176 related articles for article (PubMed ID: 12801918)
1. Localization of calpain 3 in human skeletal muscle and its alteration in limb-girdle muscular dystrophy 2A muscle.
Keira Y; Noguchi S; Minami N; Hayashi YK; Nishino I
J Biochem; 2003 May; 133(5):659-64. PubMed ID: 12801918
[TBL] [Abstract][Full Text] [Related]
2. Skeletal muscle-specific calpain, p94, and connectin/titin: their physiological functions and relationship to limb-girdle muscular dystrophy type 2A.
Sorimachi H; Ono Y; Suzuki K
Adv Exp Med Biol; 2000; 481():383-95; discussion 395-7. PubMed ID: 10987085
[TBL] [Abstract][Full Text] [Related]
3. Muscle-specific calpain, p94, responsible for limb girdle muscular dystrophy type 2A, associates with connectin through IS2, a p94-specific sequence.
Sorimachi H; Kinbara K; Kimura S; Takahashi M; Ishiura S; Sasagawa N; Sorimachi N; Shimada H; Tagawa K; Maruyama K
J Biol Chem; 1995 Dec; 270(52):31158-62. PubMed ID: 8537379
[TBL] [Abstract][Full Text] [Related]
4. The effect of calpain 3 deficiency on the pattern of muscle degeneration in the earliest stages of LGMD2A.
Vainzof M; de Paula F; Tsanaclis AM; Zatz M
J Clin Pathol; 2003 Aug; 56(8):624-6. PubMed ID: 12890817
[TBL] [Abstract][Full Text] [Related]
5. Pathophysiology of limb girdle muscular dystrophy type 2A: hypothesis and new insights into the IkappaBalpha/NF-kappaB survival pathway in skeletal muscle.
Baghdiguian S; Richard I; Martin M; Coopman P; Beckmann JS; Mangeat P; Lefranc G
J Mol Med (Berl); 2001 Jun; 79(5-6):254-61. PubMed ID: 11485017
[TBL] [Abstract][Full Text] [Related]
6. Mutations in calpain 3 associated with limb girdle muscular dystrophy: analysis by molecular modeling and by mutation in m-calpain.
Jia Z; Petrounevitch V; Wong A; Moldoveanu T; Davies PL; Elce JS; Beckmann JS
Biophys J; 2001 Jun; 80(6):2590-6. PubMed ID: 11371436
[TBL] [Abstract][Full Text] [Related]
7. Translocation of molecular chaperones to the titin springs is common in skeletal myopathy patients and affects sarcomere function.
Unger A; Beckendorf L; Böhme P; Kley R; von Frieling-Salewsky M; Lochmüller H; Schröder R; Fürst DO; Vorgerd M; Linke WA
Acta Neuropathol Commun; 2017 Sep; 5(1):72. PubMed ID: 28915917
[TBL] [Abstract][Full Text] [Related]
8. Possible functions of p94 in connectin-mediated signaling pathways in skeletal muscle cells.
Ojima K; Ono Y; Hata S; Koyama S; Doi N; Sorimachi H
J Muscle Res Cell Motil; 2005; 26(6-8):409-17. PubMed ID: 16453164
[TBL] [Abstract][Full Text] [Related]
9. Myogenic stage, sarcomere length, and protease activity modulate localization of muscle-specific calpain.
Ojima K; Ono Y; Doi N; Yoshioka K; Kawabata Y; Labeit S; Sorimachi H
J Biol Chem; 2007 May; 282(19):14493-504. PubMed ID: 17371879
[TBL] [Abstract][Full Text] [Related]
10. Myopathy phenotype of transgenic mice expressing active site-mutated inactive p94 skeletal muscle-specific calpain, the gene product responsible for limb girdle muscular dystrophy type 2A.
Tagawa K; Taya C; Hayashi Y; Nakagawa M; Ono Y; Fukuda R; Karasuyama H; Toyama-Sorimachi N; Katsui Y; Hata S; Ishiura S; Nonaka I; Seyama Y; Arahata K; Yonekawa H; Sorimachi H; Suzuki K
Hum Mol Genet; 2000 May; 9(9):1393-402. PubMed ID: 10814721
[TBL] [Abstract][Full Text] [Related]
11. Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice.
