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Literature for peptidase C02.004: calpain-3

Summary Gene structure Alignment Tree Sequences Sequence features Distribution Structure Literature Substrates

(Topics flags: S Structure, P Specificity, K Knockout, E Expression, V Review, M Mutation, I Inhibitor, R Splicing, U Therapeutic. To select only the references relevant to a single topic, click the link above. See explanation.)

    2024
  1. Mao,B., Yang,J., Zhao,X., Jia,X., Shi,X., Zhao,L., Banerjee,S., Zhang,L. and Ma,X.
    Identification and functional characterization of a novel heterozygous spliceƒ_'site mutation in the calpain 3 gene causes rare autosomal dominant limbƒ_'girdle muscular dystrophy
    Exp Ther Med27, 97-97. PubMed  Europe PubMed DOI
  2. Valls,A., Gutierrez-Gutierrez,G., Martinez,A., Ruiz-Roldan,C., Camano,P., Lopez de Munain,A. and Saenz,A.
    The CAPN3 p.Lys 254del variant is not always associated with dominant CAPN3-related muscular dystrophy
    Muscle Nerve69, 472-476. PubMed  Europe PubMed DOI
  3. Villani,K.R., Zhong,R., Henley-Beasley,C.S., Rastelli,G., Harris,E., Boncompagni,S., Barton,E.R. and Wei-LaPierre,L.
    Loss of Calpain 3 dysregulates store-operated calcium entry and its exercise response in mice
    FASEB J38, e23825-e23825. PubMed  Europe PubMed DOI
    4. 2023
  4. Joseph,R., Robinson,M.L., Lambert,L. and Srivastava,O.P.
    Lens-specific betaA3/A1-conditional knockout mice: Phenotypic characteristics and calpain activation causing protein degradation and insolubilization
    PLoS ONE18, e0281386-e0281386. PubMed  Europe PubMed DOI
  5. Ojima,K., Hata,S., Shinkai-Ouchi,F., Ono,Y. and Muroya,S.
    Calpain-3 not only proteolyzes calpain-1 and -2 but also is a substrate for calpain-1 and -2
    J Biochem174, 421-431. PubMed  Europe PubMed DOI
    6. 2022
  6. Ding,F., Huang,D., Wang,M. and Peng,J.
    An 86 amino acids motif in CAPN3 is essential for formation of the nucleolus-localized Def-CAPN3 complex
    Biochem Biophys Res Commun623, 66-73. PubMed  Europe PubMed DOI
  7. Mroczek,M., Inashkina,I., Stavusis,J., Zayakin,P., Khrunin,A., Micule,I., Kenina,V., Zdanovica,A., Zidkova,J., Fajkusova,L., Limborska,S., van der Kooi,A.J., Brusse,E., Leonardis,L., Maver,A., Pajusalu,S., Ounap,K., Puusepp,S., Dobosz,P., Sypniewski,M., Burnyte,B. and Lace,B.
    CAPN3 c.1746-20C>G variant is hypomorphic for LGMD R1 calpain 3-related
    Hum Mutat43, 1347-1353. PubMed  Europe PubMed DOI
    8. 2021
  8. Chen,L., Tang,F., Gao,H., Zhang,X., Li,X. and Xiao,D.
    CAPN3: A musclespecific calpain with an important role in the pathogenesis of diseases (Review)
    Int J Mol Med48, PubMed  Europe PubMed DOI  V
    9. 2020
  9. Hata,S., Doi,N., Shinkai-Ouchi,F. and Ono,Y.
    A muscle-specific calpain, CAPN3, forms a homotrimer
    Biochim Biophys Acta Proteins Proteom1868, 140411-140411. PubMed  Europe PubMed DOI  S
  10. Huang,W., Chen,F., Ma,Q., Xin,J., Li,J., Chen,J., Zhou,B., Chen,M., Li,J. and Peng,J.
    Ribosome biogenesis gene DEF/UTP25 is essential for liver homeostasis and regeneration
    Sci China Life Sci PubMed  Europe PubMed DOI  K
  11. Hwang,S.D., Choi,K.M., Hwang,J.Y., Kwon,M.G., Jeong,J.M., Seo,J.S., Jee,B.Y. and Park,C.I.
    Molecular genetic characterisation and expression profiling of calpain 3 transcripts in red sea bream (Pagrus major)
    Fish Shellfish Immunol98, 19-24. PubMed  Europe PubMed DOI
  12. Jahnke,V.E., Peterson,J.M., Van Der Meulen,J.H., Boehler,J., Uaesoontrachoon,K., Johnston,H.K., Defour,A., Phadke,A., Yu,Q., Jaiswal,J.K. and Nagaraju,K.
