Citations for
1ARRB2, PROKR2
Mapping the interaction site for β-arrestin-2 in the prokineticin 2 receptor. 2024 PMID:
Lattanzi R, Casella I, Fullone MR, Vincenzi M, Maftei D, Miele R.
Cell Signal. Jul;119:111175. doi: 10.1016/j.cellsig.2024.111175. Epub 2024 Apr 15. 2024
2PROKR2
Phenotypic and genotypic landscape of PROKR2 in neuroendocrine disorders
Martinez-Mayer J, Perez-Millan MI.
Front Endocrinol (Lausanne). Feb 8;14:1132787. doi: 10.3389/fendo.2023.1132787. 2023
3KAL3, PROKR2
A functional spectrum of PROKR2 mutations identified in isolated hypogonadotropic hypogonadism.
Wang X, Chen D, Zhao Y, Men M, Chen Z, Jiang F, Zheng R, Stamou MI, Plummer L, Balasubramanian R, Li JD.
Hum Mol Genet. May 5;32(10):1722-1729. doi: 10.1093/hmg/ddad014. 2023
4KAL3, PROKR2
Biallelic PROKR2 variants and congenital hypogonadotropic hypogonadism: a case report and a literature review.
Sugisawa C, Taniyama M, Sato T, Takahashi Y, Hasegawa T, Narumi S.
Endocr J. Jul 28;69(7):831-838. doi: 10.1507/endocrj.EJ21-0779. Epub 2022 Mar 2. 2022
5KAL3, PROKR2
Trafficking-defective mutant PROKR2 cycles between endoplasmic reticulum and Golgi to attenuate endoplasmic reticulum stress.
Song YB, Park SY, Park K, Hwang H, Carroll RS, Hsu VW, Kaiser UB.
Proc Natl Acad Sci U S A. Feb 22;119(8):e2102248119. doi: 10.1073/pnas.2102248119. 2022
6PROK1, PROK2, PROKR1, PROKR2
Prokineticins and their G protein-coupled receptors in health and disease.
Zhao Y, Wu J, Wang X, Jia H, Chen DN, Li JD.
Prog Mol Biol Transl Sci. 161:149-179. doi: 10.1016/bs.pmbts.2018.09.006. Epub 2018 Oct 24 2019
7PROKR2
Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early puberty.
Fukami M, Suzuki E, Izumi Y, Torii T, Narumi S, Igarashi M, Miyado M, Katsumi M, Fujisawa Y, Nakabayashi K, Hata K, Umezawa A, Matsubara Y, Yamauchi J, Ogata T.
J Cell Mol Med. Oct;21(10):2623-2626. doi: 10.1111/jcmm.13146. Epub 2017 Mar 24. 2017
8PROK1, PROKR1, PROKR2
Prokineticin1 and pregnancy.
Alfaidy N.
Ann Endocrinol (Paris). Jun;77(2):101-4. doi: 10.1016/j.ando.2016.04.014. Epub 2016 May 9. 2016
9KAL3, PROKR2
Biased signaling through G-protein-coupled PROKR2 receptors harboring missense mutations.
Sbai O, Monnier C, Dodé C, Pin JP, Hardelin JP, Rondard P.
FASEB J 28(8):3734-44. doi: 10.1096/fj.13-243402. Epub 2014 May 15. 2014
10PROKR2
Mechanisms that underlie the internalization and extracellular signal regulated kinase 1/2 activation by PKR2 receptor.
Yin W, Liu H, Peng Z, Chen D, Li J, Li JD.
Cell Signal 26(5):1118-24. doi: 10.1016/j.cellsig.2014.01.031. Epub 2014 Feb 7. 2014
11KAL3, PROKR2
Germline prokineticin receptor 2 (PROKR2) variants associated with central hypogonadism cause differental modulation of distinct intracellular pathways.
Libri DV, Kleinau G, Vezzoli V, Busnelli M, Guizzardi F, Sinisi AA, Pincelli AI, Mancini A, Russo G, Beck-Peccoz P, Loche S, Crivellaro C, Maghnie M, Krausz C, Persani L, Bonomi M; Italian Study Group on Idiopathic Central Hypogonadism (ICH).
