UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 40

Sortiert nach

Diabetes treatment in two pregnant women with permanent neonatal diabetes mellitus due to a KCNJ11 mutation

Diabetic medicine, 2020-11, Vol.37 (11), p.1956-1958

2020

Link zum Volltext

Verfügbarkeit prüfen

Neonatal hypoglycemia, early-onset diabetes and hypopituitarism due to the mutation in EIF2S3 gene causing MEHMO syndrome

Physiological research, 2018-01, Vol.67 (2), p.331-337

2018

Link zum Volltext

Verfügbarkeit prüfen

Sulfonylurea vs insulin therapy in individuals with sulfonylurea‐sensitive permanent neonatal diabetes mellitus, attributable to a KCNJ11 mutation, and poor glycaemic control

Diabetic medicine, 2018-03, Vol.35 (3), p.386-391

2018

Link zum Volltext

Verfügbarkeit prüfen

Role of β-Arrestin in Mediating Agonist-Promoted G Protein-Coupled Receptor Internalization

Science (American Association for the Advancement of Science), 1996-01, Vol.271 (5247), p.363-366

1996

Link zum Volltext

Verfügbarkeit prüfen

Differential Affinities of Visual Arrestin, βArrestin1, and βArrestin2 for G Protein-coupled Receptors Delineate Two Major Classes of Receptors

The Journal of biological chemistry, 2000-06, Vol.275 (22), p.17201-17210

2000

Link zum Volltext

Verfügbarkeit prüfen

Molecular Determinants Underlying the Formation of Stable Intracellular G Protein-coupled Receptor-β-Arrestin Complexes after Receptor Endocytosis

The Journal of biological chemistry, 2001-06, Vol.276 (22), p.19452-19460

2001

Link zum Volltext

Verfügbarkeit prüfen

Constitutive Arrestin-Mediated Desensitization of a Human Vasopressin Receptor Mutant Associated with Nephrogenic Diabetes Insipidus

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (1), p.93-98

2001

Link zum Volltext

Verfügbarkeit prüfen

Apparent Loss-of-Function Mutant GPCRs Revealed as Constitutively Desensitized Receptors

Biochemistry (Easton), 2002-10, Vol.41 (40), p.11981-11989

2002

Link zum Volltext

Verfügbarkeit prüfen

Regulation of Arrestin-3 Phosphorylation by Casein Kinase II

The Journal of biological chemistry, 2002-05, Vol.277 (19), p.16837-16846

2002

Link zum Volltext

Verfügbarkeit prüfen

PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia

Nature communications, 2020-11, Vol.11 (1), p.5903-5903, Article 5903

2020

Link zum Volltext

Verfügbarkeit prüfen

Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood

Diabetes (New York, N.Y.), 2008-04, Vol.57 (4), p.1034

2008

Link zum Volltext

Verfügbarkeit prüfen

Constitutively Active Alpha-1b Adrenergic Receptor Mutants Display Different Phosphorylation and Internalization Features

Molecular pharmacology, 1999-02, Vol.55 (2), p.339-347

1999

Link zum Volltext

Verfügbarkeit prüfen

β-Arrestin 2 Regulates Zebrafish Development through the Hedgehog Signaling Pathway

Science (American Association for the Advancement of Science), 2004-12, Vol.306 (5705), p.2264-2267

2004

Link zum Volltext

Verfügbarkeit prüfen

Role of phosphorylation in agonist-promoted beta 2-adrenergic receptor sequestration. Rescue of a sequestration-defective mutant receptor by beta ARK1

The Journal of biological chemistry, 1995-10, Vol.270 (42), p.24782-24789

1995

Link zum Volltext

Verfügbarkeit prüfen

The beta2-adrenergic receptor interacts with the Na+/H+-exchanger regulatory factor to control Na+/H+ exchange

Nature (London), 1998-04, Vol.392 (6676), p.626-630

1998

Link zum Volltext

Verfügbarkeit prüfen

Abundant contribution of short tandem repeats to gene expression variation in humans

Nature genetics, 2016-01, Vol.48 (1), p.22-29

2016

Link zum Volltext

Verfügbarkeit prüfen

Salmonella enterica Virulence Genes Are Required for Bacterial Attachment to Plant Tissue

Applied and Environmental Microbiology, 2005-10, Vol.71 (10), p.5685-5691

2005

Link zum Volltext

Verfügbarkeit prüfen

A cancer rainbow mouse for visualizing the functional genomics of oncogenic clonal expansion

Nature communications, 2019-12, Vol.10 (1), p.5490-15, Article 5490

2019

Link zum Volltext

Verfügbarkeit prüfen

Translational implications of Th17-skewed inflammation due to genetic deficiency of a cadherin stress sensor

