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