-
2
-
-
0030919488
-
The laminin α chains: Expression, developmental transitions, and chromosomal locations of α1-5, identification of hetrotrimeric laminins 8-11, and cloning of a novel α3 isoform
-
Miner J.H., Patton B.L., Lentz S.I., et al. The laminin α chains: expression, developmental transitions, and chromosomal locations of α1-5, identification of hetrotrimeric laminins 8-11, and cloning of a novel α3 isoform. J Cell Biol. 137:1997;701.
-
(1997)
J Cell Biol
, vol.137
, pp. 701
-
-
Miner, J.H.1
Patton, B.L.2
Lentz, S.I.3
-
3
-
-
0025373178
-
Merosin a tissue-specific basement membrane protein. , is a laminin-like protein
-
Ehrig K., Leivo I., Argraves W.S., Rouslahti E., Engvall E., Merosin a tissue-specific basement membrane protein. , is a laminin-like protein. Proc Nat Acad Sci (USA). 87:1990;3264-3268.
-
(1990)
Proc Nat Acad Sci (USA)
, vol.87
, pp. 3264-3268
-
-
Ehrig, K.1
Leivo, I.2
Argraves, W.S.3
Rouslahti, E.4
Engvall, E.5
-
4
-
-
0025494189
-
Distribution and isolation of four laminin variants; Tissue restricted distribution of heterotrimers assembled from five different subunits
-
Engvall E., Earwicker D., Haaparanta T., Ruoslahti E., Sanes J.R. Distribution and isolation of four laminin variants; tissue restricted distribution of heterotrimers assembled from five different subunits. Cell Regul. 1:1990;731-740.
-
(1990)
Cell Regul
, vol.1
, pp. 731-740
-
-
Engvall, E.1
Earwicker, D.2
Haaparanta, T.3
Ruoslahti, E.4
Sanes, J.R.5
-
5
-
-
0025010542
-
Molecular heterogeneity of basal laminae: Isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere
-
Sanes J.R., Engvall E., Butkowski R., Hunter D.D. Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere. J Cell Biol. 111:1990;1685-1699.
-
(1990)
J Cell Biol
, vol.111
, pp. 1685-1699
-
-
Sanes, J.R.1
Engvall, E.2
Butkowski, R.3
Hunter, D.D.4
-
7
-
-
0002270650
-
The extracellular matrix
-
A.G. Engel, Franzini-Armstrong C. New York: McGraw-Hill
-
Sanes J.R. The extracellular matrix. Engel A.G., Franzini-Armstrong C. Myology. 2:1994;242 McGraw-Hill, New York.
-
(1994)
Myology
, vol.2
, pp. 242
-
-
Sanes, J.R.1
-
8
-
-
0029794008
-
Merosin and laminin in myogenesis: Specific requirement for merosin in myotube stability and survival
-
Vachon P.H., Loechel F., Xu H., Wewer U.M., Engvall E. Merosin and laminin in myogenesis: specific requirement for merosin in myotube stability and survival. J Cell Biol. 134:1996;1483-1497.
-
(1996)
J Cell Biol
, vol.134
, pp. 1483-1497
-
-
Vachon, P.H.1
Loechel, F.2
Xu, H.3
Wewer, U.M.4
Engvall, E.5
-
9
-
-
0030909575
-
Muscular dystrophies and the dystrophin-glycoprotein complex
-
Straub V., Campbell K.P. Muscular dystrophies and the dystrophin-glycoprotein complex. Curr Opin Neurol. 10:1997;168-175.
-
(1997)
Curr Opin Neurol
, vol.10
, pp. 168-175
-
-
Straub, V.1
Campbell, K.P.2
-
10
-
-
0030724952
-
Absence of integrin α7 causes a novel form of muscular dystrophy
-
Mayer U., Saher G., Fassler R. Absence of integrin α7 causes a novel form of muscular dystrophy. Nat Genet. 17:1997;318-323.
