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Paper · 38624036

Investigating the role connective tissue fibroblasts play in the altered muscle anatomy associated with the limb abnormality, Radial Dysplasia.

Murphy GRF and 5 others. J Anat, 2024. Cited by 3 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Investigating the role connective tissue fibroblasts play in the altered muscle anatomy associated with the limb abnormality, Radial Dysplasia. Papers, record 38624036. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/38624036

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Investigating the role connective tissue fibroblasts play in the altered muscle anatomy associated with the limb abnormality, Radial Dysplasia.
PubMed
Journal
J Anat
PubMed
Year
2024
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
3
iCite
Relative citation ratio, by iCite
0.46, provisional
iCite
Revised in PubMed
2025-03-05
PubMed

Authors6

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Murphy GRFGeorge R F
2Feneck EEleanor
3Paget JJames
4Sivakumar BBranavan
5Smith GGill
6Logan MPOMalcolm P Ohttps://orcid.org/0000-0002-2068-3115

Source PubMed

Topics7

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
FibroblastsMajor topic
Connective TissueMajor topic
Muscle, SkeletalMajor topic
Humans
Male
Female
Radius

Source PubMed

Grants3

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

Grant, as the record writes itAgencyCountryNIH projectStated by
MC PC 13052Medical Research CouncilUnited KingdomPubMed
MR/S000038/1Medical Research CouncilUnited KingdomPubMed
MRX000044/1Medical Research CouncilUnited KingdomPubMed

Source PubMed

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References43

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
122,040,608Immortalized pathological human myoblasts: towards a universal tool for the study of neuromuscular disorders.Skelet Muscle2011https://conductscience.org/library/papers/22040608PubMed
238,624,036Investigating the role connective tissue fibroblasts play in the altered muscle anatomy associated with the limb abnormality, Radial Dysplasia.J Anat2024https://conductscience.org/library/papers/38624036PubMed
38,988,164Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family.Nat Genet1997https://conductscience.org/library/papers/8988164PubMed
411,466,636The incidence and epidemiology of congenital upper limb anomalies: a total population study.J Hand Surg Am2001https://conductscience.org/library/papers/11466636PubMed
525,415,508Remodelling the extracellular matrix in development and disease.Nat Rev Mol Cell Biol2014https://conductscience.org/library/papers/25415508PubMed
66,200,562Phenotypic characterization and ontogeny of mesodermal-derived and endocrine epithelial components of the human thymic microenvironment.J Exp Med1984https://conductscience.org/library/papers/6200562PubMed
731,332,239Extracellular matrix composition of connective tissues: a systematic review and meta-analysis.Sci Rep2019https://conductscience.org/library/papers/31332239PubMed
817,406,593In vitro scratch assay: a convenient and inexpensive method for analysis of cell migration in vitro.Nat Protoc2007https://conductscience.org/library/papers/17406593PubMed
912,243,004[Antegren (natalizumab). A promising new approach to therapy of multiple sclerosis].Nervenarzt2002https://conductscience.org/library/papers/12243004PubMed
1012,843,316
Mutations at the SALL4 locus on chromosome 20 result in a range of clinically overlapping phenotypes, including Okihiro syndrome, Holt-Oram syndrome, acro-renal-ocular syndrome, and patients previously reported to represent thalidomide embryopathy.
J Med Genet2003https://conductscience.org/library/papers/12843316PubMed

Cited by2

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 3 citations.

PMIDTitleJournalYearIn PapersSource
41,687,018Soft tissue abnormalities in the congenital limb malformation radial dysplasia (RD): Their clinical impact and treatment significance.J Anat2026https://conductscience.org/library/papers/41687018PubMed
38,624,036Investigating the role connective tissue fibroblasts play in the altered muscle anatomy associated with the limb abnormality, Radial Dysplasia.J Anat2024https://conductscience.org/library/papers/38624036PubMed

Genes0

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

None in this release.

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
Trials
2026-11-12
Gene search
2026-11-11
Pipelines
2026-09-18

Sources 11

  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • HGNCCC0
  • iCiteCC BY 4.0
  • NCBI GenePublic domain (US government)
  • NIH RePORTER's grant and paper linksPublic domain
  • Open TargetsCC0 1.0
  • PMC's ID filePublic domain (US government)
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • HGNCCC0: https://www.genenames.org/about/license/
  • iCiteCC BY 4.0
  • NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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