Evidence map›Paper›PMID 28778954›Full record

ArticleEMBO molecular medicine2017

β-Klotho sustains postnatal GnRH biology and spins the thread of puberty.

Micheline Misrahi

Open access · goldAbstract readComment
In one paragraph

Article in EMBO molecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.2field-weighted citation impact, top 44% of its field
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

6 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Article
  6. Nasal Placode Development, GnRH Neuronal Migration and Kallmann Syndrome.Frontiers in cell and developmental biology · 2019
    Article
4 · The record

Corrections and comments

  • Comment on
    2017
5 · Who and what money

Authors and funding

1 author at 1 institution in 1 country.

Micheline MisrahiMedical Faculty Hospital Bicêtre, Université Paris Sud, Le Kremlin Bicêtre, France.ORCID 0000-0002-5379-8859
Université Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hypogonadotropic hypogonadism is a syndrome found to be isolated (IHH) or associated with anosmia, corresponding to the Kallmann syndrome (KS). It comprises a defect in gonadotropin-releasing hormone (GnRH) secretion and absent or delayed puberty. Genetic causes have been identified with a high genetic heterogeneity. Fibroblast growth factor receptor 1 (FGFR1), a tyrosine kinase receptor, was one of the first genes whose mutations were identified as causative in KS FGFR1 is responsible for the formation of the GnRH neuron system. Studying patients has not only allowed the identification of new etiologies for this syndrome but also helped to unravel the signaling pathways involved in the development of GnRH neurons and in GnRH control and function. The FGF21/FGFR1/Klotho B (KLB) signaling pathway mediates the response to starvation and other metabolic stresses. Preventing reproduction during nutritional deprivation is an adaptive process that is essential for the survival of species. In this work, Xu

Indexed as

AnimalsDisease Models, AnimalFibroblast Growth FactorsFood DeprivationGonadotropin-Releasing HormoneHumansHypogonadismKallmann SyndromeKlotho ProteinsMembrane ProteinsMiceNeuronsPuberty, DelayedReceptor, Fibroblast Growth Factor, Type 1Sexual MaturationStarvationFGFR1 protein, humanfibroblast growth factor 21Fibroblast Growth FactorsGonadotropin-Releasing HormoneKLB protein, humanKlotho ProteinsMembrane ProteinsReceptor, Fibroblast Growth Factor, Type 1

Identifiers

PMID28778954
PMCPMC5623834
OpenAlexW2743418513

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.