Pages that link to "Q28281736"
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The following pages link to Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH) (Q28281736):
Displaying 50 items.
- Genetics of isolated hypogonadotropic hypogonadism: role of GnRH receptor and other genes (Q21296724) (← links)
- NELF is a nuclear protein involved in hypothalamic GnRH neuronal migration (Q24292996) (← links)
- WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome (Q24301463) (← links)
- Human GnRH deficiency: a unique disease model to unravel the ontogeny of GnRH neurons (Q24628946) (← links)
- From nose to brain: development of gonadotrophin-releasing hormone-1 neurones (Q24633621) (← links)
- Digenic mutations account for variable phenotypes in idiopathic hypogonadotropic hypogonadism (Q24675675) (← links)
- Central hypogonadotropic hypogonadism: genetic complexity of a complex disease (Q26852830) (← links)
- A Jacob/Nsmf Gene Knockout Results in Hippocampal Dysplasia and Impaired BDNF Signaling in Dendritogenesis (Q27309053) (← links)
- Expanding the phenotype and genotype of female GnRH deficiency (Q28386577) (← links)
- Commentary: the year in endocrine genetics for basic scientists (Q28394555) (← links)
- hypogonadotropic hypogonadism 9 with or without anosmia (Q30989720) (← links)
- Genetic determinants of pubertal timing in the general population. (Q33937715) (← links)
- TAC3/TACR3 mutations reveal preferential activation of gonadotropin-releasing hormone release by neurokinin B in neonatal life followed by reversal in adulthood (Q33984838) (← links)
- Oligogenic basis of isolated gonadotropin-releasing hormone deficiency. (Q34093958) (← links)
- Gonadotropin-releasing hormone (GnRH) neuron migration: initiation, maintenance and cessation as critical steps to ensure normal reproductive function (Q34433460) (← links)
- Cellular distribution of the NMDA-receptor activated synapto-nuclear messenger Jacob in the rat brain. (Q34641571) (← links)
- Biochemical and MRI findings of Kallmann's syndrome. (Q34691952) (← links)
- The consequences of mutations in the reproductive endocrine system (Q34804436) (← links)
- Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring (Q35108596) (← links)
- Incidence, phenotypic features and molecular genetics of Kallmann syndrome in Finland (Q35126506) (← links)
- Dysfunctional SEMA3E signaling underlies gonadotropin-releasing hormone neuron deficiency in Kallmann syndrome (Q35836124) (← links)
- When genetic load does not correlate with phenotypic spectrum: lessons from the GnRH receptor (GNRHR). (Q36201503) (← links)
- Discovering Genes Essential to the Hypothalamic Regulation of Human Reproduction Using a Human Disease Model: Adjusting to Life in the "-Omics" Era. (Q36433718) (← links)
- Responsiveness to a physiological regimen of GnRH therapy and relation to genotype in women with isolated hypogonadotropic hypogonadism (Q36589407) (← links)
- Molecular pathogenesis of Kallmann's syndrome. (Q36693337) (← links)
- Mutations along the hypothalamic-pituitary-gonadal axis affecting male reproduction (Q37026012) (← links)
- Genetics of puberty (Q37050042) (← links)
- The kisspeptin signaling pathway and its role in human isolated GnRH deficiency (Q37069536) (← links)
- New understandings of the genetic basis of isolated idiopathic central hypogonadism. (Q37074564) (← links)
- Clinical manifestations of impaired GnRH neuron development and function (Q37078042) (← links)
- Clinical assessment and genomic landscape of a consanguineous family with three Kallmann syndrome descendants (Q37084804) (← links)
- What do we learn from the murine Jacob/Nsmf gene knockout for human disease? (Q37350991) (← links)
- Nasal embryonic LHRH factor (NELF) mutations in patients with normosmic hypogonadotropic hypogonadism and Kallmann syndrome. (Q37466322) (← links)
- Differential expression of nasal embryonic LHRH factor (NELF) variants in immortalized GnRH neuronal cell lines (Q37595685) (← links)
- Deciphering genetic disease in the genomic era: the model of GnRH deficiency. (Q37605836) (← links)
- CPDadh: a new peptidase family homologous to the cysteine protease domain in bacterial MARTX toxins (Q41856688) (← links)
- Identification of two novel missense mutations in the KAL1 gene in Han Chinese subjects with Kallmann Syndrome (Q44374594) (← links)
- Olfactory ensheathing cells form the microenvironment of migrating GnRH-1 neurons during mouse development (Q45752415) (← links)
- Nasal embryonic LHRH factor plays a role in the developmental migration and projection of gonadotropin-releasing hormone 3 neurons in zebrafish. (Q47073750) (← links)
- Kallmann syndrome: phenotype and genotype of hypogonadotropic hypogonadism (Q50133432) (← links)
- Clinical assessment and molecular analysis of GnRHR and KAL1 genes in males with idiopathic hypogonadotrophic hypogonadism. (Q50459589) (← links)
- Normosmic idiopathic hypogonadotropic hypogonadism due to a novel homozygous nonsense c.C969A (p.Y323X) mutation in the KISS1R gene in three unrelated families. (Q51110573) (← links)
- [Genetics of anterior hypopituitary diseases] (Q81909612) (← links)
- Discovering Genes Essential to the Hypothalamic Regulation of Human Reproduction Using a Human Disease Model: Adjusting to Life in the "-Omics" Era (Q87993928) (← links)
- Genetics of congenital hypogonadotropic hypogonadism: peculiarities and phenotype of an oligogenic disease (Q90569848) (← links)
- An association with hypopituitarism and 9q subtelomere deletion syndrome (Q90624174) (← links)
- Molecular genetic diagnostics of hypogonadotropic hypogonadism: from panel design towards result interpretation in clinical practice (Q90722916) (← links)
- A TAC3 Missense Variant in a Domestic Shorthair Cat with Testicular Hypoplasia and Persistent Primary Dentition (Q90724638) (← links)
- Nasal Placode Development, GnRH Neuronal Migration and Kallmann Syndrome (Q92243130) (← links)
- DLG2 variants in patients with pubertal disorders (Q93271163) (← links)