المؤلفون: Ito, N., Ruegg, U.T., Kudo, A., Miyagoe-Suzuki, Y., Takeda, S.

المصدر: Channels, vol. 7, no. 3, pp. 221-224

وصف الملف: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/23584166; info:eu-repo/semantics/altIdentifier/eissn/1933-6969; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_3536D034BF529; https://serval.unil.ch/notice/serval:BIB_3536D034BF52; https://serval.unil.ch/resource/serval:BIB_3536D034BF52.P001/REF.pdf

الاتاحة: https://serval.unil.ch/notice/serval:BIB_3536D034BF52
https://doi.org/10.4161/chan.24583
https://serval.unil.ch/resource/serval:BIB_3536D034BF52.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_3536D034BF529

المؤلفون: Morise, J., Kizuka, Y., Yabuno, K., Tonoyama, Y., Hashii, N., Kawasaki, N., Manya, H., Miyagoe-Suzuki, Y., Takeda, S., Endo, T., Maeda, N., Takematsu, H., Oka, S.

المصدر: Glycobiology ; volume 24, issue 3, page 314-324 ; ISSN 0959-6658 1460-2423

الاتاحة: https://doi.org/10.1093/glycob/cwt116
http://academic.oup.com/glycob/article-pdf/24/3/314/5857240/cwt116.pdf

المؤلفون: Yuasa, K, Yoshimura, M, Urasawa, N, Ohshima, S, Howell, J M, Nakamura, A, Hijikata, T, Miyagoe-Suzuki, Y, Takeda, S

المصدر: Gene Therapy ; volume 14, issue 17, page 1249-1260 ; ISSN 0969-7128 1476-5462

الاتاحة: http://dx.doi.org/10.1038/sj.gt.3302984
https://www.nature.com/articles/3302984.pdf
https://www.nature.com/articles/3302984

المؤلفون: Yuasa, K, Sakamoto, M, Miyagoe-Suzuki, Y, Tanouchi, A, Yamamoto, H, Li, J, Chamberlain, J S, Xiao, X, Takeda, S

المصدر: Gene Therapy ; volume 9, issue 23, page 1576-1588 ; ISSN 0969-7128 1476-5462

الاتاحة: http://dx.doi.org/10.1038/sj.gt.3301829
https://www.nature.com/articles/3301829.pdf
https://www.nature.com/articles/3301829

المؤلفون: Elhussieny, A., Nogami, K., Takemura, F., Maruyama, Y., Miyagoe-Suzuki, Y., Takeda, S.

المصدر: Neuromuscular Disorders ; volume 29, page S158 ; ISSN 0960-8966

الاتاحة: http://dx.doi.org/10.1016/j.nmd.2019.06.427
https://api.elsevier.com/content/article/PII:S0960896619308156?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0960896619308156?httpAccept=text/plain

المؤلفون: Yokota, T, Lu, Q, Davies, K, Fisher, R, Sakamoto, M, Miyagoe-Suzuki, Y, Takeda, S, Partridge, T

Relation: https://ora.ox.ac.uk/objects/uuid:1c43c21b-74bd-4e6b-8eb3-19c7bdd8cc73

الاتاحة: https://ora.ox.ac.uk/objects/uuid:1c43c21b-74bd-4e6b-8eb3-19c7bdd8cc73

المؤلفون: Kanagawa, M., Yu, C.C., Ito, C., Fukada, S.I., Hozoji-Inada, M., Chiyo, T., Miyagoe-Suzuki, Y., Kobayashi, K., Okada, T., Takeda, S.I., Toda, T.

المصدر: Neuromuscular Disorders ; volume 23, issue 9-10, page 747 ; ISSN 0960-8966

الاتاحة: http://dx.doi.org/10.1016/j.nmd.2013.06.403
https://api.elsevier.com/content/article/PII:S0960896613005774?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0960896613005774?httpAccept=text/plain

المؤلفون: Kanagawa, M., Omori, Y., Kobayashi, K., Miyagoe-Suzuki, Y., Takeda, S., Endo, T., Furukawa, T., Toda, T.

المصدر: Neuromuscular Disorders ; volume 20, issue 9-10, page 600 ; ISSN 0960-8966

الاتاحة: http://dx.doi.org/10.1016/j.nmd.2010.07.018
https://api.elsevier.com/content/article/PII:S0960896610002890?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0960896610002890?httpAccept=text/plain

المؤلفون: Yuasa, K., Yoshimura, M., Urasawa, N., Ohshima, S., Howell, J.M., Nakamura, A., Hijikata, T., Miyagoe-Suzuki, Y., Takeda, S.

المصدر: Yuasa, K., Yoshimura, M., Urasawa, N., Ohshima, S., Howell, J.M. , Nakamura, A., Hijikata, T., Miyagoe-Suzuki, Y. and Takeda, S. (2007) Injection of a recombinant AAV serotype 2 into canine skeletal muscles evokes strong immune responses against transgene products. Gene Therapy, 14 (17). pp. 1249-1260.

Relation: https://researchrepository.murdoch.edu.au/id/eprint/13632/; full_text_status:none

الاتاحة: https://researchrepository.murdoch.edu.au/id/eprint/13632/

المؤلفون: Miyagoe-Suzuki, Y., Miyamoto, K., Saito, F., Matsumura, K., Manya, H., Endo, T., Takeda, S.

