Descripción del título
Protein folding and misfold...
Reviews the molecular events initiated by unfolded or misfolded proteins leading to conformational human diseases, with special emphasis on the macromolecular homo- and heteroassociations of the malfolded proteins into characteristic ultrastructures found primarily in Parkinson's and Alzheimer's diseases
Monografía
monografia Rebiun25748865 https://catalogo.rebiun.org/rebiun/record/Rebiun25748865 m o d cr cn||||||||| 090311s2009 ne ob 001 0 eng d 2008938904 GBA8D1350 bnb 311304845 317455171 437103492 526472666 646791115 756713892 1005778768 1044430975 1066429804 1067038611 1086909822 1112521740 1126420233 1136292834 1144190714 1148118289 1156025252 9781402094347 electronic bk.) 1402094345 electronic bk.) 9781402094330 geb.) 1402094337 geb.) 1281950424 9781281950420 9786611950422 6611950427 1402094337 Cloth) 10.1007/978-1-4020-9434-7 doi AU@ 000048714056 AU@ 000057999015 AU@ 000058165476 AU@ 000060410824 CDX 9713328 DEBSZ 430707290 NLGGC 325576548 NZ1 13071526 NZ1 13111611 978-1-4020-9433-0 Springer http://www.springerlink.com GW5XE eng pn GW5XE YDXCP IDEBK OCLCQ N$T MND UWW CEF CDX MERUC UAB EBLCP OCLCQ NLGGC OCLCF OHS BEDGE OCLCQ OCLCO COO DEBSZ OCLCQ E7B Z5A OCLCO MERER OCLCO OCLCQ OCLCO ESU VT2 OCLCO OCLCA OCLCQ U3W OCLCO AU@ OCLCO WYU OCLCO OCLCA ICG OCLCA YOU OCLCA UKAHL OCLCQ OCLCO W2U ERF OCLCQ OCLCA SFB OCLCQ OCLCA HEA 039110 bisacsh MED 056000 bisacsh MBGR bicssc 616.8047 22 44.46 bcl 44.90 bcl Protein folding and misfolding neurodegenerative diseases edited by Judit Ovdi, Ferenc Orosz Dordrecht London Springer 2009 Dordrecht London Dordrecht London Springer 1 online resource 1 online resource Text txt rdacontent computer c rdamedia online resource cr rdacarrier text file PDF rda Focus on structural biology 7 Includes bibliographical references and index Structural Disorder and Its Connection with Misfolding Diseases; Intrinsic Disorder in Proteins Associated with Neurodegenerative Diseases; Dynamic Role of Ubiquitination in the Management of Misfolded Proteins Associated with Neurodegenerative Diseases; Protein Misfolding and Axonal Protection in Neurodegenerative Diseases; Endoplasmic Reticulum Stress in Neurodegeneration; Involvement of Alpha-2 Domain in Prion Protein Conformationally-Induced Diseases; Synuclein Structure and Function in Parkinson's Disease Reviews the molecular events initiated by unfolded or misfolded proteins leading to conformational human diseases, with special emphasis on the macromolecular homo- and heteroassociations of the malfolded proteins into characteristic ultrastructures found primarily in Parkinson's and Alzheimer's diseases English Protein folding Proteins- Denaturation Nervous system- Degeneration- Pathophysiology Proteostasis Deficiencies Protein Folding Neurodegenerative Diseases Metabolic Diseases Biophysical Phenomena Biochemical Phenomena Nervous System Diseases Disease Chemical Phenomena Nutritional and Metabolic Diseases Neurodegenerative Diseases- physiopathology Physical Phenomena Phenomena and Processes HEALTH & FITNESS- Diseases- Nervous System (incl. Brain) MEDICAL- Neurology. Sciences de la vie. Biomédecine. Nervous system- Degeneration- Pathophysiology. Protein folding. Proteins- Denaturation. Electronic books Ovdi, Judit Orosz, Ferenc Print version Protein folding and misfolding. Dordrecht ; London : Springer, 2009 9781402094330 1402094337 (OCoLC)276224601 Focus on structural biology 7