-
(1997)
Nat Genet
, vol.17
, pp. 318-323
-
-
Mayer, U.1
Saher, G.2
Fassler, R.3
-
11
-
-
17344372250
-
Mutations in the integrin α7 gene cause congenital myopathy
-
Hayashi Y.K., Chou F.L., Engvall E. Mutations in the integrin α7 gene cause congenital myopathy. Nat Genet. 19:1998;94-97.
-
(1998)
Nat Genet
, vol.19
, pp. 94-97
-
-
Hayashi, Y.K.1
Chou, F.L.2
Engvall, E.3
-
12
-
-
85008070304
-
Laminin in animal models for muscular dystrophy: Defect of laminin-M in skeletal and cardiac muscles and peripheral nerve of the homozygous dystrophic dy/dy mice
-
Arahata K., Hayashi Y.K., Koga R., et al. Laminin in animal models for muscular dystrophy: defect of laminin-M in skeletal and cardiac muscles and peripheral nerve of the homozygous dystrophic dy/dy mice. Proc Jap Acad Biol. 69:1993;259-264.
-
(1993)
Proc Jap Acad Biol
, vol.69
, pp. 259-264
-
-
Arahata, K.1
Hayashi, Y.K.2
Koga, R.3
-
13
-
-
0028135436
-
Engvall E., Murine muscular dystrophy caused by a mutation in the laminin α2 (Lama2) gene
-
Xu H., Wu X.R., Wewer U.M. Engvall E., Murine muscular dystrophy caused by a mutation in the laminin α2 (Lama2) gene. Nat Genet. 8:1994;297-302.
-
(1994)
Nat Genet
, vol.8
, pp. 297-302
-
-
Xu, H.1
Wu, X.R.2
Wewer, U.M.3
-
14
-
-
0028318185
-
Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus
-
Sunada Y., Bernier S.M., Kozak C.A., Yamada Y., Campbell K.P. Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus. J Biol Chem. 269:1994;13729-13732.
-
(1994)
J Biol Chem
, vol.269
, pp. 13729-13732
-
-
Sunada, Y.1
Bernier, S.M.2
Kozak, C.A.3
Yamada, Y.4
Campbell, K.P.5
-
15
-
-
0028232215
-
Congenital muscular dystrophy with merosin deficiency
-
Tome F.M., Evangelista T., Leclerc A., Sunada Y., Manole E., Estournet B., Barois A., Campbell K.P., Fardeau M. Congenital muscular dystrophy with merosin deficiency. C R Acad Sci (Paris) Sciences de la vie/Life Sci. 317:1994;351-357.
-
(1994)
C R Acad Sci (Paris) Sciences de la Vie/life Sci
, vol.317
, pp. 351-357
-
-
Tome, F.M.1
Evangelista, T.2
Leclerc, A.3
Sunada, Y.4
Manole, E.5
Estournet, B.6
Barois, A.7
Campbell, K.P.8
Fardeau, M.9
-
16
-
-
0028980027
-
Mutations in the laminin α-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy
-
Helbling-Leclerc A., Zhang X., Topaloglu H., et al. Mutations in the laminin α-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy. Nat Genet. 11:1995;216-218.
-
(1995)
Nat Genet
, vol.11
, pp. 216-218
-
-
Helbling-Leclerc, A.1
Zhang, X.2
Topaloglu, H.3
-
18
-
-
0031814515
-
Congenital muscular dystrophy: From rags to riches
-
Muntoni F., Sewry C.A. Congenital muscular dystrophy: from rags to riches. Neurology. 51:1998;14-17.
-
(1998)
Neurology
, vol.51
, pp. 14-17
-
-
Muntoni, F.1
Sewry, C.A.2
-
20
-
-
0032528845
-
Merosin-deficient congenital muscular dystrophy: Partial genetic correction in two mouse models
-
Kuang W., Xu H., Vachon P.H., et al. Merosin-deficient congenital muscular dystrophy: partial genetic correction in two mouse models. J Clin Invest. 102:1998;844-852.