J Clin Endocrinol Metab 99(3):E458-63. doi: 10.1210/jc.2013-2431. Epub 2013 Nov 25. 2014
12PROK1, PROKR1, PROKR2
Endocrine gland-derived endothelial growth factor (EG-VEGF) is a potential novel regulator of human parturition.
Dunand C, Hoffmann P, Sapin V, Blanchon L, Salomon A, Sergent F, Benharouga M, Sabra S, Guibourdenche J, Lye SJ, Feige JJ, Alfaidy N.
Biol Reprod. Sep;91(3):73. doi: 10.1095/biolreprod.114.119990. Epub 2014 Aug 13 2014
13PROKR2
Functional analysis of the distal region of the third intracellular loop of PROKR2.
Zhou XT, Chen DN, Xie ZQ, Peng Z, Xia KD, Liu HD, Liu W, Su B, Li JD.
Biochem Biophys Res Commun 439(1):12-7. doi: 10.1016/j.bbrc.2013.08.039. Epub 2013 Aug 19. 2013
14PROKR2
Variations in PROKR2, but not PROK2, are associated with hypopituitarism and septo-optic dysplasia.
McCabe MJ, Gaston-Massuet C, Gregory LC, Alatzoglou KS, Tziaferi V, Sbai O, Rondard P, Masumoto KH, Nagano M, Shigeyoshi Y, Pfeifer M, Hulse T, Buchanan CR, Pitteloud N, Martinez-Barbera JP, Dattani MT.
J Clin Endocrinol Metab 98(3):E547-57. doi: 10.1210/jc.2012-3067. Epub 2013 Feb 5. 2013
15KAL3, KAL4, PROK2, PROKR2
PROK2/PROKR2 Signaling and Kallmann Syndrome.
Dodé C, Rondard P.
Front Endocrinol (Lausanne) 4:19. doi: 10.3389/fendo.2013.00019. eCollection 2013. 2013
16PROKR1, PROKR2
Prokineticin receptor variants (PKR1-I379V and PKR2-V331M) are protective genotypes in human early pregnancy.
Su MT, Lin SH, Chen YC, Wu LW, Kuo PL.
Reproduction Jun 14;146(1):63-73. doi: 10.1530/REP-13-0043. Print 2013 Jul 2013
17PROKR2
Evidence of the importance of the first intracellular loop of prokineticin receptor 2 in receptor function.
Abreu AP, Noel SD, Xu S, Carroll RS, Latronico AC, Kaiser UB.
Mol Endocrinol 26(8):1417-27. doi: 10.1210/me.2012-1102. Epub 2012 Jun 28. 2012
18PROK2, PROKR2
Prokineticin 2 potentiates acid-sensing ion channel activity in rat dorsal root ganglion neurons.
Qiu CY, Liu YQ, Qiu F, Wu J, Zhou QY, Hu WP.
J Neuroinflammation 9:108. doi: 10.1186/1742-2094-9-108. 2012
19GNRH1, PROKR2
An ancient founder mutation in PROKR2 impairs human reproduction.
Avbelj Stefanija M, Jeanpierre M, Sykiotis GP, Young J, Quinton R, Abreu AP, Plummer L, Au MG, Balasubramanian R, Dwyer AA, Florez JC, Cheetham T, Pearce SH, Purushothaman R, Schinzel A, Pugeat M, Jacobson-Dickman EE, Ten S, Latronico AC, Gusella JF, Dode C, Crowley WF Jr, Pitteloud N.
Hum Mol Genet 21(19):4314-24. doi: 10.1093/hmg/dds264. Epub 2012 Jul 5. 2012
20PROKR2
Prokr2-deficient mice display vascular dysmorphology of the fetal testes: potential implications for Kallmann syndrome aetiology.
Svingen T, McClelland KS, Masumoto K, Sujino M, Nagano M, Shigeyoshi Y, Koopman P.
Sex Dev 5(6):294-303. doi: 10.1159/000335160. Epub 2012 Jan 4. 2011
21PROKR1, PROKR2
Expression of PROKR1 and PROKR2 in human enteric neural precursor cells and identification of sequence variants suggest a role in HSCR.
Ruiz-Ferrer M, Torroglosa A, Núñez-Torres R, de Agustín JC, Antiñolo G, Borrego S.
