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PUBLICATIONS · 24793135

A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations.

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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
Nat Genet
Publication date
2014 Jun
First author
Kohsaka S

Publication notices

absence is not clearance
true
has correction metadata
false
has expression of concern metadata
false
has retraction in link
false
pubmed marks article retracted
false
pubmed marks retraction notice
false
relationships
  1. citation
    Bull Cancer. 2014 Sep;101(9):776-7. doi: 10.1684/bdc.2014.2017.
    note
    Source null
    related pmid
    25295632
    relationship
    Comment in

Authors and identifiers

  1. name
    Kohsaka S
    type
    Author
  2. name
    Shukla N
    type
    Author
  3. name
    Ameur N
    type
    Author
  4. name
    Ito T
    type
    Author
  5. name
    Ng CK
    type
    Author
  6. name
    Wang L
    type
    Author
  7. name
    Lim D
    type
    Author
  8. name
    Marchetti A
    type
    Author
  9. name
    Viale A
    type
    Author
  10. name
    Pirun M
    type
    Author
  11. name
    Socci ND
    type
    Author
  12. name
    Qin LX
    type
    Author
Complete bibliographic record and source provenance
authors
  1. name
    Kohsaka S
    type
    Author
  2. name
    Shukla N
    type
    Author
  3. name
    Ameur N
    type
    Author
  4. name
    Ito T
    type
    Author
  5. name
    Ng CK
    type
    Author
  6. name
    Wang L
    type
    Author
  7. name
    Lim D
    type
    Author
  8. name
    Marchetti A
    type
    Author
  9. name
    Viale A
    type
    Author
  10. name
    Pirun M
    type
    Author
  11. name
    Socci ND
    type
    Author
  12. name
    Qin LX
    type
    Author
bibliography ids
  1. nci-bib-5ca29ba6c9cba60db2a2d47a
book metadata
content sha256
8167ccebad4999aea13f59e62e1f56f5419e90c388b57be9aa3dffbe025bf6c4
document type
citation
dois
  1. 10.1038/ng.2969
electronic publication date
display
2014 May 4
precision
day
year
2014
evidence scope
bibliographic_metadata_only
id
pubmed:24793135
immutable id
pubmed:24793135@8167ccebad4999aea13f59e62e1f56f5419e90c388b57be9aa3dffbe025bf6c4
journal
abbreviation
Nat Genet
issn electronic
1546-1718
issn print
1061-4036
issue
6
name
Nature genetics
nlm unique id
9216904
pages
595-600
volume
46
languages
  1. eng
notices
absence is not clearance
true
has correction metadata
false
has expression of concern metadata
false
has retraction in link
false
pubmed marks article retracted
false
pubmed marks retraction notice
false
relationships
  1. citation
    Bull Cancer. 2014 Sep;101(9):776-7. doi: 10.1684/bdc.2014.2017.
    note
    Source null
    related pmid
    25295632
    relationship
    Comment in
outcomes validated
false
pmid
24793135
provenance
batch id
063b6c38419f18d4021f
provider
NCBI PubMed ESummary
record sha256
669b3e3fadb759850e75f08549e3f6748edf06638dd08ae05e215dac0e91be71
response sha256
5abcae41e9384a85f92695ef76b244ffd933f07a58a51082c160af8743d196ad
retrieved at
2026-09-09T23:47:02.607425+00:00
publication date
display
2014 Jun
precision
month
year
2014
publication types
  1. Journal Article
  2. Research Support, N.I.H., Extramural
  3. Research Support, N.I.H., Intramural
  4. Research Support, Non-U.S. Gov't
record status
PubMed - indexed for MEDLINE
schema version
1.0
source url
https://pubmed.ncbi.nlm.nih.gov/24793135/
title
A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations.

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