المؤلفون: Chung-Jiuan Jeng, Ssu-Ju Fu, Chia-Ying You, Yi-Jheng Peng, Cheng-Tsung Hsiao, Tsung-Yu Chen, Chih-Yung Tang

المصدر: Frontiers in Neurology, Vol 11 (2020)

مصطلحات موضوعية: skeletal muscle, genetic disease, mutation, channelopathy, protein quality control, protein degradation, Neurology. Diseases of the nervous system, RC346-429

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/article/10.3389/fneur.2020.00076/full; https://doaj.org/toc/1664-2295

URL الوصول: https://doaj.org/article/ff9b0382f8cd4703acbf7270b4cd1390

المؤلفون: Cheng-Tsung Hsiao, Thomas F. Tropea, Ssu-Ju Fu, Tanya M. Bardakjian, Pedro Gonzalez-Alegre, Bing-Wen Soong, Chih-Yung Tang, Chung-Jiuan Jeng

المصدر: International Journal of Molecular Sciences, Vol 22, Iss 15, p 8247 (2021)

مصطلحات موضوعية: spinocerebellar ataxia, parkinsonism, molecular genetics, channelopathy, iron homeostasis, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-0067/22/15/8247; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

URL الوصول: https://doaj.org/article/996c415dc9fb4ba39ba616c08338fe0b

المؤلفون: Ginevra Zanni, Cheng-Tsung Hsiao, Ssu-Ju Fu, Chih-Yung Tang, Alessandro Capuano, Luca Bosco, Federica Graziola, Emanuele Bellacchio, Serenella Servidei, Guido Primiano, Bing-Wen Soong, Chung-Jiuan Jeng

المصدر: International Journal of Molecular Sciences, Vol 22, Iss 9, p 4986 (2021)

مصطلحات موضوعية: KCND3, Spinocerebellar Ataxia SCA19/22, Congenital Ataxia, KV4.3, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-0067/22/9/4986; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

URL الوصول: https://doaj.org/article/15759d31a21342909ceea688dad5cfb8

المؤلفون: Ssu-Ju Fu, Meng-Chun Hu, Cheng-Tsung Hsiao, An-Ting Cheng, Tsung-Yu Chen, Chung-Jiuan Jeng, Chih-Yung Tang

المصدر: International Journal of Molecular Sciences, Vol 22, Iss 11, p 5859 (2021)

مصطلحات موضوعية: proteostasis, channelopathy, protein quality control, chaperone, co-chaperone, 17-AAG, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-0067/22/11/5859; https://doaj.org/toc/1661-6596; https://doaj.org/toc/1422-0067

URL الوصول: https://doaj.org/article/5635a4bd71404a6ab9da2c8d61dd1767

المؤلفون: Ssu-Ju Fu, Meng-Chun Hu, Yi-Jheng Peng, Hsin-Yu Fang, Cheng-Tsung Hsiao, Tsung-Yu Chen, Chung-Jiuan Jeng, Chih-Yung Tang

المصدر: Cells, Vol 9, Iss 6, p 1332 (2020)

مصطلحات موضوعية: channelopathy, cullin E3 ubiquitin ligase, polyubiquitination, proteasomal degradation, MG132, MLN4924, Cytology, QH573-671

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2073-4409/9/6/1332; https://doaj.org/toc/2073-4409

URL الوصول: https://doaj.org/article/8820b3f04a634771ac8403cf89d97a3e

المؤلفون: Yi-Jheng Peng, Yi-Ching Lee, Ssu-Ju Fu, Yun-Chia Chien, Yi-Fan Liao, Tsung-Yu Chen, Chung-Jiuan Jeng, Chih-Yung Tang

المصدر: International Journal of Molecular Sciences, Vol 19, Iss 12, p 3783 (2018)

مصطلحات موضوعية: ion channels, molecular chaperones, membrane proteins, protein stability, trafficking, skeletal muscle, Biology (General), QH301-705.5, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-0067/19/12/3783; https://doaj.org/toc/1422-0067

URL الوصول: https://doaj.org/article/c9c21f4d6820442883ee7bd7c34fd60a

المؤلفون: Ssu Ju Fu, Chung Jiuan Jeng, Cheng Tsung Hsiao, Chih Yung Tang, Thomas F. Tropea, Tanya Bardakjian, Bing Wen Soong, Pedro Gonzalez-Alegre

المصدر: International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 8247, p 8247 (2021)
Volume 22
Issue 15