The Journal of clinical investigation, 2022-02, Vol.132 (3), p.1-17

2022

Link zum Volltext

Verfügbarkeit prüfen

Acral peeling in Nagashima type palmo‐plantar keratosis patients reveals the role of serine protease inhibitor B 7 in keratinocyte adhesion

Experimental dermatology, 2022-02, Vol.31 (2), p.214-222

2022

Link zum Volltext

Verfügbarkeit prüfen

A Novel Transcription Regulatory Complex Containing Death Domain-associated Protein and the ATR-X Syndrome Protein

The Journal of biological chemistry, 2004-05, Vol.279 (19), p.20369-20377

2004

Link zum Volltext

Verfügbarkeit prüfen

The Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM Syndrome

Journal of investigative dermatology, 2020-03, Vol.140 (3), p.556-567.e9

2020

Link zum Volltext

Verfügbarkeit prüfen

Influence of prgH on the Persistence of Ingested Salmonella enterica in the Leafhopper Macrosteles quadrilineatus

Applied and environmental microbiology, 2015-09, Vol.81 (18), p.6345-6354

2015

Link zum Volltext

Verfügbarkeit prüfen

Type of bony involvement predicts genomic subgroup in sphenoid wing meningiomas

Journal of neuro-oncology, 2021-09, Vol.154 (2), p.237-246

2021

Link zum Volltext

Verfügbarkeit prüfen

1 – 25 von 40

Suche als RSS-Feed

Aktive Filter

KollektionElsevier ScienceDirect Journals Complete

SpracheKatalanisch

ThemaMutation

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(40)
Mit Volltextzugriff
(38)

Publikationsform

Artikel
(40)

Sprache

Englisch
(40)
Japanisch
(8)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Diabetes treatment in two pregnant women with permanent neonatal diabetes mellitus due to a KCNJ11 mutation

Neonatal hypoglycemia, early-onset diabetes and hypopituitarism due to the mutation in EIF2S3 gene causing MEHMO syndrome

Sulfonylurea vs insulin therapy in individuals with sulfonylurea‐sensitive permanent neonatal diabetes mellitus, attributable to a KCNJ11 mutation, and poor glycaemic control

Role of β-Arrestin in Mediating Agonist-Promoted G Protein-Coupled Receptor Internalization

Differential Affinities of Visual Arrestin, βArrestin1, and βArrestin2 for G Protein-coupled Receptors Delineate Two Major Classes of Receptors

Molecular Determinants Underlying the Formation of Stable Intracellular G Protein-coupled Receptor-β-Arrestin Complexes after Receptor Endocytosis

Constitutive Arrestin-Mediated Desensitization of a Human Vasopressin Receptor Mutant Associated with Nephrogenic Diabetes Insipidus

Apparent Loss-of-Function Mutant GPCRs Revealed as Constitutively Desensitized Receptors

Regulation of Arrestin-3 Phosphorylation by Casein Kinase II

PCM1 is necessary for focal ciliary integrity and is a candidate for severe schizophrenia

Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood

Constitutively Active Alpha-1b Adrenergic Receptor Mutants Display Different Phosphorylation and Internalization Features

β-Arrestin 2 Regulates Zebrafish Development through the Hedgehog Signaling Pathway

Role of phosphorylation in agonist-promoted beta 2-adrenergic receptor sequestration. Rescue of a sequestration-defective mutant receptor by beta ARK1

The beta2-adrenergic receptor interacts with the Na+/H+-exchanger regulatory factor to control Na+/H+ exchange

Abundant contribution of short tandem repeats to gene expression variation in humans

Salmonella enterica Virulence Genes Are Required for Bacterial Attachment to Plant Tissue

A cancer rainbow mouse for visualizing the functional genomics of oncogenic clonal expansion

Translational implications of Th17-skewed inflammation due to genetic deficiency of a cadherin stress sensor

Acral peeling in Nagashima type palmo‐plantar keratosis patients reveals the role of serine protease inhibitor B 7 in keratinocyte adhesion

Cooperation of cancer drivers with regulatory germline variants shapes clinical outcomes

A Novel Transcription Regulatory Complex Containing Death Domain-associated Protein and the ATR-X Syndrome Protein

The Role of Desmoglein 1 in Gap Junction Turnover Revealed through the Study of SAM Syndrome

Influence of prgH on the Persistence of Ingested Salmonella enterica in the Leafhopper Macrosteles quadrilineatus

Type of bony involvement predicts genomic subgroup in sphenoid wing meningiomas

Aktive Filter

Suchergebnisse filtern