    Mitochondrial dysfunction and consequences in calpain-3-deficient muscle
    Skelet Muscle10, 37-37. PubMed  Europe PubMed DOI
  13. Landires,I., Nunez-Samudio,V., Fernandez,J., Sarria,C., Villareal,V., Cordoba,F., Apraez-Ippolito,G., Martinez,S., Vidal,O.M., Velez,J.I., Arcos-Holzinger,M., Landires,S. and Arcos-Burgos,M.
    Calpainopathy: Description of a Novel Mutation and Clinical Presentation with Early Severe Contractures
    Genes (Basel)11, PubMed  Europe PubMed DOI  M
  14. Vissing,J., Dahlqvist,J.R., Roudaut,C., Poupiot,J., Richard,I., Duno,M. and Krag,T.
    A single c.1715G>C calpain 3 gene variant causes dominant calpainopathy with loss of calpain 3 expression and activity
    Hum Mutat41, 1507-1513. PubMed  Europe PubMed DOI
    15. 2019
  15. El-Khoury,R., Traboulsi,S., Hamad,T., Lamaa,M., Sawaya,R. and Ahdab-Barmada,M.
    Divergent features of mitochondrial deficiencies in LGMD2A associated with novel calpain-3 mutations
    J Neuropathol Exp Neurol78, 88-98. PubMed  Europe PubMed DOI  M
  16. Lostal,W., Roudaut,C., Faivre,M., Charton,K., Suel,L., Bourg,N., Best,H., Smith,J.E., Gohlke,J., Corre,G., Li,X., Elbeck,Z., Knoll,R., Deschamps,J.Y., Granzier,H. and Richard,I.
    Titin splicing regulates cardiotoxicity associated with calpain 3 gene therapy for limb-girdle muscular dystrophy type 2A
    Sci Transl Med11, PubMed  Europe PubMed DOI  U
    17. 2018
  17. McCartney,C.E., Ye,Q., Campbell,R.L. and Davies,P.L.
    Insertion sequence 1 from calpain-3 is functional in calpain-2 as an internal propeptide
    J Biol Chem293, 17716-17730. PubMed  Europe PubMed DOI
  18. Ye,Q., Campbell,R.L. and Davies,P.L.
    Structures of human calpain-3 protease core with and without bound inhibitor reveal mechanisms of calpain activation
    J Biol Chem293, 4056-4070. PubMed  Europe PubMed DOI  S  I
    19. 2017
  19. Pantoja-Melendez,C.A., Miranda-Duarte,A., Roque-Ramirez,B. and Zenteno,J.C.
    Epidemiological and molecular characterization of a Mexican population isolate with high prevalence of limb-girdle muscular dystrophy Type 2A due to a novel calpain-3 mutation
    PLoS ONE12, e0170280-e0170280. PubMed  Europe PubMed DOI  M
    20. 2016
  20. Fadaee,M., Kariminejad,A., Fattahi,Z., Nafissi,S., Godarzi,H.R., Beheshtian,M., Vazehan,R., Akbari,M.R., Kahrizi,K. and Najmabadi,H.
