Characterization of splice variants of the genes encoding human mitochondrial HMG-CoA lyase and HMG-CoA synthase, the main enzymes of the ketogenesis pathway - Wikidata - awgldk - TriplyDB

Characterization of splice variants of the genes encoding human mitochondrial HMG-CoA lyase and HMG-CoA synthase, the main enzymes of the ketogenesis pathway

Characterization of splice variants of the genes encoding human mitochondrial HMG-CoA lyase and HMG-CoA synthase, the main enzymes of the ketogenesis pathway

http://www.wikidata.org/entity/Q28249240

about

Characterization of a novel HMG-CoA lyase enzyme with a dual location in endoplasmic reticulum and cytosol Quantitative proteomics reveals that enzymes of the ketogenic pathway are associated with prostate cancer progression Alternative splice variants in TIM barrel proteins from human genome correlate with the structural and evolutionary modularity of this versatile protein fold Metabolic biology of 3-methylglutaconic acid-uria: a new perspective.Fatty acid transport protein 1 (FATP1) localizes in mitochondria in mouse skeletal muscle and regulates lipid and ketone body disposal.3-Hydroxy-3-methylglutaric aciduria with bilateral basal ganglia lesion: A case report Transcriptomic profiling of TK2 deficient human skeletal muscle suggests a role for the p53 signalling pathway and identifies growth and differentiation factor-15 as a potential novel biomarker for mitochondrial myopathies.Neuroketotherapeutics: A modern review of a century-old therapy.β-Hydroxybutyrate in the Brain: One Molecule, Multiple Mechanisms.Transcriptional analysis of abdominal fat in chickens divergently selected on bodyweight at two ages reveals novel mechanisms controlling adiposity: validating visceral adipose tissue as a dynamic endocrine and metabolic organ.Role of Sex Hormones on Brain Mitochondrial Function, with Special Reference to Aging and Neurodegenerative Diseases.

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P2860

Characterization of splice variants of the genes encoding human mitochondrial HMG-CoA lyase and HMG-CoA synthase, the main enzymes of the ketogenesis pathway

http://www.wikidata.org/entity/Q28249240

description

2012 nî lūn-bûn

@nan

2012 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի ապրիլին հրատարակված գիտական հոդված

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2012年の論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年論文

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2012年论文

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name

Characterization of splice var ...... mes of the ketogenesis pathway

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Characterization of splice var ...... mes of the ketogenesis pathway

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Characterization of splice var ...... mes of the ketogenesis pathway

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type

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Characterization of splice var ...... mes of the ketogenesis pathway

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Characterization of splice var ...... mes of the ketogenesis pathway

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Characterization of splice var ...... mes of the ketogenesis pathway

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Characterization of splice var ...... mes of the ketogenesis pathway

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Characterization of splice var ...... mes of the ketogenesis pathway

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Characterization of splice var ...... mes of the ketogenesis pathway

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S11033-011-1270-8

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Molecular Biology Reports

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Characterization of splice var ...... mes of the ketogenesis pathway

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Angeles Pié

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Beatriz Puisac

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Fausto G Hegardt

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Feliciano J Ramos

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Jan-Jaap Wesselink

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Juan Carlos de Karam

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Juan Pié

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María Arnedo

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María Concepción Gil-Rodríguez

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María Esperanza Teresa-Rodrigo

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P2860

Crystal structure of human 3-hydroxy-3-methylglutaryl-CoA Lyase: insights into catalysis and the molecular basis for hydroxymethylglutaric aciduria

Evidence supporting a role for histidine-235 in cation binding to human 3-hydroxy-3-methyglutaryl-CoA lyase

3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning and characterization of a mouse liver HL cDNA and subchromosomal mapping of the human and mouse HL genes

Identification of functional exonic splicing enhancer motifs recognized by individual SR proteins

A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

Crystal structures of human HMG-CoA synthase isoforms provide insights into inherited ketogenesis disorders and inhibitor design

Human mitochondrial HMG CoA synthase: liver cDNA and partial genomic cloning, chromosome mapping to 1p12-p13, and possible role in vertebrate evolution

Ten novel HMGCL mutations in 24 patients of different origin with 3-hydroxy-3-methyl-glutaric aciduria

Tissue-cell- and species-specific expression of gonadotropin-regulated long chain acyl-CoA synthetase (GR-LACS) in gonads, adrenal and brain. Identification of novel forms in the brain

RASMOL: biomolecular graphics for all

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s11033-011-1270-8

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4777-4785

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scholarly article

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4

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Paulino Gómez-Puertas

Ignacio Giménez

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2011-09-28T00:00:00Z

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