Publications by Dr Louise VB Anderson - ePrints

Browsing publications by Dr Louise VB Anderson.

Newcastle Authors	Title	Year
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