1 | EIF5A, LHCGR, MVK
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| LHCGR Expression During FSH-Induced Follicle Growth is Negatively Regulated by Eukaryotic Initiation Factor 5A.
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| Gulappa T, Menon B, Menon KMJ.
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| Endocrinology ndocrinology. 2017 Jun 9. doi: 10.1210/en.2017-00113. [Epub ahead of print]
2017
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2 | LHCGR
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| Luteinizing hormone/chorionic gonadotrophin receptor overexpressed in granulosa cells from polycystic ovary syndrome ovaries is functionally active.
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| Kanamarlapudi V, Gordon UD, López Bernal A.
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| Reprod Biomed Online 32(6):635-41. doi: 10.1016/j.rbmo.2016.03.003. Epub 2016 Mar 29.
2016
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3 | LHCGR, PPML
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| Testotoxicosis: Report of Two Cases, One with a Novel Mutation in LHCGR Gene.
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| Özcabı B, Tahmiscioğlu Bucak F, Ceylaner S, Özcan R, Büyükünal C, Ercan O, Tüysüz B, Evliyaoğlu O.
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| J Clin Res Pediatr Endocrinol 7(3):242-8. doi: 10.4274/jcrpe.2067.
2015
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4 | LHCGR, PHLCH
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| A novel inactivating mutation of the LH/chorionic gonadotrophin receptor with impaired membrane trafficking leading to Leydig cell hypoplasia type 1.
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| Rivero-Müller A, Potorac I, Pintiaux A, Daly AF, Thiry A, Rydlewski C, Nisolle M, Parent AS, Huhtaniemi I, Beckers A.
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| Eur J Endocrinol 172(6):K27-36. doi: 10.1530/EJE-14-1095. Epub 2015 Mar 20.
2015
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5 | LHCGR
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| The Presence of Human Chorionic Gonadotropin/Luteinizing Hormone Receptors in Pancreatic β-Cells.
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| Parkash J, Lei Z, Rao CV.
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| Reprod Sci 22(8):1000-7. doi: 10.1177/1933719115570910. Epub 2015 Feb 10.
2015
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6 | AHR, LHCGR
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| Transcriptional repression of the Ahr gene by LHCGR signaling in preovulatory granulosa cells is controlled by chromatin accessibility.
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| Teino I, Matvere A, Kuuse S, Ingerpuu S, Maimets T, Kristjuhan A, Tiido T.
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| Mol Cell Endocrinol 382(1):292-301. doi: 10.1016/j.mce.2013.10.011. Epub 2013 Oct 18.
2014
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7 | LHCGR, ZFP36L2
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| The RNA-binding protein, ZFP36L2, influences ovulation and oocyte maturation.
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| Ball CB, Rodriguez KF, Stumpo DJ, Ribeiro-Neto F, Korach KS, Blackshear PJ, Birnbaumer L, Ramos SB.
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| PLoS One. May 15;9(5):e97324. doi: 10.1371/journal.pone.0097324. eCollection 2014 2014
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8 | FHR, LHCGR
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| Heterodimerization between the lutropin and follitropin receptors is associated with an attenuation of hormone-dependent signaling.
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| Feng X, Zhang M, Guan R, Segaloff DL.
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| Endocrinology 154(10):3925-30. doi: 10.1210/en.2013-1407. Epub 2013 Jul 3.
2013
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9 | CYP17A1, LHCGR
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| Increased protein expression of LHCG receptor and 17α-hydroxylase/17-20-lyase in human polycystic ovaries.
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| Comim FV, Teerds K, Hardy K, Franks S.
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| Hum Reprod 28(11):3086-92. doi: 10.1093/humrep/det352. Epub 2013 Sep 5.
2013
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10 | ARF6, LHCGR
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| ARF6 activated by the LHCG receptor through the cytohesin family of guanine nucleotide exchange factors mediates the receptor internalization and signaling.
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| Kanamarlapudi V, Thompson A, Kelly E, López Bernal A.
