Menin-MLL inhibitor blocks progression of middle ear cholesteatoma in vivo
Cholesteatoma is an epithelial lesion that expands into the middle ear, resulting in bone destruction. The acceleration of the proliferative activity of epithelial stem/progenitor cells is involved in the pathogenesis of cholesteatoma. Recently, the use of a menin-mixed lineage leukemia 1 (MLL1) inh...
Ausführliche Beschreibung
Autor*in: |
Yamamoto-Fukuda, Tomomi [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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Schlagwörter: |
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Übergeordnetes Werk: |
Enthalten in: Investigation of structural analogs of hydroxychloroquine for SARS-CoV-2 main protease (Mpro): A computational drug discovery study - Reyaz, Saima ELSEVIER, 2021, Amsterdam [u.a.] |
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Übergeordnetes Werk: |
volume:140 ; year:2021 ; pages:0 |
Links: |
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DOI / URN: |
10.1016/j.ijporl.2020.110545 |
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ELV052536254 |
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10.1016/j.ijporl.2020.110545 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001243.pica (DE-627)ELV052536254 (ELSEVIER)S0165-5876(20)30688-1 DE-627 ger DE-627 rakwb eng 540 004 VZ 35.06 bkl Yamamoto-Fukuda, Tomomi verfasserin aut Menin-MLL inhibitor blocks progression of middle ear cholesteatoma in vivo 2021 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Cholesteatoma is an epithelial lesion that expands into the middle ear, resulting in bone destruction. The acceleration of the proliferative activity of epithelial stem/progenitor cells is involved in the pathogenesis of cholesteatoma. Recently, the use of a menin-mixed lineage leukemia 1 (MLL1) inhibitor, MI503, in experiments has resulted in inhibition of the growth of tumors under histone modification. In this study, we investigated the effects of the menin-MLL inhibitor against cholesteatoma growth in an in vivo model. Cholesteatoma Elsevier Level of evidence: N/A Elsevier KGF Elsevier p63 Elsevier Menin-MLL inhibitor Elsevier Akiyama, Naotaro oth Tatsumi, Norifumi oth Okabe, Masataka oth Kojima, Hiromi oth Enthalten in Elsevier Science Reyaz, Saima ELSEVIER Investigation of structural analogs of hydroxychloroquine for SARS-CoV-2 main protease (Mpro): A computational drug discovery study 2021 Amsterdam [u.a.] (DE-627)ELV006862241 volume:140 year:2021 pages:0 https://doi.org/10.1016/j.ijporl.2020.110545 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.06 Computeranwendungen Chemie VZ AR 140 2021 0 |
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10.1016/j.ijporl.2020.110545 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001243.pica (DE-627)ELV052536254 (ELSEVIER)S0165-5876(20)30688-1 DE-627 ger DE-627 rakwb eng 540 004 VZ 35.06 bkl Yamamoto-Fukuda, Tomomi verfasserin aut Menin-MLL inhibitor blocks progression of middle ear cholesteatoma in vivo 2021 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Cholesteatoma is an epithelial lesion that expands into the middle ear, resulting in bone destruction. The acceleration of the proliferative activity of epithelial stem/progenitor cells is involved in the pathogenesis of cholesteatoma. Recently, the use of a menin-mixed lineage leukemia 1 (MLL1) inhibitor, MI503, in experiments has resulted in inhibition of the growth of tumors under histone modification. In this study, we investigated the effects of the menin-MLL inhibitor against cholesteatoma growth in an in vivo model. Cholesteatoma Elsevier Level of evidence: N/A Elsevier KGF Elsevier p63 Elsevier Menin-MLL inhibitor Elsevier Akiyama, Naotaro oth Tatsumi, Norifumi oth Okabe, Masataka oth Kojima, Hiromi oth Enthalten in Elsevier Science Reyaz, Saima ELSEVIER Investigation of structural analogs of hydroxychloroquine for SARS-CoV-2 main protease (Mpro): A computational drug discovery study 2021 Amsterdam [u.a.] (DE-627)ELV006862241 volume:140 year:2021 pages:0 https://doi.org/10.1016/j.ijporl.2020.110545 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.06 Computeranwendungen Chemie VZ AR 140 2021 0 |
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10.1016/j.ijporl.2020.110545 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001243.pica (DE-627)ELV052536254 (ELSEVIER)S0165-5876(20)30688-1 DE-627 ger DE-627 rakwb eng 540 004 VZ 35.06 bkl Yamamoto-Fukuda, Tomomi verfasserin aut Menin-MLL inhibitor blocks progression of middle ear cholesteatoma in vivo 2021 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Cholesteatoma is an epithelial lesion that expands into the middle ear, resulting in bone destruction. The acceleration of the proliferative activity of epithelial stem/progenitor cells is involved in the pathogenesis of cholesteatoma. Recently, the use of a menin-mixed lineage leukemia 1 (MLL1) inhibitor, MI503, in experiments has resulted in inhibition of the growth of tumors under histone modification. In this study, we investigated the effects of the menin-MLL inhibitor against cholesteatoma growth in an in vivo model. Cholesteatoma Elsevier Level of evidence: N/A Elsevier KGF Elsevier p63 Elsevier Menin-MLL inhibitor Elsevier Akiyama, Naotaro oth Tatsumi, Norifumi oth Okabe, Masataka oth Kojima, Hiromi oth Enthalten in Elsevier Science Reyaz, Saima ELSEVIER Investigation of structural analogs of hydroxychloroquine for SARS-CoV-2 main protease (Mpro): A computational drug discovery study 2021 Amsterdam [u.a.] (DE-627)ELV006862241 volume:140 year:2021 pages:0 https://doi.org/10.1016/j.ijporl.2020.110545 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.06 Computeranwendungen Chemie VZ AR 140 2021 0 |
