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Browsing publications by
Dr Louise VB Anderson.
Newcastle Authors
Title
Year
Full text
Dr Lars Klinge
Dr Richard Charlton
Dr Juliane Mueller
Dr Louise VB Anderson
Professor Volker Straub
et al.
Late onset in dysferlinopathy widens the clinical spectrum
2008
Dr Louise VB Anderson
A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of delta-SG protein
2007
Dr Steven Laval
Dr Louise VB Anderson
Professor Volker Straub
Emerita Professor Katherine Bushby
AHNAK, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration
2007
Dr Richard Charlton
Dr Rita Barresi
Dr Louise VB Anderson
Dr Michelle Eagle
Dr Mauro Santibanez Koref
et al.
Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A
2007
Dr Louise VB Anderson
Patients with a non-dysferlin miyoshi myopathy have a novel membrane repair defect
2007
Dr Louise VB Anderson
Five year follow-up study in Miyoshi myopathy
2006
Dr Louise VB Anderson
Emerita Professor Katherine Bushby
Identification of putative
in vivo
substrates of calpain 3 by comparative proteomics of overexpressing transgenic and nontransgenic mice
2006
Emeritus Professor Clarke Slater
Dr Steven Laval
Professor Volker Straub
Emerita Professor Katherine Bushby
Dr Louise VB Anderson
et al.
Altered protein localisation during muscle regeneration in humans and rats
2005
Faye Haldane
Dr Steven Laval
Dr Louise VB Anderson
Emerita Professor Katherine Bushby
Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display
2005
Dr Steven Laval
Dr Lynsey Cree
Faye Haldane
Ilka Wappler
Dr Heiko Peters
et al.
The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice
2005
Dr Louise VB Anderson
Emerita Professor Katherine Bushby
Professor Volker Straub
A new mutation in the transmembrane domain of Caveolin-3 in a patient with percussion-induced rapid muscle contractions
2004
Dr Louise VB Anderson
Emerita Professor Katherine Bushby
Abnormalities in alpha-Dystroglycan Expression in MDC1C and LGMD21 Muscular Dystrophies
2004
Dr Steven Laval
Dr Lynsey Cree
Faye Haldane
Ilka Wappler
Professor Hanns Lochmuller
et al.
Cell culture, biochemical and microarray analyses of dysferlin
2004
Faye Haldane
Emerita Professor Katherine Bushby
Dr Louise VB Anderson
Problems associated with the detection and interpretation of dysferlin deficiency
2004
Dr Louise VB Anderson
A distinct phenotype of distal myopathy in a large Finnish family
2003
Dr Louise VB Anderson
Altered expression of the ferlins following cell membrane injury in muscle cells
2003
Dr Louise VB Anderson
Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus
2003
Dr Louise VB Anderson
Sarcoglycans of the zebrafish: Orthology and localization to the sarcolemma and myosepta of muscle
2003
Dr Lynsey Cree
Dr John Bourke
Dr Michelle Eagle
Dr Louise VB Anderson
Dr Daniel Birchall
et al.
The phenotype of limb-girdle muscular dystrophy type 2I
2003
Dr Louise VB Anderson
Emerita Professor Katherine Bushby
X-linked Emery-Dreifuss muscular dystrophy in a female with 45X/46XX mosaic constitution
2003
Dr Louise VB Anderson
Clinical variability in calpainopathy: What makes the difference?
2002
Dr Louise VB Anderson
Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice
2002
Dr Louise VB Anderson
Analysis of Protein Expression in the Muscular Dystrophies
2001
Dr Louise VB Anderson
Emerita Professor Katherine Bushby
Analysis of skeletal muscle from patients with facioscapulohumeral dystrophy
2001
Emerita Professor Katherine Bushby
Dr Louise VB Anderson
Autosomal dominant limb-girdle muscular dystrophy: description of a phenotype
2001
Dr Elizabeth Vafiadaki
Dr Alexandra Reis
Ruth Harrison
Dr Louise VB Anderson
Emerita Professor Katherine Bushby
et al.
Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation
2001
Dr Louise VB Anderson
Dysferlin protein analysis in limb-girdle muscular dystrophies
2001
Emerita Professor Katherine Bushby
Dr Louise VB Anderson
Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations
2001
Dr Louise VB Anderson
Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers
2001
Dr Louise VB Anderson
Dr Rumaisa Bashir
Professor Volker Straub
Emerita Professor Katherine Bushby
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C
2001
Dr Louise VB Anderson
Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2A
2001
Dr Louise VB Anderson
Normal calpain expression in genetically confirmed limb-girdle muscular dystrophy type 2A
2001
Dr Julie Gray
Rebecca Harrison
Dr Elizabeth Vafiadaki
Dr Robert Pogue
Emerita Professor Katherine Bushby
et al.
Secondary changes in dysferlin expression
2001
Dr Robert Pogue
Dr Louise VB Anderson
Dr Angela Pyle
Jennifer Moss
Emerita Professor Katherine Bushby
et al.
Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies
2001
Dr Louise VB Anderson
The Molecular Basis of Muscle Disease
2001
Dr Louise VB Anderson
Dr Robert Pogue
Dr Angela Pyle
Emerita Professor Katherine Bushby
The phenotype of calpainopathy: Diagnosis based on a multidisciplinary approach
2001
Dr Louise VB Anderson
Calpain3 expression during human cardiogenesis
2000
Dr Louise VB Anderson
Diagnostic protein expression in human muscle biopsies
2000
Dr Louise VB Anderson
Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family
2000
Dr Louise VB Anderson
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease
2000
Dr Louise VB Anderson
Partial α-sarcoglycan deficiency with retention of the dystrophin- glycoprotein complex in a LGMD2D family
2000
Dr Louise VB Anderson
Plenary Lecture L02: Muscular dystrophies
2000
Dr Louise VB Anderson
Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy
2000
Dr Louise VB Anderson
Ruth Harrison
Dr Robert Pogue
Dr Elizabeth Vafiadaki
Jennifer Moss
et al.
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)
2000
Dr Louise VB Anderson
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation
2000
Dr Louise VB Anderson
A splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation
1999
Dr Louise VB Anderson
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A
1999
Dr Robert Pogue
Dr Louise VB Anderson
Emerita Professor Katherine Bushby
Calpainopathy - A survey of mutations and polymorphisms
1999
Dr Louise VB Anderson
Characterization of the transmembrane molecular architecture of the dystroglycan complex in Schwann cells
1999
Dr Louise VB Anderson
Emerita Professor Katherine Bushby
Dr Robert Pogue
Dr Angela Pyle
Definition of the phenotype in limb-girdle muscular dystrophy (LGMD) 2A, (calpainopathy)
1999
Dr Louise VB Anderson
Dr Rumaisa Bashir
Dr Elizabeth Vafiadaki
Rebecca Harrison
Emerita Professor Katherine Bushby
et al.
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B
1999
Dr Louise VB Anderson
Jennifer Moss
Dr Michael Cullen
Dr Margaret Johnson
Dr Rumaisa Bashir
et al.
Dysferlin is a plasma membrane protein and is expressed early in human development
1999
Dr Rumaisa Bashir
Dr Louise VB Anderson
Jennifer Moss
Stephen Britton
Dr Elizabeth Vafiadaki
et al.
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)
1999
Dr Louise VB Anderson
Immunomarkers for molecular mass
1999
Emerita Professor Katherine Bushby
Dr Louise VB Anderson
Dr Rumaisa Bashir
Merosin-positive congenital muscular dystrophy: a large inbred family
1999
Dr Louise VB Anderson
Molecular analysis of a spontaneous dystrophin 'knockout' dog
1999
Dr Louise VB Anderson
Multiplex Western blotting system for the analysis of muscular dystrophy proteins
1999
Dr Louise VB Anderson
Dr Rumaisa Bashir
Dr Elizabeth Vafiadaki
Jennifer Moss
Rebecca Harrison
et al.
Redesignation of the SJL mouse (SJL-dysf) as a model for human dysferlin-deficient muscle disorders
1999
Dr Robert Pogue
Dr Angela Pyle
Rebecca Harrison
Dr Louise VB Anderson
Dr Ann Curtis
et al.
Strategy for mutation analysis in the autosomal recessive limb girdle muscular dystrophies
1999