Stereoselective HDAC inhibition from cysteine-derived zinc-binding groups.

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Development of histone deacetylase inhibitors as therapeutics for neurological disease Capillary microfluidic electrophoretic mobility shift assays: application to enzymatic assays in drug discovery.

P2860

Q33670661-27A32BDD-00AF-465C-8836-50922391AF04 Q38028651-1EA4314B-45D0-45A2-AFEC-DA0F1248262B

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Stereoselective HDAC inhibition from cysteine-derived zinc-binding groups.

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http://www.wikidata.org/entity/Q45955357

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2009 nî lūn-bûn

@nan

2009年の論文

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2009年学术文章

@wuu

2009年学术文章

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2009年学术文章

@zh-cn

2009年学术文章

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

2009年學術文章

@zh-hant

name

Stereoselective HDAC inhibition from cysteine-derived zinc-binding groups.

@en

Stereoselective HDAC inhibition from cysteine-derived zinc-binding groups.

@nl

type

Item

label

Stereoselective HDAC inhibition from cysteine-derived zinc-binding groups.

@en

Stereoselective HDAC inhibition from cysteine-derived zinc-binding groups.

@nl

prefLabel

Stereoselective HDAC inhibition from cysteine-derived zinc-binding groups.

@en

Stereoselective HDAC inhibition from cysteine-derived zinc-binding groups.

@nl

P1476

Stereoselective HDAC inhibition from cysteine-derived zinc-binding groups.

@en

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Alan P Kozikowski

http://www.w3.org/2001/XMLSchema#string

Kathryn McLaughlin

http://www.w3.org/2001/XMLSchema#string

Kyle V Butler

http://www.w3.org/2001/XMLSchema#string

Rong He

http://www.w3.org/2001/XMLSchema#string

P2860

Rapid evaluation and screening of interfacial reactions on self-assembled monolayers.

Targeting CREB-binding protein (CBP) loss of function as a therapeutic strategy in neurological disorders.

Deregulation of HDAC1 by p25/Cdk5 in neurotoxicity

Epigenetic targets of HDAC inhibition in neurodegenerative and psychiatric disorders.

HDAC6: a key regulator of cytoskeleton, cell migration and cell-cell interactions.

Histone deacetylase inhibitors: the Abbott experience.

Dietary agents as histone deacetylase inhibitors.

Pulse inhibition of histone deacetylases induces complete resistance to oxidative death in cortical neurons without toxicity and reveals a role for cytoplasmic p21(waf1/cip1) in cell cycle-independent neuroprotection.

Chemical origins of isoform selectivity in histone deacetylase inhibitors.

HDAC inhibitor increases histone H3 acetylation and reduces microglia inflammatory response following traumatic brain injury in rats

P304

1292-1301

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/CMDC.200900088

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Giulio Vistoli

Brett Langley

P577

2009-08-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

19551801

http://www.w3.org/2001/XMLSchema#string

P921

stereoselectivity

Stereoselective HDAC inhibition from cysteine-derived zinc-binding groups.

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P2860

P2860

Stereoselective HDAC inhibition from cysteine-derived zinc-binding groups.

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type

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P921