المؤلفون: Saki Yokoshiki, Teruyo Arato

المصدر: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-12 (2024)

مصطلحات موضوعية: Rare diseases, Orphan drugs, Non-clinical studies, Cell lines, Animal models, Biomarkers, Medicine

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1750-1172

URL الوصول: https://doaj.org/article/747077eee2d04d2a879d408591b15d6f

المؤلفون: Hiroshi Asano, Toshiyuki Isoe, Yoichi M. Ito, Naoki Nishimoto, Yudai Watanabe, Saki Yokoshiki, Hidemichi Watari

المصدر: Cancers, Vol 14, Iss 5, p 1180 (2022)

مصطلحات موضوعية: uterine leiomyosarcoma, next-generation sequencing, genomic, molecular-targeted drugs, HRD, BRCA, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2072-6694/14/5/1180; https://doaj.org/toc/2072-6694

URL الوصول: https://doaj.org/article/7a7cc1bc578443cf8f7b168b03839d16

المؤلفون: Kenji Yamada, Hideaki Shiraishi, Eishin Oki, Mika Ishige, Toshiyuki Fukao, Yusuke Hamada, Norio Sakai, Fumihiro Ochi, Asami Watanabe, Sanae Kawakami, Kazuyo Kuzume, Kenji Watanabe, Koji Sameshima, Kiyotaka Nakamagoe, Akira Tamaoka, Naoko Asahina, Saki Yokoshiki, Takashi Miyakoshi, Kota Ono, Koji Oba, Toshiyuki Isoe, Hiroshi Hayashi, Seiji Yamaguchi, Norihiro Sato

المصدر: Molecular Genetics and Metabolism Reports, Vol 15, Iss , Pp 55-63 (2018)

مصطلحات موضوعية: Medicine (General), R5-920, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2214426918300077; https://doaj.org/toc/2214-4269

URL الوصول: https://doaj.org/article/36d7a86db88242389cb8b2cc33a34d39

المؤلفون: Hideaki Shiraishi, Kenji Yamada, Eishin Oki, Mika Ishige, Toshiyuki Fukao, Yusuke Hamada, Norio Sakai, Fumihiro Ochi, Asami Watanabe, Sanae Kawakami, Kazuyo Kuzume, Kenji Watanabe, Koji Sameshima, Kiyotaka Nakamagoe, Akira Tamaoka, Naoko Asahina, Saki Yokoshiki, Takashi Miyakoshi, Koji Oba, Toshiyuki Isoe, Hiroshi Hayashi, Seiji Yamaguchi, Norihiro Sato

المصدر: Molecular Genetics and Metabolism Reports, Vol 20, Iss , Pp - (2019)

مصطلحات موضوعية: Medicine (General), R5-920, Biology (General), QH301-705.5

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2214426919300953; https://doaj.org/toc/2214-4269

URL الوصول: https://doaj.org/article/485479e07814483c920b57c0dc96b489

المؤلفون: Hideaki Shiraishi, Tsuyoshi Teramoto, Saki Yokoshiki, Jun Tohyama, Yuki Ueda, Kiyoshi Egawa, Norihiro Sato, Atsushi Manabe, Mitsuhiro Kato

المصدر: Brain and Development. 45:343-347

مصطلحات موضوعية: Developmental Neuroscience, Pediatrics, Perinatology and Child Health, Neurology (clinical), General Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::196d26283dce3f1309e7aeb73d155b1d
https://doi.org/10.1016/j.braindev.2023.02.005

المؤلفون: Koji Oba, Seiji Yamaguchi, Naoko Asahina, Saki Yokoshiki, Sanae Kawakami, Kiyotaka Nakamagoe, Mika Ishige, Toshiyuki Isoe, Kiyoshi Egawa, Koji Sameshima, Norihiro Sato, Fumihiro Ochi, Kazuyo Kuzume, Akira Tamaoka, Kenji Yamada, Hideaki Shiraishi, Asami Watanabe, Kenji Watanabe, Keiko Kobayashi, Hiroshi Hayashi, Takashi Miyakoshi

المصدر: Brain and Development. 43:214-219

مصطلحات موضوعية: Adult, Male, myalgia, medicine.medical_specialty, Mitochondrial Diseases, Gastroenterology, Lipid Metabolism, Inborn Errors, Very Long-Chain Acyl-CoA Dehydrogenase Deficiency, Mitochondrial fatty acid, 03 medical and health sciences, 0302 clinical medicine, Muscular Diseases, Developmental Neuroscience, Internal medicine, medicine, Congenital Bone Marrow Failure Syndromes, Humans, In patient, Child, Bezafibrate, business.industry, Everyday activities, Acyl-CoA Dehydrogenase, Long-Chain, General Medicine, medicine.disease, Hypotonia, Pediatrics, Perinatology and Child Health, Female, Neurology (clinical), medicine.symptom, business, Rhabdomyolysis, 030217 neurology & neurosurgery, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb1b126c5ec22fec15fea391da7cff4f
https://doi.org/10.1016/j.braindev.2020.07.019

