[HTML][HTML] The KiSS-1/GPR54 system: Essential roles in physiological homeostasis and cancer biology

N Zhu, M Zhao, Y Song, L Ding, Y Ni - Genes & diseases, 2022 - Elsevier
KiSS-1, first identified as an anti-metastasis gene in melanoma, encodes C-terminally
amidated peptide products, including kisspeptin-145, kisspeptin-54, kisspeptin-14 …

Генитальный эндометриоз

МИ Ярмолинская, ЭК Айламазян - 2017 - elibrary.ru
В книге рассматриваются современные взгляды о роли генетических, эндокринных и
иммунологических факторов в патогенезе генитального эндометриоза, обсуждаются …

KISS1R intracellular trafficking and degradation: effect of the Arg386Pro disease-associated mutation

SDC Bianco, L Vandepas, M Correa-Medina… - …, 2011 - academic.oup.com
The goal of this study was to investigate how the Arg386Pro mutation prolongs KiSS-1
receptor (KISS1R) responsiveness to kisspeptin, contributing to human central precocious …

Genetics of pubertal delay

T Saengkaew, SR Howard - Clinical endocrinology, 2022 - Wiley Online Library
The timing of pubertal development is strongly influenced by the genetic background, and
clinical presentations of delayed puberty are often found within families with clear patterns of …

Kisspeptins, estrogens and male fertility

R Chianese, G Cobellis, T Chioccarelli… - Current Medicinal …, 2016 - ingentaconnect.com
Background: The control of male fertility requires accurate endocrine, paracrine and
autocrine communications along the hypothalamus-pituitary-gonad (HPG) axis. In this …

Insights from the genetic characterization of central precocious puberty associated with multiple anomalies

APM Canton, ACV Krepischi… - Human …, 2021 - academic.oup.com
STUDY QUESTION Is there an (epi) genetic basis in patients with central precocious puberty
(CPP) associated with multiple anomalies that unmasks underlying mechanisms or reveals …

Mutational analysis of TAC3 and TACR3 genes in patients with idiopathic central pubertal disorders

C Tusset, SD Noel, EB Trarbach… - … de Endocrinologia & …, 2012 - SciELO Brasil
OBJECTIVE: To investigate the presence of variants in the TAC3 and TACR3 genes, which
encode NKB and its receptor (NK3R), respectively, in a large cohort of patients with …

Hypothalamic overexpression of makorin ring finger protein 3 results in delayed puberty in female mice

SA Roberts, L Naulé, S Chouman, T Johnson… - …, 2022 - academic.oup.com
Makorin ring finger protein 3 (MKRN3) is an important neuroendocrine player in the control
of pubertal timing and upstream inhibitor of gonadotropin-releasing hormone secretion. In …

Effects of childhood obesity and related genetic factors on precocious puberty: protocol for a multi-center prospective cohort study

T Yu, Y Yu, X Li, P Xue, X Yu, Y Chen, H Kong, C Lin… - BMC pediatrics, 2022 - Springer
Background Childhood obesity has important effects on the onset and development of
puberty. Although a number of studies have confirmed the relationship between obesity and …

A novel MKRN3 missense mutation causing familial precocious puberty

L De Vries, G Gat-Yablonski, N Dror… - Human …, 2014 - academic.oup.com
Central precocious puberty may be familial in about a quarter of the idiopathic cases.
However, little is known about the genetic causes responsible for the disorder. In this report …