    Report of limb girdle muscular dystrophy type 2a in 6 Iranian patients, one with a novel deletion in CAPN3 gene
    Neuromuscul Disord26, 277-282. PubMed  Europe PubMed DOI  M
  21. Michel,L.Y., Hoenderop,J.G. and Bindels,R.J.
    Calpain-3-mediated regulation of the Na(+)-Ca(2+) exchanger isoform 3
    Pflugers Arch468, 243-255. PubMed  Europe PubMed DOI
  22. Ono,Y., Ojima,K., Shinkai-Ouchi,F., Hata,S. and Sorimachi,H.
    An eccentric calpain, CAPN3/p94/calpain-3
    Biochimie122, 169-187. PubMed  Europe PubMed DOI  V
  23. Richard,I., Hogrel,J.Y., Stockholm,D., Payan,C.A., Fougerousse,F., Eymard,B., Mignard,C., Lopez de Munain,A., Fardeau,M. and Urtizberea,J.A.
    Natural history of LGMD2A for delineating outcome measures in clinical trials
    Ann Clin Transl Neurol3, 248-265. PubMed  Europe PubMed DOI  M
    24. 2015
  24. Dorobek,M., Ryniewicz,B., Kabzinska,D., Fidzianska,A., Styczynska,M. and Hausmanowa-Petrusewicz,I.
    The frequency of c.550delA mutation of the CANP3 gene in the Polish LGMD2A population
    Genet Test Mol Biomarkers19, 637-640. PubMed  Europe PubMed DOI  M
  25. Ermolova,N., Kramerova,I. and Spencer,M.J.
    Autolytic activation of calpain 3 proteinase is facilitated by calmodulin protein
    J Biol Chem290, 996-1004. PubMed  Europe PubMed DOI
  26. Muto,Y., Morton,J. and Palmer,D.
    Investigation of biochemical changes of the ovine calpain 3 exon-10 polymorphism
    Mol Cell Probes29, 382-388. PubMed  Europe PubMed DOI  M
  27. Ono,Y. and Sorimachi,H.
    Amino acid sequence alignment of vertebrate CAPN3/calpain-3/p94
    Data Brief5, 366-367. PubMed  Europe PubMed DOI
  28. Ramos,E., Pardo,S., Mas Rodriguez,M.F. and Velez,J.
    Limb-girdle muscular dystrophy type 2A resulting from c.C479G and c.G1818A mutations in the calpain-3 gene
    J Clin Neuromuscul Dis17, 59-62. PubMed  Europe PubMed DOI  M
  29. Ramos,E., Pardo,S., Mas,R.M.F. and Velez,J.
    Limb-girdle muscular dystrophy type 2A resulting from c.C479G and c.G1818A mutations in the calpain-3 gene
    J Clin Neuromuscul Dis17, 59-62.  M
    30. 2014
  30. Kanzaki,K., Kuratani,M., Matsunaga,S., Yanaka,N. and Wada,M.
    Three calpain isoforms are autolyzed in rat fast-twitch muscle after eccentric contractions
    J Muscle Res Cell Motil35, 179-189. PubMed  Europe PubMed DOI
  31. Nakajima,T., Shearer,T.R. and Azuma,M.
    Loss of calpastatin leads to activation of calpain in human lens epithelial cells
    Invest Ophthalmol Vis Sci55, 5278-5283. PubMed  Europe PubMed DOI  I
  32. Ojima,K., Ono,Y., Hata,S., Noguchi,S., Nishino,I. and Sorimachi,H.
    Muscle-specific calpain-3 is phosphorylated in its unique insertion region for enrichment in a myofibril fraction
    Genes Cells19, 830-841. PubMed  Europe PubMed DOI
  33. Ono,Y., Shindo,M., Doi,N., Kitamura,F., Gregorio,C.C. and Sorimachi,H.
    The N- and C-terminal autolytic fragments of CAPN3/p94/calpain-3 restore proteolytic activity by intermolecular complementation
    Proc Natl Acad Sci U S A111, E5527-E5536. PubMed  Europe PubMed DOI
  34. Partha,S.K., Ravulapalli,R., Allingham,J.S., Campbell,R.L. and Davies,P.L.
    Crystal structure of calpain-3 penta-EF-hand (PEF) domain - a homodimerized PEF family member with calcium bound at the fifth EF-hand
