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Cell cycle progression is disrupted in murine MPS VII growth plate leading to reduced chondrocyte proliferation and transition to hypertrophy

Bone (New York, N.Y.), 2020-03, Vol.132, p.115195-115195, Article 115195

2020

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Systemic scAAV9.U1a.hSGSH Delivery Corrects Brain Biochemistry in Mucopolysaccharidosis Type IIIA at Early and Later Stages of Disease

Human gene therapy, 2021-04, Vol.32 (7-8), p.420

2021

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Subregional brain distribution of simple and complex glycosphingolipids in the mucopolysaccharidosis type I (Hurler syndrome) mouse: impact of diet

Journal of neurochemistry, 2017-04, Vol.141 (2), p.287-295

2017

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Electrochemically Enhanced Antimicrobial Action of Plasma‐Activated Poly(Vinyl Alcohol) Hydrogel Dressings

Advanced functional materials, 2024-05, Vol.34 (21), p.n/a

2024

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Response to Letter to the Editor: Secondary ganglioside GM2 accumulation in mucopolysaccharidoses

Molecular genetics and metabolism reports, 2022-03, Vol.30, p.100831-100831, Article 100831

Derrick-Roberts, Ainslie L.K.

2022

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Influence of duty cycle on the physicochemical characteristics of an AC-driven argon plasma jet and its impact on hydrogen peroxide production and cell viability

Journal of physics. D, Applied physics, 2024-09, Vol.57 (37), p.375208

2024

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Correction of murine mucopolysaccharidosis type IIIA central nervous system pathology by intracerebroventricular lentiviral-mediated gene delivery

The journal of gene medicine, 2014-11, Vol.16 (11-12), p.374-387

2014

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Delayed development of ossification centers in the tibia of prenatal and early postnatal MPS VII mice

Molecular genetics and metabolism, 2018-06, Vol.124 (2), p.135-142

2018

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Altered IHH signaling contributes to reduced chondrocyte proliferation in the growth plate of MPS VII mice

Molecular genetics and metabolism reports, 2020-12, Vol.25, p.100668-100668, Article 100668

2020

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Reversal of established bone pathology in MPS VII mice following lentiviral-mediated gene therapy

Molecular genetics and metabolism, 2016-11, Vol.119 (3), p.249-257

2016

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Cell Viability Assessment of PEDOT Conducting Polymer-Coated Microneedles for Skin Sampling

ACS applied bio materials, 2023-11, Vol.6 (11), p.4662-4671

2023

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Impaired neural differentiation of MPS IIIA patient induced pluripotent stem cell-derived neural progenitor cells

Molecular genetics and metabolism reports, 2021-12, Vol.29, p.100811-100811, Article 100811

2021

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Inhibition of glycosaminoglycan synthesis using rhodamine B in a mouse model of mucopolysaccharidosis type IIIA

Pediatric research, 2006-09, Vol.60 (3), p.309-314

2006

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Selective normalisation of regional brain bis(monoacylglycero)phosphate in the mucopolysaccharidosis 1 (Hurler) mouse

Experimental neurology, 2016-03, Vol.277, p.68-75

2016

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Skeletal response to lentiviral mediated gene therapy in a mouse model of MPS VII

Molecular genetics and metabolism, 2012-06, Vol.106 (2), p.202-213

2012

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Rhodamine B and 2-acetamido-1,3,6-tri-O-acetyl-4-deoxy-4-fluoro-d-glucopyranose (F-GlcNAc) inhibit chondroitin/dermatan and keratan sulphate synthesis by different mechanisms in bovine chondrocytes

Molecular genetics and metabolism, 2012-06, Vol.106 (2), p.214-220

2012

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Mucopolysaccharidosis enzyme production by bone marrow and dental pulp derived human mesenchymal stem cells

Molecular genetics and metabolism, 2015-04, Vol.114 (4), p.584-593

2015

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Trans-generational exposure to low levels of rhodamine B does not adversely affect litter size or liver function in murine mucopolysaccharidosis type IIIA

Molecular genetics and metabolism, 2010-10, Vol.101 (2-3), p.208-213

2010

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Gastrointestinal pathology in a mouse model of mucopolysaccharidosis type IIIA

Journal of cellular physiology, 2009-05, Vol.219 (2), p.259-264

2009

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Improvement in behaviour after substrate deprivation therapy with rhodamine B in a mouse model of MPS IIIA

