Evidence map›Paper›PMID 37065626›Full record

ReviewJBMR plus2023

Hypoxia-Inducible Factor-2α Signaling in the Skeletal System.

Sarah V Mendoza, Damian C Genetos, Clare E Yellowley

Open access · goldAbstract readReview
In one paragraph

Review in JBMR plus, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. CoClBMC ophthalmology · 2026
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. The Effect of HIF-2International journal of inflammation · 2025
    Review
  9. Article
  10. Article
  11. 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 at 2 institutions in 1 country.

Sarah V MendozaDepartment of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine University of California, Davis Davis CA USA.ORCID https://orcid.org/0000-0002-0947-2755
Damian C GenetosDepartment of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine University of California, Davis Davis CA USA.ORCID https://orcid.org/0000-0002-8599-2867
Clare E YellowleyDepartment of Anatomy, Physiology, and Cell Biology, School of Veterinary Medicine University of California, Davis Davis CA USA.ORCID https://orcid.org/0000-0002-1642-513X
Cygnus (United States) · USUniversity of California, Davis · US

Funding

UC Davis MCB T32 Administrative Supplement to Recognize Excellence in Diversity, Equity, Inclusion, and Accessibility (DEIA) MentorshipT32GM007377 · NIGMS · UNIVERSITY OF CALIFORNIA DAVIS · PI CHEDIN, FREDERIC LOUIS · 1985 to 2023
$9.9M
Osteocytic Vhl: Unlocking HIF-Independent Pathways in Bone AnabolismR01AR073772 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DAMIAN C GENETOS, Clare E Yellowley-Genetos · 2019 to 2026
$3.0M
NIAMS NIH HHS R01 AR073772NIGMS NIH HHS T32 GM007377
6 · The paper itself

Abstract

Hypoxia-inducible factors (HIFs) are oxygen-dependent heterodimeric transcription factors that mediate molecular responses to reductions in cellular oxygen (hypoxia). HIF signaling involves stable HIF-β subunits and labile, oxygen-sensitive HIF-α subunits. Under hypoxic conditions, the HIF-α subunit is stabilized, complexes with nucleus-confined HIF-β subunit, and transcriptionally regulates hypoxia-adaptive genes. Transcriptional responses to hypoxia include altered energy metabolism, angiogenesis, erythropoiesis, and cell fate. Three isoforms of HIF-α-HIF-1α, HIF-2α, and HIF-3α-are found in diverse cell types. HIF-1α and HIF-2α serve as transcriptional activators, whereas HIF-3α restricts HIF-1α and HIF-2α. The structure and isoform-specific functions of HIF-1α in mediating molecular responses to hypoxia are well established across a wide range of cell and tissue types. The contributions of HIF-2α to hypoxic adaptation are often unconsidered if not outrightly attributed to HIF-1α. This review establishes what is currently known about the diverse roles of HIF-2α in mediating the hypoxic response in skeletal tissues, with specific focus on development and maintenance of skeletal fitness. © 2023 The Authors.

Indexed as

GENETIC ANIMAL MODELSOSTEOBLASTOSTEOCLASTOSTEOCYTETRANSCRIPTION FACTORS

Identifiers

PMID37065626
PMCPMC10097641
OpenAlexW4320038933

What Socratic 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 Socratic graph.