    FEBS J281, 3138-3149. PubMed  Europe PubMed DOI  S
    35. 2013
  35. Fang,Q., Forrest,R.H., Zhou,H., Frampton,C.M. and Hickford,J.G.
    Variation in exon 10 of the ovine calpain 3 gene (CAPN3) and its association with meat yield in New Zealand Romney sheep
    Meat Sci94, 388-390. PubMed  Europe PubMed DOI  M
  36. Nuaaman,M.M. and Benchimol,S.
    Proteasome-independent p53 degradation
    Cell Res23, 597-598. PubMed  Europe PubMed DOI
  37. Ono,Y., Iemura,S., Novak,S.M., Doi,N., Kitamura,F., Natsume,T., Gregorio,C.C. and Sorimachi,H.
    PLEIAD/SIMC1/C5orf25, a novel autolysis regulator for a skeletal-muscle-specific calpain, CAPN3, scaffolds a CAPN3 substrate, CTBP1
    J Mol Biol425, 2955-2972. PubMed  Europe PubMed DOI
  38. Tao,T., Shi,H., Guan,Y., Huang,D., Chen,Y., Lane,D.P., Chen,J. and Peng,J.
    Def defines a conserved nucleolar pathway that leads p53 to proteasome-independent degradation
    Cell Res23, 620-634. PubMed  Europe PubMed DOI
    39. 2012
  39. Sorimachi,H. and Ono,Y.
    Regulation and physiological roles of the calpain system in muscular disorders
    Cardiovasc Res96, 11-22. PubMed  Europe PubMed DOI  V
  40. Sorimachi,H., Hata,S. and Ono,Y.
    Muscle calpain
    [ISSN:978-0-12-407743-0]3, 2011-2017. DOI
    41. 2011
  41. Gallardo,E., Saenz,A. and Illa,I.
    Limb-girdle muscular dystrophy 2A
    Handb Clin Neurol101, 97-110. PubMed  Europe PubMed DOI  M  V
  42. Murphy,R.M., Vissing,K., Latchman,H., Lamboley,C., McKenna,M.J., Overgaard,K. and Lamb,G.D.
    Activation of skeletal muscle calpain-3 by eccentric exercise in humans does not result in its translocation to the nucleus or cytosol
    J Appl Physiol111, 1448-1458. PubMed  Europe PubMed DOI
  43. Ojima,K., Ono,Y., Ottenheijm,C., Hata,S., Suzuki,H., Granzier,H. and Sorimachi,H.
    Non-proteolytic functions of calpain-3 in sarcoplasmic reticulum in skeletal muscles
    J Mol Biol407, 439-449. PubMed  Europe PubMed DOI
  44. Saenz,A., Ono,Y., Sorimachi,H., Goicoechea,M., Leturcq,F., Blazquez,L., Garcia-Bragado,F., Marina,A., Poza,J.J., Azpitarte,M., Doi,N., Urtasun,M., Kaplan,J.C. and De Munain,A.L.
    Does the severity of the LGMD2A phenotype in compound heterozygotes depend on the combination of mutations?
    Muscle Nerve44, 710-714. PubMed  Europe PubMed DOI  M
    45. 2010
  45. Charton,K., Daniele,N., Vihola,A., Roudaut,C., Gicquel,E., Monjaret,F., Tarrade,A., Sarparanta,J., Udd,B. and Richard,I.
    Removal of the calpain 3 protease reverses the myopathology in a mouse model for titinopathies
    Hum Mol Genet19, 4608-4624. PubMed  Europe PubMed DOI
  46. de Morree,A., Lutje Hulsik,D., Impagliazzo,A., van Haagen,H.H., de Galan,P., van Remoortere,A., 't Hoen,P.A., van Ommen,G.B., Frants,R.R. and van der Maarel,S.M.