Molecular genetics and metabolism, 2007-09, Vol.92 (1), p.115-121

2007

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Electrochemically Enhanced Antimicrobial Action of Plasma‐Activated Poly(Vinyl Alcohol) Hydrogel Dressings (Adv. Funct. Mater. 21/2024)

Advanced functional materials, 2024-05, Vol.34 (21), p.n/a

2024

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Substrate Deprivation Therapy to Reduce Glycosaminoglycan Synthesis Improves Aspects of Neurological and Skeletal Pathology in MPS I Mice

Diseases, 2017-02, Vol.5 (1), p.5

2017

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Lentiviral-mediated gene therapy for murine mucopolysaccharidosis type IIIA

Molecular genetics and metabolism, 2008-04, Vol.93 (4), p.411-418

2008

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Response to Letter to the Editor: Secondary ganglioside G M2 accumulation in mucopolysaccharidoses

Molecular genetics and metabolism reports, 2022-03, Vol.30, p.100831

Derrick-Roberts, Ainslie L K

2022

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Accumulation of MPS GAG influences stem cell differentiation

Molecular genetics and metabolism, 2016-02, Vol.117 (2), p.S72-S72

2016

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Cell cycle progression is disrupted in murine MPS VII growth plate leading to reduced chondrocyte proliferation and transition to hypertrophy

Systemic scAAV9.U1a.hSGSH Delivery Corrects Brain Biochemistry in Mucopolysaccharidosis Type IIIA at Early and Later Stages of Disease

Subregional brain distribution of simple and complex glycosphingolipids in the mucopolysaccharidosis type I (Hurler syndrome) mouse: impact of diet

Electrochemically Enhanced Antimicrobial Action of Plasma‐Activated Poly(Vinyl Alcohol) Hydrogel Dressings

Response to Letter to the Editor: Secondary ganglioside GM2 accumulation in mucopolysaccharidoses

Influence of duty cycle on the physicochemical characteristics of an AC-driven argon plasma jet and its impact on hydrogen peroxide production and cell viability

Correction of murine mucopolysaccharidosis type IIIA central nervous system pathology by intracerebroventricular lentiviral-mediated gene delivery

Delayed development of ossification centers in the tibia of prenatal and early postnatal MPS VII mice

Altered IHH signaling contributes to reduced chondrocyte proliferation in the growth plate of MPS VII mice

Reversal of established bone pathology in MPS VII mice following lentiviral-mediated gene therapy

Cell Viability Assessment of PEDOT Conducting Polymer-Coated Microneedles for Skin Sampling

Impaired neural differentiation of MPS IIIA patient induced pluripotent stem cell-derived neural progenitor cells

Inhibition of glycosaminoglycan synthesis using rhodamine B in a mouse model of mucopolysaccharidosis type IIIA

Selective normalisation of regional brain bis(monoacylglycero)phosphate in the mucopolysaccharidosis 1 (Hurler) mouse

Skeletal response to lentiviral mediated gene therapy in a mouse model of MPS VII

Rhodamine B and 2-acetamido-1,3,6-tri-O-acetyl-4-deoxy-4-fluoro-d-glucopyranose (F-GlcNAc) inhibit chondroitin/dermatan and keratan sulphate synthesis by different mechanisms in bovine chondrocytes

Mucopolysaccharidosis enzyme production by bone marrow and dental pulp derived human mesenchymal stem cells

Trans-generational exposure to low levels of rhodamine B does not adversely affect litter size or liver function in murine mucopolysaccharidosis type IIIA

Gastrointestinal pathology in a mouse model of mucopolysaccharidosis type IIIA

Improvement in behaviour after substrate deprivation therapy with rhodamine B in a mouse model of MPS IIIA

Electrochemically Enhanced Antimicrobial Action of Plasma‐Activated Poly(Vinyl Alcohol) Hydrogel Dressings (Adv. Funct. Mater. 21/2024)

Substrate Deprivation Therapy to Reduce Glycosaminoglycan Synthesis Improves Aspects of Neurological and Skeletal Pathology in MPS I Mice

Lentiviral-mediated gene therapy for murine mucopolysaccharidosis type IIIA

Response to Letter to the Editor: Secondary ganglioside G M2 accumulation in mucopolysaccharidoses

Accumulation of MPS GAG influences stem cell differentiation

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