المصدر: Neuromuscular Disorders ; volume 17, issue 9-10, page 873 ; ISSN 0960-8966

الاتاحة: http://dx.doi.org/10.1016/j.nmd.2007.06.372
https://api.elsevier.com/content/article/PII:S0960896607005597?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S0960896607005597?httpAccept=text/plain

المؤلفون: Guo, L. T., Zhang, X. U., Kuang, W., Xu, H., Liu, L. A., Vilquin, J. -T., Miyagoe-Suzuki, Y., Takeda, S., Ruegg, M. A., Wewer, U. M., Engvall, E.

وصف الملف: application/pdf

Relation: https://edoc.unibas.ch/5748/1/20190220140449_5c6d507152318.pdf; Guo, L. T. and Zhang, X. U. and Kuang, W. and Xu, H. and Liu, L. A. and Vilquin, J. -T. and Miyagoe-Suzuki, Y. and Takeda, S. and Ruegg, M. A. and Wewer, U. M. and Engvall, E. (2003) Laminin alpha2 deficiency and muscular dystrophy : genotype-phenotype correlation in mutant mice. Neuromuscular Disorders, Vol. 13, H. 3. pp. 207-215.; info:pmid/12609502; urn:ISSN:0960-8966

الاتاحة: http://edoc.unibas.ch/dok/A5258397
https://edoc.unibas.ch/5748/
https://edoc.unibas.ch/5748/1/20190220140449_5c6d507152318.pdf
https://doi.org/10.1016/s0960-8966(02)00266-3

المؤلفون: Guo, L T, Zhang, X U, Kuang, W, Xu, Hong, Liu, L A, Vilquin, J-T, Miyagoe-Suzuki, Y, Takeda, S, Ruegg, M A, Wewer, U M, Engvall, E

المصدر: Guo , L T , Zhang , X U , Kuang , W , Xu , H , Liu , L A , Vilquin , J-T , Miyagoe-Suzuki , Y , Takeda , S , Ruegg , M A , Wewer , U M & Engvall , E 2003 , ' Laminin alpha2 deficiency and muscular dystrophy; genotype-phenotype correlation in mutant mice ' , Neuromuscular Disorders , vol. 13 , no. 3 , pp. 207-15 .

مصطلحات موضوعية: Animals, DNA Mutational Analysis, Desmin, Disease Models, Animal, Fluorescent Antibody Technique, Gene Expression, Genotype, Humans, Immunoblotting, Laminin, Mice, Mutant Strains, Transgenic, Muscle, Skeletal, Muscular Dystrophies, Peripheral Nerves, Phenotype, Promoter Regions, Genetic, Protein Structure, Tertiary, Protein Subunits, Recombinant Fusion Proteins

الاتاحة: https://researchprofiles.ku.dk/da/publications/laminin-alpha2-deficiency-and-muscular-dystrophy-genotypephenotype-correlation-in-mutant-mice(90653ccb-d2f4-4d3f-9891-44d67093f96a).html

المؤلفون: Guo, L.T., Zhang, X.U, Kang, W., Xu, H., Liu, L.A., Miyagoe-Suzuki, Y., Takeda, S., Ruegg, M., Wewer, Ulla M., Engvall, E.

المصدر: Guo , L T , Zhang , X U , Kang , W , Xu , H , Liu , L A , Miyagoe-Suzuki , Y , Takeda , S , Ruegg , M , Wewer , U M & Engvall , E 2003 , ' Laminin afra2 deficiency and muscular dystrophy: genotype-phenotype correlation in mutant mice. ' , Neuromuscular Disorders , no. 13 , pp. 207-215 .

الاتاحة: https://curis.ku.dk/portal/da/publications/laminin-afra2-deficiency-and-muscular-dystrophy-genotypephenotype-correlation-in-mutant-mice(f6af7b80-74c0-11db-bee9-02004c4f4f50).html

المؤلفون: Yokota, T, Lu, Q, Davies, K, Fisher, R, Sakamoto, M, Miyagoe-Suzuki, Y, Takeda, S, Partridge, T

المصدر: NEUROMUSCULAR DISORDERS. 14(8-9)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::41f5fad80d529eef7923803839722260
http://ora.ox.ac.uk/objects/uuid:1c43c21b-74bd-4e6b-8eb3-19c7bdd8cc73

المؤلفون: Takeda, S.¹, Miyagoe-Suzuki, Y.¹

المصدر: BioDrugs. 2001, Vol. 15 Issue 10, p635-644. 10p.

مصطلحات موضوعية: *DUCHENNE muscular dystrophy, *DYSTROPHIN genes, *GENE therapy

المؤلفون: Suzuki, N.^1,2, Motohashi, N.¹, Uezumi, A.¹, Fukada, S.¹, Miyagoe-Suzuki, Y.¹, Yoshimura, T.³, Itoyama, Y.², Aoki, M.², Takeda, S.¹

المصدر: Neuromuscular Disorders. Oct2006, Vol. 16 Issue 9/10, p692-693. 2p.