-
1
-
-
0027470203
-
The structure and functional diversity of dystrophin
-
Ahn AH, Kunkel LM. The structure and functional diversity of dystrophin. Nature Genet 1993; 3: 283-91
-
(1993)
Nature Genet
, vol.3
, pp. 283-291
-
-
Ahn, A.H.1
Kunkel, L.M.2
-
2
-
-
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 YK, 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 Japan Acad (Ser B) 1993; 69: 259-64
-
(1993)
Proc Japan Acad (Ser B)
, vol.69
, pp. 259-264
-
-
Arahata, K.1
Hayashi, Y.K.2
Koga, R.3
-
3
-
-
0018369721
-
Involvement of peripheral and central nerves in murine dystrophy
-
Bradley WG, Jaros E. Involvement of peripheral and central nerves in murine dystrophy. NY Acad Sci 1979; 317: 132-42
-
(1979)
NY Acad Sci
, vol.317
, pp. 132-142
-
-
Bradley, W.G.1
Jaros, E.2
-
6
-
-
0025373178
-
Merosin, a tissue specific basement membrane protein, is a laminin-like protein
-
Ehrig K, Leivo I, Argraves WS, Ruoslahti E, Engvall E, Merosin, a tissue specific basement membrane protein, is a laminin-like protein. Proc Natl Acad Sci 1990; 87: 3264-8
-
(1990)
Proc Natl Acad Sci
, vol.87
, pp. 3264-3268
-
-
Ehrig, K.1
Leivo, I.2
Argraves, W.S.3
Ruoslahti, E.4
Engvall, E.5
-
7
-
-
0029586082
-
Readjusting the localisation of merosin (laminin α2- Chain) deficient congenital muscular dystrophy locus on chromosome 6q
-
Paris
-
Helbling-Leclerc A, Topaloglu H, Tome FMS et al. Readjusting the localisation of merosin (laminin α2-chain) deficient congenital muscular dystrophy locus on chromosome 6q. C R Acad Sci (Paris) 1995; 318: 1245-52
-
(1995)
C R Acad Sci
, vol.318
, pp. 1245-1252
-
-
Helbling-Leclerc, A.1
Topaloglu, H.2
Tome, F.M.S.3
-
8
-
-
0028980027
-
Mutations in the laminin α2 chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy
-
Helbling-Leclerc A, Zhang X, Topaloglu H et al. Mutations in the laminin α2 chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy. Nature Genet 1995; 11: 216-18
-
(1995)
Nature Genet
, vol.11
, pp. 216-218
-
-
Helbling-Leclerc, A.1
Zhang, X.2
Topaloglu, H.3
-
9
-
-
0029806196
-
Congenital muscular dystrophy with laminin α2 chain deficiency: Identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry
-
Hermann R, Straub V, Meyer K, Kahn T, Wagner Voit T. Congenital muscular dystrophy with laminin α2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry. Eur J Pediatr 1996; 155: 968-76
-
(1996)
Eur J Pediatr
, vol.155
, pp. 968-976
-
-
Hermann, R.1
Straub, V.2
Meyer, K.3
Kahn, T.4
Wagner Voit, T.5
-
10
-
-
0028094441
-
Localisation of merosinnegative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping
-
Hillaire D, Leclerc A, Faure S et al. Localisation of merosinnegative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping. Hum Mol Genet 1994; 3: 1657-61
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1657-1661
-
-
Hillaire, D.1
Leclerc, A.2
Faure, S.3
-
11
-
-
0029670459
-
Laminin α2 is a component of brain capillary basement membrane: Reduced expression in dystrophic dy mice
-
Jucker M, Tian M, Norton DD, Sherman C, Kusiak JW. Laminin α2 is a component of brain capillary basement membrane: reduced expression in dystrophic dy mice. Neuroscience 1996; 71: 1153-61
-
(1996)
Neuroscience
, vol.71
, pp. 1153-1161
-
-
Jucker, M.1
Tian, M.2
Norton, D.D.3
Sherman, C.4
Kusiak, J.W.5
-
12
-
-
