-
1
-
-
0035494421
-
In vivo requirement of the alpha-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4
-
Adams ME, Mueller HA, Froehner SC (2002) In vivo requirement of the alpha-syntrophin PDZ domain for the sarcolemmal localization of nNOS and aquaporin-4. J Cell Biol 155:113-122
-
(2002)
J Cell Biol
, vol.155
, pp. 113-122
-
-
Adams, M.E.1
Mueller, H.A.2
Froehner, S.C.3
-
2
-
-
0036314393
-
Characterization of aquaporin-4 in muscle and muscular dystrophy
-
Crosbie RH, Dovico SA, Flanagan JD, Chamberlain JS, Ownby CL, Campbell KP (2002) Characterization of aquaporin-4 in muscle and muscular dystrophy. FASEB J 16:943-949
-
(2002)
FASEB J
, vol.16
, pp. 943-949
-
-
Crosbie, R.H.1
Dovico, S.A.2
Flanagan, J.D.3
Chamberlain, J.S.4
Ownby, C.L.5
Campbell, K.P.6
-
3
-
-
0033560065
-
PDZ domains: Fundamental building blocks in the organization of protein complexes at the plasma membrane
-
Fanning AS, Anderson JM (1999) PDZ domains: fundamental building blocks in the organization of protein complexes at the plasma membrane. J Clin Invest 103:767-772
-
(1999)
J Clin Invest
, vol.103
, pp. 767-772
-
-
Fanning, A.S.1
Anderson, J.M.2
-
4
-
-
0029122669
-
Localization of MIWC and GLIP water channel homologs in neuromuscular, epithelial and glandular tissues
-
Frigeri A, Gropper MA, Umenishi F, Kawashima V, Brown D, Verkman AS (1995) Localization of MIWC and GLIP water channel homologs in neuromuscular, epithelial and glandular tissues. J Cell Sci 108:2993-3002
-
(1995)
J Cell Sci
, vol.108
, pp. 2993-3002
-
-
Frigeri, A.1
Gropper, M.A.2
Umenishi, F.3
Kawashima, V.4
Brown, D.5
Verkman, A.S.6
-
5
-
-
0036636106
-
Altered aquaporin-4 expression in human muscular dystrophies: A common feature?
-
Frigeri A, Nicchia GP, Repetto S, Bado M, Minetti C, Svelto M (2002) Altered aquaporin-4 expression in human muscular dystrophies: a common feature? FASEB J 16:1120-1122
-
(2002)
FASEB J
, vol.16
, pp. 1120-1122
-
-
Frigeri, A.1
Nicchia, G.P.2
Repetto, S.3
Bado, M.4
Minetti, C.5
Svelto, M.6
-
6
-
-
0019471880
-
Congenital progressive muscular dystrophy of the Fukuyama type: Clinical, genetic and pathologic considerations
-
Fukuyama Y, Osawa M, Suzuki H (1981) Congenital progressive muscular dystrophy of the Fukuyama type: clinical, genetic and pathologic considerations. Brain Dev 3:1-29
-
(1981)
Brain Dev
, vol.3
, pp. 1-29
-
-
Fukuyama, Y.1
Osawa, M.2
Suzuki, H.3
-
7
-
-
0031974345
-
Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins
-
Gee SH, Madhavan R, Levinson SR, Caldwell JH, Sealock R, Froehner SC (1998) Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins. J Neurosci 18:128-137
-
(1998)
J Neurosci
, vol.18
, pp. 128-137
-
-
Gee, S.H.1
Madhavan, R.2
Levinson, S.R.3
Caldwell, J.H.4
Sealock, R.5
Froehner, S.C.6
-
8
-
-
0027989801
-
Molecular cloning of a mercurial-insensitive water channel expressed in selected water-transporting tissues
-
Hasegawa H, Ma T, Skach W, Matthay MA, Verkman AS (1994) Molecular cloning of a mercurial-insensitive water channel expressed in selected water-transporting tissues. J Biol Chem 269:5497-5500
-
(1994)
J Biol Chem
, vol.269
, pp. 5497-5500
-
-
Hasegawa, H.1
Ma, T.2
Skach, W.3
Matthay, M.A.4
Verkman, A.S.5
-
9
-
-
0027360897
-
Abnormal localization of laminin subunits in muscular dystrophies
-