-
(1998)
J Clin Invest
, vol.102
, pp. 844-852
-
-
Kuang, W.1
Xu, H.2
Vachon, P.H.3
-
21
-
-
0027360897
-
Abnormal localization of laminin subunits in muscular dystrophies
-
Hayashi Y.K., Engvall E., Arikawa-Hirasawa E., et al. Abnormal localization of laminin subunits in muscular dystrophies. J Neurol Sci. 119:1993;53-64.
-
(1993)
J Neurol Sci
, vol.119
, pp. 53-64
-
-
Hayashi, Y.K.1
Engvall, E.2
Arikawa-Hirasawa, E.3
-
22
-
-
0028098737
-
Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin
-
Higuchi I., Yamada H., Fukunaga H., et al. Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin. J Clin Invest. 94:1994;601-606.
-
(1994)
J Clin Invest
, vol.94
, pp. 601-606
-
-
Higuchi, I.1
Yamada, H.2
Fukunaga, H.3
-
23
-
-
0029007799
-
Expression of laminin subunits in congenital muscular dystrophy
-
Sewry C.A., Philpot J., Mahony D., et al. Expression of laminin subunits in congenital muscular dystrophy. Neuromusc Disord. 5:1995;307-316.
-
(1995)
Neuromusc Disord
, vol.5
, pp. 307-316
-
-
Sewry, C.A.1
Philpot, J.2
Mahony, D.3
-
24
-
-
0029047909
-
Laminin abnormality in severe childhood autosomal recessive muscular dystrophy
-
Yamada H., Tome F.M., Higuchi I., et al. Laminin abnormality in severe childhood autosomal recessive muscular dystrophy. Lab Invest. 72:1995;715-722.
-
(1995)
Lab Invest
, vol.72
, pp. 715-722
-
-
Yamada, H.1
Tome, F.M.2
Higuchi, I.3
-
25
-
-
0029131958
-
Increased laminin A expression in regenerating myofibers in neuromuscular disorders
-
Mundegar R.R., von Oertzen J., Zierz S. Increased laminin A expression in regenerating myofibers in neuromuscular disorders. Muscle Nerve. 18:1995;992-999.
-
(1995)
Muscle Nerve
, vol.18
, pp. 992-999
-
-
Mundegar, R.R.1
Von Oertzen, J.2
Zierz, S.3
-
26
-
-
0029396750
-
Laminin α-2 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebro-ocular dysplasia-muscular dystrophy)
-
Wewer U.M., Durkin M.E., Zhang X. Laminin α-2 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebro-ocular dysplasia-muscular dystrophy). Neurology. 45:1995;2099-2101.
-
(1995)
Neurology
, vol.45
, pp. 2099-2101
-
-
Wewer, U.M.1
Durkin, M.E.2
Zhang, X.3
-
27
-
-
0029983850
-
Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin staining
-
Connolly A.M., Pestronk A., Planer G.J., et al. Congenital muscular dystrophy syndromes distinguished by alkaline and acid phosphatase, merosin, and dystrophin staining. Neurology. 46:1996;810-814.
-
(1996)
Neurology
, vol.46
, pp. 810-814
-
-
Connolly, A.M.1
Pestronk, A.2
Planer, G.J.3
-
28
-
-
9044223654
-
Clinical heterogeneity of adhalin deficiency
-
Morandi L., Barresi R., DiBlasi C., et al. Clinical heterogeneity of adhalin deficiency. Ann Neurol. 39:1996;196-202.
-
(1996)
Ann Neurol
, vol.39
, pp. 196-202
-
-
Morandi, L.1
Barresi, R.2
Diblasi, C.3
-
29
-
-
0030879625
-
Changes of laminin α2 chain expression in congenital muscular dystrophy
-
Cohn R.D., Herrmann R., Wewer U.M., Voit T. Changes of laminin α2 chain expression in congenital muscular dystrophy. Neuromusc Disord. 7:1997;373-378.