مصطلحات موضوعية: 0301 basic medicine, Male, Pathology, Cerebellum, Action Potentials, 0302 clinical medicine, spinocerebellar ataxia, Cerebellar disorder, Biology (General), Spectroscopy, Exome sequencing, parkinsonism, Parkinsonism, Neurodegeneration, Brain, General Medicine, Computer Science Applications, Chemistry, medicine.anatomical_structure, Shal Potassium Channels, Gain of Function Mutation, Spinocerebellar ataxia, medicine.symptom, medicine.medical_specialty, QH301-705.5, Iron, Biology, Catalysis, Article, Inorganic Chemistry, 03 medical and health sciences, channelopathy, Channelopathy, Parkinsonian Disorders, Protein Domains, medicine, Humans, Spinocerebellar Ataxias, Cognitive Dysfunction, Physical and Theoretical Chemistry, QD1-999, Molecular Biology, Aged, Cerebellar ataxia, Organic Chemistry, medicine.disease, 030104 developmental biology, HEK293 Cells, nervous system, molecular genetics, iron homeostasis, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bcfeb920e03ebb3e572284c99154f27
http://europepmc.org/articles/PMC8347726

المؤلفون: Meng Chun Hu, Chung Jiuan Jeng, Tsung-Yu Chen, Ssu Ju Fu, An Ting Cheng, Cheng Tsung Hsiao, Chih Yung Tang

المصدر: International Journal of Molecular Sciences; Volume 22; Issue 11; Pages: 5859
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 22, Iss 5859, p 5859 (2021)

مصطلحات موضوعية: Male, Pelizaeus-Merzbacher Disease, Mice, Benzoquinones, Protein Isoforms, chaperone, 17-AAG, Biology (General), Spectroscopy, Mice, Knockout, Neurons, biology, Chemistry, Brain, Leydig Cells, Endoplasmic Reticulum-Associated Degradation, General Medicine, Hsp90, Computer Science Applications, Cell biology, Co-chaperone, Signal Transduction, QH301-705.5, co-chaperone, Lactams, Macrocyclic, CHO Cells, Article, Catalysis, Tacrolimus Binding Proteins, Inorganic Chemistry, Cricetulus, channelopathy, Chloride Channels, Heat shock protein, medicine, Animals, Humans, HSP70 Heat-Shock Proteins, HSP90 Heat-Shock Proteins, protein quality control, Physical and Theoretical Chemistry, QD1-999, Molecular Biology, proteostasis, urogenital system, Endoplasmic reticulum, Organic Chemistry, Leukodystrophy, medicine.disease, CLC-2 Chloride Channels, Mice, Inbred C57BL, Disease Models, Animal, HEK293 Cells, Proteostasis, Ion homeostasis, Gene Expression Regulation, Chaperone (protein), biology.protein, Molecular Chaperones

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97eaa45dedb72e931a02ec77bb407189

المؤلفون: Bing-Wen Soong, Chen Tsung Hsiao, Luca Bosco, Emanuele Bellacchio, Alessandro Capuano, Chung Jiuan Jeng, Guido Primiano, Ginevra Zanni, Serenella Servidei, Chih Yung Tang, Federica Graziola, Ssu Ju Fu

المصدر: International Journal of Molecular Sciences, Vol 22, Iss 4986, p 4986 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 9

مصطلحات موضوعية: 0301 basic medicine, Cerebellum, Ataxia, QH301-705.5, Biology, Catalysis, Inorganic Chemistry, 03 medical and health sciences, 0302 clinical medicine, Mutant protein, medicine, Missense mutation, Physical and Theoretical Chemistry, Biology (General), Molecular Biology, QD1-999, Spectroscopy, KV4.3, KCND3, Organic Chemistry, Wild type, Congenital Ataxia, General Medicine, medicine.disease, Molecular biology, Potassium channel, Computer Science Applications, Spinocerebellar Ataxia SCA19/22, Chemistry, 030104 developmental biology, medicine.anatomical_structure, Spinocerebellar ataxia, Cerebellar atrophy, medicine.symptom, 030217 neurology & neurosurgery

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab372a8768c30c9f31a2041c52011c94
https://www.mdpi.com/1422-0067/22/9/4986

المؤلفون: Ginevra, Zanni, Cheng-Tsung, Hsiao, Ssu-Ju, Fu, Chih-Yung, Tang, Alessandro, Capuano, Luca, Bosco, Federica, Graziola, Emanuele, Bellacchio, Serenella, Servidei, Guido, Primiano, Bing-Wen, Soong, Chung-Jiuan, Jeng

المصدر: International Journal of Molecular Sciences

مصطلحات موضوعية: Male, Congenital Ataxia, Middle Aged, Magnetic Resonance Imaging, Article, Spinocerebellar Ataxia SCA19/22, Xenopus laevis, HEK293 Cells, Shal Potassium Channels, KCND3, KV4.3, Mutation, Proteostasis, Animals, Humans, Spinocerebellar Ataxias, Female, Amino Acid Sequence, Child, Ion Channel Gating

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::dbcf71e4021e1e18c995598959582f9d
https://pubmed.ncbi.nlm.nih.gov/34067185