    Calpain 3 is a rapid-action, unidirectional proteolytic switch central to muscle remodeling
    PLoS ONE5, e11940-e11940. PubMed  Europe PubMed DOI
  47. Laure,L., Daniele,N., Suel,L., Marchand,S., Aubert,S., Bourg,N., Roudaut,C., Duguez,S., Bartoli,M. and Richard,I.
    A new pathway encompassing calpain 3 and its newly identified substrate cardiac ankyrin repeat protein is involved in the regulation of the nuclear factor-kappaB pathway in skeletal muscle
    FEBS J277, 4322-4337. PubMed  Europe PubMed DOI
  48. Ojima,K., Kawabata,Y., Nakao,H., Nakao,K., Doi,N., Kitamura,F., Ono,Y., Hata,S., Suzuki,H., Kawahara,H., Bogomolovas,J., Witt,C., Ottenheijm,C., Labeit,S., Granzier,H., Toyama-Sorimachi,N., Sorimachi,M., Suzuki,K., Maeda,T., Abe,K., Aiba,A. and Sorimachi,H.
    Dynamic distribution of muscle-specific calpain in mice has a key role in physical-stress adaptation and is impaired in muscular dystrophy
    J Clin Invest120, 2672-2683. PubMed  Europe PubMed DOI
  49. Ono,Y., Ojima,K., Torii,F., Takaya,E., Doi,N., Nakagawa,K., Hata,S., Abe,K. and Sorimachi,H.
    Skeletal muscle-specific calpain is an intracellular Na+-dependent protease
    J Biol Chem285, 22986-22998. PubMed  Europe PubMed DOI
  50. Stuelsatz,P., Pouzoulet,F., Lamarre,Y., Dargelos,E., Poussard,S., Leibovitch,S., Cottin,P. and Veschambre,P.
    Down-regulation of MyoD by calpain 3 promotes generation of reserve cells in C2C12 myoblasts
    J Biol Chem285, 12670-12683. PubMed  Europe PubMed DOI
    51. 2009
  51. Bertipaglia,I., Bourg,N., Richard,I., Pahlman,A.K., Andersson,L., James,P. and Carafoli,E.
    A proteomic study of calpain-3 and its involvement in limb girdle muscular dystrophy type 2a
    Cell Calcium46, 356-363. PubMed  Europe PubMed DOI  P
  52. Garnham,C.P., Hanna,R.A., Chou,J.S., Low,K.E., Gourlay,K., Campbell,R.L., Beckmann,J.S. and Davies,P.L.
    Limb-girdle muscular dystrophy type 2A can result from accelerated autoproteolytic inactivation of calpain 3
    Biochemistry48, 3457-3467. PubMed  Europe PubMed DOI
  53. Kramerova,I., Kudryashova,E., Wu,B., Germain,S., Vandenborne,K., Romain,N., Haller,R.G., Verity,M.A. and Spencer,M.J.
    Mitochondrial abnormalities, energy deficit and oxidative stress are features of calpain 3 deficiency in skeletal muscle
    Hum Mol Genet18, 3194-3205. PubMed  Europe PubMed DOI  M
  54. Moretti,D., Del Bello,B., Cosci,E., Biagioli,M., Miracco,C. and Maellaro,E.
    Novel variants of muscle calpain 3 identified in human melanoma cells: cisplatin-induced changes in vitro and differential expression in melanocytic lesions
    Carcinogenesis30, 960-967. PubMed  Europe PubMed DOI  R
  55. Vattemi,G., Tonin,P., Neri,M., Marini,M., Gualandi,F., Guglielmi,V., Ferlini,A. and Tomelleri,G.
    Calpain 3 deficiency presenting as fibre type disproportion
    Neuropathol Appl Neurobiol35, 614-617. PubMed  Europe PubMed DOI  M
    56. 2008
  56. Barendse,W., Harrison,B.E., Bunch,R.J. and Thomas,M.B.
    Variation at the calpain 3 gene is associated with meat tenderness in zebu and composite breeds of cattle
    BMC Genet9, 41-41. PubMed  Europe PubMed DOI  M
  57. Beckmann,J.S. and Spencer,M.
    Calpain 3, the "gatekeeper" of proper sarcomere assembly, turnover and maintenance
    Neuromuscul Disord18, 913-921. PubMed  Europe PubMed DOI  V
  58. Benayoun,B., Baghdiguian,S., Lajmanovich,A., Bartoli,M., Daniele,N., Gicquel,E., Bourg,N., Raynaud,F., Pasquier,M.A., Suel,L., Lochmuller,H., Lefranc,G. and Richard,I.