Richard I; Roudaut C; Marchand S; Baghdiguian S; Herasse M; Stockholm D; Ono Y; Suel L; Bourg N; Sorimachi H; Lefranc G; Fardeau M; Sébille A; Beckmann JS
J Cell Biol; 2000 Dec; 151(7):1583-90. PubMed ID: 11134085
[TBL] [Abstract][Full Text] [Related]
12. Functional defects of a muscle-specific calpain, p94, caused by mutations associated with limb-girdle muscular dystrophy type 2A.
Ono Y; Shimada H; Sorimachi H; Richard I; Saido TC; Beckmann JS; Ishiura S; Suzuki K
J Biol Chem; 1998 Jul; 273(27):17073-8. PubMed ID: 9642272
[TBL] [Abstract][Full Text] [Related]
13. Characterization of monoclonal antibodies to calpain 3 and protein expression in muscle from patients with limb-girdle muscular dystrophy type 2A.
Anderson LV; Davison K; Moss JA; Richard I; Fardeau M; Tomé FM; Hübner C; Lasa A; Colomer J; Beckmann JS
Am J Pathol; 1998 Oct; 153(4):1169-79. PubMed ID: 9777948
[TBL] [Abstract][Full Text] [Related]
14. Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures.
Mercuri E; Bushby K; Ricci E; Birchall D; Pane M; Kinali M; Allsop J; Nigro V; Sáenz A; Nascimbeni A; Fulizio L; Angelini C; Muntoni F
Neuromuscul Disord; 2005 Feb; 15(2):164-71. PubMed ID: 15694138
[TBL] [Abstract][Full Text] [Related]
15. New aspect of the research on limb-girdle muscular dystrophy 2A: a molecular biologic and biochemical approach to pathology.
Ono Y; Sorimachi H; Suzuki K
Trends Cardiovasc Med; 1999 Jul; 9(5):114-8. PubMed ID: 10639725
[TBL] [Abstract][Full Text] [Related]
16. Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A).
Spencer MJ; Tidball JG; Anderson LV; Bushby KM; Harris JB; Passos-Bueno MR; Somer H; Vainzof M; Zatz M
J Neurol Sci; 1997 Mar; 146(2):173-8. PubMed ID: 9077514
[TBL] [Abstract][Full Text] [Related]
17. Loss of calpain-3 autocatalytic activity in LGMD2A patients with normal protein expression.
Fanin M; Nascimbeni AC; Fulizio L; Trevisan CP; Meznaric-Petrusa M; Angelini C
Am J Pathol; 2003 Nov; 163(5):1929-36. PubMed ID: 14578192
[TBL] [Abstract][Full Text] [Related]
18. Muscle-specific calpain-3 is phosphorylated in its unique insertion region for enrichment in a myofibril fraction.
Ojima K; Ono Y; Hata S; Noguchi S; Nishino I; Sorimachi H
Genes Cells; 2014 Nov; 19(11):830-41. PubMed ID: 25252031
[TBL] [Abstract][Full Text] [Related]
19. Clinical, pathological, and genetic features of limb-girdle muscular dystrophy type 2A with new calpain 3 gene mutations in seven patients from three Japanese families.
Kawai H; Akaike M; Kunishige M; Inui T; Adachi K; Kimura C; Kawajiri M; Nishida Y; Endo I; Kashiwagi S; Nishino H; Fujiwara T; Okuno S; Roudaut C; Richard I; Beckmann JS; Miyoshi K; Matsumoto T
Muscle Nerve; 1998 Nov; 21(11):1493-501. PubMed ID: 9771675
[TBL] [Abstract][Full Text] [Related]
20. 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.
Baghdiguian S; Martin M; Richard I; Pons F; Astier C; Bourg N; Hay RT; Chemaly R; Halaby G; Loiselet J; Anderson LV; Lopez de Munain A; Fardeau M; Mangeat P; Beckmann JS; Lefranc G
Nat Med; 1999 May; 5(5):503-11. PubMed ID: 10229226
[No Abstract] [Full Text] [Related]
[Next] [New Search]