162 related articles for article (PubMed ID: 8706292)
41. Glu-47, which forms a salt bridge between neurophysin-II and arginine vasopressin, is deleted in patients with familial central diabetes insipidus.
Yuasa H; Ito M; Nagasaki H; Oiso Y; Miyamoto S; Sasaki N; Saito H
J Clin Endocrinol Metab; 1993 Sep; 77(3):600-4. PubMed ID: 8103767
[TBL] [Abstract][Full Text] [Related]
42. Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus.
Türkmen MÖ; Karaduman T; Tuncdemir BE; Ünal MA; Mergen H
Endocrine; 2021 Dec; 74(3):658-665. PubMed ID: 34232487
[TBL] [Abstract][Full Text] [Related]
43. Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel nonsense mutation in AVP-NPII gene.
Yang H; Yan K; Wang L; Gong F; Jin Z; Zhu H
Exp Ther Med; 2019 Aug; 18(2):1309-1314. PubMed ID: 31316622
[TBL] [Abstract][Full Text] [Related]
44. Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus.
García-Castaño A; Madariaga L; Pérez de Nanclares G; Vela A; Rica I; Gaztambide S; Martínez R; Martinez de LaPiscina I; Urrutia I; Aguayo A; Velasco O; ; Castaño L
J Clin Endocrinol Metab; 2020 Apr; 105(4):. PubMed ID: 32052034
[TBL] [Abstract][Full Text] [Related]
45. A novel AVP gene mutation in a Turkish family with neurohypophyseal diabetes insipidus.
Ilhan M; Tiryakioglu NO; Karaman O; Coskunpinar E; Yildiz RS; Turgut S; Tiryakioglu D; Toprak H; Tasan E
J Endocrinol Invest; 2016 Mar; 39(3):285-90. PubMed ID: 26208472
[TBL] [Abstract][Full Text] [Related]
46. Mutations in the AVPR2, AVP-NPII, and AQP2 genes in Turkish patients with diabetes insipidus.
Duzenli D; Saglar E; Deniz F; Azal O; Erdem B; Mergen H
Endocrine; 2012 Dec; 42(3):664-9. PubMed ID: 22644838
[TBL] [Abstract][Full Text] [Related]
47. Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene.
Patti G; Scianguetta S; Roberti D; Di Mascio A; Balsamo A; Brugnara M; Cappa M; Casale M; Cavarzere P; Cipriani S; Corbetta S; Gaudino R; Iughetti L; Martini L; Napoli F; Peri A; Salerno MC; Salerno R; Passeri E; Maghnie M; Perrotta S; Di Iorgi N
Eur J Endocrinol; 2019 Sep; 181(3):233-244. PubMed ID: 31238300
[TBL] [Abstract][Full Text] [Related]
48. Central Diabetes Insipidus Caused by Arginine Vasopressin Gene Mutation: Report of a Novel Mutation and Review of Literature.
Feldkamp LLI; Kaminsky E; Kienitz T; Quinkler M
Horm Metab Res; 2020 Nov; 52(11):796-802. PubMed ID: 32629514
[TBL] [Abstract][Full Text] [Related]
49. Familial neurohypophyseal diabetes insipidus: clinical, genetic and functional studies of novel mutations in the arginine vasopressin gene.
Alvelos MI; Francisco Â; Gomes L; Paiva I; Melo M; Marques P; Gama-de-Sousa S; Carreiro S; Quintela T; Gonçalves I; Lemos MC
Pituitary; 2021 Jun; 24(3):400-411. PubMed ID: 33433888
[TBL] [Abstract][Full Text] [Related]
50. Familial neurohypophyseal diabetes insipidus due to a novel mutation in the arginine vasopressin-neurophysin II gene.
de Fost M; van Trotsenburg AS; van Santen HM; Endert E; van den Elzen C; Kamsteeg EJ; Swaab DF; Fliers E
Eur J Endocrinol; 2011 Jul; 165(1):161-5. PubMed ID: 21498630
[TBL] [Abstract][Full Text] [Related]
51. Identification of an AVP-NPII mutation within the AVP moiety in a family with neurohypophyseal diabetes insipidus: review of the literature.
Koufaris C; Alexandrou A; Sismani C; Skordis N
Hormones (Athens); 2015; 14(3):442-6. PubMed ID: 26233932
[TBL] [Abstract][Full Text] [Related]
52. Autosomal recessive familial neurohypophyseal diabetes insipidus with continued secretion of mutant weakly active vasopressin.
Willcutts MD; Felner E; White PC
Hum Mol Genet; 1999 Jul; 8(7):1303-7. PubMed ID: 10369876
[TBL] [Abstract][Full Text] [Related]
53. A case of central diabetes insipidus due to neurophysin II gene abnormality diagnosed based on a family history of nocturnal enuresis.
Sugawara L; Nakamura T; Ishizuka Y; Maegawa H
Endocr J; 2022 Jan; 69(1):95-100. PubMed ID: 34544934
[TBL] [Abstract][Full Text] [Related]
54. Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene.
Brachet C; Birk J; Christophe C; Tenoutasse S; Velkeniers B; Heinrichs C; Rutishauser J
Eur J Endocrinol; 2011 Feb; 164(2):179-87. PubMed ID: 21088058
[TBL] [Abstract][Full Text] [Related]
55. Recurrent mutations in the vasopressin-neurophysin II gene cause autosomal dominant neurohypophyseal diabetes insipidus.
Repaske DR; Summar ML; Krishnamani MR; Gültekin EK; Arriazu MC; Roubicek ME; Blanco M; Isaac GB; Phillips JA
J Clin Endocrinol Metab; 1996 Jun; 81(6):2328-34. PubMed ID: 8964872
[TBL] [Abstract][Full Text] [Related]
56. Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a mutation in the arginine-vasopressin II gene in four generations of a Korean family.
Kim MJ; Kim YE; Ki CS; Yoo JH
Ann Pediatr Endocrinol Metab; 2014 Dec; 19(4):220-4. PubMed ID: 25654069
[TBL] [Abstract][Full Text] [Related]
57. Hyperintensity of posterior pituitary on MR T1WI in a boy with central diabetes insipidus caused by missense mutation of neurophysin II gene.
Kubota T; Yamamoto T; Ozono K; Shimotsuji T
Endocr J; 2001 Aug; 48(4):459-63. PubMed ID: 11603568
[TBL] [Abstract][Full Text] [Related]
58. Autosomal dominant familial neurohypophyseal diabetes insipidus caused by a novel missense mutation in AVP gene in a large Italian kindred.
Marzocchi C; Cantara S; Sagnella A; Castagna MG; Capezzone M
Endocrine; 2021 Oct; 74(1):188-192. PubMed ID: 34319541
[TBL] [Abstract][Full Text] [Related]
59. A novel heterozygous missense mutation in the vasopressin moiety is identified in a Japanese person with neurohypophyseal diabetes insipidus.
Kobayashi H; Fujisawa I; Ikeda K; Son C; Iwakura T; Yoshimoto A; Kasahara M; Ishihara T; Ogawa Y
J Endocrinol Invest; 2006 Mar; 29(3):252-6. PubMed ID: 16682840
[TBL] [Abstract][Full Text] [Related]
60. The molecular biology of human hereditary central diabetes insipidus.
Repaske DR; Phillips JA
Prog Brain Res; 1992; 93():295-306; discussion 306-8. PubMed ID: 1282720
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