-
(1997)
Neuromusc Disord
, vol.7
, pp. 373-378
-
-
Cohn, R.D.1
Herrmann, R.2
Wewer, U.M.3
Voit, T.4
-
30
-
-
0030810062
-
Abnormal expression of laminin b1 chain in skeletal muscle of adult-onset limb-girdle muscular dystrophy
-
Li M., Dickson D.W., Spiro A.J. Abnormal expression of laminin b1 chain in skeletal muscle of adult-onset limb-girdle muscular dystrophy. Arch Neurol. 54:1997;1457-1461.
-
(1997)
Arch Neurol
, vol.54
, pp. 1457-1461
-
-
Li, M.1
Dickson, D.W.2
Spiro, A.J.3
-
31
-
-
0030922711
-
Early onset autosomal dominant myopathy with rigidity of the spine-a possible role for laminin (1
-
Taylor J., Muntoni F., Robb S., Dubowitz V., Sewry C. Early onset autosomal dominant myopathy with rigidity of the spine-a possible role for laminin (1. Neuromusc Disord. 7:1997;211-216.
-
(1997)
Neuromusc Disord
, vol.7
, pp. 211-216
-
-
Taylor, J.1
Muntoni, F.2
Robb, S.3
Dubowitz, V.4
Sewry, C.5
-
32
-
-
0030612270
-
Presence of laminin α5 chain and lack of laminin α1 chain during human muscle development and in muscular dystrophies
-
Tiger C.-F., Champliaud M.F., Pedrosa-Domellof F., et al. Presence of laminin α5 chain and lack of laminin α1 chain during human muscle development and in muscular dystrophies. J Biol Chem. 272:1997;28590-28595.
-
(1997)
J Biol Chem
, vol.272
, pp. 28590-28595
-
-
Tiger, C.-F.1
Champliaud, M.F.2
Pedrosa-Domellof, F.3
-
33
-
-
0031594943
-
Laminin α2 chain-deficient congenital muscular dystrophy
-
Cohn R.D., Herrmann R., Sorokin L., Wewer U.M., Voit T. Laminin α2 chain-deficient congenital muscular dystrophy. Neurology. 51:1998;94-100.
-
(1998)
Neurology
, vol.51
, pp. 94-100
-
-
Cohn, R.D.1
Herrmann, R.2
Sorokin, L.3
Wewer, U.M.4
Voit, T.5
-
34
-
-
0025887362
-
Epiligrin a new cell adhesion lig. For integrin α3β1 in epithelial basement membranes
-
Carter W.G., Ryan M.C., Gahr P.J., Epiligrin a new cell adhesion lig. for integrin α3β1 in epithelial basement membranes. Cell. 65:1991;599-610.
-
(1991)
Cell
, vol.65
, pp. 599-610
-
-
Carter, W.G.1
Ryan, M.C.2
Gahr, P.J.3
-
35
-
-
0025879967
-
Kalinin: An epithelium-specific basement membrane adhesion molecule that is a component of anchoring filaments
-
Rousselle P., Lunstrum G.P., Keene D.R., Burgeson R.E. Kalinin: an epithelium-specific basement membrane adhesion molecule that is a component of anchoring filaments. J Cell Biol. 114:1991;567-576.
-
(1991)
J Cell Biol
, vol.114
, pp. 567-576
-
-
Rousselle, P.1
Lunstrum, G.P.2
Keene, D.R.3
Burgeson, R.E.4
-
36
-
-
0028307978
-
Developmental expression of nicein adhesion protein (laminin-5) subunits suggests multiple morphogenic roles
-
Aberdam M.D., Aguzzi A., Baudoin C. Developmental expression of nicein adhesion protein (laminin-5) subunits suggests multiple morphogenic roles. Cell Adhes Commun. 2:1994;115-119.
