PDF)

The Common Germline TP53-R337H Mutation Is Hypomorphic and Confers Incomplete Penetrance and Late Tumor Onset in a Mouse Model

Cancer research (Chicago, Ill.), 2021-05, Vol.81 (9), p.2442-2456

2021

Volltextzugriff (PDF)

Clinical and Functional Significance of TP53 Exon 4-Intron 4 Splice Junction Variants

Molecular cancer research, 2022-02, Vol.20 (2), p.207-216

2022

Volltextzugriff (PDF)

Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age

Clinics (São Paulo, Brazil), 2013-06, Vol.68 (6), p.785-791

2013

Volltextzugriff (PDF)

XAF1 as a modifier of p53 function and cancer susceptibility

Science advances, 2020-06, Vol.6 (26), p.eaba3231-eaba3231

2020

Volltextzugriff (PDF)

TP53-Associated Pediatric Malignancies

Genes & cancer, 2011-04, Vol.2 (4), p.485-490

2011

Volltextzugriff (PDF)

DNA Methylation Profiling Reveals Prognostically Significant Groups in Pediatric Adrenocortical Tumors: A Report From the International Pediatric Adrenocortical Tumor Registry

JCO precision oncology, 2019 (3), p.1-21

2019

Volltextzugriff (PDF)

Differential elemental distribution of retained particles along the respiratory tract

Inhalation toxicology, 2011-07, Vol.23 (8), p.459-467

2011

Volltextzugriff (PDF)

Inherited germline TP53 mutation encodes a protein with an aberrant C-terminal motif in a case of pediatric adrenocortical tumor

Familial cancer, 2011-03, Vol.10 (1), p.141-146

2011

Volltextzugriff (PDF)

Deletion Mapping of Chromosome 17 in Benign and Malignant Adrenocortical Tumors Associated with the Arg337His Mutation of the p53 Tumor Suppressor Protein

The journal of clinical endocrinology and metabolism, 2005-05, Vol.90 (5), p.2976-2981

2005

Volltextzugriff (PDF)

KDM6B Inhibition Has Anti-Tumor Activity in Anaplastic Wilms Tumor Cells Associated with WT1 And MYCN Pathway Silencing

Pediatrics (Evanston), 2021-03, Vol.147 (3_MeetingAbstract), p.914-915

2021

Volltextzugriff (PDF)

Three Novel Mutations in CYP21 Gene in Brazilian Patients with the Classical Form of 21-Hydroxylase Deficiency Due to a Founder Effect

The journal of clinical endocrinology and metabolism, 2002-09, Vol.87 (9), p.4314-4317

2002

Volltextzugriff (PDF)

Congenital Hyperinsulinism in Brazilian Neonates: A Study of Histology, KATP Channel Genes, and Proliferation of β Cells

Pediatric and developmental pathology, 2010-09, Vol.13 (5), p.375-384

2010

Volltextzugriff (PDF)

Abstract 4889: Characterizing the viromes in pediatric cancers through whole genome sequencing

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.4889-4889

2017

Volltextzugriff (PDF)

Abstract 1197: B7-H3-CAR T cells for the treatment of pediatric adrenocortical carcinoma

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.1197-1197

2023

Volltextzugriff (PDF)

iASPP: A Novel Protein Involved in Pituitary Tumorigenesis?

Frontiers of hormone research, 2010, Vol.38, p.70-76

2010

Volltextzugriff (PDF)

1 – 25 von 165

Suche als RSS-Feed

Aktive Filter

ThemaTumors

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(150)
Mit Volltextzugriff
(150)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(120)
Life Sciences & Biomedicine
(107)
Humans
(73)
Pharmacology & Pharmacy
(40)
Female
(30)
Physical Sciences
(29)
Chemistry
(27)
Chemistry, Medicinal
(27)
Male
(23)
Biochemistry & Molecular Biology
(22)
Chemistry, Multidisciplinary
(19)
Adult
(18)
Biological And Medical Sciences
(15)
Endocrinology & Metabolism
(14)
Medical Sciences
(14)
Xanthones - Pharmacology
(14)
Xanthones - Chemistry
(13)
Animals
(12)
Antineoplastic Agents - Pharmacology
(12)
Middle Aged
(12)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The E180splice mutation in the GHR gene causing Laron syndrome: Witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World?

Multiple TP53 p.R337H haplotypes and implications for tumor susceptibility

An update on the central nervous system manifestations of Li–Fraumeni syndrome

Pathological and Genetic Stratification for Management of Adrenocortical Carcinoma

Acromegaly: correlation between expression of somatostatin receptor subtypes and response to octreotide-lar treatment

Treatment of Pediatric Adrenocortical Carcinoma With Surgery, Retroperitoneal Lymph Node Dissection, and Chemotherapy: The Children's Oncology Group ARAR0332 Protocol

Familial predisposition to adrenocortical tumors: Clinical and biological features and management strategies

Genomic landscape of paediatric adrenocortical tumours

The degree of external genitalia virilization in girls with 21-hydroxylase deficiency appears to be influenced by the CAG repeats in the androgen receptor gene

The Common Germline TP53-R337H Mutation Is Hypomorphic and Confers Incomplete Penetrance and Late Tumor Onset in a Mouse Model

A Rare TP53 Mutation Predominant in Ashkenazi Jews Confers Risk of Multiple Cancers

Clinical and Functional Significance of TP53 Exon 4-Intron 4 Splice Junction Variants

Insulin-like growth factor 1 gene (CA)n repeats and a variable number of tandem repeats of the insulin gene in Brazilian children born small for gestational age

XAF1 as a modifier of p53 function and cancer susceptibility

TP53-Associated Pediatric Malignancies

DNA Methylation Profiling Reveals Prognostically Significant Groups in Pediatric Adrenocortical Tumors: A Report From the International Pediatric Adrenocortical Tumor Registry

Differential elemental distribution of retained particles along the respiratory tract

Inherited germline TP53 mutation encodes a protein with an aberrant C-terminal motif in a case of pediatric adrenocortical tumor

Deletion Mapping of Chromosome 17 in Benign and Malignant Adrenocortical Tumors Associated with the Arg337His Mutation of the p53 Tumor Suppressor Protein

KDM6B Inhibition Has Anti-Tumor Activity in Anaplastic Wilms Tumor Cells Associated with WT1 And MYCN Pathway Silencing

Three Novel Mutations in CYP21 Gene in Brazilian Patients with the Classical Form of 21-Hydroxylase Deficiency Due to a Founder Effect

Congenital Hyperinsulinism in Brazilian Neonates: A Study of Histology, KATP Channel Genes, and Proliferation of β Cells

Abstract 4889: Characterizing the viromes in pediatric cancers through whole genome sequencing

Abstract 1197: B7-H3-CAR T cells for the treatment of pediatric adrenocortical carcinoma

iASPP: A Novel Protein Involved in Pituitary Tumorigenesis?

Aktive Filter

Suchergebnisse filtern