PMC Links for Gene (Select 554) - PMC

Links from Gene

Items: 1 to 20 of 56

<< First< Prev

Page of 3

Select item 112280491.

Role of the V2R–βarrestin–Gβγ complex in promoting G protein translocation to endosomes

Badr Sokrat, Anthony H. Nguyen, Alex R. B. Thomsen, Li-Yin Huang, Hiroyuki Kobayashi, Alem W. Kahsai, Jihee Kim, Bing X. Ho, Symon Ma, John Little, IV, Catherine Ehrhart, Ian Pyne, Emmery Hammond, Michel Bouvier

Commun Biol. 2024; 7: 826. Published online 2024 Jul 7. doi: 10.1038/s42003-024-06512-y

PMCID:: PMC11228049

Abstract Article PDF–9.2M

Select item 80750692.

ARGININE VASOPRESSIN RECEPTOR 2 ACTIVATION PROMOTES MICROVASCULAR PERMEABILITY IN SEPSIS

Ernesto Lopez, Satoshi Fukuda, Katalin Modis, Osamu Fujiwara, Baigal Enkhtaivan, Raul Trujillo-Abarca, Koji Ihara, Francisco Lima-Lopez, Dannelys Perez-Bello, Csaba Szabo, Donald S. Prough, Perenlei Enkhbaatar

Pharmacol Res. Author manuscript; available in PMC 2022 Jan 1.

Published in final edited form as: Pharmacol Res. 2021 Jan; 163: 105272. Published online 2020 Nov 4. doi: 10.1016/j.phrs.2020.105272

PMCID:: PMC8075069

Abstract Article PDF–1.3M

Select item 75324663.

Characterization of five novel vasopressin V2 receptor mutants causing nephrogenic diabetes insipidus reveals a role of tolvaptan for M272R-V2R mutation

Federica Prosperi, Yoko Suzumoto, Pierluigi Marzuillo, Vincenzo Costanzo, Sabina Jelen, Anna Iervolino, Stefano Guarino, Angela La Manna, Emanuele Miraglia Del Giudice, Alessandra F. Perna, Miriam Zacchia, Emmanuelle Cordat, Giovambattista Capasso, Francesco Trepiccione

Sci Rep. 2020; 10: 16383. Published online 2020 Oct 2. doi: 10.1038/s41598-020-73089-x

PMCID:: PMC7532466

Abstract Article PDF–4.8M

Select item 72726234.

Vasopressin receptor 2 mutations in the nephrogenic syndrome of inappropriate antidiuresis show different mechanisms of constitutive activation for G protein coupled receptors

Vanessa Vezzi, Caterina Ambrosio, Maria Cristina Grò, Paola Molinari, Gökçe Süral, Tommaso Costa, H. Ongun Onaran, Susanna Cotecchia

Sci Rep. 2020; 10: 9111. Published online 2020 Jun 4. doi: 10.1038/s41598-020-65996-w

PMCID:: PMC7272623

Abstract Article PDF–4.0M

Select item 67831715.

Identification of a novel X-linked arginine-vasopressin receptor 2 mutation in nephrogenic diabetes insipidus: Case report and pedigree analysis

Danxia Peng, Ying Dai, Xuan Xu

Medicine (Baltimore) 2019 Oct; 98(40): e17359. Published online 2019 Oct 4. doi: 10.1097/MD.0000000000017359

PMCID:: PMC6783171

Abstract Article PDF–1.0M

Select item 65614676.

A novel AVPR2 splice site mutation leads to partial X-linked nephrogenic diabetes insipidus in two brothers

Marie Helene Schernthaner-Reiter, David Adams, Giampaolo Trivellin, Mary Scott Ramnitz, Margarita Raygada, Gretchen Golas, Fabio Rueda Faucz, Lars Ola Nilsson, Aikaterini A. Nella, Kavitha Dileepan, Maya Lodish, Paul Lee, Cynthia Tifft, Thomas Markello, William Gahl, Constantine A. Stratakis

Eur J Pediatr. Author manuscript; available in PMC 2019 Jun 12.

