| scholarly article | Q13442814 |
| review article | Q7318358 |
| P2093 | author name string | Ursula B Kaiser | |
| Sekoni D Noel | |||
| P2860 | cites work | The human gonadotropin releasing hormone type I receptor is a functional intracellular GPCR expressed on the nuclear membrane | Q21091123 |
| Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2 | Q21092497 | ||
| Identification of two prokineticin cDNAs: recombinant proteins potently contract gastrointestinal smooth muscle | Q24290954 | ||
| Localization and function of NK(3) subtype tachykinin receptors of layer V pyramidal neurons of the guinea-pig medial prefrontal cortex | Q46359689 | ||
| MIT(1), a black mamba toxin with a new and highly potent activity on intestinal contraction | Q46884413 | ||
| Peripheral administration of metastin induces marked gonadotropin release and ovulation in the rat. | Q47284944 | ||
| A role for kisspeptins in the regulation of gonadotropin secretion in the mouse. | Q47289867 | ||
| The KiSS-1 receptor GPR54 is essential for the development of the murine reproductive system | Q47346849 | ||
| Chromosomal localization of the gonadotropin-releasing hormone receptor gene to human chromosome 4q13.1-q21.1 and mouse chromosome 5. | Q48148662 | ||
| A novel loss-of-function mutation in GPR54/KISS1R leads to hypogonadotropic hypogonadism in a highly consanguineous family. | Q51522144 | ||
| Coding sequence analysis of GNRHR and GPR54 in patients with congenital and adult-onset forms of hypogonadotropic hypogonadism. | Q51778413 | ||
| Two novel GnRHR gene mutations in two siblings with hypogonadotropic hypogonadism. | Q51793940 | ||
| Mutations in gonadotropin-releasing hormone receptor gene cause hypogonadotropic hypogonadism. | Q55067328 | ||
| A novel homozygous splice acceptor site mutation of KISS1R in two siblings with normosmic isolated hypogonadotropic hypogonadism | Q57632449 | ||
| Loss-of-Function Mutations in the Genes Encoding Prokineticin-2 or Prokineticin Receptor-2 Cause Autosomal Recessive Kallmann Syndrome | Q57632541 | ||
| Molecular Genetic Analysis of Normosmic Hypogonadotropic Hypogonadism in a Turkish Population: Identification and Detailed Functional Characterization of a Novel Mutation in the Gonadotropin-Releasing Hormone Receptor Gene | Q57840283 | ||
| A reciprocal mutation supports helix 2 and helix 7 proximity in the gonadotropin-releasing hormone receptor | Q72258557 | ||
| Introduction: molecular chaperones of the ER: their role in protein folding and genetic disease | Q73271459 | ||
| Prevalence, phenotypic spectrum, and modes of inheritance of gonadotropin-releasing hormone receptor mutations in idiopathic hypogonadotropic hypogonadism | Q73739026 | ||
| Molecular mechanisms of G protein-coupled receptor desensitization and resensitization | Q74539372 | ||
| Molecular basis of receptor/G-protein-coupling selectivity | Q77795096 | ||
| Influence of a species-specific extracellular amino acid on expression and function of the human gonadotropin-releasing hormone receptor | Q77915046 | ||
| Neuroendocrine phenotype analysis in five patients with isolated hypogonadotropic hypogonadism due to a L102P inactivating mutation of GPR54 | Q79428657 | ||
| Kallmann syndrome | Q79790438 | ||
| The prevalence of gonadotropin-releasing hormone receptor mutations in a large cohort of patients with hypogonadotropic hypogonadism | Q81328788 | ||
| Oligogenic basis of isolated gonadotropin-releasing hormone deficiency. | Q34093958 | ||
| An mRNA surveillance mechanism that eliminates transcripts lacking termination codons | Q34120142 | ||
| Quality control of mRNA function | Q34156109 | ||
| Cloning and functional expression of a mouse gonadotropin-releasing hormone receptor | Q34237048 | ||
| Membrane trafficking of G protein-coupled receptors | Q34292577 | ||
| The human gonadotropin-releasing hormone (GnRH) receptor gene: cloning, genomic organization and chromosomal assignment | Q34325430 | ||
| Identification of highly expressed genes in metastasis-suppressed chromosome 6/human malignant melanoma hybrid cells using subtractive hybridization and differential display | Q34429046 | ||
| A family with hypogonadotropic hypogonadism and mutations in the gonadotropin-releasing hormone receptor | Q34446712 | ||
| Using automated imaging to interrogate gonadotrophin-releasing hormone receptor trafficking and function. | Q34494645 | ||
| Inactivating mutations of G protein-coupled receptors and diseases: structure-function insights and therapeutic implications. | Q34514122 | ||
| Abnormal development of the olfactory bulb and reproductive system in mice lacking prokineticin receptor PKR2 | Q34572987 | ||
| Mutations in the human gonadotropin-releasing hormone receptor: insights into receptor biology and function | Q34665597 | ||
