Christina Pacak

University of Minnesota

United States

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Articles (20)

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2025

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2020

Collaborators (12)

Carla Zingariello

Assistant Professor

UNITED STATES

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Peter Kang

University of Minnesota

UNITED STATES

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Manuela Corti

Associate Professor

University of Florida

UNITED STATES

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Chelsey Simmons

Associate Professor

University of Florida

UNITED STATES

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Jonathan Badalamenti

University of Minnesota

UNITED STATES

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Silvère M van der Maarel

Leiden University Medical Center

NETHERLANDS

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William Cade

Division Chief, Professor

Duke University School of Medicine

UNITED STATES

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Payam Mohassel

Associate Professor

Johns Hopkins University

UNITED STATES

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Atsushi Asakura

Associate Professor

University of Minnesota

UNITED STATES

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Janny Pineiro Llanes

Research Assistant Professor

University of Florida

UNITED STATES

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Alessandro Bartolomucci

University of Minnesota

UNITED STATES

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George Aslanidi

Professor

University of Minnesota

UNITED STATES

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Christina Pacak

Research Interests

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Articles (20)

Rescue of mitochondrial dysfunction through alteration of extracellular matrix composition in barth syndrome cardiac fibroblasts

The impact of Hnrnpl deficiency on transcriptional patterns of developing muscle cells

ACSS2 involved in acetyl‐CoA synthesis regulates skeletal muscle function

The D2.B10-Dmd/J mouse model of DMD exhibits a severe mitochondrial deficiency not observed in the C57BL/10ScSn-Dmd/J mouse

Cardiac Transplantation Does Not Improve Exercise Tolerance, Muscle Mass, or Substrate Metabolism in Barth Syndrome

The mouse Social Frailty Index (mSFI): a novel behavioral assessment for impaired social functioning in aging mice

Dominant stop-loss HNRNPA1 variants in juvenile-onset myopathy

AAV-DJ is superior to AAV9 for targeting brain and spinal cord, and de-targeting liver across multiple delivery routes in mice

Cognitive Decline and Other Late-Stage Neurologic Complications in Cockayne Syndrome

Cognitive Decline and Other Late-Stage Neurologic Complications in Cockayne Syndrome

Peripheral neuropathies associated with DNA repair disorders

Elevated liver glycogenolysis mediates higher blood glucose during acute exercise in Barth syndrome

Diagnostic capabilities of nanopore long-read sequencing in muscular dystrophy.

Matrix produced by diseased cardiac fibroblasts affects early myotube formation and function

The Notch signaling pathway in skeletal muscle health and disease

A review of the underlying genetics and emerging therapies for canine cardiomyopathies

A form of muscular dystrophy associated with pathogenic variants in JAG2

Resistance exercise training with protein supplementation improves skeletal muscle strength and improves quality of life in late adolescents and young adults with Barth syndrome: A pilot study.

Bioprocessing of Human Mesenchymal Stem Cells: From Planar Culture to Microcarrier-Based Bioreactors

Arginine kinetics are altered in a pilot sample of adolescents and young adults with Barth syndrome

Collaborators (12)

Carla Zingariello

Peter Kang

Manuela Corti

Chelsey Simmons

Jonathan Badalamenti

Silvère M van der Maarel

William Cade

Payam Mohassel

Atsushi Asakura

Janny Pineiro Llanes

Alessandro Bartolomucci

George Aslanidi

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