Published in final edited form as: Eur J Pediatr. 2016 May; 175(5): 727–733. Published online 2016 Jan 21. doi: 10.1007/s00431-015-2684-4

PMCID:: PMC6561467

Abstract Article PDF–306K

Select item 62803327.

A Novel Mutation in the AVPR2 Gene Causing Congenital Nephrogenic Diabetes Insipidus

Aslı Çelebi Tayfur, Tuğçe Karaduman, Merve Özcan Türkmen, Dilara Şahin, Aysun Çaltık Yılmaz, Bahar Büyükkaragöz, Ayşe Derya Buluş, Hatice Mergen

J Clin Res Pediatr Endocrinol. 2018 Dec; 10(4): 350–356. Published online 2018 Nov 29. doi: 10.4274/jcrpe.0097

PMCID:: PMC6280332

Abstract Article PDF–932K

Select item 58815698.

Identification, Characterization and Rescue of a Novel Vasopressin-2 Receptor Mutation Causing Nephrogenic Diabetes Insipidus

Sayali A. Ranadive, Baran Ersoy, Helene Favre, Clement C. Cheung, Stephen M. Rosenthal, Walter L. Miller, Christian Vaisse

Clin Endocrinol (Oxf) Author manuscript; available in PMC 2018 Apr 3.

Published in final edited form as: Clin Endocrinol (Oxf). 2009 Sep; 71(3): 388–393. Published online 2008 Dec 18. doi: 10.1111/j.1365-2265.2008.03513.x

PMCID:: PMC5881569

Abstract Article PDF–683K

Select item 57973939.

Contiguous 22.1-kb deletion embracing AVPR2 and ARHGAP4 genes at novel breakpoints leads to nephrogenic diabetes insipidus in a Chinese pedigree

Ying Bai, Yibing Chen, Xiangdong Kong

BMC Nephrol. 2018; 19: 26. Published online 2018 Feb 2. doi: 10.1186/s12882-018-0825-5

PMCID:: PMC5797393

Abstract Article PDF–816K

Select item 553655910.

A novel AVPR2 gene mutation of X-linked congenital nephrogenic diabetes insipidus in an Asian pedigree

Wei-Hong Guo, Qiang Li, Hong-Yan Wei, Hong-Yan Lu, Hui-Qi Qu, Mei Zhu

J Int Med Res. 2016 Oct; 44(5): 1131–1137. Published online 2016 Aug 25. doi: 10.1177/0300060516655642

PMCID:: PMC5536559

Abstract Article PDF–331K

Select item 534018411.

Nephrogenic Syndrome of Inappropriate Antidiuresis

Brian J. Feldman, Stephen M. Rosenthal, Gabriel A. Vargas, Raymond G. Fenwick, Eric A. Huang, Mina Matsuda-Abedini, Robert H. Lustig, Robert S. Mathias, Anthony A. Portale, Walter L. Miller, Stephen E. Gitelman

N Engl J Med. Author manuscript; available in PMC 2017 Mar 7.

Published in final edited form as: N Engl J Med. 2005 May 5; 352(18): 1884–1890. doi: 10.1056/NEJMoa042743

PMCID:: PMC5340184

Abstract Article PDF–499K

Select item 507718512.

Analysis of the V2 Vasopressin Receptor (V2R) Mutations Causing Partial Nephrogenic Diabetes Insipidus Highlights a Sustainable Signaling by a Non-peptide V2R Agonist

Noriko Makita, Tomohiko Sato, Yuki Yajima-Shoji, Junichiro Sato, Katsunori Manaka, Makiko Eda-Hashimoto, Masanori Ootaki, Naoki Matsumoto, Masaomi Nangaku, Taroh Iiri

J Biol Chem. 2016 Oct 21; 291(43): 22460–22471. Published online 2016 Sep 6. doi: 10.1074/jbc.M116.733220

PMCID:: PMC5077185

Abstract Article PDF–2.1M

Select item 496584113.