    NF-kappaB-dependent expression of the antiapoptotic factor c-FLIP is regulated by calpain 3, the protein involved in limb-girdle muscular dystrophy type 2A
    FASEB J22, 1521-1529. PubMed  Europe PubMed DOI
  59. Hayashi,C., Ono,Y., Doi,N., Kitamura,F., Tagami,M., Mineki,R., Arai,T., Taguchi,H., Yanagida,M., Hirner,S., Labeit,D., Labeit,S. and Sorimachi,H.
    Multiple molecular interactions implicate the connectin/titin N2A region as a modulating scaffold for p94/calpain 3 activity in skeletal muscle
    J Biol Chem283, 14801-14814. PubMed  Europe PubMed DOI
  60. Kramerova,I., Kudryashova,E., Wu,B., Ottenheijm,C., Granzier,H. and Spencer,M.J.
    Novel role of calpain-3 in the triad-associated protein complex regulating calcium release in skeletal muscle
    Hum Mol Genet17, 3271-3280. PubMed  Europe PubMed DOI
  61. Ono,Y., Hayashi,C., Doi,N., Tagami,M. and Sorimachi,H.
    The importance of conserved amino acid residues in p94 protease sub-domain IIb and the IS2 region for constitutive autolysis
    FEBS Lett582, 691-698. PubMed  Europe PubMed DOI
    62. 2007
  62. Chung,H., Choi,B., Jang,G., Lee,K., Kim,H., Yoon,S., Im,S., Davis,M. and Hines,H.
    Effect of variants in the ovine skeletal-muscle-specific calpain gene on body weight
    J Appl Genet48, 61-68. PubMed  Europe PubMed  M
  63. Fanin,M., Nascimbeni,A.C. and Angelini,C.
    Screening of calpain-3 autolytic activity in lgmd muscle: a functional map of capn3 gene mutations
    J Med Genet44, 38-43. PubMed  Europe PubMed DOI
  64. Hanisch,F., Muller,C.R., Grimm,D., Xue,L., Traufeller,K., Merkenschlager,A., Zierz,S. and Deschauer,M.
    Frequency of calpain-3 c.550delA mutation in limb girdle muscular dystrophy type 2 and isolated hyperCKemia in German patients
    Clin Neuropathol26, 157-163. PubMed  Europe PubMed  M
  65. Kramerova,I., Beckmann,J.S. and Spencer,M.J.
    Molecular and cellular basis of calpainopathy (limb girdle muscular dystrophy type 2A)
    Biochim Biophys Acta1772, 128-144. PubMed  Europe PubMed DOI  V
  66. Milic,A., Daniele,N., Lochmuller,H., Mora,M., Comi,G.P., Moggio,M., Noulet,F., Walter,M.C., Morandi,L., Poupiot,J., Roudaut,C., Bittner,R.E., Bartoli,M. and Richard,I.
    A third of LGMD2A biopsies have normal calpain 3 proteolytic activity as determined by an in vitro assay
    Neuromuscul Disord17, 148-156. PubMed  Europe PubMed DOI
  67. Ojima,K., Ono,Y., Doi,N., Yoshioka,K., Kawabata,Y., Labeit,S. and Sorimachi,H.
    Myogenic stage, sarcomere length, and protease activity modulate localization of muscle-specific calpain
    J Biol Chem282, 14493-14504. PubMed  Europe PubMed DOI
  68. Ono,Y., Hayashi,C., Doi,N., Kitamura,F., Shindo,M., Kudo,K., Tsubata,T., Yanagida,M. and Sorimachi,H.
    Comprehensive survey of p94/calpain 3 substrates by comparative proteomics - possible regulation of protein synthesis by p94
    Biotechnol J2, 565-576. PubMed  Europe PubMed DOI
  69. Tang,Y., Liu,X., Zoltoski,R.K., Novak,L.A., Herrera,R.A., Richard,I., Kuszak,J.R. and Kumar,N.M.
    Age-related cataracts in alpha3Cx46-knockout mice are dependent on a calpain 3 isoform
    Invest Ophthalmol Vis Sci48, 2685-2694. PubMed  Europe PubMed DOI
  70. Zhou,H., Hickford,J.G. and Fang,Q.
    Single nucleotide polymorphisms of the ovine calpain 3 (CAPN3) gene
    Mol Cell Probes21, 78-79. PubMed  Europe PubMed DOI  M
    71. 2006
  71. [YEAR:13-1-2006]Balci,B., Aurino,S., Haliloglu,G., Talim,B., Erdem,S., Akcoren,Z., Tan,E., Caglar,M., Richard,I., Nigro,V., Topaloglu,H. and Dincer,P.
