|
|
|
|
LEADER |
00000cam a2200000 a 4500 |
001 |
SCIDIR_on1344187640 |
003 |
OCoLC |
005 |
20231120010703.0 |
006 |
m o d |
007 |
cr un|---aucuu |
008 |
220912s2022 mau o 000 0 eng d |
040 |
|
|
|a YDX
|b eng
|c YDX
|d OPELS
|d EBLCP
|d OCLCF
|d OCLCQ
|
020 |
|
|
|a 9780323997812
|q (electronic bk.)
|
020 |
|
|
|a 0323997813
|q (electronic bk.)
|
020 |
|
|
|z 9780323997805
|
020 |
|
|
|z 0323997805
|
035 |
|
|
|a (OCoLC)1344187640
|
050 |
|
4 |
|a QP551
|
082 |
0 |
4 |
|a 572.645
|2 23
|
245 |
0 |
0 |
|a Disorders of protein synthesis /
|c Edited by Rossen Donev.
|
260 |
|
|
|a Cambridge, MA :
|b Academic Press,
|c 2022.
|
300 |
|
|
|a 1 online resource.
|
490 |
0 |
|
|a Advances in protein chemistry and structural biology ;
|v 132
|
588 |
0 |
|
|a Print version record.
|
505 |
0 |
|
|a Intro -- Disorders of Protein Synthesis -- Copyright -- Contents -- Contributors -- Chapter One: Translation termination codons in protein synthesis and disease -- 1. Ribosome fidelity and translation termination -- 2. Nonsense mutations and the mRNA quality control -- 3. Ribosome readthrough -- 3.1. Mechanism, programmed readthrough and natural vs premature stop codons -- 3.2. Readthrough-inducing compounds -- 3.3. The determinants of readthrough -- 3.3.1. The sequence context -- 3.3.2. The reinserted amino acid -- 4. Readthrough induction as a therapeutic approach for PTC suppression
|
505 |
8 |
|
|a 4.1. Cystic fibrosis -- 4.2. Duchenne muscular dystrophy -- 4.3. Coagulation factor deficiencies -- 4.4. Lysosomal storage disorders -- 5. Conclusions -- Author contributions -- Funding -- Conflicts of interest -- References -- Chapter Two: The disturbance of protein synthesis/degradation homeostasis is a common trait of age-related neurodegenerat ... -- 1. Introduction -- 2. Proteostasis: The balance between synthesis, folding and degradation -- 2.1. Protein re-folding and surveillance -- 2.1.1. Molecular chaperones -- 2.1.2. The unfolded protein response -- 2.1.3. The integrated stress response
|
505 |
8 |
|
|a 2.2. Protein degradation -- 2.2.1. The ubiquitin proteome system -- 2.2.2. Autophagy -- 3. The proteostasis network in the brain -- 3.1. Evidence of aberrant proteostasis in age-related neurodegenerative diseases -- 3.1.1. Alzheimer�s disease -- 3.1.2. Parkinson�s disease -- 3.1.3. Amyotrophic lateral sclerosis -- References -- Chapter Three: Computational and structural investigation of Palmitoyl-Protein Thioesterase 1 (PPT1) protein causing Neur ... -- 1. Introduction -- 2. Materials and methods -- 2.1. Sequence and mutations retrieval
|
505 |
8 |
|
|a 2.2. Deleteriousness, stability, and conservation analysis -- 2.3. Structural effects prediction -- 2.4. Molecular dynamics simulation (MDS) analysis -- 3. Results -- 3.1. Sequence and mutations retrieval -- 3.2. Deleteriousness, stability, and conservation analysis -- 3.3. Structural effects prediction -- 3.4. Molecular dynamics simulations -- 4. Discussion -- 5. Conclusion -- Acknowledgment -- Role of funding source -- Author contributions -- Conflict of interest -- References
|
505 |
8 |
|
|a Chapter Four: Translation initiation and its relationship with metabolic mechanisms in cancer development, progression an ... -- 1. Introduction -- 2. Translation initiation and its regulation -- 2.1. The formation of the preinitiation complex (PIC) -- 2.2. mRNA activation by assembly with eIF4F complex and binding to the 43S PIC -- 2.2.1. Formation of mRNA structures in 5 untranslated region (5UTR) -- 2.3. Scanning of the mRNA-bound ribosomal complex along with the 5UTR mRNA -- 2.4. Formation of the 80S ribosome -- 3. The impact of translation initiation in cancer
|
650 |
|
0 |
|a Proteins
|x Synthesis.
|
650 |
|
7 |
|a Proteins
|x Synthesis.
|2 fast
|0 (OCoLC)fst01079764
|
655 |
|
0 |
|a Electronic books.
|
700 |
1 |
|
|a Donev, Rossen.
|
776 |
0 |
8 |
|i ebook version :
|z 9780323997812
|
776 |
0 |
8 |
|c Original
|z 0323997805
|z 9780323997805
|w (OCoLC)1296534005
|
856 |
4 |
0 |
|u https://sciencedirect.uam.elogim.com/science/bookseries/18761623/132
|z Texto completo
|