Mutations of Vasopressin Receptor 2 Including Novel L312S Have Differential Effects on Trafficking

Anatoly Tiulpakov, Carl W. White, Rekhati S. Abhayawardana, Heng B. See, Audrey S. Chan, Ruth M. Seeber, Julian I. Heng, Ivan Dedov, Nathan J. Pavlos, Kevin D. G. Pfleger

Mol Endocrinol. 2016 Aug; 30(8): 889–904. Published online 2016 Jun 29. doi: 10.1210/me.2016-1002

PMCID:: PMC4965841

Abstract Article

Select item 484872214.

A novel mutation affecting the arginine‐137 residue of AVPR2 in dizygous twins leads to nephrogenic diabetes insipidus and attenuated urine exosome aquaporin‐2

Gitte R. Hinrichs, Louise H. Hansen, Maria R. Nielsen, Christina Fagerberg, Hans Dieperink, Søren Rittig, Boye L. Jensen

Physiol Rep. 2016 Apr; 4(8): e12764. Published online 2016 Apr 25. doi: 10.14814/phy2.12764

PMCID:: PMC4848722

Abstract Article PDF–483K

Select item 413715315.

Characterization of the effects of the vasopressin V2 receptor on sweating, fluid balance, and performance during exercise

Tamara Hew-Butler, Jed Hummel, Brian C. Rider, Joseph G. Verbalis

Am J Physiol Regul Integr Comp Physiol. 2014 Aug 15; 307(4): R366–R375. Published online 2014 Jun 18. doi: 10.1152/ajpregu.00120.2014

PMCID:: PMC4137153

Abstract Article

Select item 403338316.

Vasopressin-2 Receptor Signaling and Autosomal Dominant Polycystic Kidney Disease: From Bench to Bedside and Back Again

Markus M. Rinschen, Bernhard Schermer, Thomas Benzing

J Am Soc Nephrol. 2014 Jun; 25(6): 1140–1147. Published online 2014 Feb 20. doi: 10.1681/ASN.2013101037

PMCID:: PMC4033383

Abstract Article

Select item 387814217.

The Effect of Aspartate-Lysine-Isoleucine and Aspartate-Arginine-Tyrosine Mutations on the Expression and Activity of Vasopressin V2 Receptor Gene

Hossein Najafzadeh, Leila Safaeian, Hamid Mirmohammad Sadeghi, Mohammad Rabbani, Abbas Jafarian

Iran Biomed J. 2010 Jan-Apr; 14(1-2): 17–22.

PMCID:: PMC3878142

Abstract Article PDF–398K

Select item 367506918.

Characterization of Three Vasopressin Receptor 2 Variants: An Apparent Polymorphism (V266A) and Two Loss-of-Function Mutations (R181C and M311V)

Stephen P. Armstrong, Ruth M. Seeber, Mohammed Akli Ayoub, Brian J. Feldman, Kevin D. G. Pfleger

PLoS One. 2013; 8(6): e65885. Published online 2013 Jun 6. doi: 10.1371/journal.pone.0065885

PMCID:: PMC3675069

Abstract Article PDF–1.3M

Select item 361557919.

Functional polymorphisms affecting the clinically important arginine-137 residue of AVPR2 do not influence serum sodium concentration at the population level

Yi Fu, Tim Cheetham, David Bourn, Eric Orwoll, David M. Cohen

Physiol Genomics. 2013 Mar 15; 45(6): 210–216. Published online 2013 Jan 29. doi: 10.1152/physiolgenomics.00161.2012

PMCID:: PMC3615579

Abstract Article

Select item 326588920.

V2 Vasopressin Receptor (V2R) Mutations in Partial Nephrogenic Diabetes Insipidus Highlight Protean Agonism of V2R Antagonists

Kazuhiro Takahashi, Noriko Makita, Katsunori Manaka, Masataka Hisano, Yuko Akioka, Kenichiro Miura, Noriyuki Takubo, Atsuko Iida, Norishi Ueda, Makiko Hashimoto, Toshiro Fujita, Takashi Igarashi, Takashi Sekine, Taroh Iiri

J Biol Chem. 2012 Jan 13; 287(3): 2099–2106. Published online 2011 Dec 5. doi: 10.1074/jbc.M111.268797

PMCID:: PMC3265889

Abstract Article PDF–1.9M

PMC

Result Filters

Article attributes

Text availability

Publication date

Custom date range

Research Funder

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 56

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity