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Coordination-Driven Self-Assembly of Charged and Neutral Dendritic Tetrakis(ferrocenyl) Rhomboids

Organometallics, 2012-10, Vol.31 (20), p.7241-7247

2012

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Facile Self-Assembly of Supramolecular Hexakisferrocenyl Triangles via Coordination-Driven Self-Assembly and Their Electrochemical Behavior

Organometallics, 2011-07, Vol.30 (13), p.3637-3642

2011

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KNDy Cells Revisited

Endocrinology (Philadelphia), 2018-09, Vol.159 (9), p.3219-3234

2018

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Efficacy and Tolerability of Evolocumab vs Ezetimibe in Patients With Muscle-Related Statin Intolerance: The GAUSS-3 Randomized Clinical Trial

JAMA : the journal of the American Medical Association, 2016-04, Vol.315 (15), p.1580

2016

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Assessment of Systemic Delivery of rAAVrh74.MHCK7.micro-dystrophin in Children With Duchenne Muscular Dystrophy: A Nonrandomized Controlled Trial

JAMA neurology, 2020-09, Vol.77 (9), p.1122

2020

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Prenatal Testosterone Exposure Alters GABAergic Synaptic Inputs to GnRH and KNDy Neurons in a Sheep Model of Polycystic Ovarian Syndrome

Endocrinology (Philadelphia), 2019-11, Vol.160 (11), p.2529-2542

2019

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Testing preexisting antibodies prior to AAV gene transfer therapy: rationale, lessons and future considerations

Molecular therapy. Methods & clinical development, 2022-06, Vol.25, p.74-83

2022

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Delandistrogene Moxeparvovec Gene Therapy in Ambulatory Patients (Aged ≥4 to <8 Years) with Duchenne Muscular Dystrophy: 1‐Year Interim Results from Study SRP‐9001‐103 (ENDEAVOR)

Annals of neurology, 2023-11, Vol.94 (5), p.955-968

2023

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Long‐term safety and functional outcomes of delandistrogene moxeparvovec gene therapy in patients with Duchenne muscular dystrophy: A phase 1/2a nonrandomized trial

Muscle & nerve, 2024-01, Vol.69 (1), p.93-98

2024

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Evidence that synaptic plasticity of glutamatergic inputs onto KNDy neurones during the ovine follicular phase is dependent on increasing levels of oestradiol

Journal of neuroendocrinology, 2021-03, Vol.33 (3), p.e12945-n/a

2021

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Expression of SRP-9001 dystrophin and stabilization of motor function up to 2 years post-treatment with delandistrogene moxeparvovec gene therapy in individuals with Duchenne muscular dystrophy

Frontiers in cell and developmental biology, 2023-07, Vol.11, p.1167762-1167762

2023

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Abstract 1044: Single Cell RNA-sequencing Of Endothelial Cells In Atherosclerosis Reveals A Single Phenotypic Transition To A Mesenchymal Cell State

Arteriosclerosis, thrombosis, and vascular biology, 2024-05, Vol.44 (Suppl_1)

2024

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Gene therapy with bidridistrogene xeboparvovec for limb-girdle muscular dystrophy type 2E/R4: phase 1/2 trial results

Nature medicine, 2024, Vol.30 (1), p.199-206

2024

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Brief Report: A Pilot Study Examining the Effects of PEERS® for Adolescents Telehealth for Autistic Adolescents

Journal of autism and developmental disorders, 2022-12, Vol.52 (12), p.5491-5499

2022

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Chest Compression Rates and Survival Following Out-of-Hospital Cardiac Arrest

Critical care medicine, 2015-04, Vol.43 (4), p.840-848

2015

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Dizziness, Falls, and Hearing Loss in Adults Living With Sickle Cell Disease

American journal of audiology, 2022-12, Vol.31 (4), p.1178-1190

2022

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Salivary Cortisol, Equine Characteristics, and Management Factors Associated With Strongyle-Type Egg Shedding of Ohio Horses

Journal of equine veterinary science, 2021-06, Vol.101, p.103431-103431, Article 103431

2021

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Validation of a Patient Education Skills Assessment Rubric for Initial Continuous Glucose Monitor Placement

American journal of pharmaceutical education, 2024-09, Vol.88 (9), p.101075, Article 101075

2024

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Analysing otitis media resistance study

Clinical otolaryngology, 2024-01, Vol.49 (1), p.158-159

2024

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Validation of Breast Cancer Risk Models by Race/Ethnicity, Family History and Molecular Subtypes

Cancers, 2021-12, Vol.14 (1), p.45

2021

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Toward a practical method for measuring glass transition in polymers with low-frequency Raman spectroscopy

Applied physics letters, 2023-06, Vol.122 (26)

2023

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Metastatic and Malignant Phyllodes Tumors of the Breast: An Update for Current Management

The American Surgeon, 2023-12, Vol.89 (12), p.6190-6196

2023

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Gene Delivery for Limb-Girdle Muscular Dystrophy Type 2D by Isolated Limb Infusion

Human gene therapy, 2019-07, Vol.30 (7), p.794-801

2019

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Breaking Barriers to Rapid Whole Genome Sequencing in Pediatrics: Michigan's Project Baby Deer

Children (Basel), 2023-01, Vol.10 (1), p.106

2023

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Coordination-Driven Self-Assembly of Charged and Neutral Dendritic Tetrakis(ferrocenyl) Rhomboids

Facile Self-Assembly of Supramolecular Hexakisferrocenyl Triangles via Coordination-Driven Self-Assembly and Their Electrochemical Behavior

KNDy Cells Revisited

Efficacy and Tolerability of Evolocumab vs Ezetimibe in Patients With Muscle-Related Statin Intolerance: The GAUSS-3 Randomized Clinical Trial

Ibrutinib is an irreversible molecular inhibitor of ITK driving a Th1-selective pressure in T lymphocytes

Assessment of Systemic Delivery of rAAVrh74.MHCK7.micro-dystrophin in Children With Duchenne Muscular Dystrophy: A Nonrandomized Controlled Trial

Prenatal Testosterone Exposure Alters GABAergic Synaptic Inputs to GnRH and KNDy Neurons in a Sheep Model of Polycystic Ovarian Syndrome

Testing preexisting antibodies prior to AAV gene transfer therapy: rationale, lessons and future considerations

Delandistrogene Moxeparvovec Gene Therapy in Ambulatory Patients (Aged ≥4 to <8 Years) with Duchenne Muscular Dystrophy: 1‐Year Interim Results from Study SRP‐9001‐103 (ENDEAVOR)

Long‐term safety and functional outcomes of delandistrogene moxeparvovec gene therapy in patients with Duchenne muscular dystrophy: A phase 1/2a nonrandomized trial

Evidence that synaptic plasticity of glutamatergic inputs onto KNDy neurones during the ovine follicular phase is dependent on increasing levels of oestradiol

Expression of SRP-9001 dystrophin and stabilization of motor function up to 2 years post-treatment with delandistrogene moxeparvovec gene therapy in individuals with Duchenne muscular dystrophy

Abstract 1044: Single Cell RNA-sequencing Of Endothelial Cells In Atherosclerosis Reveals A Single Phenotypic Transition To A Mesenchymal Cell State

Gene therapy with bidridistrogene xeboparvovec for limb-girdle muscular dystrophy type 2E/R4: phase 1/2 trial results

Brief Report: A Pilot Study Examining the Effects of PEERS® for Adolescents Telehealth for Autistic Adolescents

Chest Compression Rates and Survival Following Out-of-Hospital Cardiac Arrest

Dizziness, Falls, and Hearing Loss in Adults Living With Sickle Cell Disease

Salivary Cortisol, Equine Characteristics, and Management Factors Associated With Strongyle-Type Egg Shedding of Ohio Horses

Validation of a Patient Education Skills Assessment Rubric for Initial Continuous Glucose Monitor Placement

Analysing otitis media resistance study

Validation of Breast Cancer Risk Models by Race/Ethnicity, Family History and Molecular Subtypes

Toward a practical method for measuring glass transition in polymers with low-frequency Raman spectroscopy

Metastatic and Malignant Phyllodes Tumors of the Breast: An Update for Current Management

Gene Delivery for Limb-Girdle Muscular Dystrophy Type 2D by Isolated Limb Infusion

Breaking Barriers to Rapid Whole Genome Sequencing in Pediatrics: Michigan's Project Baby Deer

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