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Louise Anderson

Research Profile

Disorders

Muscular Dystrophies

Anatomy

Muscle, Skeletal

Chemicals & Drugs

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TOP 3
Lars Klinge; A F Dean; W Kress; P Dixon; R Charlton; J S Müller; Louise V B Anderson; Volker Straub; Rita Barresi; Hanns Lochmüller; Kate Bushby
Late onset in dysferlinopathy widens the clinical spectrum.
Emma J Groen; Richard Charlton; Rita Barresi; Louise V B Anderson; Michelle Eagle; Judith Hudson; Mauro Santibanez Koref; Volker Straub; K M D Bushby
Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A.
Telma L F Gouveia; Patrícia M Kossugue; Julia F O Paim; Mayana Zatz; Louise V B Anderson; Vincenzo Nigro; Mariz Vainzof
A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of delta-SG protein.

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All Publications

2008: Lars Klinge; A F Dean; W Kress; P Dixon; R Charlton; J S Müller; Louise V B Anderson; Volker Straub; Rita Barresi; Hanns Lochmüller; Kate Bushby
Late onset in dysferlinopathy widens the clinical spectrum.
Neuromuscular disorders : NMD 2008;18(4):288-90.
2007: Emma J Groen; Richard Charlton; Rita Barresi; Louise V B Anderson; Michelle Eagle; Judith Hudson; Mauro Santibanez Koref; Volker Straub; K M D Bushby
Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A.
Brain : a journal of neurology 2007;130(Pt 12):3237-49.
2007: Telma L F Gouveia; Patrícia M Kossugue; Julia F O Paim; Mayana Zatz; Louise V B Anderson; Vincenzo Nigro; Mariz Vainzof
A new evidence for the maintenance of the sarcoglycan complex in muscle sarcolemma in spite of the primary absence of delta-SG protein.
Journal of molecular medicine (Berlin, Germany) 2007;85(4):415-20.
2007: Yanchao Huang; Steven H Laval; Alexandra Van Remoortere; jacques Baudier; Chriselle Benaud; Louise V B Anderson; Volker Straub; Andre Deelder; Rune R Frants; Johan T den Dunnen; Kate Bushby; Silvère M van der Maarel
AHNAK, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2007;21(3):732-42.
2007: Jyoti K Jaiswal; Gareth Marlow; Gillian Summerill; Ibrahim Mahjneh; Sebastian Mueller; Maria Hill; Katsuya Miyake; Hannelore Haase; Louise V B Anderson; Isabelle Richard; Sari Kiuru-Enari; Paul L McNeil; Sanford M Simon; Rumaisa Bashir
Patients with a non-dysferlin Miyoshi myopathy have a novel membrane repair defect.
Traffic (Copenhagen, Denmark) 2007;8(1):77-88.
2006: Niaz Cohen; Elena Kudryashova; Irina Kramerova; Louise V B Anderson; Jacques Beckmann; Katherine Bushby; Melissa J Spencer
Identification of putative in vivo substrates of calpain 3 by comparative proteomics of overexpressing transgenic and nontransgenic mice.
Proteomics 2006;6(22):6075-84.
2005: Maja von der Hagen; Steven H Laval; Lynsey M Cree; Faye Haldane; Matthew Pocock; Ilka Wappler; Heiko Peters; Herbert A Reitsamer; Harald Hoger; Maria Wiedner; Felicitas Oberndorfer; Louise V B Anderson; Volker Straub; Reginald E Bittner; K M D Bushby
The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice.
Neuromuscular disorders : NMD 2005;15(12):863-77.
2005: Yanchao Huang; Peter Verheesen; Andreas Roussis; Wendy S Frankhuizen; Ieke B Ginjaar; Faye Haldane; Steven H Laval; Louise V B Anderson; Theo Verrips; Rune R Frants; Hans de Haard; Kate Bushby; Johan T den Dunnen; Silvère M van der Maarel
Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display.
European journal of human genetics : EJHG 2005;13(6):721-30.