    Calpain-3 mutations in Turkey
    Eur J Pediatr165, 293-298. PubMed  Europe PubMed DOI  M
  72. [YEAR:19-10-2006]Cohen,N., Kudryashova,E., Kramerova,I., Anderson,L.V., Beckmann,J.S., Bushby,K. and Spencer,M.J.
    Identification of putative in vivo substrates of calpain 3 by comparative proteomics of overexpressing transgenic and nontransgenic mice
    Proteomics6, 6075-6084. PubMed  Europe PubMed DOI
  73. Duguez,S., Bartoli,M. and Richard,I.
    Calpain 3: a key regulator of the sarcomere?
    FEBS J273, 3427-3436. PubMed  Europe PubMed DOI
  74. [YEAR:21-3-2006]Garcia Diaz,B.E., Gauthier,S. and Davies,P.L.
    Ca2+ dependency of calpain 3 (p94) activation
    Biochemistry45, 3714-3722. PubMed  Europe PubMed DOI
  75. Koohmaraie,M. and Geesink,G.H.
    Contribution of postmortem muscle biochemistry to the delivery of consistent meat quality with particular focus on the calpain system
    Meat Sci74, 34-43. PubMed  Europe PubMed DOI
  76. Kramerova,I., Kudryashova,E., Wu,B. and Spencer,M.J.
    Regulation of the M-cadherin-beta-catenin complex by calpain 3 during terminal stages of myogenic differentiation
    Mol Cell Biol26, 8437-8447. PubMed  Europe PubMed DOI
  77. [YEAR:26-7-2006]Shih,M., Ma,H., Nakajima,E., David,L.L., Azuma,M. and Shearer,T.R.
    Biochemical properties of lens-specific calpain Lp85
    Exp Eye Res82, 146-152. PubMed  Europe PubMed DOI  R
    78. 2005
  78. Geesink,G.H., Taylor,R.G. and Koohmaraie,M.
    Calpain 3/p94 is not involved in postmortem proteolysis
    J Anim Sci83, 1646-1652. PubMed  Europe PubMed
  79. Jenne,D.E., Kley,R.A., Vorgerd,M., Schroder,J.M., Weis,J., Reimann,H., Albrecht,B., Nurnberg,P., Thiele,H., Muller,C.R., Meng,G., Witt,C.C. and Labeit,S.
    Limb girdle muscular dystrophy in a sibling pair with a homozygous Ser606Leu mutation in the alternatively spliced IS2 region of calpain 3
    Biol Chem386, 61-67. PubMed  Europe PubMed DOI
  80. [YEAR:16-6-2005]Kramerova,I., Kudryashova,E., Venkatraman,G. and Spencer,M.J.
    Calpain 3 participates in sarcomere remodeling by acting upstream of the ubiquitin-proteasome pathway
    Hum Mol Genet14, 2125-2134. PubMed  Europe PubMed DOI
  81. Piluso,G., Politano,L., Aurino,S., Fanin,M., Ricci,E., Ventriglia,V.M., Belsito,A., Totaro,A., Saccone,V., Topaloglu,H., Nascimbeni,A.C., Fulizio,L., Broccolini,A., Canki-Klain,N., Comi,L.I., Nigro,G., Angelini,C. and Nigro,V.
    Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes
    J Med Genet42, 686-693. PubMed  Europe PubMed DOI  M
  82. [YEAR:21-1-2005]Ravulapalli,R., Diaz,B.G., Campbell,R.L. and Davies,P.L.
    Homodimerization of calpain 3 penta-EF-hand domain
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