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, 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 1988; 85: 1544-8
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 1544-1548
-
-
Leivo, I.1
Engvall, E.2
-
13
-
-
0031026605
-
Localisation of laminin α2 chain in normal human skeletal muscle and peripheral nerve: An ultrastructural immunolabelling study
-
Malandrini A, Villanova M, Sabatelli P et al. Localisation of laminin α2 chain in normal human skeletal muscle and peripheral nerve: an ultrastructural immunolabelling study. Acta Neuropathol Berl 1997; 93: 166-72
-
(1997)
Acta Neuropathol Berl
, vol.93
, pp. 166-172
-
-
Malandrini, A.1
Villanova, M.2
Sabatelli, P.3
-
14
-
-
0342480329
-
Cardiac involvement in merosin-negative congenital muscular dystrophy
-
Muntoni F, Philpot J, Spyrou N, Camici P, Dubowitz V. Cardiac involvement in merosin-negative congenital muscular dystrophy. Dev Med Child Neurol 1995; 72: 37
-
(1995)
Dev Med Child Neurol
, vol.72
, pp. 37
-
-
Muntoni, F.1
Philpot, J.2
Spyrou, N.3
Camici, P.4
Dubowitz, V.5
-
15
-
-
0030614661
-
Refinement of the laminin α2 chain locus on chromosome 6q2 in merosin-deficient congenital muscular dystrophy
-
Naom I, D'Alessandro M, Topaloglu H et al. Refinement of the laminin α2 chain locus on chromosome 6q2 in merosin-deficient congenital muscular dystrophy. J Med Genet 1997; 34: 99-104
-
(1997)
J Med Genet
, vol.34
, pp. 99-104
-
-
Naom, I.1
D'Alessandro, M.2
Topaloglu, H.3
-
16
-
-
0024439359
-
Mouse heart laminin. Purification of the native protein and structural comparison with Engelbreth-Holm-Swarm tumour laminin
-
Paulsson M, Saladin K. Mouse heart laminin. Purification of the native protein and structural comparison with Engelbreth-Holm-Swarm tumour laminin. J Biol Chem 1989; 264; 18726-52
-
(1989)
J Biol Chem
, vol.264
, pp. 18726-18752
-
-
Paulsson, M.1
Saladin, K.2
-
17
-
-
0025991750
-
Structure of laminin variants. The 300 kDa chains of merosin and bovine heart laminin are related to the human placenta merosin heavy chain and replace the a chain in some laminin variants
-
Paulsson M, Saladin K, Kngvall E. Structure of laminin variants. The 300 kDa chains of merosin and bovine heart laminin are related to the human placenta merosin heavy chain and replace the a chain in some laminin variants. J Biol Chem 1991; 266: 17545-51
-
(1991)
J Biol Chem
, vol.266
, pp. 17545-17551
-
-
Paulsson, M.1
Saladin, K.2
Kngvall, E.3
-
18
-
-
0029061267
-
Clinical phenotype in congenital muscular dystrophy: Correlation with expression of merosin in skeletal muscle
-
Philpot J, Sewry C, Pennock J, Dubowitz V. Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal muscle. Neuromusc Disord 1995; 5: 301-5
-
(1995)
Neuromusc Disord
, vol.5
, pp. 301-305
-
-
Philpot, J.1
Sewry, C.2
Pennock, J.3
Dubowitz, V.4
-
19
-
-
0029582766
-
Expression of laminin isoforms in mouse myogenic cells in vitro and in vivo
-
Schuler F, Sorokin LM. Expression of laminin isoforms in mouse myogenic cells in vitro and in vivo. J Cell Sci 1995; 108: 3795-804
-
(1995)
J Cell Sci
, vol.108
, pp. 3795-3804
-
-
Schuler, F.1
Sorokin, L.M.2
-
20
-
-
0030918601
-
Variable phenotype in merosin-deficient congenital muscular dystrophy and differential immunolabelling of two fragments of the laminin α2 chain
-
