-
1
-
-
0024369426
-
Molecular cloning of a novel mammalian calcium-dependent protease distinct from both m- and mu-type: Specific expression of the mRNA in skeletal muscle
-
Sorimachi H., et al. Molecular cloning of a novel mammalian calcium-dependent protease distinct from both m- and mu-type: specific expression of the mRNA in skeletal muscle. J. Biol. Chem. 264:1989;20106-20111
-
(1989)
J. Biol. Chem.
, vol.264
, pp. 20106-20111
-
-
Sorimachi, H.1
-
2
-
-
0033050067
-
Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional events
-
Herasse M., et al. Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional events. Mol. Cell. Biol. 19:1999;4047-4055
-
(1999)
Mol. Cell. Biol.
, vol.19
, pp. 4047-4055
-
-
Herasse, M.1
-
3
-
-
13344285357
-
Muscle-specific calpain, p94, responsible for limb girdle muscular dystrophy type 2A, associates with connectin through IS2, a p94-specific sequence
-
Sorimachi H., et al. Muscle-specific calpain, p94, responsible for limb girdle muscular dystrophy type 2A, associates with connectin through IS2, a p94-specific sequence. J. Biol. Chem. 270:1995;31158-31162
-
(1995)
J. Biol. Chem.
, vol.270
, pp. 31158-31162
-
-
Sorimachi, H.1
-
4
-
-
0031172869
-
Muscle-specific calpain, p94, interacts with the extreme C-terminal region of connectin, a unique region flanked by two immunoglobulin C2 motifs
-
Kinbara K., Sorimachi H., Ishiura S., Suzuki K. Muscle-specific calpain, p94, interacts with the extreme C-terminal region of connectin, a unique region flanked by two immunoglobulin C2 motifs. Arch. Biochem. Biophys. 342:1997;99-107
-
(1997)
Arch. Biochem. Biophys.
, vol.342
, pp. 99-107
-
-
Kinbara, K.1
Sorimachi, H.2
Ishiura, S.3
Suzuki, K.4
-
5
-
-
0028905205
-
Mutations in the proteolytic enzyme, calpain 3, cause limb-girdle muscular dystrophy type 2A
-
Richard I., et al. Mutations in the proteolytic enzyme, calpain 3, cause limb-girdle muscular dystrophy type 2A. Cell. 81:1995;27-40
-
(1995)
Cell
, vol.81
, pp. 27-40
-
-
Richard, I.1
-
6
-
-
0030481058
-
Chromosome 15-linked limb-girdle muscular dystrophy: Clinical phenotypes in Reunion Island and French metropolitan communities
-
Fardeau M., Eymard B., Mignard C., Tome F.M., Richard I., Beckmann J.S. Chromosome 15-linked limb-girdle muscular dystrophy: clinical phenotypes in Reunion Island and French metropolitan communities. Neuromusc. Disord. 6:1996;447-453
-
(1996)
Neuromusc. Disord.
, vol.6
, pp. 447-453
-
-
Fardeau, M.1
Eymard, B.2
Mignard, C.3
Tome, F.M.4
Richard, I.5
Beckmann, J.S.6
-
7
-
-
0032941594
-
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., et al. 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. Nat. Med. 5:1999;503-511
-
(1999)
Nat. Med.
, vol.5
, pp. 503-511
-
-
Baghdiguian, S.1
-
8
-
-
0034739841
-
Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice
-
Richard I., et al. Loss of calpain 3 proteolytic activity leads to muscular dystrophy and to apoptosis-associated IkappaBalpha/nuclear factor kappaB pathway perturbation in mice. J. Cell Biol. 151:2000;1583-1590
-
(2000)
