Louise V.B. Anderson

Author

Also Known As

L. V. B. Anderson, L.V.B Anderson, L.V.B. Anderson, LOUISE V. B. ANDERSON, Louise Anderson, Louise V B Anderson, Louise V. B. Anderson, Louise V.B Anderson, Louise V.B. Anderson, Louise VB Anderson

Publications

4.4K

Citations

H-Index

Concepts

All Affiliations

Newcastle University North Tyneside General Hospital Genethon (France)Centre for Life Universidade de São Paulo

About

Louise V.B. Anderson is an author at Newcastle University specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	24	29	2.1K
2	Health Sciences	4	4	386
3	Natural Sciences	3	3	308
4	Engineering	1	1	171
5	Anatomy	1	1	19

Louise V.B. Anderson

Publications

Citations

H-Index

Page 1

	Year	Citations
Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development Louise V.B. Anderson, Kenneth Davison, Jessica Moss, Human Molecular Genetics	1999	292
Calpain 3 deficiency is associated with myonuclear apoptosis and profound perturbation of the IκBα/NF-κB pathway in limb-girdle muscular dystrophy type 2A Stephen Baghdiguian, Marianne Martin, Isabelle Richard, Nature Medicine Signal TransductionMolecular PhysiologySkeletal MuscleMyonuclear ApoptosisMedicine	1999	275
Calpainopathy—A Survey of Mutations and Polymorphisms Isabelle Richard, Carinne Roudaut, Amets Sáenz, The American Journal of Human Genetics Genetic DisorderGeneticsGenetic EpidemiologyPathologyGenetic Variation	1999	206
AHNAK a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration Yanchao Huang, Steven H. Laval, Alexandra van Remoortere, The FASEB Journal Muscle FunctionCytoskeletonDysferlin Protein ComplexCellular PhysiologyMiyoshi Myopathy	2006	180
Identical Mutation in Patients with Limb Girdle Muscular Dystrophy Type 2B Or Miyoshi Myopathy Suggests a Role for Modifier Gene(s) Tracey Weiler, R. Bashir, Louise V.B. Anderson, Human Molecular Genetics Miyoshi MyopathyRare DiseasesOr Miyoshi MyopathyMendelian DisorderGenetic Disorder	1999	179
Abnormalities in α-Dystroglycan Expression in MDC1C and LGMD2I Muscular Dystrophies S. Brown, Silvia Torelli, Martin Brockington, American Journal Of Pathology PathologyDegenerative Diseaseα-Dystroglycan ExpressionMedicineCell Biology	2004	171
Multiplex Western Blotting System for the Analysis of Muscular Dystrophy Proteins Louise V.B. Anderson, Keith Davison American Journal Of Pathology Protein FunctionEngineeringSkeletal MuscleProtein FoldingNatural Sciences	1999	171
Characterization of Monoclonal Antibodies to Calpain 3 and Protein Expression in Muscle from Patients with Limb-Girdle Muscular Dystrophy Type 2A Louise V.B. Anderson, Keith Davison, Jennifer A. Moss, American Journal Of Pathology Muscle PhysiologyMuscle FunctionKinesiologyProtein ExpressionSkeletal Muscle	1998	166
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies) Louise V.B. Anderson, Ruth M Harrison, Robert Pogue, Neuromuscular Disorders Miyoshi MyopathyCalpain 3Skeletal MusclePhysiologySecondary Reduction	2000	163
Molecular analysis of a spontaneous dystrophin `knockout' dog Scott J. Schatzberg, Natasha J. Olby, Matthew Breen, Neuromuscular Disorders Animal PhysiologyPhysiologyVeterinary PathologyVeterinary SciencePathology	1999	118

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