Related references
Note: Only part of the references are listed.Organelle-targeted delivery of biological macromolecules using the protein transduction domain: Potential applications for peptide aptamer delivery into the nucleus
Tomoaki Yoshikawa et al.
JOURNAL OF MOLECULAR BIOLOGY (2008)
Cellular uptake and lysosomal delivery of galactocerebrosidase tagged with the HIV Tat protein transduction domain
Xian-Yang Zhang et al.
JOURNAL OF NEUROCHEMISTRY (2008)
TAT-mediated delivery of LAD restores pyruvate dehydrogenase complex activity in the mitochondria of patients with LAD deficiency
Matan Rapoport et al.
MOLECULAR THERAPY (2008)
Therapeutic approaches in glycogen storage disease type II/Pompe disease
Benedikt Schoser et al.
NEUROTHERAPEUTICS (2008)
Current Strategies in the Management of Lysosomal Storage Diseases
Bryce A. Heese
SEMINARS IN PEDIATRIC NEUROLOGY (2008)
The role of amino acids T148 and R281 in human dihydrolipoamide dehydrogenase
Yi-Chun Wang et al.
JOURNAL OF BIOMEDICAL SCIENCE (2008)
Molecular dynamics simulations suggest a mechanism for translocation of the HIV-1 TAT peptide across lipid membranes
Henry D. Herce et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
TAT transduction: the molecular mechanism and therapeutic prospects
Jacob M. Gump et al.
TRENDS IN MOLECULAR MEDICINE (2007)
Histochemical staining and quantification of dihydrolipoamide dehydrogenase diaphorase activity using blue native PAGE
Liang-Jun Yan et al.
ELECTROPHORESIS (2007)
The role of N286 and D320 in the reaction mechanism of human dihydrolipoamide dehydrogenase (E3) center domain
Yi-Chun Wang et al.
JOURNAL OF BIOMEDICAL SCIENCE (2007)
Molecular architecture of the pyruvate dehydrogenase complex: bridging the gap
M. Smolle et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2006)
TAT-mediated intracellular delivery of purine nucleoside phosphorylase corrects its deficiency in mice
Ana Toro et al.
JOURNAL OF CLINICAL INVESTIGATION (2006)
Novel mutations in dihydrolipoamide dehydrogenase deficiency in two cousins with borderline-normal PDH complex activity
Jessie M. Cameron et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
A new level of architectural complexity in the human pyruvate dehydrogenase complex
Michaela Smolle et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
The kinetics and tissue distribution of protein transduction in mice
SR Cai et al.
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2006)
How dihydrolipoamide dehydrogenase-binding protein binds dihydrolipoamide dehydrogenase in the human pyruvate dehydrogenase complex
EM Ciszak et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2006)
Crystal structure of human dihydrolipoamide dehydrogenase:: NAD+/NADH binding and the structural basis of disease-causing mutations
CA Brautigam et al.
JOURNAL OF MOLECULAR BIOLOGY (2005)
Short-term, high dose enzyme replacement therapy in sialidosis mice
DN Wang et al.
MOLECULAR GENETICS AND METABOLISM (2005)
Mice deficient in dihydrolipoamide dehydrogenase show increased vulnerability to MPTP, malonate and 3-nitropropionic acid neurotoxicity
P Klivenyi et al.
JOURNAL OF NEUROCHEMISTRY (2004)
Enzyme-replacement therapy for metabolic storage disorders
RO Brady et al.
LANCET NEUROLOGY (2004)
Targeting proteins to mitochondria using TAT
V Del Gaizo et al.
MOLECULAR GENETICS AND METABOLISM (2003)
Mitochondria
PF Chinnery et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2003)
Mechanisms of disease: Mitochondrial respiratory-chain diseases
S DiMauro et al.
NEW ENGLAND JOURNAL OF MEDICINE (2003)
A novel TAT-mitochondrial signal sequence fusion protein is processed, stays in mitochondria, and crosses the placenta
V Del Gaizo et al.
MOLECULAR THERAPY (2003)
TAT-mediated protein transduction into mammalian cells
M Becker-Hapak et al.
METHODS (2001)
Arginine-rich peptides - An abundant source of membrane-permeable peptides having potential as carriers for intracellular protein delivery
S Futaki et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2001)
Protein transduction: unrestricted delivery into all cells?
SR Schwarze et al.
TRENDS IN CELL BIOLOGY (2000)
ATP synthesis in lipoamide dehydrogenase deficiency
A Saada et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2000)