Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
My NCBI Filters
Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1989 1
1992 7
1993 4
1994 7
1995 1
1996 3
1997 4
1998 3
1999 2
2000 7
2001 2
2002 11
2003 3
2004 5
2005 6
2006 8
2007 7
2008 12
2009 12
2010 12
2011 8
2012 9
2013 7
2014 4
2015 1
2016 9
2017 1
2018 4
2019 2
2020 2
Text availability
Article attribute
Article type
Publication date

gene_pubmed for PMID: 554

148 results
Results by year
Filters applied: . Clear all
Page 1
Gain-of-function mutations of the V2 vasopressin receptor in nephrogenic syndrome of inappropriate antidiuresis (NSIAD): a cell-based assay to assess constitutive water reabsorption.
Ranieri M, Tamma G, Pellegrino T, Vezzi V, Ambrosio C, Grò C, Di Mise A, Costa T, Valenti G, Cotecchia S. Ranieri M, et al. Pflugers Arch. 2019 Oct;471(10):1291-1304. doi: 10.1007/s00424-019-02307-x. Epub 2019 Sep 5. Pflugers Arch. 2019. PMID: 31486901
A Novel Mutation in the AVPR2 Gene Causing Congenital Nephrogenic Diabetes Insipidus.
Çelebi Tayfur A, Karaduman T, Özcan Türkmen M, Şahin D, Çaltık Yılmaz A, Büyükkaragöz B, Buluş AD, Mergen H. Çelebi Tayfur A, et al. J Clin Res Pediatr Endocrinol. 2018 Nov 29;10(4):350-356. doi: 10.4274/jcrpe.0097. Epub 2018 Jul 11. J Clin Res Pediatr Endocrinol. 2018. PMID: 29991464 Free PMC article.
Novel and recurrent variants in AVPR2 in 19 families with X-linked congenital nephrogenic diabetes insipidus.
Joshi S, Kvistgaard H, Kamperis K, Færch M, Hagstrøm S, Gregersen N, Rittig S, Christensen JH. Joshi S, et al. Eur J Pediatr. 2018 Sep;177(9):1399-1405. doi: 10.1007/s00431-018-3132-z. Epub 2018 Mar 28. Eur J Pediatr. 2018. PMID: 29594432
Analysis of the V2 Vasopressin Receptor (V2R) Mutations Causing Partial Nephrogenic Diabetes Insipidus Highlights a Sustainable Signaling by a Non-peptide V2R Agonist.
Makita N, Sato T, Yajima-Shoji Y, Sato J, Manaka K, Eda-Hashimoto M, Ootaki M, Matsumoto N, Nangaku M, Iiri T. Makita N, et al. J Biol Chem. 2016 Oct 21;291(43):22460-22471. doi: 10.1074/jbc.M116.733220. Epub 2016 Sep 6. J Biol Chem. 2016. PMID: 27601473 Free PMC article.
[Analysis of AVPR2 gene mutation in a pedigree affected with congenital nephrogenic diabetes insipidus].
Dai Z, Ruan L, Jin J, Qian Y, Wang L, Shi Z, Wu C. Dai Z, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016 Oct;33(5):666-9. doi: 10.3760/cma.j.issn.1003-9406.2016.05.019. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2016. PMID: 27577218 Chinese.
Mutations of Vasopressin Receptor 2 Including Novel L312S Have Differential Effects on Trafficking.
Tiulpakov A, White CW, Abhayawardana RS, See HB, Chan AS, Seeber RM, Heng JI, Dedov I, Pavlos NJ, Pfleger KD. Tiulpakov A, et al. Mol Endocrinol. 2016 Aug;30(8):889-904. doi: 10.1210/me.2016-1002. Epub 2016 Jun 29. Mol Endocrinol. 2016. PMID: 27355191 Free PMC article.
148 results
Jump to page
Feedback