MARC

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040 |a N$T  |b eng  |e rda  |e pn  |c N$T  |d EBLCP  |d N$T  |d OPELS  |d UKMGB  |d OCLCF  |d YDX  |d UKAHL  |d OCLCQ  |d ERF  |d LVT  |d UX1  |d VT2  |d OCLCO  |d OCLCA  |d OCLCQ  |d OCLCO  |d COM  |d OCL  |d OCLCQ  |d CASUM  |d OCLCO 
015 |a GBB9A7073  |2 bnb 
016 7 |a 019425787  |2 Uk 
019 |a 1102804516  |a 1229425118  |a 1235833002 
020 |a 9780128137970  |q (electronic bk.) 
020 |a 0128137975  |q (electronic bk.) 
020 |z 9780128137963 
020 |z 0128137967 
035 |a (OCoLC)1102638944  |z (OCoLC)1102804516  |z (OCoLC)1229425118  |z (OCoLC)1235833002 
050 4 |a QH599 
060 4 |a 2019 F-939 
060 4 |a WL 140 
072 7 |a SCI  |x 007000  |2 bisacsh 
082 0 4 |a 572.87  |2 23 
245 0 0 |a Chromatin signaling and neurological disorders /  |c edited by Olivier Binda. 
264 1 |a London :  |b Academic Press,  |c [2019] 
264 4 |c �2019 
300 |a 1 online resource 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a Translational epigenetics series ;  |v v. 12 
500 |a Includes index. 
588 0 |a Online resource; title from PDF title page (EBSCO, viewed June 3, 2019). 
505 0 |a Front Cover; Chromatin Signaling and Neurological Disorders; Translational Epigenetics Series; Chromatin Signaling and Neurological Disorders; Copyright; Contents; Contributors; Preface; Chromatin and epigenetics; Chromatin signaling and neurological diseases; References; 1 -- Chromatin and epigenetic signaling pathways; 1.1 Chromatin signaling and epigenetics; 1.2 Chromatin organization; 1.3 Histone posttranslational modifications and the histone code; 1.4 Functions of histone posttranslational modifications; 1.5 DNA methylation; 1.6 Writers, erasers, and readers; 1.6.1 Histone writers 
505 8 |a 1.6.2 DNA writers1.6.3 Histone erasers; 1.6.4 DNA erasers; 1.6.5 Histone readers; 1.6.6 DNA readers; 1.7 Modification cross talk; 1.8 Effects of metabolism on histone and DNA modifications; 1.9 Epigenetic inheritance; 1.10 Summary; References; 1 -- Neurodegenerative disorders; 2 -- Into the unknown: chromatin signaling in spinal muscular atrophy; 2.1 Spinal muscular atrophy: prevalence, genetic basis, clinical features, and pathogenesis; 2.2 The survival motor neuron protein: localization, structure, and function; 2.3 Epigenetic landscape in spinal muscular atrophy pathogenesis 
505 8 |a 2.4 Targeting epigenetic factors as potential therapeutics in spinal muscular atrophy2.4.1 Histone deacetylase inhibitors as regulators of the survival motor neuron gene; 2.4.2 The nonspecific effect of histone deacetylase inhibitors; 2.4.3 The potential protective effect of histone deacetylase inhibitors in the pathogenesis of spinal muscular atrophy; 2.5 Conclusion; Acronyms and abbreviations; Acknowledgments; References; 3 -- Charcot-Marie-Tooth disease; 3.1 Introduction; 3.2 Epigenetic regulation of Schwann cell development; 3.3 Epigenetic regulation of dosage-sensitive genes 
505 8 |a 3.4 Epigenetic regulators targeted by CMT mutations3.4.1 DNMT1; 3.4.2 LMNA; 3.4.3 SYNE1; 3.4.4 MED25; 3.4.5 SETX; 3.4.6 MORC2; 3.4.7 PRDM12; 3.5 Novel mechanisms for CMT mutations; 3.6 Summary; Acknowledgments; References; 4 -- Epigenetic mechanisms in Huntington's disease; 4.1 Introduction; 4.2 Huntington's disease; 4.2.1 Neuropathology of HD; 4.3 Transcriptional dysregulation in HD; 4.4 Altered epigenetic marks in HD; 4.4.1 Histone modifications; 4.4.1.1 Histone acetylation; 4.4.1.2 Histone acetylation alterations in HD; 4.4.1.3 Histone methylation; 4.4.1.4 Histone methylation changes in HD 
505 8 |a 4.4.1.5 Histone phosphorylation4.4.1.6 Histone phosphorylation and HD; 4.4.1.7 Histone ubiquitination; 4.4.1.8 Altered histone ubiquitination in HD; 4.4.2 DNA methylation; 4.4.3 DNA methylation changes in HD; 4.4.3.1 Global DNA methylation changes; 4.4.3.2 Gene-specific DNA methylation changes; 4.4.3.3 Implicating DNA methylation enzymes; 4.5 Epigenetic-based therapies; 4.5.1 HDAC inhibitors as a treatment for HD; 4.5.2 Methylation-inhibiting drugs; 4.6 Concluding remarks; 4.7 Abbreviations; References; 5 -- The epigenetics of multiple sclerosis 
504 |a Includes bibliographical references and index. 
650 0 |a Chromatin. 
650 0 |a Nervous system  |x Diseases. 
650 0 |a Genetic regulation. 
650 1 2 |a Nervous System Diseases  |x genetics  |0 (DNLM)D009422Q000235 
650 1 2 |a Chromatin  |x metabolism  |0 (DNLM)D002843Q000378 
650 2 2 |a Histones  |x metabolism  |0 (DNLM)D006657Q000378 
650 2 2 |a Signal Transduction  |x genetics  |0 (DNLM)D015398Q000235 
650 2 2 |a Chromatin Assembly and Disassembly  |0 (DNLM)D042002 
650 2 2 |a Gene Expression Regulation  |0 (DNLM)D005786 
650 2 2 |a Epigenesis, Genetic  |0 (DNLM)D044127 
650 2 |a Chromatin  |0 (DNLM)D002843 
650 2 |a Nervous System Diseases  |0 (DNLM)D009422 
650 6 |a Chromatine.  |0 (CaQQLa)201-0062726 
650 6 |a Syst�eme nerveux  |x Maladies.  |0 (CaQQLa)201-0007359 
650 6 |a R�egulation g�en�etique.  |0 (CaQQLa)201-0028678 
650 7 |a SCIENCE  |x Life Sciences  |x Biochemistry.  |2 bisacsh 
650 7 |a Genetic regulation  |2 fast  |0 (OCoLC)fst00940086 
650 7 |a Chromatin  |2 fast  |0 (OCoLC)fst00859922 
650 7 |a Nervous system  |x Diseases  |2 fast  |0 (OCoLC)fst01036098 
655 4 |a Dictionaries. 
655 4 |a Internet Resources. 
700 1 |a Binda, Olivier,  |e editor. 
776 0 8 |i Print version:  |t Chromatin signaling and neurological disorders.  |d London : Academic Press, [2019]  |z 0128137967  |z 9780128137963  |w (OCoLC)1022787494 
830 0 |a Translational epigenetics series ;  |v v. 12. 
856 4 0 |u https://sciencedirect.uam.elogim.com/science/book/9780128137963  |z Texto completo