المؤلفون: Asami Watanabe, Yusuke Hamada, Saki Yokoshiki, Kenji Watanabe, Kiyotaka Nakamagoe, Takashi Miyakoshi, Hideaki Shiraishi, Norihiro Sato, Fumihiro Ochi, Seiji Yamaguchi, Naoko Asahina, Kota Ono, Toshiyuki Isoe, Koji Oba, Toshiyuki Fukao, Mika Ishige, Hiroshi Hayashi, Norio Sakai, Kazuyo Kuzume, Akira Tamaoka, Kenji Yamada, Eishin Oki, Koji Sameshima, Sanae Kawakami

المصدر: Molecular Genetics and Metabolism Reports, Vol 15, Iss, Pp 55-63 (2018)
Molecular Genetics and Metabolism Reports

مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Visual analogue scale, Carnitine palmitoyltransferase-II (CPT-2) deficiency, Population, Gastroenterology, 03 medical and health sciences, 0302 clinical medicine, Endocrinology, Quality of life, Bezafibrate, Fatty acid oxidation disorders (FAODs), Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency, Clinical trial, Internal medicine, Genetics, Clinical endpoint, medicine, Carnitine, education, Molecular Biology, lcsh:QH301-705.5, education.field_of_study, lcsh:R5-920, biology, business.industry, 030104 developmental biology, lcsh:Biology (General), biology.protein, Creatine kinase, business, lcsh:Medicine (General), 030217 neurology & neurosurgery, Research Paper, medicine.drug

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f806d3c4347e3a27aff092270b28c1fb
http://www.sciencedirect.com/science/article/pii/S2214426918300077

المؤلفون: Masukazu Inoie, Saki Yokoshiki, Yasuyuki Fujita, Toshifumi Nomura, Kota Ono, Norihiro Sato, Hiroshi Shimizu, Hideki Nakamura, Riichiro Abe, Satoru Shinkuma, Shotaro Suzuki, Hiroshi Hayashi, Shota Takashima, Chihiro Nakayama, Hideki Goto, Wakana Matsumura

المصدر: Journal of Investigative Dermatology. 139:2115-2124.e11

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Pathology, medicine.medical_specialty, Time Factors, Revertant, Pilot Projects, Dermatology, Immunofluorescence, Risk Assessment, Severity of Illness Index, Biochemistry, 03 medical and health sciences, 0302 clinical medicine, Japan, Recessive dystrophic epidermolysis bullosa, medicine, Clinical endpoint, Humans, Autografts, Child, Molecular Biology, Cells, Cultured, Wound treatment, Wound Healing, integumentary system, medicine.diagnostic_test, business.industry, Biopsy, Needle, Causative gene, Skin Transplantation, Cell Biology, Middle Aged, Immunohistochemistry, digestive system diseases, Epidermolysis Bullosa Dystrophica, Transplantation, Treatment Outcome, 030104 developmental biology, Epidermal Cells, 030220 oncology & carcinogenesis, Female, Epidermis, business, Follow-Up Studies, Donor skin

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c527573c408a78e9a34003bb3c439ada
https://doi.org/10.1016/j.jid.2019.03.1155

المؤلفون: Toshiyuki Fukao, Mika Ishige, Hiroshi Hayashi, Hideaki Shiraishi, Asami Watanabe, Takashi Miyakoshi, Koji Oba, Yusuke Hamada, Seiji Yamaguchi, Norihiro Sato, Fumihiro Ochi, Naoko Asahina, Norio Sakai, Eishin Oki, Akira Tamaoka, Kenji Yamada, Kazuyo Kuzume, Sanae Kawakami, Koji Sameshima, Saki Yokoshiki, Toshiyuki Isoe, Kiyotaka Nakamagoe, Kenji Watanabe

المصدر: Molecular Genetics and Metabolism Reports, Vol 20, Iss, Pp-(2019)
Molecular Genetics and Metabolism Reports

مصطلحات موضوعية: Quality of life, medicine.medical_specialty, Carnitine palmitoyltransferase-II (CPT-2) deficiency, Endocrinology, Internal medicine, Genetics, medicine, In patient, Carnitine, lcsh:QH301-705.5, Molecular Biology, Beta oxidation, lcsh:R5-920, Bezafibrate, business.industry, Mental health, Fatty acid oxidation disorders (FAODs), Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency, Clinical trial, lcsh:Biology (General), Open label, lcsh:Medicine (General), business, Research Paper, medicine.drug

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91988820fd4d7c411908d0c148a6b0f0
http://hdl.handle.net/2115/76033