PLoS One 6(8):e23475. doi: 10.1371/journal.pone.0023475. Epub 2011 Aug 12. 2011
22PROKR2
Evidence that prokineticin receptor 2 exists as a dimer in vivo.
Marsango S, Bonaccorsi di Patti MC, Barra D, Miele R.
Cell Mol Life Sci 68(17):2919-29. doi: 10.1007/s00018-010-0601-6. Epub 2010 Dec 14. Erratum in: Cell Mol Life Sci. 2011 Sep;68(17):2931. 2011
23CDH7, FGF8, FGFR1, GNRHR, IHH1, IHH2GNRH1, KAL1, KAL1, KAL2, KAL3, KAL4, KISS1R, PCC, PROK2, PROKR2, TAC3, TACR3
Genetics basis for GnRH-dependent pubertal disorders in humans.
Silveira LF, Trarbach EB, Latronico AC.
Mol Cell Endocrinol 324(1-2):30-8. Epub 2010 Feb 25. Review.PMID: 20188792 2010
24PROK2, PROKR1, PROKR2
Divergent roles of prokineticin receptors in the endothelial cells: angiogenesis and fenestration.
Guilini C, Urayama K, Turkeri G, Dedeoglu DB, Kurose H, Messaddeq N, Nebigil CG.
Am J Physiol Heart Circ Physiol 298(3):H844-52. doi: 10.1152/ajpheart.00898.2009. Epub 2009 Dec 18. 2010
25KAL3, PROKR2
PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity.
Monnier C, Dodé C, Fabre L, Teixeira L, Labesse G, Pin JP, Hardelin JP, Rondard P.
Hum Mol Genet 18(1):75-81. Epub 2008 Sep 29. 2009
26KAL3, KAL4, PROK2, PROKR2
Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum.
Cole LW, Sidis Y, Zhang C, Quinton R, Plummer L, Pignatelli D, Hughes VA, Dwyer AA, Raivio T, Hayes FJ, Seminara SB, Huot C, Alos N, Speiser P, Takeshita A, Van Vliet G, Pearce S, Crowley WF Jr, Zhou QY, Pitteloud N.
J Clin Endocrinol Metab 93(9):3551-9. Epub 2008 Jun 17. 2008
27KAL3, KAL4, PROK2, PROKR2
Loss-of-function mutations in the genes encoding prokineticin-2 or prokineticin receptor-2 cause autosomal recessive Kallmann syndrome.
Abreu AP, Trarbach EB, de Castro M, Frade Costa EM, Versiani B, Matias Baptista MT, Garmes HM, Mendonca BB, Latronico AC.
J Clin Endocrinol Metab 93(10):4113-8. Epub 2008 Aug 5. 2008
28PROKR2, PROK2
Prokineticin receptor 2 (Prokr2) is essential for the regulation of circadian behavior by the suprachiasmatic nuclei.
Prosser HM, Bradley A, Chesham JE, Ebling FJ, Hastings MH, Maywood ES.
Proc Natl Acad Sci U S A 104(2):648-53. Epub 2007 Jan 3. 2007
29KAL1, KAL2, KAL3, KAL4, PROK2, PROKR2
Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2.
Dode C, Teixeira L, Levilliers J, Fouveaut C, Bouchard P, Kottler ML, Lespinasse J, Lienhardt-Roussie A, Mathieu M, Moerman A, Morgan G, Murat A, Toublanc JE, Wolczynski S, Delpech M, Petit C, Young J, Hardelin JP.
PLoS Genet 2(10):e175. Epub 2006 Sep 1. 2006
30PROKR2
Identification and molecular characterization of two closely related Gprotein-coupled receptors activated by prokineticins/endocrine gland vascularendothelial growth factor.
Lin DC, Bullock CM, Ehlert FJ, Chen JL, Tian H, Zhou QY.
J Biol Chem 277(22):19276-80. 2002
31PROK1, PROK2, PROKR1, PROKR2
Molecular cloning and characterization of prokineticin receptors.
Soga T, Matsumoto S, Oda T, Saito T, Hiyama H, Takasaki J, Kamohara M, Ohishi T, Matsushime H, Furuichi K.
Biochim Biophys Acta 1579(2-3):173-9. 2002