Sewry CA, Naom I, D'Alessandro M et al. Variable phenotype in merosin-deficient congenital muscular dystrophy and differential immunolabelling of two fragments of the laminin α2 chain. Neuromusc Disord 1997; 7: 169-75
-
(1997)
Neuromusc Disord
, vol.7
, pp. 169-175
-
-
Sewry, C.A.1
Naom, I.2
D'Alessandro, M.3
-
21
-
-
0029007799
-
Expression of laminin subunits in congenital muscular dystrophy
-
Sewry CA, Philpot J, Mahony D, Wilson LA, Muntoni F, Dubowitz V. Expression of laminin subunits in congenital muscular dystrophy. Neuromusc Disord 1995; 5: 307-16
-
(1995)
Neuromusc Disord
, vol.5
, pp. 307-316
-
-
Sewry, C.A.1
Philpot, J.2
Mahony, D.3
Wilson, L.A.4
Muntoni, F.5
Dubowitz, V.6
-
22
-
-
0030053280
-
Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy
-
Sewry CA, Philpot J. Sorokin L et al. Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy. Lancet 1996; 347: 582-4
-
(1996)
Lancet
, vol.347
, pp. 582-584
-
-
Sewry, C.A.1
Philpot, J.2
Sorokin, L.3
-
23
-
-
0028788685
-
Peripheral nerve involvement in congenital muscular dystrophy
-
Shorer Z, Philpot J, Muntoni F, Sewry C, Dubowitz V. Peripheral nerve involvement in congenital muscular dystrophy. J Child Neurol 1995; 10: 472-5
-
(1995)
J Child Neurol
, vol.10
, pp. 472-475
-
-
Shorer, Z.1
Philpot, J.2
Muntoni, F.3
Sewry, C.4
Dubowitz, V.5
-
24
-
-
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, Campbell KP. Deficiency of merosin in dystrophic dy mice and genetic linkage of laminin M chain gene to dy locus. J Biol Chem 1994; 269: 13729-52
-
(1994)
J Biol Chem
, vol.269
, pp. 13729-13752
-
-
Sunada, Y.1
Bernier, S.M.2
Kozak, C.A.3
Yamada, Y.4
Campbell, K.P.5
-
26
-
-
0030990635
-
Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency
-
Tan E, Topaloglu H, Sewry C et al. Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency. Neuromusc Disord 1997; 7: 85-90
-
(1997)
Neuromusc Disord
, vol.7
, pp. 85-90
-
-
Tan, E.1
Topaloglu, H.2
Sewry, C.3
-
28
-
-
0030019062
-
Localization of merosin in normal human brain: Implications for congenital muscular dystrophy with merosin deficiency
-
Villanova M, Malandrini A, Toti P et al. Localization of merosin in normal human brain: implications for congenital muscular dystrophy with merosin deficiency. J Submicrosc Cytol Pathol 1996; 28: 1-4
-
(1996)
J Submicrosc Cytol Pathol
, vol.28
, pp. 1-4
-
-
Villanova, M.1
Malandrini, A.2
Toti, P.3
-
29
-
-
0030465319
-
Merosin/laminin-2 and muscular dystrophy
-
Wewer U, Engvall E, Merosin/laminin-2 and muscular dystrophy. Neuromusc Disord 1996; 6: 409-18
-
(1996)
Neuromusc Disord
, vol.6
, pp. 409-418
-
-
Wewer, U.1
Engvall, E.2
-
30
-
-
0028334735
-
Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse
-
Xu H, Christmas P, Wu X-R, Wewer U, Engvall E. Defective muscle basement membrane and lack of M-laminin in the dystrophic dy/dy mouse. Proc Natl Acad Sci USA 1994; 91: 5572-6
-
(1994)
Proc Natl Acad Sci USA
, vol.91
, pp. 5572-5576
-
-
Xu, H.1
Christmas, P.2
Wu, X.-R.3
Wewer, U.4
Engvall, E.5
-
31
-
-
0028135436
-
Murine muscular dystrophy caused by a mutation in the laminin α2 (Lama2) gene
-
Xu H, Wu X-R, Wewer UM, Engvall E, Murine muscular dystrophy caused by a mutation in the laminin α2 (Lama2) gene. Nature Genet 1994; 8: 297-302
-
(1994)
Nature Genet
, vol.8
, pp. 297-302
-
-
Xu, H.1
Wu, X.-R.2
Wewer, U.M.3
Engvall, E.4
|