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Monoclonal antibodies for clinical trials of Duchenne muscular dystrophy therapy

Neuromuscular disorders : NMD, 2014-03, Vol.24 (3), p.195-200

2014

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A two-site ELISA can quantify upregulation of SMN protein by drugs for spinal muscular atrophy

Neurology, 2008-11, Vol.71 (22), p.1757

2008

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Resolving the Equal Number Density Puzzle: Molecular Picture from Simulations of LiCl(aq) and NaCl(aq)

The journal of physical chemistry. B, 2021-04, Vol.125 (12), p.3153-3162

2021

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A systematic review on the global occurrence of Taenia hydatigena in pigs and cattle

Veterinary parasitology, 2016-08, Vol.226, p.97-103

2016

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In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide

Nature biotechnology, 2000-06, Vol.18 (6), p.615-622

2000

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The exon 2b region of the spinal muscular atrophy protein, SMN, is involved in self-association and SIP1 binding

Human molecular genetics, 2000-11, Vol.9 (19), p.2869-2877

2000

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Structure, stability and interactions in the complexes of carbonyls with cyanides

Theoretical chemistry accounts, 2017, Vol.136 (1), p.1-12, Article 10

2017

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An insight into Csp-H... pi hydrogen bonds and stability of complexes formed by acetylene and its substituted derivatives with benzene and borazine

RSC advances, 2016-01, Vol.6 (108), p.106662-106670

2016

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Contributions to the biodiversity of Vietnam - Results of VIETBIO inventory work and field training in Cuc Phuong National Park

Biodiversity data journal, 2022, Vol.10, p.e77025-e77025

2022

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Distribution of Emerin and Lamins in the Heart and Implications for Emery-Dreifuss Muscular Dystrophy

Human molecular genetics, 1999-02, Vol.8 (2), p.353-359

1999

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Localization of the DMDL Gene-Encoded Dystrophin-Related Protein Using a Panel of Nineteen Monoclonal Antibodies: Presence at Neuromuscular Junctions, in the Sarcolemma of Dystrophic Skeletal Muscle, in Vascular and Other Smooth Muscles, and in Proliferating Brain Cell Lines

The Journal of cell biology, 1991-12, Vol.115 (6), p.1695-1700

1991

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Mapping the pork value chain in Vietnam: a systematic review

Tropical animal health and production, 2020-11, Vol.52 (6), p.2799-2808

2020

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Monitoring duchenne muscular dystrophy gene therapy with epitope-specific monoclonal antibodies

Methods in molecular biology (Clifton, N.J.), 2011, Vol.709, p.39

2011

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A lamin A/C beta-strand containing the site of lipodystrophy mutations is a major surface epitope for a new panel of monoclonal antibodies

Biochimica et biophysica acta, 2004-03, Vol.1671 (1), p.87-92

2004

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Detection of the dystroglycanopathy protein, fukutin, using a new panel of site-specific monoclonal antibodies

Biochemical and biophysical research communications, 2012-07, Vol.424 (2), p.354-357

2012

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The Relationship between SMN, the Spinal Muscular Atrophy Protein, and Nuclear Coiled Bodies in Differentiated Tissues and Cultured Cells

Experimental cell research, 2000-05, Vol.256 (2), p.365-374

2000

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Helminth infections in dogs in Phu Tho Province, northern Vietnam

Current research in parasitology & vector-borne diseases, 2022-01, Vol.2, p.100091-100091, Article 100091

2022

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An insight into CH···N hydrogen bond and stability of the complexes formed by trihalomethanes with ammonia and its monohalogenated derivatives

International journal of quantum chemistry, 2017-03, Vol.117 (6), p.n/a

2017

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P.10.20 Recent and future additions to the MDA Monoclonal Antibody Resource for Neuromuscular Disorders

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.794-795

2013

Volltextzugriff (PDF)

The Emery-Dreifuss Muscular Dystrophy Protein, Emerin, is a Nuclear Membrane Protein

Human molecular genetics, 1996-06, Vol.5 (6), p.801-808

1996

Volltextzugriff (PDF)

Nuclear Gems and Cajal (Coiled) Bodies in Fetal Tissues: Nucleolar Distribution of the Spinal Muscular Atrophy Protein, SMN

Experimental cell research, 2001-05, Vol.265 (2), p.252-261

2001

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Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo

Journal of cell science, 2003-07, Vol.116 (Pt 14), p.3027-3035

2003

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Localization of Myotonic Dystrophy Protein Kinase in Human and Rabbit Tissues using a new Panel of Monoclonal Antibodies

Human molecular genetics, 1998-11, Vol.7 (12), p.1957-1965

1998

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Storytelling Pedagogy in Australia and Asia

1, 2021

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A novel dystrophin isoform is required for normal retinal electrophysiology

Human molecular genetics, 1995-05, Vol.4 (5), p.837-842

1995

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Monoclonal antibodies for clinical trials of Duchenne muscular dystrophy therapy

A two-site ELISA can quantify upregulation of SMN protein by drugs for spinal muscular atrophy

Resolving the Equal Number Density Puzzle: Molecular Picture from Simulations of LiCl(aq) and NaCl(aq)

A systematic review on the global occurrence of Taenia hydatigena in pigs and cattle

In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide

The exon 2b region of the spinal muscular atrophy protein, SMN, is involved in self-association and SIP1 binding

Structure, stability and interactions in the complexes of carbonyls with cyanides

An insight into Csp-H... pi hydrogen bonds and stability of complexes formed by acetylene and its substituted derivatives with benzene and borazine

Contributions to the biodiversity of Vietnam - Results of VIETBIO inventory work and field training in Cuc Phuong National Park

Distribution of Emerin and Lamins in the Heart and Implications for Emery-Dreifuss Muscular Dystrophy

Localization of the DMDL Gene-Encoded Dystrophin-Related Protein Using a Panel of Nineteen Monoclonal Antibodies: Presence at Neuromuscular Junctions, in the Sarcolemma of Dystrophic Skeletal Muscle, in Vascular and Other Smooth Muscles, and in Proliferating Brain Cell Lines

Mapping the pork value chain in Vietnam: a systematic review

Monitoring duchenne muscular dystrophy gene therapy with epitope-specific monoclonal antibodies

A lamin A/C beta-strand containing the site of lipodystrophy mutations is a major surface epitope for a new panel of monoclonal antibodies

Detection of the dystroglycanopathy protein, fukutin, using a new panel of site-specific monoclonal antibodies

The Relationship between SMN, the Spinal Muscular Atrophy Protein, and Nuclear Coiled Bodies in Differentiated Tissues and Cultured Cells

Helminth infections in dogs in Phu Tho Province, northern Vietnam

An insight into CH···N hydrogen bond and stability of the complexes formed by trihalomethanes with ammonia and its monohalogenated derivatives

P.10.20 Recent and future additions to the MDA Monoclonal Antibody Resource for Neuromuscular Disorders

The Emery-Dreifuss Muscular Dystrophy Protein, Emerin, is a Nuclear Membrane Protein

Nuclear Gems and Cajal (Coiled) Bodies in Fetal Tissues: Nucleolar Distribution of the Spinal Muscular Atrophy Protein, SMN

Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo

Localization of Myotonic Dystrophy Protein Kinase in Human and Rabbit Tissues using a new Panel of Monoclonal Antibodies

Storytelling Pedagogy in Australia and Asia

A novel dystrophin isoform is required for normal retinal electrophysiology

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