Results 81 to 90 of about 3,243 (180)
Genetic Polymorphisms of Prokineticins and Prokineticin Receptors Associated with Human Disease
Prokineticins (PKs) are low molecular weight proteins that exert their effects by binding to two seven-transmembrane G-protein-coupled receptors (prokineticin receptors, PKRs).
Roberta Lattanzi, Rossella Miele
doaj +1 more source
Targeted Gene Panel Sequencing for Molecular Diagnosis of Kallmann Syndrome and Normosmic Idiopathic Hypogonadotropic Hypogonadism [PDF]
Ja Hye Kim +7 more
openalex +1 more source
Testicular ultrasound in a patient with Kallmann syndrome: A case report
Daniela Donat +5 more
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Profiling, Bioinformatic, and Functional Data on the Developing Olfactory/GnRH System Reveal Cellular and Molecular Pathways Essential for This Process and Potentially Relevant for the Kallmann Syndrome [PDF]
Giulia Garaffo +10 more
openalex +1 more source
Hypogonadotropic Hypogonadism Revisited
Impaired testicular function, i.e., hypogonadism, can result from a primary testicular disorder (hypergonadotropic) or occur secondary to hypothalamic-pituitary dysfunction (hypogonadotropic).
Renato Fraietta +2 more
doaj
Kallmann综合征(Kallmann Syndrome,KS)又称促性腺激素分泌不足的性腺功能减退伴嗅觉丧失症,是一种先天性的遗传病。早期发现并及时给予激素替代治疗可使患者恢复性腺功能,部分患者可恢复生育力。本院在2008年收治两例KS患者,经KAL1基因分子筛查分析发现两例患者KAL1基因均有异常,现就两例KAL1基因突变的KS患者的临床表现及治疗进行报道如下。
李志 +5 more
doaj
The Kallmann syndrome gene product expressed in COS cells is cleaved on the cell surface to yield a diffusible component [PDF]
Elena I. Rugarli
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Kallmann syndrome is defined as the association of hypogonadotropic hypogonadism and anosmia or hyposmia caused by abnormal migration of olfactory axons and neurons producing gonadotropin-releasing hormone.
Azlansyah Azlansyah +6 more
doaj +1 more source
Olfactory Agenesis in Kallmann Syndrome (KS) [PDF]
Sahana Shetty +3 more
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