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Items: 1 to 20 of 99

1.

Genetic Variations of the KISS1R Gene in Korean Girls with Central Precocious Puberty.

Oh YJ, Rhie YJ, Nam HK, Kim HR, Lee KH.

J Korean Med Sci. 2017 Jan;32(1):108-114. doi: 10.3346/jkms.2017.32.1.108.

2.

Prevalence of KISS1 Receptor mutations in a series of 603 patients with normosmic congenital hypogonadotrophic hypogonadism and characterization of novel mutations: a single-centre study.

Francou B, Paul C, Amazit L, Cartes A, Bouvattier C, Albarel F, Maiter D, Chanson P, Trabado S, Brailly-Tabard S, Brue T, Guiochon-Mantel A, Young J, Bouligand J.

Hum Reprod. 2016 Jun;31(6):1363-74. doi: 10.1093/humrep/dew073. Epub 2016 Apr 19.

PMID:
27094476
3.

KISS1R signaling promotes invadopodia formation in human breast cancer cell via β-arrestin2/ERK.

Goertzen CG, Dragan M, Turley E, Babwah AV, Bhattacharya M.

Cell Signal. 2016 Mar;28(3):165-176. doi: 10.1016/j.cellsig.2015.12.010. Epub 2015 Dec 23.

PMID:
26721186
4.

Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated families.

Demirbilek H, Ozbek MN, Demir K, Kotan LD, Cesur Y, Dogan M, Temiz F, Mengen E, Gurbuz F, Yuksel B, Topaloglu AK.

Clin Endocrinol (Oxf). 2015 Mar;82(3):429-38. doi: 10.1111/cen.12618. Epub 2014 Nov 7.

PMID:
25262569
5.

KISS1 receptor is preferentially expressed in clinically non-functioning pituitary tumors.

Yaron M, Renner U, Gilad S, Stalla GK, Stern N, Greenman Y.

Pituitary. 2015 Jun;18(3):306-11. doi: 10.1007/s11102-014-0572-y.

PMID:
24817066
6.

PRR repeats in the intracellular domain of KISS1R are important for its export to cell membrane.

Chevrier L, de Brevern A, Hernandez E, Leprince J, Vaudry H, Guedj AM, de Roux N.

Mol Endocrinol. 2013 Jun;27(6):1004-14. doi: 10.1210/me.2012-1386. Epub 2013 Apr 22.

7.

Molecular biology of the kisspeptin receptor: signaling, function, and mutations.

Bianco SD, Kaiser UB.

Adv Exp Med Biol. 2013;784:133-58. doi: 10.1007/978-1-4614-6199-9_7. Review.

PMID:
23550005
8.

Two families with normosmic congenital hypogonadotropic hypogonadism and biallelic mutations in KISS1R (KISS1 receptor): clinical evaluation and molecular characterization of a novel mutation.

Brioude F, Bouligand J, Francou B, Fagart J, Roussel R, Viengchareun S, Combettes L, Brailly-Tabard S, Lombès M, Young J, Guiochon-Mantel A.

PLoS One. 2013;8(1):e53896. doi: 10.1371/journal.pone.0053896. Epub 2013 Jan 18.

9.

Value of metastin receptor immunohistochemistry in predicting metastasis after radical nephrectomy for pT1 clear cell renal cell carcinoma.

Shoji S, Nakano M, Tomonaga T, Kim H, Hanai K, Usui Y, Nagata Y, Miyazawa M, Sato H, Tang XY, Osamura YR, Uchida T, Terachi T, Takeya K.

Clin Exp Metastasis. 2013 Jun;30(5):607-14. doi: 10.1007/s10585-012-9564-3. Epub 2013 Jan 1.

PMID:
23277422
10.

Single-cell analyses reveal that KISS1R-expressing cells undergo sustained kisspeptin-induced signaling that is dependent upon an influx of extracellular Ca2+.

Babwah AV, Pampillo M, Min L, Kaiser UB, Bhattacharya M.

Endocrinology. 2012 Dec;153(12):5875-87. doi: 10.1210/en.2012-1747. Epub 2012 Oct 15.

11.

A novel severe N-terminal splice site KISS1R gene mutation causes hypogonadotropic hypogonadism but enables a normal development of neonatal external genitalia.

Breuer O, Abdulhadi-Atwan M, Zeligson S, Fridman H, Renbaum P, Levy-Lahad E, Zangen DH.

Eur J Endocrinol. 2012 Aug;167(2):209-16. doi: 10.1530/EJE-12-0127. Epub 2012 May 22.

PMID:
22619348
12.
13.

KISS1R intracellular trafficking and degradation: effect of the Arg386Pro disease-associated mutation.

Bianco SD, Vandepas L, Correa-Medina M, Gereben B, Mukherjee A, Kuohung W, Carroll R, Teles MG, Latronico AC, Kaiser UB.

Endocrinology. 2011 Apr;152(4):1616-26. doi: 10.1210/en.2010-0903. Epub 2011 Feb 1.

14.

GPR54 is a target for suppression of metastasis in endometrial cancer.

Kang HS, Baba T, Mandai M, Matsumura N, Hamanishi J, Kharma B, Kondoh E, Yoshioka Y, Oishi S, Fujii N, Murphy SK, Konishi I.

Mol Cancer Ther. 2011 Apr;10(4):580-90. doi: 10.1158/1535-7163.MCT-10-0763. Epub 2011 Jan 31.

15.

A novel loss-of-function mutation in GPR54/KISS1R leads to hypogonadotropic hypogonadism in a highly consanguineous family.

Nimri R, Lebenthal Y, Lazar L, Chevrier L, Phillip M, Bar M, Hernandez-Mora E, de Roux N, Gat-Yablonski G.

J Clin Endocrinol Metab. 2011 Mar;96(3):E536-45. doi: 10.1210/jc.2010-1676. Epub 2010 Dec 30.

PMID:
21193544
16.

Human diseases associated with GPR54 mutations.

Teles MG, Silveira LF, Bianco S, Latronico AC.

Prog Mol Biol Transl Sci. 2009;88:33-56. doi: 10.1016/S1877-1173(09)88002-2. Epub 2009 Oct 7. Review.

PMID:
20374724
17.

A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism.

Teles MG, Trarbach EB, Noel SD, Guerra-Junior G, Jorge A, Beneduzzi D, Bianco SD, Mukherjee A, Baptista MT, Costa EM, De Castro M, Mendonça BB, Kaiser UB, Latronico AC.

Eur J Endocrinol. 2010 Jul;163(1):29-34. doi: 10.1530/EJE-10-0012. Epub 2010 Apr 6.

PMID:
20371656
18.

Disease-causing mutation in GPR54 reveals the importance of the second intracellular loop for class A G-protein-coupled receptor function.

Wacker JL, Feller DB, Tang XB, Defino MC, Namkung Y, Lyssand JS, Mhyre AJ, Tan X, Jensen JB, Hague C.

J Biol Chem. 2008 Nov 7;283(45):31068-78. doi: 10.1074/jbc.M805251200. Epub 2008 Sep 4.

19.

GPR54 polymorphisms in Chinese girls with central precocious puberty.

Luan X, Yu H, Wei X, Zhou Y, Wang W, Li P, Gan X, Wei D, Xiao J.

Neuroendocrinology. 2007;86(2):77-83. Epub 2007 Aug 15.

PMID:
17700012
20.

Human genetics of GPR54.

Cerrato F, Seminara SB.

Rev Endocr Metab Disord. 2007 Mar;8(1):47-55. Review.

PMID:
17334928

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