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Potential phosphorus eutrophication mitigation strategy: Biochar carbon composition, thermal stability and pH influence phosphorus sorption

Chemosphere (Oxford), 2017-08, Vol.180, p.201-211

2017

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Axin2+ PDL Cells Directly Contribute to New Alveolar Bone Formation in Response to Orthodontic Tension Force

Journal of dental research, 2022-06, Vol.101 (6), p.695-703

2022

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Towards a locally constructed multi-element ultrasound imaging transducer for resource poor environments

IPEM-translation, 2024-03, Vol.9, p.100023, Article 100023

2024

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Mitochondrial Disease—Its Impact, Etiology, and Pathology

Current Topics in Developmental Biology, 2007, Vol.77, p.113-155

2007

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Relationship of arsenic and chromium availability with carbon functional groups, aluminum and iron in Little Washita River Experimental Watershed Reservoirs, Oklahoma, USA

Ecotoxicology and environmental safety, 2021-01, Vol.207, p.111468, Article 111468

2021

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Organic matter composition and thermal stability influence greenhouse gases production in subtropical peatland under different vegetation types

Heliyon, 2022-11, Vol.8 (11), p.e11547-e11547, Article e11547

2022

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Understanding the mechanisms contributing to Alpers’ neuropathology

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S19-S20

2017

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Dynamic and static tests of balance and postural sway in boys: effects of previous wrist bone fractures and high adiposity

Gait & posture, 2003-04, Vol.17 (2), p.136-141

2003

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P31 Genotypic and phenotypic heterogeneity in adult-onset progressive external ophthalmoplegia (PEO) with mitochondrial DNA instability: a systematic review

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S15-S15

2014

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Using a quantitative quadruple immunofluorescent assay to detect isolated Complex I deficiency

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S23-S23

2017

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P39. Assigning pathogenicity to three novel mt-tRNA mutations associated with different mitochondrial disease presentations

Clinical neurophysiology, 2015-08, Vol.126 (8), p.e115-e115

2015

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P28 Investigating mitochondrial dysfunction in the myofibrillar and other protein aggregate myopathies

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S14-S14

2014

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A national cohort study of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) – implications to clinical practice and therapeutic study

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S21-S21

2017

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Novel GFM2 variants identified in two cases of early-onset mitochondrial disease cause impaired expression of mtDNA encoded OXPHOS subunits

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S22-S22

2017

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A feasibility study of bezafibrate in mitochondrial myopathy

Neuromuscular disorders : NMD, 2017-03, Vol.27, p.S18-S18

2017

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P56 Mitochondrial DNA deletions do not have a replicative advantage in human muscle

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S22-S22

2012

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P68 A proposed consensus panel of organisms for determining evolutionary conservation of mt-tRNA point mutations

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S26-S26

2012

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P66 Changes in mitochondrial function over time and with exercise in patients with mitochondrial disease

Neuromuscular disorders : NMD, 2012-03, Vol.22, p.S25-S25

2012

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G.P.116 Late onset Muscle Mitochondrial Disease due to a p.R357P Twinkle mutation in an Irish family

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.890-890

2012

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222 SUPEROXIDE DISMUTASE 2 DOWNREGULATION AND MITOCHONDRIA RESPIRATION IN OSTEOARTHRITIS

Osteoarthritis and cartilage, 2010, Vol.18, p.S103-S104

2010

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P73 Mitochondrial abnormalities in inclusion body myositis

Neuromuscular disorders : NMD, 2011, Vol.21, p.S27-S28

2011

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P56 Why does mitochondrial disease progress? From molecular genetics to patient phenotype

Neuromuscular disorders : NMD, 2011, Vol.21, p.S22-S22

2011

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Initial development and validation of a mitochondrial disease quality of life scale

Neuromuscular disorders : NMD, 2013-04, Vol.23 (4), p.324-329

2013

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O5 Determination of mutation loads in preimplantation embryos to assess the effectiveness of preimplantation genetic diagnosis (PGD) for mitochondrial DNA (mtDNA) inherited disorders

Reproductive biomedicine online, 2012-05, Vol.24, p.S41-S41

2012

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P26 Can aerobic exercise improve function in patients with mitochondrial disease?

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S13-S14

2014

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Potential phosphorus eutrophication mitigation strategy: Biochar carbon composition, thermal stability and pH influence phosphorus sorption

Axin2+ PDL Cells Directly Contribute to New Alveolar Bone Formation in Response to Orthodontic Tension Force

Towards a locally constructed multi-element ultrasound imaging transducer for resource poor environments

Mitochondrial Disease—Its Impact, Etiology, and Pathology

Relationship of arsenic and chromium availability with carbon functional groups, aluminum and iron in Little Washita River Experimental Watershed Reservoirs, Oklahoma, USA

Organic matter composition and thermal stability influence greenhouse gases production in subtropical peatland under different vegetation types

Understanding the mechanisms contributing to Alpers’ neuropathology

Dynamic and static tests of balance and postural sway in boys: effects of previous wrist bone fractures and high adiposity

P31 Genotypic and phenotypic heterogeneity in adult-onset progressive external ophthalmoplegia (PEO) with mitochondrial DNA instability: a systematic review

Using a quantitative quadruple immunofluorescent assay to detect isolated Complex I deficiency

P39. Assigning pathogenicity to three novel mt-tRNA mutations associated with different mitochondrial disease presentations

P28 Investigating mitochondrial dysfunction in the myofibrillar and other protein aggregate myopathies

A national cohort study of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) – implications to clinical practice and therapeutic study

Novel GFM2 variants identified in two cases of early-onset mitochondrial disease cause impaired expression of mtDNA encoded OXPHOS subunits

A feasibility study of bezafibrate in mitochondrial myopathy

P56 Mitochondrial DNA deletions do not have a replicative advantage in human muscle

P68 A proposed consensus panel of organisms for determining evolutionary conservation of mt-tRNA point mutations

P66 Changes in mitochondrial function over time and with exercise in patients with mitochondrial disease

G.P.116 Late onset Muscle Mitochondrial Disease due to a p.R357P Twinkle mutation in an Irish family

222 SUPEROXIDE DISMUTASE 2 DOWNREGULATION AND MITOCHONDRIA RESPIRATION IN OSTEOARTHRITIS

P73 Mitochondrial abnormalities in inclusion body myositis

P56 Why does mitochondrial disease progress? From molecular genetics to patient phenotype

Initial development and validation of a mitochondrial disease quality of life scale

O5 Determination of mutation loads in preimplantation embryos to assess the effectiveness of preimplantation genetic diagnosis (PGD) for mitochondrial DNA (mtDNA) inherited disorders

P26 Can aerobic exercise improve function in patients with mitochondrial disease?

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