-
1
-
-
0018823476
-
Morphology of connective tissue in skeletal muscle
-
Borg TK and Caulfield JB. Morphology of connective tissue in skeletal muscle. Tissue Cell 12: 197-207, 1980.
-
(1980)
Tissue Cell
, vol.12
, pp. 197-207
-
-
Borg, T.K.1
Caulfield, J.B.2
-
2
-
-
0033675485
-
Biaxial constitutive relations for the passive canine diaphragm
-
Boriek AM, Kelly NG, Rodarte JR, and Wilson TA. Biaxial constitutive relations for the passive canine diaphragm. J Appl Physiol 89: 2187-2190, 2000.
-
(2000)
J Appl Physiol
, vol.89
, pp. 2187-2190
-
-
Boriek, A.M.1
Kelly, N.G.2
Rodarte, J.R.3
Wilson, T.A.4
-
4
-
-
0006057179
-
Inferences on passive diaphragm mechanics from gross anatomy
-
Boriek AM and Rodarte JR. Inferences on passive diaphragm mechanics from gross anatomy. J Appl Physiol 84: 318-326, 1994.
-
(1994)
J Appl Physiol
, vol.84
, pp. 318-326
-
-
Boriek, A.M.1
Rodarte, J.R.2
-
6
-
-
85039673912
-
Desmin may contribute to the transverse inextensibility of the dog costal diaphragm
-
Boriek AM and Tidball JG. Desmin may contribute to the transverse inextensibility of the dog costal diaphragm. Am J Respir Crit Care Med 151: A585, 1995.
-
(1995)
Am J Respir Crit Care Med
, vol.151
-
-
Boriek, A.M.1
Tidball, J.G.2
-
7
-
-
0028158834
-
Displacements and strains in the costal diaphragm of the dog
-
Boriek AM, Wilson TA, and Rodarte JR. Displacements and strains in the costal diaphragm of the dog. J Appl Physiol 76: 223-229, 1994.
-
(1994)
J Appl Physiol
, vol.76
, pp. 223-229
-
-
Boriek, A.M.1
Wilson, T.A.2
Rodarte, J.R.3
-
9
-
-
0028914964
-
Three muscular dystrophies: Loss of cytoskeleton-extracellular matrix linkage
-
Campbell KP. Three muscular dystrophies: loss of cytoskeleton-extracellular matrix linkage. Cell 80: 675-679, 1995.
-
(1995)
Cell
, vol.80
, pp. 675-679
-
-
Campbell, K.P.1
-
10
-
-
0024600620
-
Association of dystrophin and an integral membrane glycoprotein
-
Campbell KP and Kahl SD. Association of dystrophin and an integral membrane glycoprotein. Nature 338: 259-262, 1989.
-
(1989)
Nature
, vol.338
, pp. 259-262
-
-
Campbell, K.P.1
Kahl, S.D.2
-
11
-
-
0031769060
-
Diaphragm compliance is increased in the cardiomyopathic Syrian hamster
-
Coirault C, Samuel JL, Chemla D, Pourny JC, Lambert F, Marotte F, and Lecarpentier Y. Diaphragm compliance is increased in the cardiomyopathic Syrian hamster. J Appl Physiol 1762-1769, 1998.
-
(1998)
J Appl Physiol
, pp. 1762-1769
-
-
Coirault, C.1
Samuel, J.L.2
Chemla, D.3
Pourny, J.C.4
Lambert, F.5
Marotte, F.6
Lecarpentier, Y.7
-
12
-
-
0034810216
-
Three mouse models of muscular dystrophy: The natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin α2-deficient mice
-
Connolly AM, Keeling RM, Mehta S, Pestronk A, and Sanes JR. Three mouse models of muscular dystrophy: the natural history of strength and fatigue in dystrophin-, dystrophin/utrophin-, and laminin α2-deficient mice. Neuromuscul Disord 703-712, 2001.
-
(2001)
Neuromuscul Disord
, pp. 703-712
-
-
Connolly, A.M.1
Keeling, R.M.2
Mehta, S.3
Pestronk, A.4
Sanes, J.R.5
-
13
-
-
0029751853
-
Effect of ramipril and losartan on collagen expression in right and left heart after myocardial infarction
-
Dixon IM, Ju H, Jassal DS, and Peterson DJ. Effect of ramipril and losartan on collagen expression in right and left heart after myocardial infarction. Mol Cell Biochem 165: 31-45, 1996.
-
(1996)
Mol Cell Biochem
, vol.165
, pp. 31-45
-
-
Dixon, I.M.1
Ju, H.2
Jassal, D.S.3
Peterson, D.J.4
-
15
-
-
0036157115
-
Nonmuscular involvement in merosin-negative congenital muscular dystrophy
-
Gilhuis HJ, ten Donkelaar HJ, Tanke RB, Vingerhoets DM, Zwarts MJ, Verrips A, and Gabreels FJ. Nonmuscular involvement in merosin-negative congenital muscular dystrophy. Pediatr Neurol 26: 30-36, 2002.
