ミトキサントロン (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "ミトキサントロン" in Japanese language version.

refsWebsite

Global rank Japanese rank

4^th place

24^th place

2^nd place

6^th place

6,690^th place

394^th place

5^th place

19^th place

447^th place

1,043^rd place

low place

low place

1nrcresearchpress.com

low place

low place

actabp.pl (Global: low place; Japanese: low place)

Mazerski J, Martelli S, Borowski E (1998). “The geometry of intercalation complex of antitumor mitoxantrone and ametantrone with DNA: molecular dynamics simulations.”. Acta Biochim. Pol. 45 (1): 1–11. PMID 9701490.

doi.org (Global: 2^nd place; Japanese: 6^th place)

Parker C, Waters R, Leighton C, Hancock J, Sutton R, Moorman AV, Ancliff P, Morgan M, Masurekar A, Goulden N, Green N, Révész T, Darbyshire P, Love S, Saha V (2010). “Effect of mitoxantrone on outcome of children with first relapse of acute lymphoblastic leukaemia (ALL R3): an open-label randomised trial”. Lancet 376 (9757): 2009–2017. doi:10.1016/S0140-6736(10)62002-8. PMC 3010035. PMID 21131038.
Fox E (2006). “Management of worsening multiple sclerosis with mitoxantrone: a review”. Clin Ther 28 (4): 461–74. doi:10.1016/j.clinthera.2006.04.013. PMID 16750460.
Wu, C. -C.; Li, Y. -C.; Wang, Y. -R.; Li, T. -K.; Chan, N. -L. (2013). “On the structural basis and design guidelines for type II topoisomerase-targeting anticancer drugs”. Nucleic Acids Research 41 (22): 10630–10640. doi:10.1093/nar/gkt828. PMID 24038465.
Baron M, Giorgi-Renault S, Renault J, et al. (1984). “Heterocycles with a quinone function.5.An abnormal reaction of butanedione with 1,2-diaminoanthraquinone - Crystalline structure obtained from naphto(2,3-f) quinoxaline-7,12 dione” (French). Can. J. Chem. 62 (3): 526–530. doi:10.1139/v84-087.

fda.gov (Global: 447^th place; Japanese: 1,043^rd place)

“Mitoxantrone Hydrochloride (marketed as Novantrone and generics) - Healthcare Professional Sheet text version”. U.S. Food and Drug Administration. 2014年9月19日閲覧。

nih.gov (Global: 4^th place; Japanese: 24^th place)

pubmed.ncbi.nlm.nih.gov

Parker C, Waters R, Leighton C, Hancock J, Sutton R, Moorman AV, Ancliff P, Morgan M, Masurekar A, Goulden N, Green N, Révész T, Darbyshire P, Love S, Saha V (2010). “Effect of mitoxantrone on outcome of children with first relapse of acute lymphoblastic leukaemia (ALL R3): an open-label randomised trial”. Lancet 376 (9757): 2009–2017. doi:10.1016/S0140-6736(10)62002-8. PMC 3010035. PMID 21131038.
Fox E (2006). “Management of worsening multiple sclerosis with mitoxantrone: a review”. Clin Ther 28 (4): 461–74. doi:10.1016/j.clinthera.2006.04.013. PMID 16750460.
Wu, C. -C.; Li, Y. -C.; Wang, Y. -R.; Li, T. -K.; Chan, N. -L. (2013). “On the structural basis and design guidelines for type II topoisomerase-targeting anticancer drugs”. Nucleic Acids Research 41 (22): 10630–10640. doi:10.1093/nar/gkt828. PMID 24038465.
Mazerski J, Martelli S, Borowski E (1998). “The geometry of intercalation complex of antitumor mitoxantrone and ametantrone with DNA: molecular dynamics simulations.”. Acta Biochim. Pol. 45 (1): 1–11. PMID 9701490.

pmc.ncbi.nlm.nih.gov

Parker C, Waters R, Leighton C, Hancock J, Sutton R, Moorman AV, Ancliff P, Morgan M, Masurekar A, Goulden N, Green N, Révész T, Darbyshire P, Love S, Saha V (2010). “Effect of mitoxantrone on outcome of children with first relapse of acute lymphoblastic leukaemia (ALL R3): an open-label randomised trial”. Lancet 376 (9757): 2009–2017. doi:10.1016/S0140-6736(10)62002-8. PMC 3010035. PMID 21131038.

nrcresearchpress.com (Global: low place; Japanese: low place)

Baron M, Giorgi-Renault S, Renault J, et al. (1984). “Heterocycles with a quinone function.5.An abnormal reaction of butanedione with 1,2-diaminoanthraquinone - Crystalline structure obtained from naphto(2,3-f) quinoxaline-7,12 dione” (French). Can. J. Chem. 62 (3): 526–530. doi:10.1139/v84-087.

pmda.go.jp (Global: 6,690^th place; Japanese: 394^th place)

info.pmda.go.jp

“ノバントロン注10mg／ノバントロン注20mg 添付文書” (2016年9月). 2016年11月6日閲覧。

worldcat.org (Global: 5^th place; Japanese: 19^th place)

Katzung, Bertram G. (2006). “Cancer Chemotherapy”. Basic and clinical pharmacology (10th ed.). New York: McGraw-Hill Medical Publishing Division. ISBN 0-07-145153-6. OCLC 157011367