(Q46685505)

24 December 2017

title

TAT-mediated delivery of LAD restores pyruvate dehydrogenase complex activity in the mitochondria of patients with LAD deficiency (English)

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24 December 2017

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2

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24 December 2017

author name string

Matan Rapoport

series ordinal

1

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24 December 2017

Orly Elpeleg

series ordinal

3

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24 December 2017

Haya Lorberboum-Galski

series ordinal

4

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24 December 2017

publication date

5 February 2008

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24 December 2017

published in

Molecular Therapy

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24 December 2017

volume

16

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24 December 2017

issue

4

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24 December 2017

page(s)

691-697

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24 December 2017

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7 January 2021

Mitochondrial respiratory-chain diseases

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7 January 2021

Crystal structure of human dihydrolipoamide dehydrogenase: NAD+/NADH binding and the structural basis of disease-causing mutations

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7 January 2021

Molecular architecture of the pyruvate dehydrogenase complex: bridging the gap

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7 January 2021

A new level of architectural complexity in the human pyruvate dehydrogenase complex

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7 January 2021

Structural insight into interactions between dihydrolipoamide dehydrogenase (E3) and E3 binding protein of human pyruvate dehydrogenase complex

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7 January 2021

ATP synthesis in lipoamide dehydrogenase deficiency.

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7 January 2021

Molecular basis of lipoamide dehydrogenase deficiency in Ashkenazi Jews

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7 January 2021

Lipoamide Dehydrogenase Deficiency Due to a Novel Mutation in the Interface Domain

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7 January 2021

Identification of two missense mutations in a dihydrolipoamide dehydrogenase-deficient patient

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7 January 2021

Deficiency of dihydrolipoamide dehydrogenase due to two mutant alleles (E340K and G101del). Analysis of a family and prenatal testing

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7 January 2021

Identification of two mutations in a compound heterozygous child with dihydrolipoamide dehydrogenase deficiency

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7 January 2021

Mitochondrial disorders

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7 January 2021

Enzyme-replacement therapy for metabolic storage disorders

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7 January 2021

Short-term, high dose enzyme replacement therapy in sialidosis mice

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7 January 2021

Enzyme replacement for lysosomal diseases

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7 January 2021

Arginine-rich peptides. An abundant source of membrane-permeable peptides having potential as carriers for intracellular protein delivery

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7 January 2021

Biological applications of protein transduction technology

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7 January 2021

Transducing proteins to manipulate intracellular targets

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7 January 2021

Autonomous functional domains of chemically synthesized human immunodeficiency virus tat trans-activator protein

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7 January 2021

Cellular uptake of the tat protein from human immunodeficiency virus

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7 January 2021

In vivo protein transduction: delivery of a biologically active protein into the mouse

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7 January 2021

Transduction of functionally active TAT fusion proteins into cornea.

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7 January 2021

The kinetics and tissue distribution of protein transduction in mice

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7 January 2021

A novel approach for enzyme replacement therapy. The use of phenylalanine hydroxylase-based fusion proteins for the treatment of phenylketonuria

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7 January 2021

Targeting proteins to mitochondria using TAT.

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7 January 2021

A novel TAT-mitochondrial signal sequence fusion protein is processed, stays in mitochondria, and crosses the placenta

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7 January 2021

Regulation of the activity of the pyruvate dehydrogenase complex

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7 January 2021

Lipoamide dehydrogenase activity in lymphocytes

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7 January 2021

Lipoamide dehydrogenase deficiency: a new cause for recurrent myoglobinuria

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7 January 2021

Mitochondrial dysfunction and oxidative damage in parkin-deficient mice

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7 January 2021

The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosis

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7 January 2021

Identifiers

DOI

10.1038/MT.2008.4

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24 December 2017

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24 December 2017