-
(2002)
Pediatr Neurol
, vol.26
, pp. 30-36
-
-
Gilhuis, H.J.1
Ten Donkelaar, H.J.2
Tanke, R.B.3
Vingerhoets, D.M.4
Zwarts, M.J.5
Verrips, A.6
Gabreels, F.J.7
-
16
-
-
0028282605
-
Passive length-force properties of senescent diaphragm: Relationship with collagen characteristics
-
Gosselin LE, Martinez DA, Vailas AC, and Sieck GC. Passive length-force properties of senescent diaphragm: relationship with collagen characteristics. J Appl Physiol 76: 2680-2685, 1994.
-
(1994)
J Appl Physiol
, vol.76
, pp. 2680-2685
-
-
Gosselin, L.E.1
Martinez, D.A.2
Vailas, A.C.3
Sieck, G.C.4
-
17
-
-
0032759070
-
Laminins during muscle development and in muscular dystrophies
-
Gullberg D, Tiger CF, and Velling T. Laminins during muscle development and in muscular dystrophies. Cell Mol Life Sci 56:442-460, 1999.
-
(1999)
Cell Mol Life Sci
, vol.56
, pp. 442-460
-
-
Gullberg, D.1
Tiger, C.F.2
Velling, T.3
-
18
-
-
0028980027
-
Mutations in the laminin α2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy
-
Helbling-Leclerc A, Zhang X, TH, Cruaud C, Tesson F, Weissenbach J, Tome FM, Schwartz K, Fardeau M, Tryggvason K, and Guicheny P. Mutations in the laminin α2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy. Nat Genet 11: 216-218, 1995.
-
(1995)
Nat Genet
, vol.11
, pp. 216-218
-
-
Helbling-Leclerc, A.1
Zhang, X.2
Cruaud, C.3
Tesson, F.4
Weissenbach, J.5
Tome, F.M.6
Schwartz, K.7
Fardeau, M.8
Tryggvason, K.9
Guicheny, P.10
-
19
-
-
0030809116
-
Altered expression of the α7β1 integrin in human and murine muscular dystrophies
-
Hodges BL, Hayashi YK, Nonaka I, Wang W, Arahata K, and Kaufman SJ. Altered expression of the α7β1 integrin in human and murine muscular dystrophies. J Cell Sci 19: 2873-2881, 1997.
-
(1997)
J Cell Sci
, vol.19
, pp. 2873-2881
-
-
Hodges, B.L.1
Hayashi, Y.K.2
Nonaka, I.3
Wang, W.4
Arahata, K.5
Kaufman, S.J.6
-
20
-
-
0033040088
-
Vinculin, talin, integrin α6β1 and laminin can serve as components of attachment complex mediating contraction force transmission from cardiomyocytes to extracellular matrix
-
Imanaka-Yoshida K, Enomoto-Iwamoto M, Yoshida T, and Sakakura T. Vinculin, talin, integrin α6β1 and laminin can serve as components of attachment complex mediating contraction force transmission from cardiomyocytes to extracellular matrix. Cell Motil Cytoskeleton 42: 1-11, 1999.
-
(1999)
Cell Motil Cytoskeleton
, vol.42
, pp. 1-11
-
-
Imanaka-Yoshida, K.1
Enomoto-Iwamoto, M.2
Yoshida, T.3
Sakakura, T.4
-
21
-
-
0037195860
-
Distinct signaling pathways are activated in response to mechanical signaling stress applied axially and transversely to skeletal muscle fibers
-
Kumar A, Chaudhry I, Reid MB, and Boriek AM. Distinct signaling pathways are activated in response to mechanical signaling stress applied axially and transversely to skeletal muscle fibers. J Biol Chem 277: 46493-46503, 2002.
-
(2002)
J Biol Chem
, vol.277
, pp. 46493-46503
-
-
Kumar, A.1
Chaudhry, I.2
Reid, M.B.3
Boriek, A.M.4
-
22
-
-
0023970247
-
Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development
-
Leivo I and Engvall E. Merosin, a protein specific for basement membranes of Schwann cells, striated muscle, and trophoblast, is expressed late in nerve and muscle development. Proc Natl Acad Sci USA 85: 1544-1548, 1988.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 1544-1548
-
-
Leivo, I.1
Engvall, E.2
-
23
-
-
0003605027
-
-
Cary, NC: SAS Institute
-
Littel RC, Milliken GA, Stroup WW, and Wolfinger RD. SAS System for Mixed Models. Cary, NC: SAS Institute, 1996.
