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Louise Anderson

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Disorders

Muscular Dystrophies

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Skeletal Muscle

Chemicals & Drugs

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TOP 3
Klinge L; Dean A F; Kress W; Dixon P; Charlton R; Müller J S; Anderson L V; Straub V; Barresi R; Lochmüller H; Bushby K
Late onset in dysferlinopathy widens the clinical spectrum.
Groen Emma J; Charlton Richard; Barresi Rita; Anderson Louise V; Eagle Michelle; Hudson Judith; Koref Mauro Santibanez; Straub Volker; Bushby Katharine M D
Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A.
Gouveia Telma L F; Kossugue Patrícia M; Paim Julia F; Zatz Mayana; Anderson Louise V B; Nigro Vincenzo; Vainzof Mariz
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: Klinge L; Dean A F; Kress W; Dixon P; Charlton R; Müller J S; Anderson L V; Straub V; Barresi R; Lochmüller H; Bushby K
Late onset in dysferlinopathy widens the clinical spectrum.
Neuromuscular disorders : NMD 2008;18(4):288-90.
2007: Groen Emma J; Charlton Richard; Barresi Rita; Anderson Louise V; Eagle Michelle; Hudson Judith; Koref Mauro Santibanez; Straub Volker; Bushby Katharine M D
Analysis of the UK diagnostic strategy for limb girdle muscular dystrophy 2A.
Brain : a journal of neurology 2007;130(Pt 12):3237-49.
2007: Gouveia Telma L F; Kossugue Patrícia M; Paim Julia F; Zatz Mayana; Anderson Louise V B; Nigro Vincenzo; Vainzof Mariz
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: Huang Yanchao; Laval Steven H; van Remoortere Alexandra; Baudier Jacques; Benaud Chriselle; Anderson Louise V B; Straub Volker; Deelder Andre; Frants Rune R; den Dunnen Johan T; Bushby Kate; van der Maarel Silvère M
AHNAK, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration.
The FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2007;21(3):732-42.
2007: Jaiswal Jyoti K; Marlow Gareth; Summerill Gillian; Mahjneh Ibrahim; Mueller Sebastian; Hill Maria; Miyake Katsuya; Haase Hannelore; Anderson Louise V B; Richard Isabelle; Kiuru-Enari Sari; McNeil Paul L; Simon Sanford M; Bashir Rumaisa
Patients with a non-dysferlin Miyoshi myopathy have a novel membrane repair defect.
Traffic (Copenhagen, Denmark) 2007;8(1):77-88.
2006: Cohen Niaz; Kudryashova Elena; Kramerova Irina; Anderson Louise V B; Beckmann Jacques S; Bushby Katherine; Spencer Melissa J
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: von der Hagen Maja; Laval Steven H; Cree Lynsey M; Haldane Faye; Pocock Matthew; Wappler Ilka; Peters Heiko; Reitsamer Herbert A; Hoger Harald; Wiedner Maria; Oberndorfer Felicitas; Anderson Louise V B; Straub Volker; Bittner Reginald E; Bushby Kate M D
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: Huang Yanchao; Verheesen Peter; Roussis Andreas; Frankhuizen Wendy; Ginjaar Ieke; Haldane Faye; Laval Steve; Anderson Louise V B; Verrips Theo; Frants Rune R; de Haard Hans; Bushby Kate; den Dunnen Johan; van der Maarel Silvère M
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: von Tell Désirée; Bruder Carl E G; Anderson Louise V B; Anvret Maria; Ahlberg Gabrielle
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: Mahjneh I; Haravuori H; Paetau A; Anderson L V B; Saarinen A; Udd B; Somer H
A distinct phenotype of distal myopathy in a large Finnish family.
Neurology 2003;61(1):87-92.
2003: Poppe M; Cree L; Bourke J; Eagle M; Anderson L V B; Birchall D; Brockington M; Buddles M; Busby M; Muntoni F; Wills A; Bushby K
The phenotype of limb-girdle muscular dystrophy type 2I.
Neurology 2003;60(8):1246-51.
2003: Chambers Stephen P; Anderson Louise V B; Maguire Giselle M; Dodd Andrew; Love Donald R
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: Leriche-Guérin K; Anderson L V B; Wrogemann K; Roy B; Goulet M; Tremblay J P
