نتایج جستجو برای: kallmann syndrome

تعداد نتایج: 621960  

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2011
Paolo Emanuele Forni Carol Taylor-Burds Vida Senkus Melvin Trevor Williams Susan Wray

The origin of GnRH-1 cells and olfactory ensheathing cells has been controversial. Genetic Cre-lox lineage tracing of the neural crest (NC) versus ectodermal contribution to the developing nasal placode was performed using two complementary mouse models, the NC-specific Wnt1Cre mouse line and an ectodermal-specific Crect mouse line. Using these lines we prove that the NC give rise to the olfact...

Journal: :Reproductive biology 2011
Alessandro D Genazzani Susanna Santagni Elisa Chierchia Erika Rattighieri Annalisa Campedelli Alessia Prati Federica Ricchieri Tommaso Simoncini

Three Kallmann syndrome (KS) patients were examined to assess characteristics of LH response to GnRH bolus, with and without GnRH sensitization using Instantaneous Secretory Rate (ISR) computation before and after estriol treatment (60 days, 2 mg/day). Six healthy women were enrolled as controls and underwent GnRH bolus during the early follicular phase (days 3-5 of the menstrual cycle). After ...

Journal: :Biochimie 2021

Prokineticins are family of small proteins involved in many important biological processes including food intake and control energy balance. The prokineticin 2 (PROK2) is expressed several peripheral tissues areas the central nervous system. PROK2 activates G protein-coupled receptors, namely, receptor 1 (PROKR1) (PROKR2). Preclinical models exhibiting disturbances pathway (at level or its rece...

Atefeh Ahmadzadeh, Elahe Ghods, Majid Mojarrad, Mohammad Hassanzadeh Nazarabadi, Mojgan Afkhamizadeh, Robab Aboutorabi, Seyed Morteza Taghavi, Shokoofeh Bonakdaran, Zohreh Mosavi,

Idiopathic hypogonadotropic hypogonadism (IHH) is a condition caused by low doses of hypothalamic gonadotropin-releasing hormone (GnRH) leading to absence or incomplete sexual maturation. One of the disorders leading to IHH is Kallmann syndrome which is characterized by GnRH deficiency with anosmia or hyposmia. This disorder generally occurs as a hereditary syndrome with X-linked recessive inhe...

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