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PUBLICATIONS · 30543698

A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children's Oncology Group study.

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Bibliographic metadata only. No full-text article or abstract is reproduced. Absence of a captured notice is not confirmation that a publication is clear of corrections or retractions.

Journal
PLoS One
Publication date
2018
First author
Armstrong AE

Publication notices

absence is not clearance
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has correction metadata
false
has expression of concern metadata
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has retraction in link
false
pubmed marks article retracted
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pubmed marks retraction notice
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relationships

    Authors and identifiers

    1. name
      Armstrong AE
      type
      Author
    2. name
      Gadd S
      type
      Author
    3. name
      Huff V
      type
      Author
    4. name
      Gerhard DS
      type
      Author
    5. name
      Dome JS
      type
      Author
    6. name
      Perlman EJ
      type
      Author
    Complete bibliographic record and source provenance
    authors
    1. name
      Armstrong AE
      type
      Author
    2. name
      Gadd S
      type
      Author
    3. name
      Huff V
      type
      Author
    4. name
      Gerhard DS
      type
      Author
    5. name
      Dome JS
      type
      Author
    6. name
      Perlman EJ
      type
      Author
    bibliography ids
    1. nci-bib-3c36be856659f6f95684eba3
    book metadata
    content sha256
    3fd1bcba02c0f6830703e19a08ab1d87c264571e2764356ec9fd2032b2092a76
    document type
    citation
    dois
    1. 10.1371/journal.pone.0208936
    electronic publication date
    display
    2018 Dec 13
    precision
    day
    year
    2018
    evidence scope
    bibliographic_metadata_only
    id
    pubmed:30543698
    immutable id
    pubmed:30543698@3fd1bcba02c0f6830703e19a08ab1d87c264571e2764356ec9fd2032b2092a76
    journal
    abbreviation
    PLoS One
    issn electronic
    1932-6203
    issn print
    Source null
    issue
    12
    name
    PloS one
    nlm unique id
    101285081
    pages
    e0208936
    volume
    13
    languages
    1. eng
    notices
    absence is not clearance
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    has correction metadata
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    has expression of concern metadata
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    has retraction in link
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    pubmed marks article retracted
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    pubmed marks retraction notice
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    relationships
      outcomes validated
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      pmid
      30543698
      provenance
      batch id
      438b2803888025c6cf56
      provider
      NCBI PubMed ESummary
      record sha256
      4814e5a18bc8d0e660f2b42ce0be52a8af2325b0cef8749b5da1eee11eec07fc
      response sha256
      0adf5ff07d3aa03a45feef5e4b7998e2ddea370eb9d1c6aa9134c5fd329767e6
      retrieved at
      2026-09-09T23:47:36.359220+00:00
      publication date
      display
      2018
      precision
      year
      year
      2018
      publication types
      1. Journal Article
      2. Research Support, N.I.H., Extramural
      record status
      PubMed - indexed for MEDLINE
      schema version
      1.0
      source url
      https://pubmed.ncbi.nlm.nih.gov/30543698/
      title
      A unique subset of low-risk Wilms tumors is characterized by loss of function of TRIM28 (KAP1), a gene critical in early renal development: A Children's Oncology Group study.

      Preserved source evidence · Independent clinical review pending · Not medical advice