J. Cell Biol.
, vol.151
, pp. 1583-1590
-
-
Richard, I.1
-
9
-
-
0025780879
-
Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl protooncogene
-
Tybulewicz V.L., Crawford C.E., Jackson P.K., Bronson R.T., Mulligan R.C. Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl protooncogene. Cell. 65:1991;1153-1163
-
(1991)
Cell
, vol.65
, pp. 1153-1163
-
-
Tybulewicz, V.L.1
Crawford, C.E.2
Jackson, P.K.3
Bronson, R.T.4
Mulligan, R.C.5
-
10
-
-
0031855858
-
Assessing protein coding region integrity in cDNA sequencing projects
-
Salamov A.A., Nishikawa T., Swindells M.B. Assessing protein coding region integrity in cDNA sequencing projects. Bioinformatics. 14:1998;384-390
-
(1998)
Bioinformatics
, vol.14
, pp. 384-390
-
-
Salamov, A.A.1
Nishikawa, T.2
Swindells, M.B.3
-
11
-
-
0034876289
-
Bidirectional transcriptional activity of PGK-neomycin and unexpected embryonic lethality in heterozygote chimeric knockout mice
-
Scacheri P.C., et al. Bidirectional transcriptional activity of PGK-neomycin and unexpected embryonic lethality in heterozygote chimeric knockout mice. Genesis. 30:2001;259-263
-
(2001)
Genesis
, vol.30
, pp. 259-263
-
-
Scacheri, P.C.1
-
12
-
-
0025295251
-
Limited bidirectional activity of two housekeeping gene promoters: Human HPRT and PGK
-
Johnson P., Friedmann T. Limited bidirectional activity of two housekeeping gene promoters: human HPRT and PGK. Gene. 88:1990;207-213
-
(1990)
Gene
, vol.88
, pp. 207-213
-
-
Johnson, P.1
Friedmann, T.2
-
13
-
-
0019881849
-
Immunofluorescent localization of PGK-1 and PGK-2 isozymes within specific cells of the mouse testis
-
Kramer J.M. Immunofluorescent localization of PGK-1 and PGK-2 isozymes within specific cells of the mouse testis. Dev. Biol. 87:1981;30-36
-
(1981)
Dev. Biol.
, vol.87
, pp. 30-36
-
-
Kramer, J.M.1
-
14
-
-
0025161837
-
Transcription switch of two phosphoglycerate kinase genes during spermatogenesis as determined with mouse testis sections in situ
-
Goto M., et al. Transcription switch of two phosphoglycerate kinase genes during spermatogenesis as determined with mouse testis sections in situ. Exp. Cell Res. 186:1990;273-278
-
(1990)
Exp. Cell Res.
, vol.186
, pp. 273-278
-
-
Goto, M.1
-
15
-
-
0034457922
-
A targeted partial invalidation of the insulin-like growth factor I receptor gene in mice causes a postnatal growth deficit
-
Holzenberger M., et al. A targeted partial invalidation of the insulin-like growth factor I receptor gene in mice causes a postnatal growth deficit. Endocrinology. 141:2000;2557-2566
-
(2000)
Endocrinology
, vol.141
, pp. 2557-2566
-
-
Holzenberger, M.1
-
16
-
-
0029993449
-
Know your neighbors: Three phenotypes in null mutants of the myogenic bHLH gene MRF4
-
Olson E.N., Arnold H.H., Rigby P.W., Wold B.J. Know your neighbors: three phenotypes in null mutants of the myogenic bHLH gene MRF4. Cell. 85:1996;1-4
-
(1996)
Cell
, vol.85
, pp. 1-4
-
-
Olson, E.N.1
Arnold, H.H.2
Rigby, P.W.3
Wold, B.J.4
-
17
-
-
0029091902
-
Targeted deletion of 5′HS2 of the murine beta-globin LCR reveals that it is not essential for proper regulation of the beta-globin locus
-
Fiering S. Targeted deletion of 5′HS2 of the murine beta-globin LCR reveals that it is not essential for proper regulation of the beta-globin locus. Genes Dev. 9:1995;2203-2213
-
(1995)
Genes Dev.
, vol.9
, pp. 2203-2213
-
-
Fiering, S.1
-
18
-
-
0029847228
-
Long-range disruption of gene expression by a selectable marker cassette
-
Pham C.T., MacIvor D.M., Hug B.A., Heusel J.W., Ley T.J. Long-range disruption of gene expression by a selectable marker cassette. Proc. Natl. Acad. Sci. USA. 93:1996;13090-13095
-
(1996)
Proc. Natl. Acad. Sci. USA
, vol.93
, pp. 13090-13095
-
-
Pham, C.T.1
MacIvor, D.M.2
Hug, B.A.3
Heusel, J.W.4
Ley, T.J.5
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