Misfolded proteins recognition strategies of E3 ubiquitin ligases and neurodegenerative diseases. - Test2 - elhamkhani - TriplyDB

Misfolded proteins recognition strategies of E3 ubiquitin ligases and neurodegenerative diseases.

Misfolded proteins recognition strategies of E3 ubiquitin ligases and neurodegenerative diseases.

http://www.wikidata.org/entity/Q38045837

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A Decade of Boon or Burden: What Has the CHIP Ever Done for Cellular Protein Quality Control Mechanism Implicated in Neurodegeneration and Aging?Protein quality control system in neurodegeneration: a healing company hard to beat but failure is fatal.Autophagy coupling interplay: can improve cellular repair and aging?Chaperoning proteins for destruction: diverse roles of Hsp70 chaperones and their co-chaperones in targeting misfolded proteins to the proteasome Mahogunin ring finger-1 (MGRN1) suppresses chaperone-associated misfolded protein aggregation and toxicity.Mahogunin Ring Finger-1 (MGRN1), a Multifaceted Ubiquitin Ligase: Recent Unraveling of Neurobiological Mechanisms.Indomethacin elicits proteasomal dysfunctions develops apoptosis through mitochondrial abnormalities.Ubiquitin ligase ITCH recruitment suppresses the aggregation and cellular toxicity of cytoplasmic misfolded proteins.Human Telomerase Reverse Transcriptase (hTERT) Positively Regulates 26S Proteasome Activity.Co-expression Patterns between ATN1 and ATXN2 Coincide with Brain Regions Affected in Huntington's Disease.Proteasomal Dysfunction Induced By Diclofenac Engenders Apoptosis Through Mitochondrial Pathway.

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P2860

Misfolded proteins recognition strategies of E3 ubiquitin ligases and neurodegenerative diseases.

http://www.wikidata.org/entity/Q38045837

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artigo científico

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artikel ilmiah

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Misfolded proteins recognition ...... nd neurodegenerative diseases.

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Misfolded proteins recognition ...... nd neurodegenerative diseases.

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Misfolded proteins recognition ...... nd neurodegenerative diseases.

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S12035-012-8351-0

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Molecular Neurobiology

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Misfolded proteins recognition ...... nd neurodegenerative diseases.

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Amit Mishra

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Deepak Chhangani

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Nihar Ranjan Jana

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A SMAD ubiquitin ligase targets the BMP pathway and affects embryonic pattern formation

Identification of CHIP, a novel tetratricopeptide repeat-containing protein that interacts with heat shock proteins and negatively regulates chaperone functions.

The ubiquitin-proteasome proteolytic pathway: destruction for the sake of construction

The RBCC gene RFP2 (Leu5) encodes a novel transmembrane E3 ubiquitin ligase involved in ERAD

The E3 ligase Smurf1 regulates Wolfram syndrome protein stability at the endoplasmic reticulum

Membrane topology of the yeast endoplasmic reticulum-localized ubiquitin ligase Doa10 and comparison with its human ortholog TEB4 (MARCH-VI)

Parkin is recruited into aggresomes in a stress-specific manner: over-expression of parkin reduces aggresome formation but can be dissociated from parkin's effect on neuronal survival

Insights into Lafora disease: malin is an E3 ubiquitin ligase that ubiquitinates and promotes the degradation of laforin.

Cloning of human and mouse cDNAs encoding novel zinc finger proteins expressed in cerebellum and hippocampus

Parkin accumulation in aggresomes due to proteasome impairment

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s12035-012-8351-0

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302-312

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scholarly article

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10.1007/S12035-012-8351-0

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1

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47

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2012-09-22T00:00:00Z

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1024919377

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23001884

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neurodegeneration