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Organizing biological data
Genome sequencing reveals novel causative structural and single nucleotide variants in Pakistani families with congenital hypogonadotropic hypogonadism
novel CHH causing variants found in Pakistani families
Stem Leydig cells support macrophage immunological homeostasis through intercellular mitochondria transfer in a TRPM7-mediated manner in the testis
Illuminating the terminal nerve: Uncovering the link between GnRH-1 neuron and olfactory development
A case of Culler-Jones syndrome caused by a novel mutation of GLI2 gene and literature review
Intra-pituitary follicle-stimulating hormone signaling regulates hepatic lipid metabolism
Homo sapiens
Gene analysis of a patient with combined pituitary hormone deficiency
Transcriptomic analysis of MA-10 Leydig cells treated with sinapic acid phenethyl ester
Precise Correction of Lhcgr Mutation in Stem Leydig Cells by Prime Editing Rescues Hereditary Primary Hypogonadism in Mice
Convergent pathways underlying the Kallmann syndrome-linked genes Hs6st1 and Fgfr1
Steroidogenic factor 1 regulates transcription of the inhibin B co-receptor in pituitary gonadotrope cells
Hypoganodotropic hypogonadism diagnosis by NGS
Mus musculus
Transcriptomic analysis of MA-10 Leydig cells treated with gigantol
Rattus norvegicus strain:SD
Targeted epigenetic reprogramming of endogenous loci by CRISPR/Cas9-based transcriptional activators directly converts fibroblasts to Leydig cells
Rattus norvegicus breed:Sprague-Dawley
Rattus norvegicus breed:Sprague-Dawley Raw sequence reads
Effect of Xq28 deletion on hypergonadotropic hypogonadism
Genetic etiologies of GnRH deficiency
RNA and cell free miRNA in one family of Kallmann's syndrome
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