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10.1016/j.ijporl.2020.110545 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001243.pica (DE-627)ELV052536254 (ELSEVIER)S0165-5876(20)30688-1 DE-627 ger DE-627 rakwb eng 540 004 VZ 35.06 bkl Yamamoto-Fukuda, Tomomi verfasserin aut Menin-MLL inhibitor blocks progression of middle ear cholesteatoma in vivo 2021 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Cholesteatoma is an epithelial lesion that expands into the middle ear, resulting in bone destruction. The acceleration of the proliferative activity of epithelial stem/progenitor cells is involved in the pathogenesis of cholesteatoma. Recently, the use of a menin-mixed lineage leukemia 1 (MLL1) inhibitor, MI503, in experiments has resulted in inhibition of the growth of tumors under histone modification. In this study, we investigated the effects of the menin-MLL inhibitor against cholesteatoma growth in an in vivo model. Cholesteatoma Elsevier Level of evidence: N/A Elsevier KGF Elsevier p63 Elsevier Menin-MLL inhibitor Elsevier Akiyama, Naotaro oth Tatsumi, Norifumi oth Okabe, Masataka oth Kojima, Hiromi oth Enthalten in Elsevier Science Reyaz, Saima ELSEVIER Investigation of structural analogs of hydroxychloroquine for SARS-CoV-2 main protease (Mpro): A computational drug discovery study 2021 Amsterdam [u.a.] (DE-627)ELV006862241 volume:140 year:2021 pages:0 https://doi.org/10.1016/j.ijporl.2020.110545 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.06 Computeranwendungen Chemie VZ AR 140 2021 0 |
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10.1016/j.ijporl.2020.110545 doi /cbs_pica/cbs_olc/import_discovery/elsevier/einzuspielen/GBV00000000001243.pica (DE-627)ELV052536254 (ELSEVIER)S0165-5876(20)30688-1 DE-627 ger DE-627 rakwb eng 540 004 VZ 35.06 bkl Yamamoto-Fukuda, Tomomi verfasserin aut Menin-MLL inhibitor blocks progression of middle ear cholesteatoma in vivo 2021 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Cholesteatoma is an epithelial lesion that expands into the middle ear, resulting in bone destruction. The acceleration of the proliferative activity of epithelial stem/progenitor cells is involved in the pathogenesis of cholesteatoma. Recently, the use of a menin-mixed lineage leukemia 1 (MLL1) inhibitor, MI503, in experiments has resulted in inhibition of the growth of tumors under histone modification. In this study, we investigated the effects of the menin-MLL inhibitor against cholesteatoma growth in an in vivo model. Cholesteatoma Elsevier Level of evidence: N/A Elsevier KGF Elsevier p63 Elsevier Menin-MLL inhibitor Elsevier Akiyama, Naotaro oth Tatsumi, Norifumi oth Okabe, Masataka oth Kojima, Hiromi oth Enthalten in Elsevier Science Reyaz, Saima ELSEVIER Investigation of structural analogs of hydroxychloroquine for SARS-CoV-2 main protease (Mpro): A computational drug discovery study 2021 Amsterdam [u.a.] (DE-627)ELV006862241 volume:140 year:2021 pages:0 https://doi.org/10.1016/j.ijporl.2020.110545 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U SSG-OLC-PHA 35.06 Computeranwendungen Chemie VZ AR 140 2021 0 |
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Cholesteatoma is an epithelial lesion that expands into the middle ear, resulting in bone destruction. The acceleration of the proliferative activity of epithelial stem/progenitor cells is involved in the pathogenesis of cholesteatoma. Recently, the use of a menin-mixed lineage leukemia 1 (MLL1) inhibitor, MI503, in experiments has resulted in inhibition of the growth of tumors under histone modification. In this study, we investigated the effects of the menin-MLL inhibitor against cholesteatoma growth in an in vivo model. |
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Cholesteatoma is an epithelial lesion that expands into the middle ear, resulting in bone destruction. The acceleration of the proliferative activity of epithelial stem/progenitor cells is involved in the pathogenesis of cholesteatoma. Recently, the use of a menin-mixed lineage leukemia 1 (MLL1) inhibitor, MI503, in experiments has resulted in inhibition of the growth of tumors under histone modification. In this study, we investigated the effects of the menin-MLL inhibitor against cholesteatoma growth in an in vivo model. |
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Cholesteatoma is an epithelial lesion that expands into the middle ear, resulting in bone destruction. The acceleration of the proliferative activity of epithelial stem/progenitor cells is involved in the pathogenesis of cholesteatoma. Recently, the use of a menin-mixed lineage leukemia 1 (MLL1) inhibitor, MI503, in experiments has resulted in inhibition of the growth of tumors under histone modification. In this study, we investigated the effects of the menin-MLL inhibitor against cholesteatoma growth in an in vivo model. |
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