Dysferlin expression after normal myoblast transplantation in SCID and in SJL mice.
Neuromuscular disorders : NMD 2002;12(2):167-73.
2001: Brockington M; Yuva Y; Prandini P; Brown S C; Torelli S; Benson M A; Herrmann R; Anderson L V; Bashir R; Burgunder J M; Fallet S; Romero N; Fardeau M; Straub V; Storey G; Pollitt C; Richard I; Sewry C A; Bushby K; Voit T; Blake D J; Muntoni F
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: Vainzof M; Anderson L V; McNally E M; Davis D B; Faulkner G; Valle G; Moreira E S; Pavanello R C; Passos-Bueno M R; Zatz M
Dysferlin protein analysis in limb-girdle muscular dystrophies.
Journal of molecular neuroscience : MN 2001;17(1):71-80.
2001: Pollitt C; Anderson L V; Pogue R; Davison K; Pyle A; Bushby K M
The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach.
Neuromuscular disorders : NMD 2001;11(3):287-96.
2001: Vafiadaki E; Reis A; Keers S; Harrison R; Anderson L V; Raffelsberger T; Ivanova S; Hoger H; Bittner R E; Bushby K; Bashir R
Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation.
Neuroreport 2001;12(3):625-9.
2001: Pogue R; Anderson L V; Pyle A; Sewry C; Pollitt C; Johnson M A; Davison K; Moss J A; Mercuri E; Muntoni F; Bushby K M
Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies.
Neuromuscular disorders : NMD 2001;11(1):80-7.
2001: Olby N J; Sharp N J; Anderson L V; Kunkel L M; Bönnemann C G
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: Mahjneh I; Marconi G; Bushby K; Anderson L V; Tolvanen-Mahjneh H; Somer H
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: Anderson L V; Harrison R M; Pogue R; Vafiadaki E; Pollitt C; Davison K; Moss J A; Keers S; Pyle A; Shaw P J; Mahjneh I; Argov Z; Greenberg C R; Wrogemann K; Bertorini T; Goebel H H; Beckmann J S; Bashir R; Bushby K M
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: Ginjaar I B; Kneppers A L; v d Meulen J D; Anderson L V; Bremmer-Bout M; van Deutekom J C; Weegenaar J; den Dunnen J T; Bakker E
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: Ginjaar H B; van der Kooi A J; Ceelie H; Kneppers A L; van Meegen M; Barth P G; Busch H F; Wokke J H; Anderson L V; Bönnemann C G; Jeanpierre M; Bolhuis P A; Moorman A F; de Visser M; Bakker E; Ommen G J
Sarcoglycanopathies in Dutch patients with autosomal recessive limb girdle muscular dystrophy.
Journal of neurology 2000;247(7):524-9.
2000: Vainzof M; Moreira E S; Canovas M; Anderson L V; Pavanello R C; Passos-Bueno M R; Zatz M
Partial alpha-sarcoglycan deficiency with retention of the dystrophin-glycoprotein complex in a LGMD2D family.
Muscle & nerve 2000;23(6):984-8.
2000: Fougerousse F; Anderson L V; Delezoide A L; Suel L; Durand M; Beckmann J S
Calpain3 expression during human cardiogenesis.
Neuromuscular disorders : NMD 2000;10(4-5):251-6.
2000: McNally E M; Ly C T; Rosenmann H; Mitrani Rosenbaum S; Jiang W; Anderson L V; Soffer D; Argov Z
Splicing mutation in dysferlin produces limb-girdle muscular dystrophy with inflammation.
American journal of medical genetics 2000;91(4):305-12.
2000: Auranen M; Rapola J; Pihko H; Haltia M; Leivo I; Soinila S; Virtanen I; Kalimo H; Anderson L V; Santavuori P; Somer H
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease.
Neuromuscular disorders : NMD 2000;10(1):16-23.
1999: Anderson L V
Immunomarkers for molecular mass.
Neuromuscular disorders : NMD 1999;9(6-7):421-2.
1999: Bittner R E; Anderson L V; Burkhardt E; Bashir R; Vafiadaki E; Ivanova S; Raffelsberger T; Maerk I; Höger H; Jung M; Karbasiyan M; Storch M; Lassmann H; Moss J A; Davison K; Harrison R; Bushby K M; Reis A
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: Schatzberg S J; Olby N J; Breen M; Anderson L V; Langford C F; Dickens H F; Wilton S D; Zeiss C J; Binns M M; Kornegay J N; Morris G E; Sharp N J
