The kisspeptin system in and beyond reproduction: Exploring intricate pathways and potential links between endometriosis and polycystic ovary syndrome

N Salmeri, P Viganò, P Cavoretto, R Marci… - Reviews in endocrine …, 2024 - Springer
Endometriosis and polycystic ovary syndrome (PCOS) are two common female reproductive
disorders with a significant impact on the health and quality of life of women affected. A …

The emerging therapeutic potential of kisspeptin and neurokinin B

B Patel, K Koysombat, EG Mills, J Tsoutsouki… - Endocrine …, 2024 - academic.oup.com
Kisspeptin (KP) and neurokinin B (NKB) are neuropeptides that govern the reproductive
endocrine axis through regulating hypothalamic gonadotropin-releasing hormone (GnRH) …

[HTML][HTML] Mini-Puberty, Physiological and Disordered: Consequences, and Potential for Therapeutic Replacement

J Rohayem, EC Alexander, S Heger… - Endocrine …, 2024 - academic.oup.com
There are 3 physiological waves of central hypothalamic-pituitary-gonadal (HPG) axis
activity over the lifetime. The first occurs during fetal life, the second—termed “mini-puberty” …

Molecular mechanisms in the etiology of polycystic ovary syndrome (PCOS): a multifaceted hypothesis towards the disease with potential therapeutics

KU Nisa, N Tarfeen, SA Mir, AA Waza… - Indian Journal of Clinical …, 2024 - Springer
Among the premenopausal women, Polycystic Ovary Syndrome (PCOS) is the most
prevalent endocrinopathy affecting the reproductive system and metabolic rhythms leading …

Diagnosis, Treatment, and Outcomes of Males with Central Precocious Puberty

R Robilliard, PA Lee, LS Topor - … and Metabolism Clinics, 2024 - endo.theclinics.com
The typical timing of male puberty begins between 9 and 14 years old, at an average age of
11.6 Æ 0.9 years. 1 Luteinizing hormone (LH), measured via an ultrasensitive assay, acts as …

The Genetic Etiology is a Relevant Cause of Central Precocious Puberty

APM Canton, CE Seraphim… - European Journal of …, 2024 - academic.oup.com
Objectives The etiology of central precocious puberty (CPP) has expanded with
identification of new genetic causes, including the monogenic deficiency of MKRN3. We …

[PDF][PDF] Altered pubertal timing in 7q11. 23 copy number variations and associated genetic mechanisms

SM Wei, MD Gregory, T Nash, AA e Gouvêa, CB Mervis… - Iscience, 2024 - cell.com
Pubertal timing, including age at menarche (AAM), is a heritable trait linked to lifetime health
outcomes. Here, we investigate genetic mechanisms underlying AAM by combining GWAS …

[HTML][HTML] Human-specific epigenomic states in spermatogenesis

C Liao, BW Walters, M DiStasio, BJ Lesch - Computational and Structural …, 2024 - Elsevier
Infertility is becoming increasingly common, affecting one in six people globally. Half of
these cases can be attributed to male factors, many driven by abnormalities in the process of …

Relevance of augmented kisspeptin signaling through H364 KISS1R in central precocious puberty

AA Banerjee, SR Bhanarkar, R Keshwani, S Pande… - Gene, 2024 - Elsevier
Understanding the pathophysiology of idiopathic central precocious puberty (ICPP) is
essential, in view of its consequences on reproductive health and metabolic disorders in …

Novel variants ensued genomic imprinting in familial central precocious puberty

V Karaman, E Karakilic-Ozturan, S Poyrazoglu… - Journal of …, 2024 - Springer
Methods Eighteen familial CPP cases were investigated by Sanger sequencing for five CPP-
related genes; DLK1, KISS1, KISS1R, MKRN3, and PROKR2. Segregation analysis was …