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Peroxisomesbiogenesis, function, and...
~
Imanaka, Tsuneo.
Peroxisomesbiogenesis, function, and role in human disease /
紀錄類型:
書目-電子資源 : Monograph/item
正題名/作者:
Peroxisomesedited by Tsuneo Imanaka, Nobuyuki Shimozawa.
其他題名:
biogenesis, function, and role in human disease /
其他作者:
Imanaka, Tsuneo.
出版者:
Singapore :Springer Singapore :2019.
面頁冊數:
xii, 279 p. :ill., digital ;24 cm.
Contained By:
Springer eBooks
標題:
Peroxisomes.
電子資源:
https://doi.org/10.1007/978-981-15-1169-1
ISBN:
9789811511691$q(electronic bk.)
Peroxisomesbiogenesis, function, and role in human disease /
Peroxisomes
biogenesis, function, and role in human disease /[electronic resource] :edited by Tsuneo Imanaka, Nobuyuki Shimozawa. - Singapore :Springer Singapore :2019. - xii, 279 p. :ill., digital ;24 cm.
Part 1 Biogenesis and Function of peroxisome -- 1 The history of peroxisomal research -- 2 Peroxisome Biogenesis -- 3 Peroxisome Degradation and Its Molecular Machinery -- 4 The function of the peroxisome -- Part 2 Dysfunction of Peroxisome and Human Disease -- 5 Peroxisomal disorders -- 6 Model organisms used to understand peroxisomal disorders -- 7 Diagnosis of peroxisomal disorders -- 8 Therapeutic strategies for X-linked adrenoleukodystrophy, a representative peroxisome disease -- Part 3 Topics in Peroxisome Research -- 9 The isolation of peroxisomes -- 10 Structure Biology of peroxisomal proteins, peroxins -- 11 Lipidomics of peroxisomal disorders -- 12 Neurophysiology and neuropsychology for X-ALD.
This book provides readers with a comprehensive overview of peroxisomes and their role in human diseases. It starts by describing the history of peroxisome research and then examines in detail the current understanding of the biogenesis and function of peroxisomes. It then focuses on peroxisomal disorders and the involvement of peroxisomes in cancer and age-related diseases, discussing in detail the use of model organisms to elucidate the pathogenesis of peroxisomal disorders and the physiological importance of peroxisomal proteins. Further, the book examines diagnostic and therapeutic strategies in peroxisomal disorders as well as significant recent advances. Lastly, it addresses various topics in peroxisome research, including the isolation of peroxisomes from mammalian tissues and cells, the structural biology of peroxisomal proteins, the lipidomics of peroxisomal disorders, the value of exome sequencing, and neuropsychological testing in X-linked adrenoleukodystrophy. Given its scope, the book is a valuable resource for postgraduate students and researchers in the life sciences and clinicians in the fields of internal medicine, pediatrics, and neurology.
ISBN: 9789811511691$q(electronic bk.)
Standard No.: 10.1007/978-981-15-1169-1doiSubjects--Topical Terms:
683524
Peroxisomes.
LC Class. No.: QH603.P47 / P47 2019
Dewey Class. No.: 571.655
Peroxisomesbiogenesis, function, and role in human disease /
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Part 1 Biogenesis and Function of peroxisome -- 1 The history of peroxisomal research -- 2 Peroxisome Biogenesis -- 3 Peroxisome Degradation and Its Molecular Machinery -- 4 The function of the peroxisome -- Part 2 Dysfunction of Peroxisome and Human Disease -- 5 Peroxisomal disorders -- 6 Model organisms used to understand peroxisomal disorders -- 7 Diagnosis of peroxisomal disorders -- 8 Therapeutic strategies for X-linked adrenoleukodystrophy, a representative peroxisome disease -- Part 3 Topics in Peroxisome Research -- 9 The isolation of peroxisomes -- 10 Structure Biology of peroxisomal proteins, peroxins -- 11 Lipidomics of peroxisomal disorders -- 12 Neurophysiology and neuropsychology for X-ALD.
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This book provides readers with a comprehensive overview of peroxisomes and their role in human diseases. It starts by describing the history of peroxisome research and then examines in detail the current understanding of the biogenesis and function of peroxisomes. It then focuses on peroxisomal disorders and the involvement of peroxisomes in cancer and age-related diseases, discussing in detail the use of model organisms to elucidate the pathogenesis of peroxisomal disorders and the physiological importance of peroxisomal proteins. Further, the book examines diagnostic and therapeutic strategies in peroxisomal disorders as well as significant recent advances. Lastly, it addresses various topics in peroxisome research, including the isolation of peroxisomes from mammalian tissues and cells, the structural biology of peroxisomal proteins, the lipidomics of peroxisomal disorders, the value of exome sequencing, and neuropsychological testing in X-linked adrenoleukodystrophy. Given its scope, the book is a valuable resource for postgraduate students and researchers in the life sciences and clinicians in the fields of internal medicine, pediatrics, and neurology.
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