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Modification of splicing in the dystrophin gene in cultured Mdx muscle cells by antisense oligoribonucleotides

Human molecular genetics, 1998-07, Vol.7 (7), p.1083-1090

1998

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Spontaneous peritoneal closure after orchidopexy in children: Comment to: Orchidopexy without ligation of the processus vaginalis is not associated with an increased risk of inguinal hernia. Ceccanti S, Zani A, Mele E and Cozzi DA (2013)

Hernia : the journal of hernias and abdominal wall surgery, 2014-06, Vol.18 (3), p.343-344

2014

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Bifunctional Antisense Oligonucleotides Provide a Trans-Acting Splicing Enhancer That Stimulates SMN2 Gene Expression in Patient Fibroblasts

Proceedings of the National Academy of Sciences - PNAS, 2003-04, Vol.100 (7), p.4114-4119

2003

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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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Objective Risk-scoring Systems for Repair of Abdominal Aortic Aneurysms: Applicability in Endovascular Repair?

European journal of vascular and endovascular surgery, 2008-08, Vol.36 (2), p.172-177

2008

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Device-specific Outcomes Following Endovascular Aortic Aneurysm Repair

European journal of vascular and endovascular surgery, 2008-12, Vol.36 (6), p.661-667

2008

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Lipofection of cultured mouse muscle cells : A direct comparison of lipofectamine and DOSPER

Gene therapy, 1998-04, Vol.5 (4), p.542-551

1998

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Endovascular Management of Chronic Type B Dissecting Aortic Aneurysm Utilizing Aortic and Renal Stents

Cardiovascular and interventional radiology, 2008-07, Vol.31 (Suppl 2), p.67-71

2008

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Objective Risk-scoring Systems for Repair of Abdominal Aortic Aneurysms: Applicability in Endovascular Repair?

Journal of vascular surgery, 2008, Vol.48 (2), p.502-503

2008

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Variability in the presentation of complicated jejunal diverticulosis

JRSM open, 2023-07, Vol.14 (7), p.20542704231183247

2023

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Is it acceptable to approach colorectal cancer patients at diagnosis to discuss genetic testing? A pilot study

British journal of cancer, 2003-10, Vol.89 (8), p.1400-1402

2003

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Characterisation of novel point mutations in the survival motor neuron gene SMN, in three patients with SMA

Human genetics, 2001-04, Vol.108 (4), p.356-357

2001

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Julius

The Journal of continuing education in the health professions, 2005, Vol.25 (2), p.127-128

Dunckley, Carol M.

2005

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Direct retroviral-mediated transfer of a dystrophin minigene into mdx mouse muscle in vivo

Human molecular genetics, 1993-06, Vol.2 (6), p.717-723

1993

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What is important to measure in the last months and weeks of life?: A modified nominal group study

International journal of nursing studies, 2006-05, Vol.43 (4), p.393-403

2006

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Electric vehicles — are they a realistic option for the future?

Journal of power sources, 1993-01, Vol.42 (1), p.291-295

Dunckley, M.

1993

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Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: in vitro mimicking and antisense modulation of the splicing abnormality

Gene, 2003-06, Vol.311, p.25-33

2003

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Intramuscular injection of a plasmid vector expressing human apolipoprotein E limits progression of xanthoma and aortic atheroma in apoE-deficient mice

Human molecular genetics, 2000-10, Vol.9 (17), p.2545-2551

2000

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Efficient coexpression and secretion of anti-atherogenic human apolipoprotein AI and lecithin-cholesterol acyltransferase by cultured muscle cells using adeno-associated virus plasmid vectors

Gene therapy, 1998-10, Vol.5 (10), p.1434-1440

1998

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Retroviral-mediated transfer of a dystrophin minigene into mdx mouse myoblasts in vitro

FEBS letters, 1992-01, Vol.296 (2), p.128-134

1992

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Project to impROve management of terminal illnEss (PROMOTE)

Journal of interprofessional care, 2001-11, Vol.15 (4), p.398-399

2001

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Human dystrophin expression corrects the myopathic phenotype in transgenic mdx mice

Human molecular genetics, 1992-04, Vol.1 (1), p.35-40

1992

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Coronary Artery Bypass Grafting: Patients' and Health Professionals' Views of Recovery After Hospital Discharge

European journal of cardiovascular nursing : journal of the Working Group on Cardiovascular Nursing of the European Society of Cardiology, 2008-03, Vol.7 (1), p.36-42

2008

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Independent localization of dystrophin N- and C-terminal regions to the sarcolemma of mdx mouse myofibres in vivo

Journal of cell science, 1994-06, Vol.107 (6), p.1469-1475

1994

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Adenovirus-based targeting in myoblasts is hampered by nonhomologous vector integration

Human gene therapy, 2008-10, Vol.19 (10), p.1000-1008

2008

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Modification of splicing in the dystrophin gene in cultured Mdx muscle cells by antisense oligoribonucleotides

Spontaneous peritoneal closure after orchidopexy in children: Comment to: Orchidopexy without ligation of the processus vaginalis is not associated with an increased risk of inguinal hernia. Ceccanti S, Zani A, Mele E and Cozzi DA (2013)

Bifunctional Antisense Oligonucleotides Provide a Trans-Acting Splicing Enhancer That Stimulates SMN2 Gene Expression in Patient Fibroblasts

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

Objective Risk-scoring Systems for Repair of Abdominal Aortic Aneurysms: Applicability in Endovascular Repair?

Device-specific Outcomes Following Endovascular Aortic Aneurysm Repair

Lipofection of cultured mouse muscle cells : A direct comparison of lipofectamine and DOSPER

Endovascular Management of Chronic Type B Dissecting Aortic Aneurysm Utilizing Aortic and Renal Stents

Objective Risk-scoring Systems for Repair of Abdominal Aortic Aneurysms: Applicability in Endovascular Repair?

Variability in the presentation of complicated jejunal diverticulosis

Is it acceptable to approach colorectal cancer patients at diagnosis to discuss genetic testing? A pilot study

Characterisation of novel point mutations in the survival motor neuron gene SMN, in three patients with SMA

Julius

Direct retroviral-mediated transfer of a dystrophin minigene into mdx mouse muscle in vivo

What is important to measure in the last months and weeks of life?: A modified nominal group study

Electric vehicles — are they a realistic option for the future?

Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: in vitro mimicking and antisense modulation of the splicing abnormality

Intramuscular injection of a plasmid vector expressing human apolipoprotein E limits progression of xanthoma and aortic atheroma in apoE-deficient mice

Efficient coexpression and secretion of anti-atherogenic human apolipoprotein AI and lecithin-cholesterol acyltransferase by cultured muscle cells using adeno-associated virus plasmid vectors

Retroviral-mediated transfer of a dystrophin minigene into mdx mouse myoblasts in vitro

Project to impROve management of terminal illnEss (PROMOTE)

Human dystrophin expression corrects the myopathic phenotype in transgenic mdx mice

Coronary Artery Bypass Grafting: Patients' and Health Professionals' Views of Recovery After Hospital Discharge

Independent localization of dystrophin N- and C-terminal regions to the sarcolemma of mdx mouse myofibres in vivo

Adenovirus-based targeting in myoblasts is hampered by nonhomologous vector integration

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