Molecular analysis of a spontaneous dystrophin 'knockout' dog.
Neuromuscular disorders : NMD 1999;9(5):289-95.
1999: Richard I; Roudaut C; Saenz A; Pogue R; Grimbergen J E; Anderson L V; Beley C; Cobo A M; de Diego C; Eymard B; Gallano P; Ginjaar H B; Lasa A; Pollitt C; Topaloglu H; Urtizberea J A; de Visser M; van der Kooi A; Bushby K; Bakker E; Lopez de Munain A; Fardeau M; Beckmann J S
Calpainopathy-a survey of mutations and polymorphisms.
American journal of human genetics 1999;64(6):1524-40.
1999: Baghdiguian S; Martin M; Richard I; Pons F; Astier C; Bourg N; Hay R T; Chemaly R; Halaby G; Loiselet J; Anderson L V; Lopez de Munain A; Fardeau M; Mangeat P; Beckmann J S; Lefranc G
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: Weiler T; Bashir R; Anderson L V; Davison K; Moss J A; Britton S; Nylen E; Keers S; Vafiadaki E; Greenberg C R; Bushby C R; Wrogemann K
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: Anderson L V; Davison K; Moss J A; Young C; Cullen M J; Walsh J; Johnson M A; Bashir R; Britton S; Keers S; Argov Z; Mahjneh I; Fougerousse F; Beckmann J S; Bushby K M
Dysferlin is a plasma membrane protein and is expressed early in human development.
Human molecular genetics 1999;8(5):855-61.
1999: Anderson L V; Davison K
Multiplex Western blotting system for the analysis of muscular dystrophy proteins.
The American journal of pathology 1999;154(4):1017-22.
1998: Anderson L V; Davison K; Moss J A; Richard I; Fardeau M; Tomé F M; Hübner C; Lasa A; Colomer J; Beckmann J S
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: Schatzberg S J; Anderson L V; Wilton S D; Kornegay J N; Mann C J; Solomon G G; Sharp N J
Alternative dystrophin gene transcripts in golden retriever muscular dystrophy.
Muscle & nerve 1998;21(8):991-8.
1998: Vater R; Young C; Anderson L V; Lindsay S; Blake D J; Davies K E; Zuellig R; Slater C R
Utrophin mRNA expression in muscle is not restricted to the neuromuscular junction.
Molecular and cellular neurosciences 1998;10(5-6):229-42.
1998: Bushby K; Anderson L V; Pollitt C; Naom I; Muntoni F; Bindoff L
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: Slater C R; Young C; Wood S J; Bewick G S; Anderson L V; Baxter P; Fawcett P R; Roberts M; Jacobson L; Kuks J; Vincent A; Newsom-Davis J
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: Metzinger L; Blake D J; Squier M V; Anderson L V; Deconinck A E; Nawrotzki R; Hilton-Jones D; Davies K E
Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophy.
Human molecular genetics 1997;6(7):1185-91.
1997: Spencer M J; Tidball J G; Anderson L V; Bushby K M; Harris J B; Passos-Bueno M R; Somer H; Vainzof M; Zatz M
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A).
Journal of the neurological sciences 1997;146(2):173-8.
1996: Sewry C A; Taylor J; Anderson L V; Ozawa E; Pogue R; Piccolo F; Bushby K; Dubowitz V; Muntoni F
Abnormalities in alpha-, beta- and gamma-sarcoglycan in patients with limb-girdle muscular dystrophy.
Neuromuscular disorders : NMD 1996;6(6):467-74.
1996: Vainzof M; Passos-Bueno M R; Canovas M; Moreira E S; Pavanello R C; Marie S K; Anderson L V; Bonnemann C G; McNally E M; Nigro V; Kunkel L M; Zatz M
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.
Human molecular genetics 1996;5(12):1963-9.
1995: Bushby K M; Appleton R; Anderson L V; Welch J L; Kelly P; Gardner-Medwin D
Deletion status and intellectual impairment in Duchenne muscular dystrophy.
Developmental medicine and child neurology 1995;37(3):260-9.
1994: Heald A; Anderson L V; Bushby K M; Shaw P J
Becker muscular dystrophy with onset after 60 years.
Neurology 1994;44(12):2388-90.

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Louise Anderson

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