Hayashi YK, Engvall E, Arikawa-Hirasawa E, Goto K, Koga R, Nonaka I, Sugita H, Arahata K (1993) Abnormal localization of laminin subunits in muscular dystrophies. J Neurol Sci 119: 53-64
-
(1993)
J Neurol Sci
, vol.119
, pp. 53-64
-
-
Hayashi, Y.K.1
Engvall, E.2
Arikawa-Hirasawa, E.3
Goto, K.4
Koga, R.5
Nonaka, I.6
Sugita, H.7
Arahata, K.8
-
10
-
-
0030982138
-
Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy
-
Ishii H, Hayashi YK, Nonaka I, Arahata K (1997) Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy. Neuromusc Disord 7:191-197
-
(1997)
Neuromusc Disord
, vol.7
, pp. 191-197
-
-
Ishii, H.1
Hayashi, Y.K.2
Nonaka, I.3
Arahata, K.4
-
11
-
-
0034666299
-
Aquaporin 4: Lack of mRNA expression in the rat regenerating muscle fiber under denervation
-
Jimi T, Wakayama Y, Murahashi M, Shibuya S, Inoue M, Hara H, Matsuzaki Y, Uemura N (2000) Aquaporin 4: lack of mRNA expression in the rat regenerating muscle fiber under denervation. Neurosci Lett 291:93-96
-
(2000)
Neurosci Lett
, vol.291
, pp. 93-96
-
-
Jimi, T.1
Wakayama, Y.2
Murahashi, M.3
Shibuya, S.4
Inoue, M.5
Hara, H.6
Matsuzaki, Y.7
Uemura, N.8
-
12
-
-
0032560851
-
An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy
-
Kobayashi K, Nakahori Y, Miyake M, Matsumura K, Kondolida E, Nomura Y, Segawa M, Yoshioka M, Saito K, Osawa M, Hamano K, Sakakihara Y, Nonaka I, Nakagome Y, Kanazawa I, Nakamura Y, Tokunaga K, Toda T (1998) An ancient retrotransposal insertion causes Fukuyama-type congenital muscular dystrophy. Nature 394:388-392
-
(1998)
Nature
, vol.394
, pp. 388-392
-
-
Kobayashi, K.1
Nakahori, Y.2
Miyake, M.3
Matsumura, K.4
Kondolida, E.5
Nomura, Y.6
Segawa, M.7
Yoshioka, M.8
Saito, K.9
Osawa, M.10
Hamano, K.11
Sakakihara, Y.12
Nonaka, I.13
Nakagome, Y.14
Kanazawa, I.15
Nakamura, Y.16
Tokunaga, K.17
Toda, T.18
-
13
-
-
0033559273
-
Immunohistochemical studies of aquaporin 4 in the skeletal muscle of mdx mouse
-
Liu JW, Wakayama Y, Inoue M, Shibuya S, Kojima H, Jimi T, Oniki H (1999) Immunohistochemical studies of aquaporin 4 in the skeletal muscle of mdx mouse. J Neurol Sci 164:24-28
-
(1999)
J Neurol Sci
, vol.164
, pp. 24-28
-
-
Liu, J.W.1
Wakayama, Y.2
Inoue, M.3
Shibuya, S.4
Kojima, H.5
Jimi, T.6
Oniki, H.7
-
14
-
-
0037173670
-
Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies
-
Michele DE, Barresi R, Kanagawa M, Saito F, Cohn RD, Satz JS, Dollar J, Nishino I, Kelley RI, Somer H, Straub V, Mathews KD, Moore SA, Campbell KP (2002) Post-translational disruption of dystroglycan-ligand interactions in congenital muscular dystrophies. Nature 418:417-422
-
(2002)
Nature
, vol.418
, pp. 417-422
-
-
Michele, D.E.1
Barresi, R.2
Kanagawa, M.3
Saito, F.4
Cohn, R.D.5
Satz, J.S.6
Dollar, J.7
Nishino, I.8
Kelley, R.I.9
Somer, H.10
Straub, V.11
Mathews, K.D.12
Moore, S.A.13
Campbell, K.P.14
-
15
-
-
0030031292
-
Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? -pathological study of the cerebral cortex of an FCMD fetus
-
Berl
-
Nakano I, Funahashi M, Takada K, Toda T (1996) Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? -pathological study of the cerebral cortex of an FCMD fetus. Acta Neuropathol (Berl) 91:313-321
-
(1996)
Acta Neuropathol
, vol.91
, pp. 313-321
-
-
Nakano, I.1
Funahashi, M.2
Takada, K.3
Toda, T.4
-
16
-
-
0032578454
-