2003: Désirée von Tell; Carl Bruder; Louise V B Anderson; Maria Anvret; Gabrielle Ahlberg
Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locus.
Neurogenetics 2003;4(4):173-7.
2003: Ibrahim Mahjneh; Henna Haravuori; Anders Paetau; Louise V B Anderson; A Saarinen; Bjarne Udd; Hannu Somer
A distinct phenotype of distal myopathy in a large Finnish family.
Neurology 2003;61(1):87-92.
2003: Maja Poppe; Lynsey M Cree; John Bourke; Michelle Eagle; Louise V B Anderson; Daniel Birchall; Martin Brockington; MR Buddles; M Busby; Francesco Muntoni; A Wills; Kate Bushby
The phenotype of limb-girdle muscular dystrophy type 2I.
Neurology 2003;60(8):1246-51.
2003: Stephen P Chambers; Louise V B Anderson; Giselle M Maguire; Andrew Dodd; Donald R Love
Sarcoglycans of the zebrafish: orthology and localization to the sarcolemma and myosepta of muscle.
Biochemical and biophysical research communications 2003;303(2):488-95.
2002: K Leriche-Guérin; Louise V B Anderson; Klaus Wrogemann; Brigitte Roy; Marlyne Goulet; Jacques P Tremblay
Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice.
Neuromuscular disorders : NMD 2002;12(2):167-73.
2001: Martin Brockington; Yeliz Yuva; Paola Prandini; Susan C Brown; Silvia Torelli; Matthew A Benson; Ralf Herrmann; Louise V B Anderson; Rumaisa Bashir; Jean-Marc Burgunder; S Fallet; Norma B Romero; M Fardeau; Volker Straub; G Storey; C Pollitt; Isabelle Richard; Caroline A Sewry; Kate Bushby; Thomas Voit; Derek J Blake; Francesco Muntoni
Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C.
Human molecular genetics 2001;10(25):2851-9.
2001: Mariz Vainzof; Louise V B Anderson; Elizabeth McNally; Dawn Belt Davis; Georgine Faulkner; Georgio Valle; Eloisa S Moreira; Rita C M Pavanello; Maria Rita Passos-Bueno; Mayana Zatz
Dysferlin protein analysis in limb-girdle muscular dystrophies.
Journal of molecular neuroscience : MN 2001;17(1):71-80.
2001: C Pollitt; Louise V B Anderson; R Pogue; K Davison; Angela Pyle; K M D Bushby
The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach.
Neuromuscular disorders : NMD 2001;11(3):287-96.
2001: E Vafiadaki; A Reis; Sharon M Keers; R Harrison; Louise V B Anderson; Thomas Raffelsberger; S Ivanova; H Hoger; Reginald E Bittner; Kate Bushby; Rumaisa Bashir
Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation.
Neuroreport 2001;12(3):625-9.
2001: R Pogue; Louise V B Anderson; Angela Pyle; C Sewry; C Pollitt; MA Johnson; K Davison; JA Moss; E Mercuri; Francesco Muntoni; K M D Bushby
Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies.
Neuromuscular disorders : NMD 2001;11(1):80-7.
2001: Natasha Olby; Nicholas J H Sharp; Louise V B Anderson; Louis Kunkel; Carsten G Bönnemann
Evaluation of the dystrophin-glycoprotein complex, alpha-actinin, dysferlin and calpain 3 in an autosomal recessive muscular dystrophy in Labrador retrievers.
Neuromuscular disorders : NMD 2001;11(1):41-9.
2001: Ibrahim Mahjneh; Giampiero Marconi; Kate Bushby; Louise V B Anderson; H Tolvanen-Mahjneh; Hannu Somer
Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations.
Neuromuscular disorders : NMD 2001;11(1):20-6.
2000: Louise V B Anderson; R M Harrison; R Pogue; E Vafiadaki; C Pollitt; K Davison; JA Moss; Sharon M Keers; Angela Pyle; Pamela J Shaw; Ibrahim Mahjneh; Zohar Argov; Cheryl R Greenberg; Klaus Wrogemann; Tulio Bertorini; H H Goebel; Jacques Beckmann; Rumaisa Bashir; K M D Bushby
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).
Neuromuscular disorders : NMD 2000;10(8):553-9.