-
(1996)
SAS System for Mixed Models
-
-
Littel, R.C.1
Milliken, G.A.2
Stroup, W.W.3
Wolfinger, R.D.4
-
24
-
-
0016718398
-
Genetically determined defect of Schwann cell basement membrane in dystrophic mouse
-
Madrid RE, Jaros E, Cullen MJ, and Bradley WG. Genetically determined defect of Schwann cell basement membrane in dystrophic mouse. Nature 257: 319-321, 1975.
-
(1975)
Nature
, vol.257
, pp. 319-321
-
-
Madrid, R.E.1
Jaros, E.2
Cullen, M.J.3
Bradley, W.G.4
-
25
-
-
0014936580
-
Muscular dystrophy in the mouse caused by an allele at the dy-locus
-
Meier H and Southard JL. Muscular dystrophy in the mouse caused by an allele at the dy-locus. Life Sci 137-144, 1970.
-
(1970)
Life Sci
, pp. 137-144
-
-
Meier, H.1
Southard, J.L.2
-
26
-
-
0037131559
-
Muscular dystrophy with laminin deficiency decreases the content of butyrylcholinesterase tetramers in sciatic nerves of Lama2dy mice
-
Moral-Naranjo M, Cabezas-Herrera J, Vidal C, and Campoy F. Muscular dystrophy with laminin deficiency decreases the content of butyrylcholinesterase tetramers in sciatic nerves of Lama2dy mice. Neurosci Lett 331: 155, 2002.
-
(2002)
Neurosci Lett
, vol.331
, pp. 155
-
-
Moral-Naranjo, M.1
Cabezas-Herrera, J.2
Vidal, C.3
Campoy, F.4
-
28
-
-
0026419948
-
The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy
-
Stedman HH, Sweeney HL, Shrager JB, Maguire HC, Panattieri RA, Petrof B, Narusawa M, Leferovich JM, Sladky JT, and Kelly AM. The mdx mouse diaphragm reproduces the degenerative changes of Duchenne muscular dystrophy. Nature 352: 536-539, 1991.
-
(1991)
Nature
, vol.352
, pp. 536-539
-
-
Stedman, H.H.1
Sweeney, H.L.2
Shrager, J.B.3
Maguire, H.C.4
Panattieri, R.A.5
Petrof, B.6
Narusawa, M.7
Leferovich, J.M.8
Sladky, J.T.9
Kelly, A.M.10
-
29
-
-
0028318185
-
Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus
-
Sunada Y, Bernier SM, Kozak CA, Yamada Y, and Campbell KP. Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus. J Biol Chem 13: 13732, 1994.
-
(1994)
J Biol Chem
, vol.13
, pp. 13732
-
-
Sunada, Y.1
Bernier, S.M.2
Kozak, C.A.3
Yamada, Y.4
Campbell, K.P.5
-
30
-
-
0022618526
-
Successful treatment of murine muscular dystrophy with the protease inhibitor bestatin
-
Tsuji S and Matsushita H. Successful treatment of murine muscular dystrophy with the protease inhibitor bestatin. J Neurol Sci 72: 183-194, 1986.
-
(1986)
J Neurol Sci
, vol.72
, pp. 183-194
-
-
Tsuji, S.1
Matsushita, H.2
-
31
-
-
0030610576
-
Integrins (α7β1) in muscle function and survival. Disrupted expression in merosindeficient congenital muscular dystrophy
-
Vachon PH, Xu H, Liu L, Loechel F, Hayashi Y, Arahata K, Reed JC, Wewer UM, and Engvall E. Integrins (α7β1) in muscle function and survival. Disrupted expression in merosindeficient congenital muscular dystrophy. J Clin Invest 90: 1870-1881, 1997.
-
(1997)
J Clin Invest
, vol.90
, pp. 1870-1881
-
-
Vachon, P.H.1
Xu, H.2
Liu, L.3
Loechel, F.4
Hayashi, Y.5
Arahata, K.6
Reed, J.C.7
Wewer, U.M.8
Engvall, E.9
-
32
-
-
0028334735
-
Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse
-
Xu H, Christmas P, Wu XR, Wewer UM, and Engvall E. Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse. Proc Natl Acad Sci USA 91: 5572-5576, 1994.
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 5572-5576
-
-
Xu, H.1
Christmas, P.2
Wu, X.R.3
Wewer, U.M.4
Engvall, E.5
-
33
-
-
0028135436
-
Murine muscular dystrophy caused by a mutation in the laminin α2 (Lama2) gene
-
Xu H, Wu XR, Wewer UM, and Engvall E. Murine muscular dystrophy caused by a mutation in the laminin α2 (Lama2) gene. Nat Genet 8: 297-302, 1994.
-
(1994)
Nat Genet
, vol.8
, pp. 297-302
-
-
Xu, H.1
Wu, X.R.2
Wewer, U.M.3
Engvall, E.4
|