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Rad51 inhibition is an effective means of targeting DNA repair in glioma models and CD133+ tumor-derived cells

Neuro-oncology (Charlottesville, Va.), 2011-05, Vol.13 (5), p.487-499

2011

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Factors influencing pursuit of residency training

American journal of health-system pharmacy, 2005-11, Vol.62 (21), p.2226, 35-2235

2005

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Simian Immunodeficiency Virus-Infected Macaques Treated with Highly Active Antiretroviral Therapy Have Reduced Central Nervous System Viral Replication and Inflammation but Persistence of Viral DNA

The Journal of infectious diseases, 2010-07, Vol.202 (1), p.161-170

2010

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DUX4-induced gene expression is the major molecular signature in FSHD skeletal muscle

Human molecular genetics, 2014-10, Vol.23 (20), p.5342-5352

2014

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MRI-informed muscle biopsies correlate MRI with pathology and DUX4 target gene expression in FSHD

Human molecular genetics, 2019-02, Vol.28 (3), p.476-486

2019

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Longitudinal measures of RNA expression and disease activity in FSHD muscle biopsies

Human molecular genetics, 2020-04, Vol.29 (6), p.1030-1043

2020

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Model systems of DUX4 expression recapitulate the transcriptional profile of FSHD cells

Human molecular genetics, 2016-10, Vol.25 (20), p.4419-4431

2016

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A novel cell-based high-throughput screen for inhibitors of HIV-1 gene expression and budding identifies the cardiac glycosides

Journal of antimicrobial chemotherapy, 2014-04, Vol.69 (4), p.988-994

2014

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HIV-1 DNA Is Detected in Bone Marrow Populations Containing CD4⁺ T Cells but Is not Found in Purified CD34⁺ Hematopoietic Progenitor Cells in Most Patients on Antiretroviral Therapy

The Journal of infectious diseases, 2012-03, Vol.205 (6), p.1014-1018

2012

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Predictors of functional outcomes in patients with facioscapulohumeral muscular dystrophy

Brain (London, England : 1878), 2021-12, Vol.144 (11), p.3451-3460

2021

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RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy

Human molecular genetics, 2009-07, Vol.18 (13), p.2414-2430

2009

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A senior surgical resident can safely perform complex esophageal cancer surgery after surgical mentoring program-experience of a European high-volume center

Diseases of the esophagus, 2024-07, Vol.37 (7)

2024

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High-resolution breakpoint junction mapping of proximally extended D4Z4 deletions in FSHD1 reveals evidence for a founder effect

Human molecular genetics, 2022-03, Vol.31 (5), p.748-760

2022

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Reply: Wheelchair use in genetically-confirmed FSHD1 from a large cohort study in Chinese population

Brain (London, England : 1878), 2022-06, Vol.145 (6), p.e55-e56

2022

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Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2

Human molecular genetics, 2015-02, Vol.24 (3), p.659-669

2015

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Single-cell RNA sequencing in facioscapulohumeral muscular dystrophy disease etiology and development

Human molecular genetics, 2019-04, Vol.28 (7), p.1064-1075

2019

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Elevated plasma complement components in facioscapulohumeral dystrophy

Human molecular genetics, 2022-06, Vol.31 (11), p.1821-1829

2022

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Regional and bilateral MRI and gene signatures in facioscapulohumeral dystrophy: implications for clinical trial design and mechanisms of disease progression

Human molecular genetics, 2024-04, Vol.33 (8), p.698-708

2024

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Hereditary ferritinopathy : A novel mutation, its cellular pathology, and pathogenetic insights

Journal of neuropathology and experimental neurology, 2005-04, Vol.64 (4), p.280-294

2005

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Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophy

Brain (London, England : 1878), 2024-02, Vol.147 (2), p.414-426

2024

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Wnt/β-catenin signaling suppresses DUX4 expression and prevents apoptosis of FSHD muscle cells

Human molecular genetics, 2013-12, Vol.22 (23), p.4661-4672

2013

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Cis D4Z4 repeat duplications associated with facioscapulohumeral muscular dystrophy type 2

Human molecular genetics, 2018-10, Vol.27 (20), p.3488-3497

2018

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Facioscapulohumeral Dystrophy

Physical therapy, 2008-01, Vol.88 (1), p.105-113

2008

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Fecal Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-Cov-2) RNA Is Associated With Decreased Coronavirus Disease 2019 (COVID-19) Survival

Clinical infectious diseases, 2022-03, Vol.74 (6), p.1081-1084

2022

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DICER/AGO-dependent epigenetic silencing of D4Z4 repeats enhanced by exogenous siRNA suggests mechanisms and therapies for FSHD

Human molecular genetics, 2015-09, Vol.24 (17), p.4817-4828

2015

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Rad51 inhibition is an effective means of targeting DNA repair in glioma models and CD133+ tumor-derived cells

Factors influencing pursuit of residency training

Simian Immunodeficiency Virus-Infected Macaques Treated with Highly Active Antiretroviral Therapy Have Reduced Central Nervous System Viral Replication and Inflammation but Persistence of Viral DNA

DUX4-induced gene expression is the major molecular signature in FSHD skeletal muscle

MRI-informed muscle biopsies correlate MRI with pathology and DUX4 target gene expression in FSHD

Longitudinal measures of RNA expression and disease activity in FSHD muscle biopsies

Model systems of DUX4 expression recapitulate the transcriptional profile of FSHD cells

A novel cell-based high-throughput screen for inhibitors of HIV-1 gene expression and budding identifies the cardiac glycosides

HIV-1 DNA Is Detected in Bone Marrow Populations Containing CD4⁺ T Cells but Is not Found in Purified CD34⁺ Hematopoietic Progenitor Cells in Most Patients on Antiretroviral Therapy

Predictors of functional outcomes in patients with facioscapulohumeral muscular dystrophy

RNA transcripts, miRNA-sized fragments and proteins produced from D4Z4 units: new candidates for the pathophysiology of facioscapulohumeral dystrophy

A senior surgical resident can safely perform complex esophageal cancer surgery after surgical mentoring program-experience of a European high-volume center

High-resolution breakpoint junction mapping of proximally extended D4Z4 deletions in FSHD1 reveals evidence for a founder effect

Reply: Wheelchair use in genetically-confirmed FSHD1 from a large cohort study in Chinese population

Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2

Single-cell RNA sequencing in facioscapulohumeral muscular dystrophy disease etiology and development

Elevated plasma complement components in facioscapulohumeral dystrophy

Regional and bilateral MRI and gene signatures in facioscapulohumeral dystrophy: implications for clinical trial design and mechanisms of disease progression

Hereditary ferritinopathy : A novel mutation, its cellular pathology, and pathogenetic insights

Autosomal dominant in cis D4Z4 repeat array duplication alleles in facioscapulohumeral dystrophy

Wnt/β-catenin signaling suppresses DUX4 expression and prevents apoptosis of FSHD muscle cells

Cis D4Z4 repeat duplications associated with facioscapulohumeral muscular dystrophy type 2

Facioscapulohumeral Dystrophy

Fecal Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-Cov-2) RNA Is Associated With Decreased Coronavirus Disease 2019 (COVID-19) Survival

DICER/AGO-dependent epigenetic silencing of D4Z4 repeats enhanced by exogenous siRNA suggests mechanisms and therapies for FSHD

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