-
(1994)
Cell Adhes Commun
, vol.2
, pp. 115-119
-
-
Aberdam, M.D.1
Aguzzi, A.2
Baudoin, C.3
-
37
-
-
0027936342
-
Al-Imara, L., Carter, N.P., Localization of the gene (LAMA4) to chromosome 6q21 and isolation of a partial cDNA encoding a variant laminin A chain
-
Richards A.J. Al-Imara, L., Carter, N.P., Localization of the gene (LAMA4) to chromosome 6q21 and isolation of a partial cDNA encoding a variant laminin A chain. Genomics. 22:1994;237-239.
-
(1994)
Genomics
, vol.22
, pp. 237-239
-
-
Richards, A.J.1
-
38
-
-
0029008416
-
Primary structure and expression of a novel human laminin α4 chain
-
Iivanainen A., Sainio K., Sariola H., Tryggvason K. Primary structure and expression of a novel human laminin α4 chain. FEBS Lett. 365:1995;183-188.
-
(1995)
FEBS Lett
, vol.365
, pp. 183-188
-
-
Iivanainen, A.1
Sainio, K.2
Sariola, H.3
Tryggvason, K.4
-
39
-
-
0031456144
-
Distribution and function of laminins in the neuromuscular system of developing, adult and mutant mice
-
Patton B.L., Miner J.H., Chiu A.Y., Sanes J.R. Distribution and function of laminins in the neuromuscular system of developing, adult and mutant mice. J Cell Biol. 139:1997;1507-1521.
-
(1997)
J Cell Biol
, vol.139
, pp. 1507-1521
-
-
Patton, B.L.1
Miner, J.H.2
Chiu, A.Y.3
Sanes, J.R.4
-
41
-
-
0027985787
-
Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy
-
Bione S., Maestrini E., Rivella S., Mancini M., Regis S., Romeo G., Toniolo D. Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophy. Nat Genet. 8:1994;323-327.
-
(1994)
Nat Genet
, vol.8
, pp. 323-327
-
-
Bione, S.1
Maestrini, E.2
Rivella, S.3
Mancini, M.4
Regis, S.5
Romeo, G.6
Toniolo, D.7
-
42
-
-
0029874852
-
Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy
-
Nagano A., Koga R., Ogawa M., et al. Emerin deficiency at the nuclear membrane in patients with Emery-Dreifuss muscular dystrophy. Nat Genet. 12:1996;254-259.
-
(1996)
Nat Genet
, vol.12
, pp. 254-259
-
-
Nagano, A.1
Koga, R.2
Ogawa, M.3
-
43
-
-
0031686034
-
Al-Lozi, M., Primary α-sarcoglycan deficiency responsive to immunosuppression over three years
-
Connolly A.M., Pestronk A., Mehta S. Al-Lozi, M., Primary α-sarcoglycan deficiency responsive to immunosuppression over three years. Muscle Nerve. 1998;in press.
-
(1998)
Muscle Nerve
-
-
Connolly, A.M.1
Pestronk, A.2
Mehta, S.3
-
44
-
-
0031042885
-
Mutations in the sarcoglycan genes in patients with myopathy
-
Duggan D.J., Gorospe R., Fanin M.S., et al. Mutations in the sarcoglycan genes in patients with myopathy. N Engl J Med. 336:1997;618-624.
-
(1997)
N Engl J Med
, vol.336
, pp. 618-624
-
-
Duggan, D.J.1
Gorospe, R.2
Fanin, M.S.3
-
45
-
-
0030848338
-
Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: A model for Duchenne muscular dystrophy
-
Grady R.M., Teng H., Nichol M.C., et al. Skeletal and cardiac myopathies in mice lacking utrophin and dystrophin: a model for Duchenne muscular dystrophy. Cell. 90:1997;729-738.
-
(1997)
Cell
, vol.90
, pp. 729-738
-
-
Grady, R.M.1
Teng, H.2
Nichol, M.C.3
-
46
-
-
0014838245
-
Three 'myosin adenosine triphosphatase' systems: The nature of their pH lability and sulfhydryl dependence
-
Brooke M.H., Kaiser K.K. Three 'myosin adenosine triphosphatase' systems: the nature of their pH lability and sulfhydryl dependence. J Histochem Cytochem. 18:1970;670-672.