2000: Ieke B Ginjaar; A L J Kneppers; J D v d Meulen; Louise V B Anderson; Mattie Bremmer-Bout; Judith C T van Deutekom; Jitske Weegenaar; Johan T den Dunnen; Egbert Bakker
Dystrophin nonsense mutation induces different levels of exon 29 skipping and leads to variable phenotypes within one BMD family.
European journal of human genetics : EJHG 2000;8(10):793-6.
2000: HB Ginjaar; Anneke J van der Kooi; Huib Ceelie; A L J Kneppers; MT van Meegen; Peter G Barth; H F M Busch; J H J Wokke; Louise V B Anderson; Carsten G Bönnemann; M Jeanpierre; PA Bolhuis; A F Moorman; Marianne De Visser; Egbert Bakker; G J Ommen
Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy.
Journal of neurology 2000;247(7):524-9.
2000: Mariz Vainzof; Eloisa S Moreira; Marta Canovas; Louise V B Anderson; Rita C M Pavanello; Maria Rita Passos-Bueno; Mayana Zatz
Partial alpha-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family.
Muscle & nerve 2000;23(6):984-8.
2000: Françoise Fougerousse; Louise V B Anderson; A L Delezoide; Laurence Suel; Muriel Durand; Jacques Beckmann
Calpain3 expression during human cardiogenesis.
Neuromuscular disorders : NMD 2000;10(4-5):251-6.
2000: Elizabeth McNally; CT Ly; Hanna Rosenmann; Stella Mitrani-Rosenbaum; W Jiang; Louise V B Anderson; Dov Soffer; Zohar Argov
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation.
American journal of medical genetics 2000;91(4):305-12.
2000: Mari Auranen; Juhani Rapola; Helena Pihko; Matti Haltia; Ilmo V V Leivo; Seppo Soinila; Ismo Virtanen; Hannu Kalimo; Louise V B Anderson; Pirkko Santavuori; Hannu Somer
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease.
Neuromuscular disorders : NMD 2000;10(1):16-23.
1999: Louise V B Anderson
Immunomarkers for molecular mass.
Neuromuscular disorders : NMD 1999;9(6-7):421-2.
1999: Reginald E Bittner; Louise V B Anderson; E Burkhardt; Rumaisa Bashir; E Vafiadaki; S Ivanova; Thomas Raffelsberger; I Maerk; Harald Höger; M Jung; M Karbasiyan; M Storch; Hans Lassmann; JA Moss; K Davison; R Harrison; K M D Bushby; A Reis
Dysferlin deletion in SJL mice (SJL-Dysf) defines a natural model for limb girdle muscular dystrophy 2B.
Nature genetics 1999;23(2):141-2.
1999: Scott J Schatzberg; Natasha Olby; Matthew Breen; Louise V B Anderson; Cordelia F Langford; HF Dickens; Stephen D Wilton; C J Zeiss; Matthew M Binns; Joe Kornegay; Glenn E Morris; Nicholas J H Sharp
Molecular analysis of a spontaneous dystrophin 'knockout' dog.
Neuromuscular disorders : NMD 1999;9(5):289-95.
1999: Isabelle Richard; Carinne Roudaut; A Saenz; R Pogue; J E Grimbergen; Louise V B Anderson; C Beley; Anna Maria Cobo; C de Diego; Bruno Eymard; Pía Gallano; HB Ginjaar; Adriana Lasa; C Pollitt; Haluk Topaloglu; J Andoni Urtizberea; Marianne De Visser; Anneke J van der Kooi; Kate Bushby; Egbert Bakker; Adolfo Lopez de Munain; M Fardeau; Jacques Beckmann
Calpainopathy-a survey of mutations and polymorphisms.
American journal of human genetics 1999;64(6):1524-40.
1999: Stephen Baghdiguian; M Martin; Isabelle Richard; F Pons; Catherine Astier; Nathalie Bourg; Ron Thomas Hay; Raymond Chemaly; Georges Halaby; Jacques Loiselet; Louise V B Anderson; Adolfo Lopez de Munain; M Fardeau; Paul Mangeat; Jacques Beckmann; Gérard Lefranc
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IkappaB alpha/NF-kappaB pathway in limb-girdle muscular dystrophy type 2A.
Nature medicine 1999;5(5):503-11.