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| J Biol Chem 287(24):20443-55. doi: 10.1074/jbc.M112.362087. Epub 2012 Apr 20.
2012
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11 | DENND1A, LHCGR
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| Variants in DENND1A and LHCGR are associated with endometrioid adenocarcinoma.
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| Wang Z, Li T, Zhang W, You L, Zhao Y, Xia M, Zhao H, Chen ZJ.
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| Gynecol Oncol 127(2):403-5. doi: 10.1016/j.ygyno.2012.08.007. Epub 2012 Aug 14.
2012
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12 | LHCGR
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| Inherited mutation of the luteinizing hormone/choriogonadotropin receptor (LHCGR) in empty follicle syndrome.
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| Yariz KO, Walsh T, Uzak A, Spiliopoulos M, Duman D, Onalan G, King MC, Tekin M.
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| Fertil Steril 96(2):e125-30. doi: 10.1016/j.fertnstert.2011.05.057. Epub 2011 Jun 17.
2011
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13 | LHCGR
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| A cell surface inactive mutant of the human lutropin receptor (hLHR) attenuates signaling of wild-type or constitutively active receptors via heterodimerization.
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| Zhang M, Feng X, Guan R, Hébert TE, Segaloff DL.
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| Cell Signal 21(11):1663-71. Epub 2009 Jul 16.PMID: 19616090 2009
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14 | LHCGR, PHLCH
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| A splice site mutation combined with a novel missense mutation of LHCGR cause male pseudohermaphroditism.
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| Qiao J, Han B, Liu BL, Chen X, Ru Y, Cheng KX, Chen FG, Zhao SX, Liang J, Lu YL, Tang JF, Wu YX, Wu WL, Chen JL, Chen MD, Song HD.
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| Hum Mutat 30(9):E855-65.PMID: 19551906 2009
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15 | LHCGR
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| Association of luteinizing hormone receptor gene expression with cell cycle progression in granulosa cells.
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| Cannon JD, Seekallu SV, Vandevoort CA, Chaffin CL.
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| Am J Physiol Endocrinol Metab 296(6):E1392-9. Epub 2009 Mar 17.PMID: 19293332 2009
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16 | LHCGR, PHLCH
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| A luteinizing hormone receptor intronic variant is significantly associated with decreased risk of Alzheimer's disease in males carrying an apolipoprotein E epsilon4 allele.
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| Haasl RJ, Ahmadi MR, Meethal SV, Gleason CE, Johnson SC, Asthana S, Bowen RL, Atwood CS.
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| BMC Med Genet 9:37.PMID: 18439297 2008
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17 | LHCGR, MVK
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| Regulation of luteinizing hormone receptor mRNA expression by mevalonate kinase--role of the catalytic center in mRNA recognition.
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| Nair AK, Young MA, Menon KM.
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| FEBS J 275(13):3397-407. doi: 10.1111/j.1742-4658.2008.06490.x. Epub 2008 May 20.
2008
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18 | LHCGR, PPML
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| Natural antisense LHCGR could make sense of hypogonadism, male-limited precocious puberty and pre-eclampsia.
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| Chambers AE, Banerjee S.
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| Mol Cell Endocrinol 241(1-2):1-9. Review.PMID: 16087288 2005
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19 | ARR3, FSHR, LHCGR
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| The association of arrestin-3 with the follitropin receptor depends on receptor activation and phosphorylation.
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| Krishnamurthy H, Galet C, Ascoli M.
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| Mol Cell Endocrinol 204(1-2):127-40.
2003
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20 | LHCGR, PHLCH
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| Homozygous mutation within the conserved Ala-Phe-Asn-Glu-Thr motif of exon 7 of the LH receptor causes male pseudohermaphroditism.
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| Gromoll J, Schulz A, Borta H, Gudermann T, Teerds KJ, Greschniok A, Nieschlag E, Seif FJ.
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| Eur J Endocrinol 147(5):597-608. 2002
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21 | LHCGR, PPML
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| A novel luteinizing hormone receptor mutation in a patient with familial male-limited precocious puberty : effect of the size of a critical amino acid on receptor activity.