-
(1970)
J Histochem Cytochem
, vol.18
, pp. 670-672
-
-
Brooke, M.H.1
Kaiser, K.K.2
-
48
-
-
0024815139
-
Immunoreactivity in patients with Xp21 muscular dystrophy
-
Nicholson L.V.B., Davison K., Johnson M.A. Immunoreactivity in patients with Xp21 muscular dystrophy. J Neurol Sci. 94:1989;137-146.
-
(1989)
J Neurol Sci
, vol.94
, pp. 137-146
-
-
Nicholson, L.V.B.1
Davison, K.2
Johnson, M.A.3
-
49
-
-
0025780738
-
Primary structures of the human laminin A chain: Limited expression in human tissues
-
Nissinen M., Vuolteenaho R., Boot-Handford R., Kallunki P., Tryggvason K. Primary structures of the human laminin A chain: limited expression in human tissues. Biochem J. 276:1991;369-379.
-
(1991)
Biochem J
, vol.276
, pp. 369-379
-
-
Nissinen, M.1
Vuolteenaho, R.2
Boot-Handford, R.3
Kallunki, P.4
Tryggvason, K.5
-
50
-
-
0030899672
-
Neural targeting of mycobacterium leprae mediated by the G domain of the laminin-α2 chain
-
Rambukkana A., Salzer J.L., Yurchenco P.D., Tuomanen E.I. Neural targeting of mycobacterium leprae mediated by the G domain of the laminin-α2 chain. Cell. 88:1997;811-821.
-
(1997)
Cell
, vol.88
, pp. 811-821
-
-
Rambukkana, A.1
Salzer, J.L.2
Yurchenco, P.D.3
Tuomanen, E.I.4
-
51
-
-
0024535958
-
Sanes J.R., Laminin-like adhesive protein concentrated in the synaptic cleft of the neuromuscular junction
-
Hunter D.D., Shah V., Merlie J.P. Sanes J.R., Laminin-like adhesive protein concentrated in the synaptic cleft of the neuromuscular junction. Nature. 338:1989;229-234.
-
(1989)
Nature
, vol.338
, pp. 229-234
-
-
Hunter, D.D.1
Shah, V.2
Merlie, J.P.3
-
52
-
-
0030612954
-
Absence of laminin α1 chain in the skeletal muscle of dystrophic dy/dy mice
-
Tiger C.-F., Gullberg D. Absence of laminin α1 chain in the skeletal muscle of dystrophic dy/dy mice. Muscle Nerve. 20:1997;1515-1524.
-
(1997)
Muscle Nerve
, vol.20
, pp. 1515-1524
-
-
Tiger, C.-F.1
Gullberg, D.2
-
53
-
-
0026631140
-
Monoclonal antibodies against laminin A chain fragment E3 and their effects on binding to cells and proteoglycan and on kidney development
-
Sorokin L.M., Conzelmann S., Ekblom P., et al. Monoclonal antibodies against laminin A chain fragment E3 and their effects on binding to cells and proteoglycan and on kidney development. Exp Cell Res. 201:1992;137-144.
-
(1992)
Exp Cell Res
, vol.201
, pp. 137-144
-
-
Sorokin, L.M.1
Conzelmann, S.2
Ekblom, P.3
-
54
-
-
0024788014
-
Selective immunoreactivities of kidney basement membranes to monoclonal antibodies against laminin: Localization of the end of the long arm and the short arms to discrete microdomains
-
Abrahamson D.R., Irwin M.H., St. John P.L., et al. Selective immunoreactivities of kidney basement membranes to monoclonal antibodies against laminin: localization of the end of the long arm and the short arms to discrete microdomains. J Cell Biol. 109:1989;3477-3491.
-
(1989)
J Cell Biol
, vol.109
, pp. 3477-3491
-
-
Abrahamson, D.R.1
Irwin, M.H.2
St. John, P.L.3
-
55
-
-
0029122801
-
A synaptic localization domain in the synaptic cleft protein laminin β2 (s-laminin)
-
Martin P.T., Ettinger A.J., Sanes J.R. A synaptic localization domain in the synaptic cleft protein laminin β2 (s-laminin). Science. 269:1995;413-416.