1999: Tracey Weiler; Rumaisa Bashir; Louise V B Anderson; K Davison; JA Moss; S Britton; Edward Nylen; Sharon M Keers; E Vafiadaki; Cheryl R Greenberg; C R Bushby; Klaus Wrogemann
Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s).
Human molecular genetics 1999;8(5):871-7.
1999: Louise V B Anderson; K Davison; JA Moss; C Young; M J Cullen; J Walsh; MA Johnson; Rumaisa Bashir; S Britton; Sharon M Keers; Zohar Argov; Ibrahim Mahjneh; Françoise Fougerousse; Jacques Beckmann; K M D Bushby
Dysferlin is a plasma membrane protein and is expressed early in human development.
Human molecular genetics 1999;8(5):855-61.
1999: Louise V B Anderson; K Davison
Multiplex Western blotting system for the analysis of muscular dystrophy proteins.
The American journal of pathology 1999;154(4):1017-22.
1998: Louise V B Anderson; K Davison; JA Moss; I Richard; M Fardeau; F M Tomé; C Hübner; Adriana Lasa; Jaume Colomer; Jacques Beckmann
Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A.
The American journal of pathology 1998;153(4):1169-79.
1998: Scott J Schatzberg; Louise V B Anderson; Stephen D Wilton; Joe Kornegay; Christopher J Mann; G G Solomon; Nicholas J H Sharp
Alternative dystrophin gene transcripts in golden retriever muscular dystrophy.
Muscle & nerve 1998;21(8):991-8.
1998: R Vater; Carol Young; Louise V B Anderson; S Lindsay; Derek J Blake; Kay E Davies; R Zuellig; Clarke Slater
Utrophin mRNA expression in muscle is not restricted to the neuromuscular junction.
Molecular and cellular neurosciences 1998;10(5-6):229-42.
1998: Kate Bushby; Louise V B Anderson; C Pollitt; IS Naom; Francesco Muntoni; Laurence A Bindoff
Abnormal merosin in adults. A new form of late onset muscular dystrophy not linked to chromosome 6q2.
Brain : a journal of neurology 1998;121 ( Pt 4)():581-8.
1997: Clarke Slater; Carol Young; S J Wood; Guy S Bewick; Louise V B Anderson; P Baxter; Peter R W Fawcett; M Roberts; L Jacobson; J Kuks; A Vincent; John Newsom-Davis
Utrophin abundance is reduced at neuromuscular junctions of patients with both inherited and acquired acetylcholine receptor deficiencies.
Brain : a journal of neurology 1997;120 ( Pt 9)():1513-31.
1997: L Metzinger; Derek J Blake; MV Squier; Louise V B Anderson; AE Deconinck; RA Nawrotzki; David Hilton-Jones; Kay E Davies
Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophy.
Human molecular genetics 1997;6(7):1185-91.
1997: Melissa J Spencer; James G Tidball; Louise V B Anderson; K M D Bushby; J B Harris; M R Passos-Bueno; Hannu Somer; Mariz Vainzof; M Zatz
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A).
Journal of the neurological sciences 1997;146(2):173-8.
1996: C A Sewry; J Taylor; Louise V B Anderson; E Ozawa; R Pogue; F Piccolo; K Bushby; V Dubowitz; Francesco Muntoni
Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy.
Neuromuscular disorders : NMD 1996;6(6):467-74.
1996: Mariz Vainzof; Maria Rita Passos-Bueno; M Canovas; Eloisa S Moreira; Rita C M Pavanello; Suely K N Marie; Louise V B Anderson; Carsten G Bönnemann; Elizabeth McNally; Vincenzo Nigro; Louis Kunkel; Mayana Zatz
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.
Human molecular genetics 1996;5(12):1963-9.
1995: K M Bushby; Richard E Appleton; Louise V B Anderson; J L Welch; P Kelly; D Gardner-Medwin
Deletion status and intellectual impairment in Duchenne muscular dystrophy.
Developmental medicine and child neurology 1995;37(3):260-9.
1994: A Heald; Louise V B Anderson; K M Bushby; Pamela J Shaw
Becker muscular dystrophy with onset after 60 years.
Neurology 1994;44(12):2388-90.