The Episodic secretion of hormones |
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Insight Into the Ontogeny of GnRH Neurons From Patients Born Without a Nose |
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Insights into hypothalamic-pituitary dysfunction in polycystic ovary syndrome. |
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Interpulse interval of GnRH stimulation independently modulates LH secretion |
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Interpulse interval sequence of LH in normal men essentially constitutes a renewal process |
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Is GnRH reduced at the midcycle surge in the human? Evidence from a GnRH-deficient model. |
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Isolated GnRH deficiency: a disease model serving as a unique prism into the systems biology of the GnRH neuronal network |
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Kisspeptin and GPR54: discovery of a novel pathway in reproduction |
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Kisspeptin resets the hypothalamic GnRH clock in men. |
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The longitudinal study of adrenal maturation during gonadal suppression: evidence that adrenarche is a gradual process |
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Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism |
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Luteinizing hormone-secreting pituitary tumor: biosynthetic characterization and clinical studies |
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Mass spectrometric and physiological validation of a sensitive, automated, direct immunoassay for serum estradiol using the Architect |
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The midcycle gonadotropin surge in normal women occurs in the face of an unchanging gonadotropin-releasing hormone pulse frequency |
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Modeling mutant/wild-type interactions to ascertain pathogenicity of PROKR2 missense variants in patients with isolated GnRH deficiency. |
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Modes of action of GnRH and GnRH analogs |
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Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay |
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Mutations in FGF17, IL17RD, DUSP6, SPRY4, and FLRT3 are identified in individuals with congenital hypogonadotropic hypogonadism |
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Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin-releasing hormone deficiency: molecular genetics and clinical spectrum. |
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The natural history of autonomous gonadal function, adrenarche, and central puberty in gonadotropin-independent precocious puberty. |
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Neuroendocrine-gonadal axis in men: frequent sampling of LH, FSH, and testosterone |
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Neuroendocrine, gonadal, placental, and obstetric phenotypes in patients with IHH and mutations in the G-protein coupled receptor, GPR54. |
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Neuroendocrine regulation of the corpus luteum in the human. Evidence for pulsatile progesterone secretion |
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New genes controlling human reproduction and how you find them |
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An overview of LHRH and its analogues: clinical uses |
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Perifused pituitary cultures: a model for LHRH regulation of LH secretion |
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Perifusion of rat pituitary cells with gonadotropin-releasing hormone, activin, and inhibin reveals distinct effects on gonadotropin gene expression and secretion |
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Perspective: the importance of genetic defects in humans in elucidating the complexities of the hypothalamic-pituitary-gonadal axis |
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Pituitary and gonadal responsiveness is enhanced during GnRH-induced puberty |
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Pituitary luteinizing hormone responses to intravenous and subcutaneous administration of gonadotropin-releasing hormone in men. |
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Polycystic ovarian morphology with regular ovulatory cycles: insights into the pathophysiology of polycystic ovarian syndrome |
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Potential for fertility with replacement of hypothalamic gonadotropin-releasing hormone in long term female survivors of cranial tumors |
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Precursors of alpha-inhibin modulate follicle-stimulating hormone receptor binding and biological activity |
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Predictors of outcome of long-term GnRH therapy in men with idiopathic hypogonadotropic hypogonadism. |
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Prioritizing genetic testing in patients with Kallmann syndrome using clinical phenotypes |
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Pubertal timing predicts adult psychosexuality: Evidence from typically developing adults and adults with isolated GnRH deficiency |
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Pulsatile gonadotropin-releasing hormone modifies polyadenylation of gonadotropin subunit messenger ribonucleic acids |
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Relative roles of inhibin B and sex steroids in the negative feedback regulation of follicle-stimulating hormone in men across the full spectrum of seminiferous epithelium function |
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Relatively low levels of dimeric inhibin circulate in men and women with polycystic ovarian syndrome using a specific two-site enzyme-linked immunosorbent assay |
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The Reproductive Endocrine Associates of the Massachusetts General Hospital: fifteen years of integrated clinical practice and investigation. |
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Reproductive endocrine phenotypes relating to CHD7 mutations in humans. |
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Responsiveness to a physiological regimen of GnRH therapy and relation to genotype in women with isolated hypogonadotropic hypogonadism |
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Reversible kallmann syndrome, delayed puberty, and isolated anosmia occurring in a single family with a mutation in the fibroblast growth factor receptor 1 gene |
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A role for kisspeptins in the regulation of gonadotropin secretion in the mouse. |
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The role of prior pubertal development, biochemical markers of testicular maturation, and genetics in elucidating the phenotypic heterogeneity of idiopathic hypogonadotropic hypogonadism |
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Role of seminiferous tubular development in determining the FSH versus LH responsiveness to GnRH in early sexual maturation |
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The role of the prokineticin 2 pathway in human reproduction: evidence from the study of human and murine gene mutations |
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Safety of frequent venous blood sampling in a pediatric research population |
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SAT-LB071 Loss of Function |
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Sensitivity differences in reproductive/endocrine organs to chronically administered LHRH agonists in female rats |
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Simulation of the normal menstrual cycle in Kallman's syndrome by pulsatile administration of luteinizing hormone-releasing hormone (LHRH) |
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SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome |
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Spatial ability in androgen-deficient men. |
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The spectrum of abnormal patterns of gonadotropin-releasing hormone secretion in men with idiopathic hypogonadotropic hypogonadism: clinical and laboratory correlations |
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The study of GnRH control of reproductive function |
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Successful use of pulsatile gonadotropin-releasing hormone (GnRH) for ovulation induction and pregnancy in a patient with GnRH receptor mutations |
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SUN-219 Human Congenital Arhinia Is Associated with GnRH Deficiency and Primary Testicular Defects. |
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TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood |
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TCF12 haploinsufficiency causes autosomal dominant Kallmann syndrome and reveals network-level interactions between causal loci |
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Timing of peripubertal steroid exposure predicts visuospatial cognition in men: Evidence from three samples |
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Trial of recombinant follicle-stimulating hormone pretreatment for GnRH-induced fertility in patients with congenital hypogonadotropic hypogonadism |
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Utility of free alpha-subunit as an alternative neuroendocrine marker of gonadotropin-releasing hormone (GnRH) stimulation of the gonadotroph in the human: evidence from normal and GnRH-deficient men. |
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Validation of highly specific and sensitive radioimmunoassays for lutropin, follitropin, and free alpha subunit in unextracted urine |
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Variable tolerance of the developing follicle and corpus luteum to gonadotropin-releasing hormone antagonist-induced gonadotropin withdrawal in the human |
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Variants in DENND1A are associated with polycystic ovary syndrome in women of European ancestry |
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When genetic load does not correlate with phenotypic spectrum: lessons from the GnRH receptor (GNRHR). |
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