-
(1995)
Science
, vol.269
, pp. 413-416
-
-
Martin, P.T.1
Ettinger, A.J.2
Sanes, J.R.3
-
56
-
-
8244233831
-
Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2 chain
-
Allamand V., Sunada Y., Salih M.A., et al. Mild congenital muscular dystrophy in two patients with an internally deleted laminin α2 chain. Hum Mol Genet. 6:1997;747-752.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 747-752
-
-
Allamand, V.1
Sunada, Y.2
Salih, M.A.3
-
57
-
-
0344081866
-
D'Alessandro, M., Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin α2 chain
-
Sewry C.A., Naom I., et al. D'Alessandro, M., Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin α2 chain. Neuromusc Disord. 5:1995;307-316.
-
(1995)
Neuromusc Disord
, vol.5
, pp. 307-316
-
-
Sewry, C.A.1
Naom, I.2
-
58
-
-
0031572281
-
Frieser M., Developmental regulation of the laminin α5 chain suggests a role in epithelial and endothelial cell maturation
-
Sorokin L.M., Pausch F., et al. Frieser M., Developmental regulation of the laminin α5 chain suggests a role in epithelial and endothelial cell maturation. Dev Biol. 189:1997;285-300.
-
(1997)
Dev Biol
, vol.189
, pp. 285-300
-
-
Sorokin, L.M.1
Pausch, F.2
-
59
-
-
0019966026
-
Fetal myosin heavy chains in regenerating muscle
-
Sartore S., Gorza L., Schiaffino S. Fetal myosin heavy chains in regenerating muscle. Nature. 298:1982;294-296.
-
(1982)
Nature
, vol.298
, pp. 294-296
-
-
Sartore, S.1
Gorza, L.2
Schiaffino, S.3
-
60
-
-
0002841587
-
The satellite cell and muscle regeneration
-
A.G. Engel, Franzini-Armstrong C. New York: McGraw-Hill
-
Bischoff R. The satellite cell and muscle regeneration. Engel A.G., Franzini-Armstrong C. Myology. 1:1994;97 McGraw-Hill, New York.
-
(1994)
Myology
, vol.1
, pp. 97
-
-
Bischoff, R.1
-
61
-
-
0016553546
-
Regeneration in free grafts of normal and denervated muscles in the rat: Morphology and histochemistry
-
Carlson B.M., Gutmann E. Regeneration in free grafts of normal and denervated muscles in the rat: morphology and histochemistry. Anat Rec. 183:1975;47-62.
-
(1975)
Anat Rec
, vol.183
, pp. 47-62
-
-
Carlson, B.M.1
Gutmann, E.2
-
62
-
-
0026478180
-
Muscle regeneration and aging
-
Carlson B.M. Muscle regeneration and aging. Monogr Dev Biol. 23:1992;189-195.
-
(1992)
Monogr Dev Biol
, vol.23
, pp. 189-195
-
-
Carlson, B.M.1
-
63
-
-
0030848969
-
Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy
-
Deconinck A.E., Rafael J.A., Skinner J.A. Utrophin-dystrophin-deficient mice as a model for Duchenne muscular dystrophy. Cell. 90:1997;717-727.
-
(1997)
Cell
, vol.90
, pp. 717-727
-
-
Deconinck, A.E.1
Rafael, J.A.2
Skinner, J.A.3
-
64
-
-
0029124239
-
Expression of laminin subunits in human fetal skeletal muscle
-
Sewry C.A., Chevallay M., Tome F.M.S. Expression of laminin subunits in human fetal skeletal muscle. Histochem J. 27:1995;497-504.
