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arginine vasopressin and Genetic Diseases, X-Chromosome Linked

arginine vasopressin has been researched along with Genetic Diseases, X-Chromosome Linked in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Armstrong, SP; Ayoub, MA; Feldman, BJ; Pfleger, KD; Seeber, RM	1

Other Studies

1 other study(ies) available for arginine vasopressin and Genetic Diseases, X-Chromosome Linked

Article	Year
Characterization of three vasopressin receptor 2 variants: an apparent polymorphism (V266A) and two loss-of-function mutations (R181C and M311V). PloS one, 2013, Volume: 8, Issue:6 Topics: Animals; Aquaporin 2; Arginine Vasopressin; Arrestins; beta-Arrestins; Chlorocebus aethiops; COS Cells; Cyclic AMP; Diabetes Insipidus, Nephrogenic; Gene Expression Regulation; Genetic Diseases, X-Linked; GTP-Binding Protein alpha Subunits, Gs; HEK293 Cells; Humans; Inappropriate ADH Syndrome; Inositol Phosphates; Mutation; Polymorphism, Genetic; Receptors, Vasopressin; Signal Transduction	2013

Article

Year

Characterization of three vasopressin receptor 2 variants: an apparent polymorphism (V266A) and two loss-of-function mutations (R181C and M311V).

PloS one, 2013, Volume: 8, Issue:6

Topics: Animals; Aquaporin 2; Arginine Vasopressin; Arrestins; beta-Arrestins; Chlorocebus aethiops; COS Cells; Cyclic AMP; Diabetes Insipidus, Nephrogenic; Gene Expression Regulation; Genetic Diseases, X-Linked; GTP-Binding Protein alpha Subunits, Gs; HEK293 Cells; Humans; Inappropriate ADH Syndrome; Inositol Phosphates; Mutation; Polymorphism, Genetic; Receptors, Vasopressin; Signal Transduction

2013