Anderson LV - Search Results

1

The differential gene expression profiles of proximal and distal muscle groups are altered in pre-pathological dysferlin-deficient mice.

von der Hagen M, Laval SH, Cree LM, Haldane F, Pocock M, Wappler I, Peters H, Reitsamer HA, Hoger H, Wiedner M, Oberndorfer F, Anderson LV, Straub V, Bittner RE, Bushby KM. von der Hagen M, et al. Among authors: anderson lv. Neuromuscul Disord. 2005 Dec;15(12):863-77. doi: 10.1016/j.nmd.2005.09.002. Epub 2005 Nov 8. Neuromuscul Disord. 2005. PMID: 16288871

2

Cloning of the mouse dysferlin gene and genomic characterization of the SJL-Dysf mutation.

Vafiadaki E, Reis A, Keers S, Harrison R, Anderson LV, Raffelsberger T, Ivanova S, Hoger H, Bittner RE, Bushby K, Bashir R. Vafiadaki E, et al. Among authors: anderson lv. Neuroreport. 2001 Mar 5;12(3):625-9. doi: 10.1097/00001756-200103050-00039. Neuroreport. 2001. PMID: 11234777

3

Late onset in dysferlinopathy widens the clinical spectrum.

Klinge L, Dean AF, Kress W, Dixon P, Charlton R, Müller JS, Anderson LV, Straub V, Barresi R, Lochmüller H, Bushby K. Klinge L, et al. Among authors: anderson lv. Neuromuscul Disord. 2008 Apr;18(4):288-90. doi: 10.1016/j.nmd.2008.01.004. Neuromuscul Disord. 2008. PMID: 18396043

4

AHNAK, a novel component of the dysferlin protein complex, redistributes to the cytoplasm with dysferlin during skeletal muscle regeneration.

Huang Y, Laval SH, van Remoortere A, Baudier J, Benaud C, Anderson LV, Straub V, Deelder A, Frants RR, den Dunnen JT, Bushby K, van der Maarel SM. Huang Y, et al. Among authors: anderson lv. FASEB J. 2007 Mar;21(3):732-42. doi: 10.1096/fj.06-6628com. Epub 2006 Dec 21. FASEB J. 2007. PMID: 17185750

5

Dysferlin associates with the developing T-tubule system in rodent and human skeletal muscle.

Klinge L, Harris J, Sewry C, Charlton R, Anderson L, Laval S, Chiu YH, Hornsey M, Straub V, Barresi R, Lochmüller H, Bushby K. Klinge L, et al. Muscle Nerve. 2010 Feb;41(2):166-73. doi: 10.1002/mus.21166. Muscle Nerve. 2010. PMID: 20082313

6

Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies).

Anderson LV, Harrison RM, Pogue R, Vafiadaki E, Pollitt C, Davison K, Moss JA, Keers S, Pyle A, Shaw PJ, Mahjneh I, Argov Z, Greenberg CR, Wrogemann K, Bertorini T, Goebel HH, Beckmann JS, Bashir R, Bushby KM. Anderson LV, et al. Neuromuscul Disord. 2000 Dec;10(8):553-9. doi: 10.1016/s0960-8966(00)00143-7. Neuromuscul Disord. 2000. PMID: 11053681

7

Strategy for mutation analysis in the autosomal recessive limb-girdle muscular dystrophies.

Pogue R, Anderson LV, Pyle A, Sewry C, Pollitt C, Johnson MA, Davison K, Moss JA, Mercuri E, Muntoni F, Bushby KM. Pogue R, et al. Among authors: anderson lv. Neuromuscul Disord. 2001 Jan;11(1):80-7. doi: 10.1016/s0960-8966(00)00154-1. Neuromuscul Disord. 2001. PMID: 11166169

8

The phenotype of calpainopathy: diagnosis based on a multidisciplinary approach.

Pollitt C, Anderson LV, Pogue R, Davison K, Pyle A, Bushby KM. Pollitt C, et al. Among authors: anderson lv. Neuromuscul Disord. 2001 Apr;11(3):287-96. doi: 10.1016/s0960-8966(00)00197-8. Neuromuscul Disord. 2001. PMID: 11297944

9

Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutations.

Mahjneh I, Marconi G, Bushby K, Anderson LV, Tolvanen-Mahjneh H, Somer H. Mahjneh I, et al. Among authors: anderson lv. Neuromuscul Disord. 2001 Jan;11(1):20-6. doi: 10.1016/s0960-8966(00)00157-7. Neuromuscul Disord. 2001. PMID: 11166162

10

Protein studies in dysferlinopathy patients using llama-derived antibody fragments selected by phage display.

Huang Y, Verheesen P, Roussis A, Frankhuizen W, Ginjaar I, Haldane F, Laval S, Anderson LV, Verrips T, Frants RR, de Haard H, Bushby K, den Dunnen J, van der Maarel SM. Huang Y, et al. Among authors: anderson lv. Eur J Hum Genet. 2005 Jun;13(6):721-30. doi: 10.1038/sj.ejhg.5201414. Eur J Hum Genet. 2005. PMID: 15827562

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