-
(1995)
Histochem J
, vol.27
, pp. 497-504
-
-
Sewry, C.A.1
Chevallay, M.2
Tome, F.M.S.3
-
65
-
-
0022447078
-
Fetal myosin immunoreactivity in human dystrophic muscle
-
Schiaffino S., Gorza L., Dones I., Cornelio F., Sartore S. Fetal myosin immunoreactivity in human dystrophic muscle. Muscle Nerve. 9:1986;51-58.
-
(1986)
Muscle Nerve
, vol.9
, pp. 51-58
-
-
Schiaffino, S.1
Gorza, L.2
Dones, I.3
Cornelio, F.4
Sartore, S.5
-
66
-
-
0023832469
-
Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy
-
Webster C., Silberstein L., Hays A.P., Blau H.M. Fast muscle fibers are preferentially affected in Duchenne muscular dystrophy. Cell. 52:1988;503-513.
-
(1988)
Cell
, vol.52
, pp. 503-513
-
-
Webster, C.1
Silberstein, L.2
Hays, A.P.3
Blau, H.M.4
-
67
-
-
0026403408
-
Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers
-
Marini J.F., Pons F., Leger J., Loffreda N., Anoal M., Chevallay M., Fardeau M., Leger J.J. Expression of myosin heavy chain isoforms in Duchenne muscular dystrophy patients and carriers. Neuromusc Disord. 1:1991;397-409.
-
(1991)
Neuromusc Disord
, vol.1
, pp. 397-409
-
-
Marini, J.F.1
Pons, F.2
Leger, J.3
Loffreda, N.4
Anoal, M.5
Chevallay, M.6
Fardeau, M.7
Leger, J.J.8
-
68
-
-
0030783172
-
Animal models for muscular dystrophy show different patterns of sarcolemmal disruption
-
Straub V., Rafael J.A., Chamberlain J.S., Campbell K.P. Animal models for muscular dystrophy show different patterns of sarcolemmal disruption. J Cell Biol. 139:1997;375-385.
-
(1997)
J Cell Biol
, vol.139
, pp. 375-385
-
-
Straub, V.1
Rafael, J.A.2
Chamberlain, J.S.3
Campbell, K.P.4
-
69
-
-
17344366176
-
Identification of a new locus for a peculiar form of congenital muscular dystrophy with early rigidity of the spine, on chromosome IP35-36
-
Moghadaszadeh B., Desguerre I., Topaloglu H., et al. Identification of a new locus for a peculiar form of congenital muscular dystrophy with early rigidity of the spine, on chromosome IP35-36. Am J Hum Genet. 62:1998;1439-1445.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1439-1445
-
-
Moghadaszadeh, B.1
Desguerre, I.2
Topaloglu, H.3
-
70
-
-
0345367513
-
Congenital myasthenic syndromes in two kinships with end-plate acetylcholine receptor and utrophin deficiency
-
Sieb J.P., Dorfler P., Tzartos S., Wewer U.M., Ruegg M.A., Meyer D., Baumann I., Lindemuth R., Jakschik J., Ries F. Congenital myasthenic syndromes in two kinships with end-plate acetylcholine receptor and utrophin deficiency. Neurology. 50:1998;54-61.
-
(1998)
Neurology
, vol.50
, pp. 54-61
-
-
Sieb, J.P.1
Dorfler, P.2
Tzartos, S.3
Wewer, U.M.4
Ruegg, M.A.5
Meyer, D.6
Baumann, I.7
Lindemuth, R.8
Jakschik, J.9
Ries, F.10
-
71
-
-
0032533384
-
Motor neurons and Schwann cells distinguish between synaptic and extrasynaptic isoforms of laminin
-
Cho S.I., Ko J., Patton B.L., Sanes J.R., Chiu A.Y. Motor neurons and Schwann cells distinguish between synaptic and extrasynaptic isoforms of laminin. J Neurobiol. 37:1998;339-358.
-
(1998)
J Neurobiol
, vol.37
, pp. 339-358
-
-
Cho, S.I.1
Ko, J.2
Patton, B.L.3
Sanes, J.R.4
Chiu, A.Y.5
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