進行性骨化性線維異形成症 (Japanese Wikipedia)

Analysis of information sources in references of the Wikipedia article "進行性骨化性線維異形成症" in Japanese language version.

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4doi.org

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bmj.com

jmg.bmj.com

Connor JM, Evans DA (1982). “Genetic aspects of fibrodysplasia ossificans progressiva” (abstract). J. Med. Genet. 19 (1): 35–39. doi:10.1136/jmg.19.1.35. PMC 1048816. PMID 7069743.

doi.org

Maruyama, Rika; Nguyen, Quynh; Roshmi, Rohini Roy; Touznik, Aleksander; Yokota, Toshifumi (2022-06). “Allele-Selective LNA Gapmers for the Treatment of Fibrodysplasia Ossificans Progressiva Knock Down the Pathogenic ACVR1R206H Transcript and Inhibit Osteogenic Differentiation”. Nucleic Acid Therapeutics 32 (3): 185–193. doi:10.1089/nat.2021.0009. ISSN 2159-3345. PMID 35085461.
Connor JM, Evans DA (1982). “Genetic aspects of fibrodysplasia ossificans progressiva” (abstract). J. Med. Genet. 19 (1): 35–39. doi:10.1136/jmg.19.1.35. PMC 1048816. PMID 7069743.
Shore EM, Xu M, Feldman GJ et al. (2006). “A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva” (abstract). Nat. Genet. 38 (5): 525–527. doi:10.1038/ng1783. PMID 16642017.
Dinther et al. (2010). “ALK2 R206H mutation linked to fibrodysplasia ossificans progressiva confers constitutive activity to the BMP type I receptor and sensitizes mesenchymal cells to BMP-induced osteoblast differentiation and bone formation”. Journal of Bone and Mineral Research: 091211115834058–35. doi:10.1359/jbmr.091110.

jiji.com

難病１７歳「ゴールまだ先」＝ｉＰＳ研究に協力－兵庫 - 時事ドットコム^{[リンク切れ]}

kobe-np.co.jp

“iPS創薬の治験開始　骨の難病、明石のYさんに世界初”. 神戸新聞. (2017年10月5日) 2017年10月5日閲覧。 ^{[リンク切れ]}

kyoto-np.co.jp

"９月にもｉＰＳ創薬治験　山中京大教授「活発化に期待」". 京都新聞. (2017年8月1日). http://www.kyoto-np.co.jp/environment/article/20170801000094^{[リンク切れ]}

muttermuseum.org

memento.muttermuseum.org

“Fibrodysplasia Ossificans Progressiva” (英語). Mütter Museum. 2022年9月13日閲覧。※ムッター博物館による解説。

nature.com

Shore EM, Xu M, Feldman GJ et al. (2006). “A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva” (abstract). Nat. Genet. 38 (5): 525–527. doi:10.1038/ng1783. PMID 16642017.

nih.gov

pubmed.ncbi.nlm.nih.gov

Maruyama, Rika; Nguyen, Quynh; Roshmi, Rohini Roy; Touznik, Aleksander; Yokota, Toshifumi (2022-06). “Allele-Selective LNA Gapmers for the Treatment of Fibrodysplasia Ossificans Progressiva Knock Down the Pathogenic ACVR1R206H Transcript and Inhibit Osteogenic Differentiation”. Nucleic Acid Therapeutics 32 (3): 185–193. doi:10.1089/nat.2021.0009. ISSN 2159-3345. PMID 35085461.
Connor JM, Evans DA (1982). “Genetic aspects of fibrodysplasia ossificans progressiva” (abstract). J. Med. Genet. 19 (1): 35–39. doi:10.1136/jmg.19.1.35. PMC 1048816. PMID 7069743.
Shore EM, Xu M, Feldman GJ et al. (2006). “A recurrent mutation in the BMP type I receptor ACVR1 causes inherited and sporadic fibrodysplasia ossificans progressiva” (abstract). Nat. Genet. 38 (5): 525–527. doi:10.1038/ng1783. PMID 16642017.

pmc.ncbi.nlm.nih.gov

Connor JM, Evans DA (1982). “Genetic aspects of fibrodysplasia ossificans progressiva” (abstract). J. Med. Genet. 19 (1): 35–39. doi:10.1136/jmg.19.1.35. PMC 1048816. PMID 7069743.

nikkei.com

sankei.com

“「新薬の治験に参加したい」皮膚を提供のFOP患者、Yさん、京都大の研究グループに期待”. 産経新聞. (2017年8月1日) 2017年8月3日閲覧。

upenn.edu

uphs.upenn.edu

News Release of FOP's Cause^{[リンク切れ]}

web.archive.org

“iPS使い創薬、初の治験へ＝骨の難病患者に－9月以降、4大学病院で・京大”. 時事通信社. (2017年8月1日) 2017年8月1日閲覧。 ^{[リンク切れ]}

wiley.com

onlinelibrary.wiley.com

Dinther et al. (2010). “ALK2 R206H mutation linked to fibrodysplasia ossificans progressiva confers constitutive activity to the BMP type I receptor and sensitizes mesenchymal cells to BMP-induced osteoblast differentiation and bone formation”. Journal of Bone and Mineral Research: 091211115834058–35. doi:10.1359/jbmr.091110.

worldcat.org

search.worldcat.org

Maruyama, Rika; Nguyen, Quynh; Roshmi, Rohini Roy; Touznik, Aleksander; Yokota, Toshifumi (2022-06). “Allele-Selective LNA Gapmers for the Treatment of Fibrodysplasia Ossificans Progressiva Knock Down the Pathogenic ACVR1R206H Transcript and Inhibit Osteogenic Differentiation”. Nucleic Acid Therapeutics 32 (3): 185–193. doi:10.1089/nat.2021.0009. ISSN 2159-3345. PMID 35085461.