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Gαs and Gαq/11 protein coupling bias of two AVPR2 mutants (R68W and V162A) that cause nephrogenic diabetes insipidus

Journal of receptors and signal transduction, 2022-11, Vol.42 (6), p.573-579

Erdem Tuncdemir, Beril

2022

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Can tolvaptan usage cause cytotoxicity? An in vitro study

The European research journal, 2023-05, Vol.9 (3), p.454-460

ERDEM TUNÇDEMİR, Beril

2023

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Evaluation of pharmacochaperone-mediated rescue of mutant V2 receptor proteins

European journal of pharmacology, 2019-12, Vol.865, p.172803-172803, Article 172803

2019

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Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus

Endocrine, 2021-12, Vol.74 (3), p.658-665

2021

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Design and Development of Gold-Loaded and Boron-Attached Multicore Manganese Ferrite Nanoparticles as a Potential Agent in Biomedical Applications

ACS omega, 2022-06, Vol.7 (23), p.20195-20203

2022

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Effects of N-acetyl cysteine, vitamin E and vitamin C on liver glutathione levels following amiodarone treatment in rats

Kardiochirurgia i torakochirurgia polska, 2019-01, Vol.16 (2), p.88-92

2019

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Functional characterization of AVPR2 mutants found in Turkish patients with nephrogenic diabetes insipidus

Endocrine Connections, 2018-01, Vol.7 (1), p.56-64

2018

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Functional analysis of AQP2 mutants found in patients with diabetes insipidus

Biológia, 2021-09, Vol.76 (9), p.2767-2776

2021

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May toxicity of amiodarone be prevented by antioxidants? A cell-culture study

Journal of cardiothoracic surgery, 2012-06, Vol.7 (1), p.61-61, Article 61

2012

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Composition of the colon microbiota in the individuals with inflammatory bowel disease and colon cancer

Folia microbiologica, 2024-04, Vol.69 (2), p.333-345

2024

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Mutations in the AVPR2, AVP-NPII, and AQP2 genes in Turkish patients with diabetes insipidus

Endocrine, 2012-12, Vol.42 (3), p.664-669

2012

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A large deletion of the AVPR2 gene causing severe nephrogenic diabetes insipidus in a Turkish family

Endocrine, 2014-05, Vol.46 (1), p.148-153

2014

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Association of VNTR polymorphisms in DRD4, 5-HTT and DAT1 genes with obesity

Archives of physiology and biochemistry, 2015-05, Vol.121 (2), p.75-79

2015

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Identification of a Novel Deletion in AVP-NPII Gene in a Patient with Central Diabetes Insipidus

Annals of clinical and laboratory science, 2015-09, Vol.45 (5), p.588-592

2015

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Promoter hypermethylation of p16 and APC in gastrointestinal cancer patients

The Turkish journal of gastroenterology, 2014-10, Vol.25 (5), p.512-517

2014

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Evaluation of MUC1, CK20, and hTERT expression in peripheral blood of gastrointestinal cancer patients in search of diagnostic criteria

Turkish journal of biology, 2014, Vol.38, p.848-857

2014

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Pharmacological chaperones for rescue of the mutant AVPR2s

Endocrine Abstracts, 2018-05

2018

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Tolvaptan; OPC-41 061, Mozavaptan; OPC-31 260, OPC-21 268 as pharmacological chaperones to rescue of mutant AVPR2s

Endocrine Abstracts, 2018-05

2018

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Rescue study of trapped AVPR2 mutants with chemicals

Endocrine Abstracts, 2017-05

2017

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CHEMICAL CHAPERONE EFFECTS ON ARGININE-VASOPRESSIN RECEPTOR 2 MUTANTS

Hacettepe Journal of Biology and Chemistry, 2022-01, Vol.50 (1), p.37-43

2022

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Functional characterization of a large deletion in the AVPR2 gene causing severe nephrogenic diabetes insipidus in a Turkish family

Endocrine Abstracts, 2016-05

2016

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Functional analysis of G12E mutation of AVPR2 gene in Turkish patients with diabetes insipidus

Endocrine Abstracts, 2016-05

2016

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A novel p.H80Y mutation in the AVPR2 gene causing congenital nephrogenic diabetes insipidus

Endocrine Abstracts, 2017-05

2017

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Functional analysis of four mutants of the V2 receptor

Endocrine Abstracts, 2015-05

2015

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A novel E108D mutation of AVP-NPII gene in a Turkish patient with central diabetes insipidus

Endocrine Abstracts, 2016-05

2016

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Gαs and Gαq/11 protein coupling bias of two AVPR2 mutants (R68W and V162A) that cause nephrogenic diabetes insipidus

Can tolvaptan usage cause cytotoxicity? An in vitro study

Evaluation of pharmacochaperone-mediated rescue of mutant V2 receptor proteins

Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus

Design and Development of Gold-Loaded and Boron-Attached Multicore Manganese Ferrite Nanoparticles as a Potential Agent in Biomedical Applications

Effects of N-acetyl cysteine, vitamin E and vitamin C on liver glutathione levels following amiodarone treatment in rats

Functional characterization of AVPR2 mutants found in Turkish patients with nephrogenic diabetes insipidus

Functional analysis of AQP2 mutants found in patients with diabetes insipidus

May toxicity of amiodarone be prevented by antioxidants? A cell-culture study

Composition of the colon microbiota in the individuals with inflammatory bowel disease and colon cancer

Mutations in the AVPR2, AVP-NPII, and AQP2 genes in Turkish patients with diabetes insipidus

A large deletion of the AVPR2 gene causing severe nephrogenic diabetes insipidus in a Turkish family

Association of VNTR polymorphisms in DRD4, 5-HTT and DAT1 genes with obesity

Identification of a Novel Deletion in AVP-NPII Gene in a Patient with Central Diabetes Insipidus

Promoter hypermethylation of p16 and APC in gastrointestinal cancer patients

Evaluation of MUC1, CK20, and hTERT expression in peripheral blood of gastrointestinal cancer patients in search of diagnostic criteria

Pharmacological chaperones for rescue of the mutant AVPR2s

Tolvaptan; OPC-41 061, Mozavaptan; OPC-31 260, OPC-21 268 as pharmacological chaperones to rescue of mutant AVPR2s

Rescue study of trapped AVPR2 mutants with chemicals

CHEMICAL CHAPERONE EFFECTS ON ARGININE-VASOPRESSIN RECEPTOR 2 MUTANTS

Functional characterization of a large deletion in the AVPR2 gene causing severe nephrogenic diabetes insipidus in a Turkish family

Functional analysis of G12E mutation of AVPR2 gene in Turkish patients with diabetes insipidus

A novel p.H80Y mutation in the AVPR2 gene causing congenital nephrogenic diabetes insipidus

Functional analysis of four mutants of the V2 receptor

A novel E108D mutation of AVP-NPII gene in a Turkish patient with central diabetes insipidus

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