Journal
Molecular cancer research : MCR
ISSN: 1557-3125
Titre abrégé: Mol Cancer Res
Pays: United States
ID NLM: 101150042
Informations de publication
Date de publication:
02 2019
02 2019
Historique:
received:
24
07
2018
revised:
06
09
2018
accepted:
15
10
2018
pubmed:
26
10
2018
medline:
28
1
2020
entrez:
26
10
2018
Statut:
ppublish
Résumé
Melanoma is one of the most highly mutated cancer types. To identify functional drivers of melanoma, we searched for cross-species conserved mutations utilizing a mouse melanoma model driven by loss of PTEN and CDKN2A, and identified mutations in
Identifiants
pubmed: 30355677
pii: 1541-7786.MCR-18-0777
doi: 10.1158/1541-7786.MCR-18-0777
pmc: PMC6386183
mid: NIHMS1510302
doi:
Substances chimiques
Braf protein, mouse
EC 2.7.11.1
Proto-Oncogene Proteins B-raf
EC 2.7.11.1
Protein Tyrosine Phosphatase, Non-Receptor Type 11
EC 3.1.3.48
Ptpn11 protein, mouse
EC 3.1.3.48
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
583-593Subventions
Organisme : NICHD NIH HHS
ID : U01 HD087198
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL125353
Pays : United States
Organisme : BLRD VA
ID : I01 BX001792
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA076292
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI139072
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA225520
Pays : United States
Organisme : BLRD VA
ID : IK6 BX004603
Pays : United States
Informations de copyright
©2018 American Association for Cancer Research.
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