Evidence map›Paper›PMID 35328752›Full record

ReviewInternational journal of molecular sciences2022

Aberrant Notch Signaling Pathway as a Potential Mechanism of Central Precocious Puberty.

Young Suk Shim, Hae Sang Lee, Jin Soon Hwang

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Review
  2. Association Study BetweenInternational journal of molecular sciences · 2026
    Article
  3. Role of astrocytes in the pathogenesis of perinatal brain injury.Molecular medicine (Cambridge, Mass.) · 2025
    Review
  4. Current research of the Notch pathway in hepatocellular carcinoma.European journal of medical research · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. MFNG is an independent prognostic marker for osteosarcoma.European journal of medical research · 2023
    Article
  11. Review
  12. Gonadotropin Cell Transduction Mechanisms.International journal of molecular sciences · 2022
    Article
  13. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Young Suk ShimDepartment of Pediatrics, Ajou University School of Medicine, Suwon 164999, Korea.
Hae Sang LeeDepartment of Pediatrics, Ajou University School of Medicine, Suwon 164999, Korea.ORCID 0000-0002-9684-4042
Jin Soon HwangDepartment of Pediatrics, Ajou University School of Medicine, Suwon 164999, Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Notch signaling pathway is highly conserved during evolution. It has been well documented that Notch signaling regulates cell proliferation, migration, and death in the nervous, cardiac, and endocrine systems. The Notch pathway is relatively simple, but its activity is regulated by numerous complex mechanisms. Ligands bind to Notch receptors, inducing their activation and cleavage. Various post-translational processes regulate Notch signaling by affecting the synthesis, secretion, activation, and degradation of Notch pathway-related proteins. Through such post-translational regulatory processes, Notch signaling has versatile effects in many tissues, including the hypothalamus. Recently, several studies have reported that mutations in genes related to the Notch signaling pathway were found in patients with central precocious puberty (CPP). CPP is characterized by the early activation of the hypothalamus-pituitary-gonadal (HPG) axis. Although genetic factors play an important role in CPP development, few associated genetic variants have been identified. Aberrant Notch signaling may be associated with abnormal pubertal development. In this review, we discuss the current knowledge about the role of the Notch signaling pathway in puberty and consider the potential mechanisms underlying CPP.

Indexed as

Puberty, PrecociousHumansMutationPubertyReceptors, NotchSignal TransductionReceptors, Notchcentral precocious pubertyetiologyNotch signaling pathwaypuberty

Identifiers

PMID35328752
PMCPMC8950842

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.