| KISS1R intracellular trafficking and degradation: effect of the Arg386Pro disease-associated mutation. | Q34697009 | ||
| Postmenopausal hypertrophy of neurons expressing the estrogen receptor gene in the human hypothalamus | Q34736716 | ||
| Biochemical mechanism of pathogenesis of human gonadotropin-releasing hormone receptor mutants Thr104Ile and Tyr108Cys associated with familial hypogonadotropic hypogonadism | Q34774581 | ||
| Protein aggregation in disease: a role for folding intermediates forming specific multimeric interactions | Q34815754 | ||
| TAC3 and TACR3 mutations in familial hypogonadotropic hypogonadism reveal a key role for Neurokinin B in the central control of reproduction | Q34902985 | ||
| Hypogonadotropic hypogonadism due to a novel missense mutation in the first extracellular loop of the neurokinin B receptor. | Q35014404 | ||
| A homozygous R262Q mutation in the gonadotropin-releasing hormone receptor presenting as constitutional delay of growth and puberty with subsequent borderline oligospermia | Q35783009 | ||
| Olfactory bulb hypoplasia in Prokr2 null mice stems from defective neuronal progenitor migration and differentiation. | Q36432101 | ||
| Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum. | Q36938312 | ||
| Menopause and the human hypothalamus: evidence for the role of kisspeptin/neurokinin B neurons in the regulation of estrogen negative feedback | Q37076705 | ||
| Non-syndromic congenital hypogonadotropic hypogonadism: clinical presentation and genotype-phenotype relationships | Q37704009 | ||
| Mechanism of action of gonadotropin releasing hormone | Q39501715 | ||
| The molecular basis of gonadotropin-releasing hormone (GnRH) action in the pituitary gonadotrope | Q39508463 | ||
| Disease-causing mutation in GPR54 reveals the importance of the second intracellular loop for class A G-protein-coupled receptor function | Q39943167 | ||
| Seminal anti-Müllerian hormone level is a marker of spermatogenic response during long-term gonadotropin therapy in male hypogonadotropic hypogonadism. | Q40113395 | ||
| Mutation Ala(171)Thr stabilizes the gonadotropin-releasing hormone receptor in its inactive conformation, causing familial hypogonadotropic hypogonadism. | Q40657960 | ||
| Structure and function of receptors coupled to G proteins | Q40668280 | ||
| Studies of gonadotropin-releasing hormone (GnRH) action using GnRH receptor-expressing pituitary cell lines | Q41130838 | ||
| Two novel mutations in the gonadotropin-releasing hormone receptor gene in Brazilian patients with hypogonadotropic hypogonadism and normal olfaction. | Q42505552 | ||
| A comparative phenotypic study of kallmann syndrome patients carrying monoallelic and biallelic mutations in the prokineticin 2 or prokineticin receptor 2 genes | Q43214533 | ||
| The fertile eunuch variant of idiopathic hypogonadotropic hypogonadism: spontaneous reversal associated with a homozygous mutation in the gonadotropin-releasing hormone receptor | Q43633820 | ||
| Spontaneous pregnancy in a patient who was homozygous for the Q106R mutation in the gonadotropin-releasing hormone receptor gene | Q44022898 | ||
| Rescue of hypogonadotropic hypogonadism-causing and manufactured GnRH receptor mutants by a specific protein-folding template: misrouted proteins as a novel disease etiology and therapeutic target | Q44055174 | ||
| Four naturally occurring mutations in the human GnRH receptor affect ligand binding and receptor function | Q44532281 | ||
| GNRHR mutations in a woman with idiopathic hypogonadotropic hypogonadism highlight the differential sensitivity of luteinizing hormone and follicle-stimulating hormone to gonadotropin-releasing hormone | Q44968726 | ||
| Two novel missense mutations in g protein-coupled receptor 54 in a patient with hypogonadotropic hypogonadism. | Q45187029 | ||
| Suppression of metastasis in human breast carcinoma MDA-MB-435 cells after transfection with the metastasis suppressor gene, KiSS-1 | Q24311474 | ||
| Cloning and characterization of the human GnRH receptor | Q24314839 | ||
| PROKR2 missense mutations associated with Kallmann syndrome impair receptor signalling activity | Q24317396 | ||
| Increased hypothalamic GPR54 signaling: a potential mechanism for initiation of puberty in primates | Q24556670 | ||
| I-TASSER: a unified platform for automated protein structure and function prediction | Q24605680 | ||
| Mutations of the KISS1 gene in disorders of puberty | Q24618754 | ||
| Hypogonadotropic hypogonadism due to loss of function of the KiSS1-derived peptide receptor GPR54 | Q24685744 | ||
| Exosome-mediated recognition and degradation of mRNAs lacking a termination codon | Q27939297 | ||
| Identification of G protein-coupled receptor genes from the human genome sequence | Q28202262 | ||
