Degradation of functional triose phosphate isomerase protein underlies sugarkill pathology (Q36724350)

15 August 2017

Degradation of functional triose phosphate isomerase protein underlies sugarkill pathology (English)

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15 August 2017

Jacquelyn L Seigle

1

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15 August 2017

Alicia M Celotto

series ordinal

2

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15 August 2017

Michael J Palladino

series ordinal

3

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15 August 2017

language of work or name

English

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publication date

5 May 2008

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15 August 2017

8

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inferred from page(s)

published in

Genetics

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15 August 2017

179

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15 August 2017

2

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15 August 2017

855-862

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describes a project that uses

15 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2429879/fullTextXML

inferred from PubMed Central ID database lookup

cites work

Triosephosphate isomerase deficiency: facts and doubts

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Mechanisms of disease II: cellular protein quality control.

30 September 2017

1 reference

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Triose phosphate isomerase deficiency is caused by altered dimerization--not catalytic inactivity--of the mutant enzymes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

wasted away, a Drosophila mutation in triosephosphate isomerase, causes paralysis, neurodegeneration, and early death

30 September 2017

1 reference

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Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy

30 September 2017

1 reference

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Ubiquitin-proteasome system and Parkinson's disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

A genetic suppressor of two dominant temperature-sensitive lethal proteasome mutants of Drosophila melanogaster is itself a mutated proteasome subunit gene

30 September 2017

1 reference

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The unfolded protein response: a stress signaling pathway critical for health and disease.

30 September 2017

1 reference

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Proteasome dysfunction in mammalian aging: steps and factors involved

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Triosephosphate isomerase deficiency: consequences of an inherited mutation at mRNA, protein and metabolic levels

30 September 2017

1 reference

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Navigating the chaperone network: an integrative map of physical and genetic interactions mediated by the hsp90 chaperone

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Advanced glycation end products and RAGE: a common thread in aging, diabetes, neurodegeneration, and inflammation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Pathways of chaperone-mediated protein folding in the cytosol

30 September 2017

1 reference

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Roles of molecular chaperones in protein misfolding diseases

30 September 2017

1 reference

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Functional aspects of cellular microcompartmentation in the development of neurodegeneration: mutation induced aberrant protein-protein associations

30 September 2017

1 reference

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Genetic modifiers of tauopathy in Drosophila.

30 September 2017

1 reference

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HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY

30 September 2017

1 reference

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Temperature-sensitive paralytic mutants are enriched for those causing neurodegeneration in Drosophila.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

The proteasome in brain aging

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Triosephosphate isomerase deficiency: a neurodegenerative misfolding disease

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Molecular chaperones in the cytosol: from nascent chain to folded protein

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Triosephosphate isomerase deficiency: historical perspectives and molecular aspects

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Reversal of metabolic block in glycolysis by enzyme replacement in triosephosphate isomerase-deficient cells.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

The dominant temperature-sensitive lethal DTS7 of Drosophila melanogaster encodes an altered 20S proteasome beta-type subunit.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Search for the pathogenesis of the differing phenotype in two compound heterozygote Hungarian brothers with the same genotypic triosephosphate isomerase deficiency

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

PEST sequences and regulation by proteolysis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Identification of an essential gene, l(3)73Ai, with a dominant temperature-sensitive lethal allele, encoding a Drosophila proteasome subunit

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Crystal structure of recombinant human triosephosphate isomerase at 2.8 A resolution. Triosephosphate isomerase-related human genetic disorders and comparison with the trypanosomal enzyme

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Amino acid sequences common to rapidly degraded proteins: the PEST hypothesis

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Human triose-phosphate isomerase deficiency: a single amino acid substitution results in a thermolabile enzyme

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Characterization of triosephosphate isomerase mutants with reduced enzyme activity in Mus musculus

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Drosophila mutants with opposing effects on nerve excitability: genetic and spatial interactions in repetitive firing

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Functional hemizygosity in the human genome: direct estimate from twelve erythrocyte enzyme loci.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activity.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Generalized brain and skin proteasome inhibition in Huntington's disease

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Increased formation of methylglyoxal and protein glycation, oxidation and nitrosation in triosephosphate isomerase deficiency

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

The ubiquitin proteasome system acutely regulates presynaptic protein turnover and synaptic efficacy

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Neural dysfunction and neurodegeneration in Drosophila Na+/K+ ATPase alpha subunit mutants.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Distinct behavior of mutant triosephosphate isomerase in hemolysate and in isolated form: molecular basis of enzyme deficiency

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Identification of genes that modify ataxin-1-induced neurodegeneration.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2429879

Impaired proteasome function in Alzheimer's disease

5 September 2018

1 reference

12 December 2020

Elevated frequency of carriers for triosephosphate isomerase deficiency in newborn infants

1 reference

12 December 2020

Triosephosphate isomerase deficiency: 2 new cases

1 reference

12 December 2020

Evidence for founder effect of the Glu104Asp substitution and identification of new mutations in triosephosphate isomerase deficiency

1 reference

12 December 2020

The mechanism of the triosephosphate isomerase reaction.

1 reference

12 December 2020

Proteasome inhibition induces reversible impairments in protein synthesis.

1 reference

12 December 2020

Proteasome inhibitor-induced model of Parkinson's disease

1 reference

12 December 2020

Diminished Blood Levels of Reduced Glutathione and α-Tocopherol in Two Triosephosphate Isomerase-Deficient Brothers

1 reference

12 December 2020

10.1534/GENETICS.108.087551

Identifiers

DOI

1 reference

15 August 2017

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15 August 2017

PubMed publication ID

18458110

1 reference