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Protein arginine methyltransferase 5 is essential for growth of lung cancer cells.

Gu, Z ; Gao, S ; et al.
In: The Biochemical journal, Jg. 446 (2012-09-01), Heft 2, S. 235-41
academicJournal

Titel:
Protein arginine methyltransferase 5 is essential for growth of lung cancer cells.
Autor/in / Beteiligte Person: Gu, Z ; Gao, S ; Zhang, F ; Wang, Z ; Ma, W ; Davis, RE
Zeitschrift: The Biochemical journal, Jg. 446 (2012-09-01), Heft 2, S. 235-41
Veröffentlichung: London, UK : Published by Portland Press on behalf of the Biochemical Society, 2012
Medientyp: academicJournal
ISSN: 1470-8728 (electronic)
DOI: 10.1042/BJ20120768
Schlagwort:
  • Adenocarcinoma metabolism
  • Adenocarcinoma pathology
  • Animals
  • Carcinoma, Squamous Cell enzymology
  • Carcinoma, Squamous Cell metabolism
  • Carcinoma, Squamous Cell pathology
  • Cell Line, Tumor
  • Cell Proliferation
  • Gene Expression Profiling
  • Gene Silencing
  • Humans
  • Lung metabolism
  • Lung pathology
  • Lung Neoplasms metabolism
  • Lung Neoplasms pathology
  • Mice
  • Mice, Nude
  • Mutant Proteins antagonists & inhibitors
  • Mutant Proteins metabolism
  • Neoplasm Proteins antagonists & inhibitors
  • Neoplasm Proteins genetics
  • Neoplasm Transplantation
  • Protein-Arginine N-Methyltransferases antagonists & inhibitors
  • Protein-Arginine N-Methyltransferases genetics
  • RNA, Small Interfering
  • Receptor, Fibroblast Growth Factor, Type 3 antagonists & inhibitors
  • Receptor, Fibroblast Growth Factor, Type 3 genetics
  • Receptor, Fibroblast Growth Factor, Type 3 metabolism
  • Recombinant Proteins antagonists & inhibitors
  • Recombinant Proteins metabolism
  • Signal Transduction
  • Small Cell Lung Carcinoma enzymology
  • Small Cell Lung Carcinoma metabolism
  • Small Cell Lung Carcinoma pathology
  • Tumor Burden
  • Adenocarcinoma enzymology
  • Lung enzymology
  • Lung Neoplasms enzymology
  • Neoplasm Proteins metabolism
  • Protein-Arginine N-Methyltransferases metabolism
Sonstiges:
  • Nachgewiesen in: MEDLINE
  • Sprachen: English
  • Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
  • Language: English
  • [Biochem J] 2012 Sep 01; Vol. 446 (2), pp. 235-41.
  • MeSH Terms: Adenocarcinoma / *enzymology ; Lung / *enzymology ; Lung Neoplasms / *enzymology ; Neoplasm Proteins / *metabolism ; Protein-Arginine N-Methyltransferases / *metabolism ; Adenocarcinoma / metabolism ; Adenocarcinoma / pathology ; Animals ; Carcinoma, Squamous Cell / enzymology ; Carcinoma, Squamous Cell / metabolism ; Carcinoma, Squamous Cell / pathology ; Cell Line, Tumor ; Cell Proliferation ; Gene Expression Profiling ; Gene Silencing ; Humans ; Lung / metabolism ; Lung / pathology ; Lung Neoplasms / metabolism ; Lung Neoplasms / pathology ; Mice ; Mice, Nude ; Mutant Proteins / antagonists & inhibitors ; Mutant Proteins / metabolism ; Neoplasm Proteins / antagonists & inhibitors ; Neoplasm Proteins / genetics ; Neoplasm Transplantation ; Protein-Arginine N-Methyltransferases / antagonists & inhibitors ; Protein-Arginine N-Methyltransferases / genetics ; RNA, Small Interfering ; Receptor, Fibroblast Growth Factor, Type 3 / antagonists & inhibitors ; Receptor, Fibroblast Growth Factor, Type 3 / genetics ; Receptor, Fibroblast Growth Factor, Type 3 / metabolism ; Recombinant Proteins / antagonists & inhibitors ; Recombinant Proteins / metabolism ; Signal Transduction ; Small Cell Lung Carcinoma / enzymology ; Small Cell Lung Carcinoma / metabolism ; Small Cell Lung Carcinoma / pathology ; Tumor Burden
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  • Grant Information: P30 CA016672 United States CA NCI NIH HHS; CA16672 United States CA NCI NIH HHS
  • Substance Nomenclature: 0 (Mutant Proteins) ; 0 (Neoplasm Proteins) ; 0 (RNA, Small Interfering) ; 0 (Recombinant Proteins) ; EC 2.1.1.319 (PRMT5 protein, human) ; EC 2.1.1.319 (Protein-Arginine N-Methyltransferases) ; EC 2.7.10.1 (FGFR3 protein, human) ; EC 2.7.10.1 (Receptor, Fibroblast Growth Factor, Type 3)
  • Entry Date(s): Date Created: 20120620 Date Completed: 20121029 Latest Revision: 20211021
  • Update Code: 20240513
  • PubMed Central ID: PMC3865921

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