M. Soustek

发表

Peripheral nerve and neuromuscular junction pathology in Pompe disease.

B. Byrne, D. Fuller, Sooyeon Lee, 2015, Human molecular genetics.

Increased mtDNA Abundance and Improved Function in Human Barth Syndrome Patient Fibroblasts Following AAV-TAZ Gene Delivery

B. Byrne, P. Kang, C. A. Pacak, 2019, International journal of molecular sciences.

Inhibition of the ER stress IRE1α inflammatory pathway protects against cell death in mitochondrial complex I mutant cells

Rutger O. Vogel, P. Puigserver, S. Gygi, 2018, Cell Death & Disease.

Comparative impact of AAV and enzyme replacement therapy on respiratory and cardiac function in adult Pompe mice

B. Byrne, D. Fuller, N. Clément, 2015, Molecular Therapy: Methods & Clinical Development.

Adeno-associated virus-mediated gene therapy for metabolic myopathy.

B. Byrne, Angela L McCall, C. Mah, 2013, Human gene therapy.

Characterization of a transgenic short hairpin RNA-induced murine model of Tafazzin deficiency.

B. Byrne, C. Mah, M. Schlame, 2011, Human gene therapy.

Intrapleural administration of AAV9 improves neural and cardiorespiratory function in Pompe disease.

B. Byrne, D. Fuller, M. ElMallah, 2013, Molecular therapy : the journal of the American Society of Gene Therapy.

Interrupting synoviolin play at the ER: a plausible action to elevate mitochondrial energetics and silence obesity

P. Puigserver, M. Soustek, 2015, The EMBO journal.

Brown Adipose YY1 Deficiency Activates Expression of Secreted Proteins Linked to Energy Expenditure and Prevents Diet-Induced Obesity

P. Puigserver, Joeva J. Barrow, M. Soustek, 2015, Molecular and Cellular Biology.

Bromodomain Inhibitors Correct Bioenergetic Deficiency Caused by Mitochondrial Disease Complex I Mutations.

Rutger O. Vogel, P. Puigserver, S. Gygi, 2016, Molecular cell.

AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome.

B. Byrne, P. Kang, C. A. Pacak, 2019, Human gene therapy.

AAV9-TAZ Gene Replacement Ameliorates Cardiac TMT Proteomic Profiles in a Mouse Model of Barth Syndrome

B. Byrne, P. Kang, C. A. Pacak, 2019, Molecular therapy. Methods & clinical development.

ER and Nutrient Stress Promote Assembly of Respiratory Chain Supercomplexes through the PERK-eIF2α Axis.

P. Puigserver, S. Gygi, Mark P. Jedrychowski, 2019, Molecular cell.

Inhibition of the ER stress IRE1α inflammatory pathway protects against cell death in mitochondrial complex I mutant cells

Rutger O. Vogel, P. Puigserver, S. Gygi, 2018, Cell Death & Disease.

Endurance training ameliorates complex 3 deficiency in a mouse model of Barth syndrome

B. Byrne, G. Walter, A. Lewin, 2015, Journal of Inherited Metabolic Disease.

Interrupting synoviolin play at the ER: a plausible action to elevate mitochondrial energetics and silence obesity

P. Puigserver, M. Soustek, 2015, The EMBO journal.