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| Wu SM, et al.
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| Mol Genet Metab 66 : 68-73. 1999
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22 | LHCGR, PPML
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| A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty.
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| Kremer H, et al.
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| J Clin Endocrinol Metab 84(3):1136-40. 1999
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23 | PHLCH, LHCGR, PPML
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| Naturally Occurring Mutations of the Luteinizing-Hormone Receptor: Lessons Learned about Reproductive Physiology and G Protein-Coupled Receptors.
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| Latronico AC, et al.
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| Am J Hum Genet 65(4):949-958. No abstract available 1999
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24 | LHCGR
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| Leydig-Cell Tumors Caused by An Activating Mutation of the Gene Encoding the Luteinizing Hormone Receptor.
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| Liu G, Duranteau L, Carel JC, Monroe J, Doyle DA, Shenker A.
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| N Engl J Med 341(23):1731-1736. No abstract available 1999
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25 | D2S123, D2S1248, D2S2153, D2S2227, D2S2251, D2S2292, D2S2378, D2S391, FSHR, LHCGR, MSH2, MSH6, PIGF, RPS27A, SPTBN1, VRK2
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| Genomic mapping of chromosomal region 2p15-p21 (D2S378-D2S391): integration of Genemap'98 within a framework of yeast and bacterial artificial chromosomes.
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| Kirschner LS, Taymans SE, Pack S, Pak E, Pike BL, Chandrasekharappa SC, Zhuang Z, Stratakis CA.
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| Genomics 62(1):21-33 1999
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26 | LHCGR, PPML
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| A mutation in the first transmembrane domain of the lutropin receptor causes male precocious puberty.
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| Gromoll J, Partsch CJ, Simoni M, Nordhoff V, Sippell WG, Nieschlag E, Saxena BB.
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| J Clin Endocrinol Metab 83(2):476-80. 1998
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27 | LHCGR, PHLCH
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| A homozygous microdeletion in helix 7 of the luteinizing hormone receptor associated with familial testicular and ovarian resistance is due to both decreased cell surface expression and impaired effector activation by the cell surface receptor.
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| Latronico AC, Chai Y, Arnhold IJ, Liu X, Mendonca BB, Segaloff DL.
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| Mol Endocrinol 12(3):442-50. 1998
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28 | LHCGR, PPML
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| Severe testotoxicosis phenotype associated with Asp578-Tyr mutation of the lutrophin/choriogonadotrophin receptor gene.
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| Mller J, et al.
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| J Med Genet 35 : 340-341. 1998
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29 | LHCGR, PHLCH
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| A homozygous mutation in the luteinizing hormone receptor causes partial Leydig cell hypoplasia : correlation between receptor activity and phenotype.
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| Martens JW, et al.
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| Mol Endocrinol 12 : 775-784. 1998
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30 | LHCGR, PPML
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| A unique constitutively activating mutation in third transmembrane helix of luteinizing hormone receptor causes sporadic male gonadotropin-independent precocious puberty.
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| Latronico AC, et al.
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| J Clin Endocrinol Metab 83 : 2435-2440. 1998
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31 | LHCGR, PPML
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| A new point mutation in the luteinising hormone receptor gene in familial and sporadic male limited precocious puberty : genotype does not always correlate with phenotype.
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| Evans BAJ, et al.
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| J Med Genet 33 : 143-147. 1996
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32 | LHCGR, PPML
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| A missense (T577I) mutation in the luteinizing hormone receptor gene associated with familial male-limited precocious puberty.
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| Cocco S, et al.
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| Hum Mutat 7 : 164-166. 1996
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33 | LHCGR, PPML
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| Testicular and ovarian resistance to luteinizing hormone caused by inactivating mutations of the luteinizing hormone-receptor gene.
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| Latronico AC, et al.
