Results 71 to 80 of about 2,190 (162)
INSL3 Variation in Dogs Following Suppression and Recovery of the HPG Axis
Insulin-like peptide 3 (INSL3) is a constitutive product of mature, adult-type Leydig cells of the testes and consequently in most mammals is an ideal biomarker with which to monitor pubertal development.
Ravinder Anand-Ivell +5 more
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Biomarcadores de hipogonadismo masculino en la infancia y la adolescencia
El eje hipotálamo-hipófiso-testicular es activo en la vida fetal y durante los primeros meses de la vida posnatal: la hipófisis secreta hormona luteinizante (LH) y folículo-estimulante (FSH), mientras que el testículo produce testosterona y factor ...
Rey Rodolfo A.
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Relaxin family peptide receptor 2 (RXFP2) is a GPCR known for its role in reproductive function. It is structurally related to the human relaxin receptor RXFP1 and can be activated by human gene-2 (H2) relaxin as well as its cognate ligand insulin-like ...
Shoni Bruell +9 more
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Relaxin, a heterodimeric polypeptide hormone, is a key regulator of collagen metabolism and multiple vascular control pathways in humans and rodents.
Linda eChan +17 more
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Background In recent years, the relaxin family of signaling molecules has been shown to play diverse roles in mammalian physiology, but little is known about its diversity or physiology in teleosts, an infraclass of the bony fishes comprising ~ 50% of ...
Glen Peter +6 more
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Testicular Dysgenesis Syndrome (TDS) encompasses a spectrum of male reproductive disorders that originate during fetal development. Among the critical players in testicular morphogenesis, fetal Leydig cells perform essential functions through the ...
Ajitha E. Veluthakunju +9 more
doaj +1 more source
Proliferation and differentiation of adult Leydig cells are mainly completed in puberty. In many studies, apart from normal postnatal development process, it is widely indicated that, through administrating EDS, Leydig cell population is eliminated and ...
Gulfidan Coskun +5 more
doaj +1 more source
Novel INSL3 variants cause male infertility with cryptorchidism
Cryptorchidism is one of the most prevalent male congenital abnormalities, affecting 1.6%-9% of newborn males, and it poses substantial risks to male fertility. INSL3 and its receptor RXFP2 play a major role in the first phase of the biphasic testicular descent process.
Chunjia Wei +10 more
openaire +2 more sources
Prenatal di(2-ethylhexyl) phthalate (DEHP) exposure can produce reproductive toxicity in animal models. Only limited data exist from human studies on maternal DEHP exposure and its effects on infants.
Atsuko Araki +10 more
doaj +1 more source
Cryptorchidism, a common congenital condition in male children, has been associated with impaired testicular function and increased risk of infertility.
Derya Ayvaci +4 more
doaj +1 more source

