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...

TREM-1 orchestrates angiotensin II-induced monocyte trafficking and promotes experimental abdominal aortic aneurysm

The Journal of clinical investigation, 2021-01, Vol.131 (2), p.1-14

2021

Volltextzugriff (PDF)

Severe Arterial Hypertension from Cullin 3 Mutations Is Caused by Both Renal and Vascular Effects

Journal of the American Society of Nephrology, 2019-05, Vol.30 (5), p.811-823

2019

Volltextzugriff (PDF)

Gene Expression Profiling Reveals a New Classification of Adrenocortical Tumors and Identifies Molecular Predictors of Malignancy and Survival

Journal of clinical oncology, 2009-03, Vol.27 (7), p.1108-1115

2009

Volltextzugriff (PDF)

Cullin 3 Exon 9 Deletion in Familial Hyperkalemic Hypertension Impairs Cullin3-Ring-E3 Ligase (CRL3) Dynamic Regulation and Cycling

International journal of molecular sciences, 2022-05, Vol.23 (9), p.5151

2022

Volltextzugriff (PDF)

Mutations in Regulatory Subunit Type 1A of Cyclic Adenosine 5′-Monophosphate-Dependent Protein Kinase (PRKAR1A): Phenotype Analysis in 353 Patients and 80 Different Genotypes

The journal of clinical endocrinology and metabolism, 2009-06, Vol.94 (6), p.2085-2091

2009

Volltextzugriff (PDF)

Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis

The Journal of clinical investigation, 2020-12, Vol.130 (12), p.6379-6394

2020

Volltextzugriff (PDF)

Role of angiotensin II AT1 receptor activation in cardiovascular diseases

Kidney international, 2008-12, Vol.74 (11), p.1379-1384

2008

Volltextzugriff (PDF)

Cullin 3 targets the tumor suppressor gene ARMC5 for ubiquitination and degradation

Endocrine-related cancer, 2020-04, Vol.27 (4), p.221-230

2020

Volltextzugriff (PDF)

Mutations and polymorphisms in the gene encoding regulatory subunit type 1-alpha of protein kinase A (PRKAR1A): an update

Human mutation, 2010-04, Vol.31 (4), p.369-379

2010

Volltextzugriff (PDF)

Functional Characterization of PRKAR1A Mutations Reveals a Unique Molecular Mechanism Causing Acrodysostosis but Multiple Mechanisms Causing Carney Complex

The Journal of biological chemistry, 2015-11, Vol.290 (46), p.27816-27828

2015

Volltextzugriff (PDF)

IGF2 promotes growth of adrenocortical carcinoma cells, but its overexpression does not modify phenotypic and molecular features of adrenocortical carcinoma

PloS one, 2014-08, Vol.9 (8), p.e103744-e103744

2014

Volltextzugriff (PDF)

Aberrant cortisol regulations in bilateral macronodular adrenal hyperplasia: a frequent finding in a prospective study of 32 patients with overt or subclinical Cushing's syndrome

European journal of endocrinology, 2010-07, Vol.163 (1), p.129-138

2010

Volltextzugriff (PDF)

Lessons from constitutively active mutants of G protein-coupled receptors

Trends in Endocrinology & Metabolism, 2002-10, Vol.13 (8), p.336-343

2002

Volltextzugriff (PDF)

Mass-array screening of frequent mutations in cancers reveals RB1 alterations in aggressive adrenocortical carcinomas

European journal of endocrinology, 2014-03, Vol.170 (3), p.385-391

2014

Volltextzugriff (PDF)

Mechanisms of Cell-surface Rerouting of an Endoplasmic Reticulum-retained Mutant of the Vasopressin V1b/V3 Receptor by a Pharmacological Chaperone

The Journal of biological chemistry, 2005-12, Vol.280 (51), p.42198-42206

2005

Volltextzugriff (PDF)

Gain-of-function mutant of angiotensin II receptor, type 1A, causes hypertension and cardiovascular fibrosis in mice

The Journal of clinical investigation, 2007-07, Vol.117 (7), p.1914-1925

2007

Volltextzugriff (PDF)

A Novel C-terminal Motif Is Necessary for the Export of the Vasopressin V1b/V3 Receptor to the Plasma Membrane

The Journal of biological chemistry, 2005-01, Vol.280 (3), p.2300-2308

2005

Volltextzugriff (PDF)

Constitutive Internalization of Constitutively Active Angiotensin II AT1A Receptor Mutants Is Blocked by Inverse Agonists

The Journal of biological chemistry, 2002-02, Vol.277 (8), p.5891-5901

2002

Volltextzugriff (PDF)

Prevalence of Hyperkalemia and Familial Hyperkalemic Hypertension in 5100 Patients Referred to a Tertiary Hypertension Unit

Hypertension (Dallas, Tex. 1979), 2024-11, Vol.81 (11), p.2275-2285

2024

Volltextzugriff (PDF)

