Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy (Q24676326)

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English	Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy	scientific article

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instance of

scholarly article

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title

Drosophila model of human inherited triosephosphate isomerase deficiency glycolytic enzymopathy (English)

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main subject

Drosophila

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Triose phosphate isomerase Dmel_CG2171

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stated in

GOA release 2020-03-11

triosephosphate isomerase deficiency

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based on heuristic

inferred from title

author name string

Alicia M Celotto

series ordinal

1

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Adam C Frank

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2

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Jacquelyn L Seigle

series ordinal

3

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Michael J Palladino

series ordinal

4

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language of work or name

English

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publication date

November 2006

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published in

Genetics

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volume

174

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issue

3

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page(s)

1237-46

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cites work

Molecular analysis of a series of alleles in humans with reduced activity at the triosephosphate isomerase locus

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

7 April 2017

Human triosephosphate isomerase deficiency resulting from mutation of Phe-240

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

7 April 2017

Human triosephosphate isomerase cDNA and protein structure. Studies of triosephosphate isomerase deficiency in man

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

7 April 2017

Refined 1.83 A structure of trypanosomal triosephosphate isomerase crystallized in the presence of 2.4 M-ammonium sulphate. A comparison with the structure of the trypanosomal triosephosphate isomerase-glycerol-3-phosphate complex

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

7 April 2017

Primary structure of human triosephosphate isomerase

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

7 April 2017

HEREDITARY HEMOLYTIC ANEMIA WITH TRIOSEPHOSPHATE ISOMERASE DEFICIENCY

2 references

stated in

PubMed Central

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

7 April 2017

Triosephosphate isomerase deficiency: historical perspectives and molecular aspects

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

7 April 2017

Structure of chicken muscle triose phosphate isomerase determined crystallographically at 2.5Å resolution: using amino acid sequence data

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

7 April 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

7 April 2017

Population genetics of the metabolically related Adh, Gpdh and Tpi polymorphisms in Drosophila melanogaster : II. Temporal and Spatial Variation in an Orchard Population

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 September 2017

Structure of a high-resolution crystal form of human triosephosphate isomerase: improvement of crystals using the gel-tube method

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 September 2017

Drosophila: a "model" model system to study neurodegeneration

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 September 2017

Structure of triosephosphate isomerase from Escherichia coli determined at 2.6 A resolution

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 September 2017

Triosephosphate isomerase deficiency: a neurodegenerative misfolding disease

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 September 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 September 2017

Premature translation termination mediates triosephosphate isomerase mRNA degradation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 September 2017

Genetic and cytogenetic studies of four glycolytic enzymes in Drosophila melanogaster: Aldolase, triosephosphate isomerase, 3-phosphoglycerate kinase, and phosphoglucomutase

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 September 2017

A-to-I pre-mRNA editing in Drosophila is primarily involved in adult nervous system function and integrity

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

30 May 2018

Neuroprotective effects of creatine and cyclocreatine in animal models of Huntington's disease.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

30 May 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

30 May 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

30 May 2018

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.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

30 May 2018

Structure and expression of the triose phosphate isomerase (Tpi) gene of Drosophila melanogaster

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

30 May 2018

Mitochondrial encephalomyopathy in Drosophila.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 November 2018

Neuroprotective mechanisms of creatine occur in the absence of mitochondrial creatine kinase

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 November 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 November 2018

Nucleotide variation in the triosephosphate isomerase (Tpi) locus of Drosophila melanogaster and Drosophila simulans

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 November 2018

Molecular analysis of four ENU induced triosephosphate isomerase null mutants in Mus musculus

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 November 2018

Myopathy with altered mitochondria due to a triosephosphate isomerase (TPI) deficiency.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1667072

retrieved

28 November 2018

Synaptic physiology and ultrastructure in comatose mutants define an in vivo role for NSF in neurotransmitter release

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16980388

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triose phosphate isomerase deficiency in 3 French families: two novel null alleles, a frameshift mutation (TPI Alfortville) and an alteration in the initiation codon (TPI Paris)

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16980388

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Elevated frequency of carriers for triosephosphate isomerase deficiency in newborn infants

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16980388

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis of triosephosphate isomerase deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16980388

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16980388

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16980388

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The mechanism of the triosephosphate isomerase reaction.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16980388

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Crystallization of yeast triose phosphate isomerase from polyethylene glycol. Protein crystal formation following phase separation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16980388

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Triosephosphate isomerase deficiency: 2 new cases

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16980388

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Refined 1.83 Å structure of trypanosomal triosephosphate isomerase crystallized in the presence of 2.4 m-ammonium sulphate

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1534%2FGENETICS.106.063206

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Triosephosphate isomerase deficiency: a neurodegenerative misfolding disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1534%2FGENETICS.106.063206

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1534/GENETICS.106.063206

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4982888

OpenCitations bibliographic resource ID

4982888

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4982888

PMC publication ID

1667072

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4982888

PubMed publication ID

16980388

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

4982888

ResearchGate publication ID

6814638

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