| Molecular chaperones in the cytosol: from nascent chain to folded protein | Q28205903 | ||
| The GPR54 gene as a regulator of puberty | Q28211950 | ||
| Human genetics of GPR54 | Q28291184 | ||
| Tachykinins: receptor to effector | Q28297263 | ||
| KiSS-1, a novel human malignant melanoma metastasis-suppressor gene | Q28298463 | ||
| Molecular cloning and expression of cDNA encoding the murine gonadotropin-releasing hormone receptor | Q28326858 | ||
| The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations | Q28385113 | ||
| Prokineticin 2 transmits the behavioural circadian rhythm of the suprachiasmatic nucleus | Q28509233 | ||
| Cloning, sequencing, and expression of human gonadotropin releasing hormone (GnRH) receptor | Q28645650 | ||
| The structure and function of G-protein-coupled receptors | Q29616792 | ||
| Setting the standards: quality control in the secretory pathway | Q29620321 | ||
| Biological activity and pathological implications of misfolded proteins. | Q30322243 | ||
| I-TASSER: fully automated protein structure prediction in CASP8 | Q30380936 | ||
| Unraveling the structure and function of G protein-coupled receptors through NMR spectroscopy. | Q30383769 | ||
| Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism | Q30442563 | ||
| Importance of the extracellular loops in G protein-coupled receptors for ligand recognition and receptor activation | Q30522852 | ||
| Regulation of GPR54 signaling by GRK2 and {beta}-arrestin | Q33642051 | ||
| GPR54 regulates ERK1/2 activity and hypothalamic gene expression in a Gα(q/11) and β-arrestin-dependent manner | Q33707710 | ||
| A GPR54-activating mutation in a patient with central precocious puberty. | Q33811648 | ||
| The genetic and molecular basis of idiopathic hypogonadotropic hypogonadism | Q33830319 | ||
| Activation of MAPK cascades by G-protein-coupled receptors: the case of gonadotropin-releasing hormone receptor | Q33856613 | ||
| Complete hypogonadotropic hypogonadism associated with a novel inactivating mutation of the gonadotropin-releasing hormone receptor | Q33877145 | ||
| TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood | Q33984838 | ||
| The year in G protein-coupled receptor research | Q34088801 | ||
| P433 | issue | 1-2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | G protein-coupled receptor | Q38173 |
| P304 | page(s) | 91-101 | |
| P577 | publication date | 2011-06-29 | |
| P1433 | published in | Molecular and Cellular Endocrinology | Q1573600 |
| P1476 | title | G protein-coupled receptors involved in GnRH regulation: molecular insights from human disease | |
| P478 | volume | 346 |
| Q38755269 | Characterization of Gonadotrope Secretoproteome Identifies Neurosecretory Protein VGF-derived Peptide Suppression of Follicle-stimulating Hormone Gene Expression |
| Q36385294 | Computational Analysis of Missense Variants of G Protein-Coupled Receptors Involved in the Neuroendocrine Regulation of Reproduction |
| Q44838301 | Declining age of puberty of school girls in southern Thailand |
| Q87993928 | Discovering Genes Essential to the Hypothalamic Regulation of Human Reproduction Using a Human Disease Model: Adjusting to Life in the "-Omics" Era |
| Q36433718 | Discovering Genes Essential to the Hypothalamic Regulation of Human Reproduction Using a Human Disease Model: Adjusting to Life in the "-Omics" Era. |
| Q27342884 | GPCRs Direct Germline Development and Somatic Gonad Function in Planarians |
| Q47656518 | Gain-of-function mutations in G-protein-coupled receptor genes associated with human endocrine disorders. |
| Q47157987 | GnRH receptor gene mutations in adolescents and young adults presenting with signs of partial gonadotropin deficiency |
| Q55262023 | GnRH-(1-5) Inhibits TGF-β Signaling to Regulate the Migration of Immortalized Gonadotropin-Releasing Hormone Neurons. |
| Q36463613 | Mechanisms underlying the tissue-specific and regulated activity of the Gnrhr promoter in mammals. |
| Q41992967 | Paradoxical gain-of-function mutant of the G-protein-coupled receptor PROKR2 promotes early puberty |
| Q52608499 | STAT6, PBX2, and PBRM1 Emerge as Predicted Regulators of 452 Differentially Expressed Genes Associated With Puberty in Brahman Heifers. |
| Q36989279 | The Novel Actions of the Metabolite GnRH-(1-5) are Mediated by a G Protein-Coupled Receptor. |
| Q41134167 | The retinoblastoma protein regulates hypoxia-inducible genetic programs, tumor cell invasiveness and neuroendocrine differentiation in prostate cancer cells |
| Q28485191 | Two families with normosmic congenital hypogonadotropic hypogonadism and biallelic mutations in KISS1R (KISS1 receptor): clinical evaluation and molecular characterization of a novel mutation |
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