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| N Engl J Med 334 : 507-512. 1996
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34 | PPML, LHCGR
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| A case of male-limited precocious puberty caused by a point mutation in the second transmembrane domain of the luteinizing hormone choriogonadotropin receptor gene.
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| Yano K, et al.
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| Biochem Biophys Res Commun 220 : 1036-1042. 1996
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35 | LHCGR, PHLCH
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| Compound heterozygous mutations of the luteinizing hormone receptor gene in Leydig cell hypoplasia.
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| Laue LL, et al.
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| Mol Endocrinol 10 : 987-997. 1996
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36 | LHCGR
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| An inactivating mutation of the luteinizing hormone receptor causes amenorrhea in a 46,XX female.
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| Toledo SPA, et al.
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| J Clin Endocrinol Metab 81 : 3850-3854. 1996
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37 | PPML, LHCGR
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| Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene.
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| Kremer H, et al.
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| Nat Genet 9 : 160-164. 1995
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38 | LHCGR, PPML
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| Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious puberty.
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| Kosugi S, et al.
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| Hum Mol Genet 4 : 183-188. 1995
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39 | LHCGR, PPML
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| A novel mutation of the luteinizing hormone receptor gene causing male gonadotropin-independent precocious puberty.
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| Latronico AC, et al.
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| J Clin Endocrinol Metab 80 : 2490-2494. 1995
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40 | PPML, LHCGR
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| A missense mutation in the second transmembrane segment of the luteinizing hormone receptor causes familial male-limited precocious puberty.
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| Kraaij R, et al.
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| J Clin Endocrinol Metab 80 : 3168-3172. 1995
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41 | LHCGR, PPML
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| Identification of constitutively activating mutation of the luteinising hormone receptor in a family with male limited gonadotrophin independent precocious puberty (testotoxicosis).
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| Kawate N, et al.
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| J Med Genet 32 : 553-554. 1995
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42 | LHCGR, PHLCH
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| A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasia.
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| Laue L, et al.
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| Hum Mol Genet 4 : 1429-1433. 1995
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43 | LHCGR
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| Genetic heterogeneity of activating mutations of the luteinizing hormone receptor gene in familial male-limited precocious puberty. (abstr)
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| Laue L, et al.
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| Am J Hum Genet 55 : A228. 1994
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44 | LHCGR, PPML
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| Cosegregation of missense mutations of the luteinizing hormone receptor gene with familial male-limited precocious puberty.
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| Kremer H, et al.
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| Hum Mol Genet 2 : 1779-1783. 1993
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45 | LHCGR
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| A constitutively activating mutation of the luteinizing hormone receptor in familial male precocious puberty.
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| Shenker A, et al.
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| Nature 365 : 652-654. 1993
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46 | LHCGR, FSHR
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| The chromosomal localization of the human follicle-stimulating hormone receptor gene (FSHR) on 2p21-p16 is similar to that of the luteinizing hormone receptor gene.
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| Rousseau-Merck MF, et al.
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| Genomics 15 : 222-224. 1993
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47 | LHCGR
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| Localization of the human luteinizing hormone/chriogonadotropin receptor gene (LHCGR) to chromosome 2p21.
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| Rousseau-Merck MF, et al.
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| Cytogenet Cell Genet 54 : 77-79. 1990
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48 | LHCGR
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| Isolation of TSH and LH/CG receptor cDNAs from human thyroid: regulation by tissue specific splicing.
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| Frazier AL, Robbins LS, Stork PJ, Sprengel R, Segaloff DL, Cone RD.
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| Mol Endocrinol 4(8):1264-76. 1990
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49 | LHCGR
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| Cloning and sequencing of human LH/hCG receptor cDNA.
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| Minegishi T, Nakamura K, Takakura Y, Miyamoto K, Hasegawa Y, Ibuki Y, Igarashi M, Minegish T [corrected to Minegishi T.
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| Biochem Biophys Res Commun 172(3):1049-54. Erratum in: Biochem Biophys Res Commun 1994 Jun 15;201(2):1057. PMID: 2244890 1990
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