Role of angiotensin II AT receptor activation in cardiovascular diseases

Kidney international, 2008-12, Vol.74 (11), p.1379-1384

2008

Volltextzugriff (PDF)

Steroidogenesis in Aldosterone-Producing Adenoma Revisited by Transcriptome Analysis

The journal of clinical endocrinology and metabolism, 2005-12, Vol.90 (12), p.6638-6649

2005

Volltextzugriff (PDF)

Systematic Identification of Mutations That Constitutively Activate the Angiotensin II Type 1A Receptor by Screening a Randomly Mutated cDNA Library with an Original Pharmacological Bioassay

Proceedings of the National Academy of Sciences - PNAS, 2000-06, Vol.97 (13), p.7615-7620

2000

Volltextzugriff (PDF)

Cloning and characterization of the human V3 pituitary vasopressin receptor

FEBS letters, 1994-12, Vol.356 (2), p.215-220

1994

Volltextzugriff (PDF)

1 – 25 von 192

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(177)
Mit Volltextzugriff
(164)

Publikationsform

Artikel
(190)
Bücher
(2)

Sprache

Englisch
(181)
Französisch
(10)

Erscheinungsjahr

n.n

Thema

Science & Technology
(106)
Life Sciences & Biomedicine
(97)
Humans
(95)
Animals
(53)
Biological And Medical Sciences
(44)
Female
(39)
Male
(37)
Mutation
(35)
Fundamental And Applied Biological Sciences. Psychology
(33)
Biochemistry & Molecular Biology
(26)
Endocrinology & Metabolism
(25)
Molecular Sequence Data
(25)
Amino Acid Sequence
(24)
Adult
(23)
Cricetinae
(22)
Life Sciences
(21)
Rats
(19)
Base Sequence
(18)
Medical Sciences
(18)
Middle Aged
(18)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Integrated genomic characterization of adrenocortical carcinoma

TREM-1 orchestrates angiotensin II-induced monocyte trafficking and promotes experimental abdominal aortic aneurysm

Severe Arterial Hypertension from Cullin 3 Mutations Is Caused by Both Renal and Vascular Effects

Gene Expression Profiling Reveals a New Classification of Adrenocortical Tumors and Identifies Molecular Predictors of Malignancy and Survival

Cullin 3 Exon 9 Deletion in Familial Hyperkalemic Hypertension Impairs Cullin3-Ring-E3 Ligase (CRL3) Dynamic Regulation and Cycling

Mutations in Regulatory Subunit Type 1A of Cyclic Adenosine 5′-Monophosphate-Dependent Protein Kinase (PRKAR1A): Phenotype Analysis in 353 Patients and 80 Different Genotypes

Mutation affecting the conserved acidic WNK1 motif causes inherited hyperkalemic hyperchloremic acidosis

Role of angiotensin II AT1 receptor activation in cardiovascular diseases

Cullin 3 targets the tumor suppressor gene ARMC5 for ubiquitination and degradation

Mutations and polymorphisms in the gene encoding regulatory subunit type 1-alpha of protein kinase A (PRKAR1A): an update

Functional Characterization of PRKAR1A Mutations Reveals a Unique Molecular Mechanism Causing Acrodysostosis but Multiple Mechanisms Causing Carney Complex

IGF2 promotes growth of adrenocortical carcinoma cells, but its overexpression does not modify phenotypic and molecular features of adrenocortical carcinoma

Aberrant cortisol regulations in bilateral macronodular adrenal hyperplasia: a frequent finding in a prospective study of 32 patients with overt or subclinical Cushing's syndrome

Lessons from constitutively active mutants of G protein-coupled receptors

Mass-array screening of frequent mutations in cancers reveals RB1 alterations in aggressive adrenocortical carcinomas

Mechanisms of Cell-surface Rerouting of an Endoplasmic Reticulum-retained Mutant of the Vasopressin V1b/V3 Receptor by a Pharmacological Chaperone

Adrenal GIPR expression and chromosome 19q13 microduplications in GIP-dependent Cushing's syndrome

Gain-of-function mutant of angiotensin II receptor, type 1A, causes hypertension and cardiovascular fibrosis in mice

A Novel C-terminal Motif Is Necessary for the Export of the Vasopressin V1b/V3 Receptor to the Plasma Membrane

Constitutive Internalization of Constitutively Active Angiotensin II AT1A Receptor Mutants Is Blocked by Inverse Agonists

Prevalence of Hyperkalemia and Familial Hyperkalemic Hypertension in 5100 Patients Referred to a Tertiary Hypertension Unit

Role of angiotensin II AT receptor activation in cardiovascular diseases

Steroidogenesis in Aldosterone-Producing Adenoma Revisited by Transcriptome Analysis

Systematic Identification of Mutations That Constitutively Activate the Angiotensin II Type 1A Receptor by Screening a Randomly Mutated cDNA Library with an Original Pharmacological Bioassay

Cloning and characterization of the human V3 pituitary vasopressin receptor

Suchergebnisse filtern