These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

242 related articles for article (PubMed ID: 1303271)

  • 1. Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus.
    van den Ouweland AM; Dreesen JC; Verdijk M; Knoers NV; Monnens LA; Rocchi M; van Oost BA
    Nat Genet; 1992 Oct; 2(2):99-102. PubMed ID: 1303271
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in the V2 vasopressin receptor gene are associated with X-linked nephrogenic diabetes insipidus.
    Pan Y; Metzenberg A; Das S; Jing B; Gitschier J
    Nat Genet; 1992 Oct; 2(2):103-6. PubMed ID: 1303257
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two novel mutations in the vasopressin V2 receptor gene in unrelated Japanese kindreds with nephrogenic diabetes insipidus.
    Tsukaguchi H; Matsubara H; Aritaki S; Kimura T; Abe S; Inada M
    Biochem Biophys Res Commun; 1993 Dec; 197(2):1000-10. PubMed ID: 8267567
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Congenital nephrogenic diabetes insipidus].
    Thibonnier M
    Rev Prat; 1994 May; 44(9):1169-72. PubMed ID: 7939338
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in the vasopressin V2 receptor gene in families with nephrogenic diabetes insipidus and functional expression of the Q-2 mutant.
    Rosenthal W; Seibold A; Antaramian A; Gilbert S; Birnbaumer M; Bichet DG; Arthus MF; Lonergan M
    Cell Mol Biol (Noisy-le-grand); 1994 May; 40(3):429-36. PubMed ID: 7920187
    [TBL] [Abstract][Full Text] [Related]  

  • 6. V2 vasopressin receptor dysfunction in nephrogenic diabetes insipidus caused by different molecular mechanisms.
    Schöneberg T; Schulz A; Biebermann H; Grüters A; Grimm T; Hübschmann K; Filler G; Gudermann T; Schultz G
    Hum Mutat; 1998; 12(3):196-205. PubMed ID: 9711877
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Vasopressin receptor mutations causing nephrogenic diabetes insipidus.
    Bichet DG; Turner M; Morin D
    Proc Assoc Am Physicians; 1998; 110(5):387-94. PubMed ID: 9756088
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Brief report: a mutation in the vasopressin V2-receptor gene in a kindred with X-linked nephrogenic diabetes insipidus.
    Merendino JJ; Speigel AM; Crawford JD; O'Carroll AM; Brownstein MJ; Lolait SJ
    N Engl J Med; 1993 May; 328(21):1538-41. PubMed ID: 8479491
    [No Abstract]   [Full Text] [Related]  

  • 9. [Identification of mutations in the arginine vasopressin receptor 2 gene in congenital nephrogenic diabetes insipidus patients].
    Gu F; Shi Y; Deng J; Jin Z
    Zhonghua Yi Xue Za Zhi; 2002 Oct; 82(20):1401-5. PubMed ID: 12509923
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cloning and characterization of a vasopressin V2 receptor and possible link to nephrogenic diabetes insipidus.
    Lolait SJ; O'Carroll AM; McBride OW; Konig M; Morel A; Brownstein MJ
    Nature; 1992 May; 357(6376):336-9. PubMed ID: 1534150
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Pathological aspects of water transport in the collecting ducts].
    Bichet DG
    Nephrologie; 1996; 17(7):417-22. PubMed ID: 9019668
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two novel mutations in the vasopressin V2 receptor gene in patients with congenital nephrogenic diabetes insipidus.
    Oksche A; Dickson J; Schülein R; Seyberth HW; Müller M; Rascher W; Birnbaumer M; Rosenthal W
    Biochem Biophys Res Commun; 1994 Nov; 205(1):552-7. PubMed ID: 7999078
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular genetic study of congenital nephrogenic diabetes insipidus and rescue of mutant vasopressin V2 receptor by chemical chaperones.
    Cheong HI; Cho HY; Park HW; Ha IS; Choi Y
    Nephrology (Carlton); 2007 Apr; 12(2):113-7. PubMed ID: 17371330
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Three novel AVPR2 mutations in three Japanese families with X-linked nephrogenic diabetes insipidus.
    Tajima T; Nakae J; Takekoshi Y; Takahashi Y; Yuri K; Nagashima T; Fujieda K
    Pediatr Res; 1996 Mar; 39(3):522-6. PubMed ID: 8929875
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A Null mutation in the vasopressin V2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus in the Hopewell kindred.
    Holtzman EJ; Kolakowski LF; O'Brien D; Crawford JD; Ausiello DA
    Hum Mol Genet; 1993 Aug; 2(8):1201-4. PubMed ID: 8401502
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of mutations in the arginine vasopressin receptor 2 gene causing nephrogenic diabetes insipidus in Chinese patients.
    Chen CH; Chen WY; Liu HL; Liu TT; Tsou AP; Lin CY; Chao T; Qi Y; Hsiao KJ
    J Hum Genet; 2002; 47(2):66-73. PubMed ID: 11916004
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Binding-, intracellular transport-, and biosynthesis-defective mutants of vasopressin type 2 receptor in patients with X-linked nephrogenic diabetes insipidus.
    Tsukaguchi H; Matsubara H; Taketani S; Mori Y; Seido T; Inada M
    J Clin Invest; 1995 Oct; 96(4):2043-50. PubMed ID: 7560098
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Nephrogenic diabetes insipidus caused by mutation of Tyr205: a key residue of V2 vasopressin receptor function.
    Sangkuhl K; Römpler H; Busch W; Karges B; Schöneberg T
    Hum Mutat; 2005 May; 25(5):505. PubMed ID: 15841479
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Partial nephrogenic diabetes insipidus caused by a novel mutation in the AVPR2 gene.
    Faerch M; Christensen JH; Corydon TJ; Kamperis K; de Zegher F; Gregersen N; Robertson GL; Rittig S
    Clin Endocrinol (Oxf); 2008 Mar; 68(3):395-403. PubMed ID: 17941907
    [TBL] [Abstract][Full Text] [Related]  

  • 20. C112R, W323S, N317K mutations in the vasopressin V2 receptor gene in patients with nephrogenic diabetes insipidus. Mutations in brief no. 165. Online.
    Szalai C; Triga D; Czinner A
    Hum Mutat; 1998; 12(2):137-8. PubMed ID: 10694923
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.