Differential HMG-CoA lyase expression in human tissues provides clues about 3-hydroxy-3-methylglutaric aciduria (Q33992645)

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English	Differential HMG-CoA lyase expression in human tissues provides clues about 3-hydroxy-3-methylglutaric aciduria	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

30 July 2017

Differential HMG-CoA lyase expression in human tissues provides clues about 3-hydroxy-3-methylglutaric aciduria (English)

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Europe PubMed Central

PubMed publication ID

30 July 2017

author name string

Beatriz Puisac

1

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30 July 2017

María Arnedo

2

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30 July 2017

Cesar H Casale

3

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30 July 2017

María Pilar Ribate

4

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30 July 2017

Tomás Castiella

5

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30 July 2017

Feliciano J Ramos

6

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30 July 2017

Antonia Ribes

7

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PubMed publication ID

30 July 2017

Celia Pérez-Cerdá

8

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PubMed publication ID

30 July 2017

Nuria Casals

9

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Europe PubMed Central

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30 July 2017

Fausto G Hegardt

10

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30 July 2017

Juan Pié

11

1 reference

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PubMed publication ID

30 July 2017

publication date

8 June 2010

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30 July 2017

Journal of Inherited Metabolic Disease

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Europe PubMed Central

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30 July 2017

33

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Europe PubMed Central

PubMed publication ID

30 July 2017

4

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Europe PubMed Central

PubMed publication ID

30 July 2017

405-410

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Europe PubMed Central

PubMed publication ID

30 July 2017

describes a project that uses

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Europe PubMed Central

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2903694/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

A Case of Dilated Cardiomyopathy Associated with 3-Hydroxy-3-Methylglutaryl-Coenzyme A (HMG CoA) Lyase Deficiency

1 reference

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

1 reference

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Role of oxidative stress in pancreatic inflammation

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Feasibility of pathways for transfer of acyl groups from mitochondria to the cytosol to form short chain acyl-CoAs in the pancreatic beta cell

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A Nonsense Mutation in the Exon 2 of the 3-Hydroxy- 3-methylglutaryl Coenzyme A Lyase (HL) Gene Producing Three Mature mRNAs Is the Main Cause of 3-Hydroxy-3-methylglutaric Aciduria in European Mediterranean Patients

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3-Hydroxy-3-methylglutaryl-CoA lyase is present in mouse and human liver peroxisomes

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Cytosolic 3-hydroxy-3-methyl glutaryl coenzyme a synthase in rat brain: Properties and developmental change

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Atypical presentation and neuropathological studies in 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

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3-Hydroxy-3-methylglutaryl-coenzyme a lyase deficiency: a review

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3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: review of 18 reported patients

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3-Hydroxy-3-methylglutaryl-CoA lyase in human skin fibroblasts: study of its properties and deficient activity in 3-hydroxy-3-methylglutaric aciduria patients using a simple spectrophotometric method

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10.1007/S10545-010-9097-3

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Europe PubMed Central

PubMed publication ID

30 July 2017

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Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

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Europe PubMed Central

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30 July 2017

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