Direct immunogold labelling of aquaporin-4 in square arrays of astrocyte and ependymocyte plasma membranes in rat brain and spinal cord
-
Rash JE, Yasumura T, Hudson CS, Agre P, Nielsen S (1998) Direct immunogold labelling of aquaporin-4 in square arrays of astrocyte and ependymocyte plasma membranes in rat brain and spinal cord. Proc Natl Acad Sci U S A 95:11981-11986
-
(1998)
Proc Natl Acad Sci U S A
, vol.95
, pp. 11981-11986
-
-
Rash, J.E.1
Yasumura, T.2
Hudson, C.S.3
Agre, P.4
Nielsen, S.5
-
17
-
-
0019449011
-
Freeze fracture studies of muscle plasma membrane in human muscular dystrophy
-
Berl
-
Schotland DL, Bonilla E, Wakayama Y (1981) Freeze fracture studies of muscle plasma membrane in human muscular dystrophy. Acta Neuropathol (Berl) 54:189-197
-
(1981)
Acta Neuropathol
, vol.54
, pp. 189-197
-
-
Schotland, D.L.1
Bonilla, E.2
Wakayama, Y.3
-
18
-
-
0030981854
-
A comparative freeze-fracture study of plasma membrane of dystrophic skeletal muscles in dy/dy mice with merosin (laminin 2) deficiency and mdx mice with dystrophin deficiency
-
Shibuya S, Wakayama Y, Oniki H, Kojima H, Saito M, Etou T, Nonaka I (1997) A comparative freeze-fracture study of plasma membrane of dystrophic skeletal muscles in dy/dy mice with merosin (laminin 2) deficiency and mdx mice with dystrophin deficiency. Neuropathol Appl Neurobiol 23:123-131
-
(1997)
Neuropathol Appl Neurobiol
, vol.23
, pp. 123-131
-
-
Shibuya, S.1
Wakayama, Y.2
Oniki, H.3
Kojima, H.4
Saito, M.5
Etou, T.6
Nonaka, I.7
-
19
-
-
0008560190
-
Identification of aquaporin 4 molecule in the replica of normal rat sarcolemma: Fracture-label immunoelectron microscopin study
-
Shibuya S, Wakayama Y, Inoue M (1999) Identification of aquaporin 4 molecule in the replica of normal rat sarcolemma: fracture-label immunoelectron microscopin study (abstract). Ann Neurol 46:460
-
(1999)
Ann Neurol
, vol.46
, pp. 460
-
-
Shibuya, S.1
Wakayama, Y.2
Inoue, M.3
-
20
-
-
0038045645
-
Postsynaptic density-95 mimics and occludes hippocampal long-term potentiation and enhances long-term depression
-
Stein V, House DR, Bredt DS, Nicoll RA (2003) Postsynaptic density-95 mimics and occludes hippocampal long-term potentiation and enhances long-term depression. J Neurosci 23:5503-5506
-
(2003)
J Neurosci
, vol.23
, pp. 5503-5506
-
-
Stein, V.1
House, D.R.2
Bredt, D.S.3
Nicoll, R.A.4
-
21
-
-
0036133518
-
Deficiency of a 180-kDa extracellular matrix protein in Fukuyama type congenital muscular dystrophy skeletal muscle
-
Sunada Y, Saito F, Higuchi I, Matsumura K, Shimizu T (2002) Deficiency of a 180-kDa extracellular matrix protein in Fukuyama type congenital muscular dystrophy skeletal muscle. Neuromusc Disord 12:117-120
-
(2002)
Neuromusc Disord
, vol.12
, pp. 117-120
-
-
Sunada, Y.1
Saito, F.2
Higuchi, I.3
Matsumura, K.4
Shimizu, T.5
-
22
-
-
0027364850
-
Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33
-
Toda T, Segawa M, Nomura Y, Nonaka I, Masuda K, Ishihara T, Suzuki M, Tomita I, Origuchi Y, Ohno K, Misugi N, Sasaki Y, Takeda K, Kawai M, Otani K, Murakami T, Saito K, Fukuyama Y, Shimizu T, Kanazawa I, Nakamura Y (1993) Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33. Nat Genet 5:283-286
-
(1993)
Nat Genet
, vol.5
, pp. 283-286
-
-
Toda, T.1
Segawa, M.2
Nomura, Y.3
Nonaka, I.4
Masuda, K.5
Ishihara, T.6
Suzuki, M.7
Tomita, I.8
Origuchi, Y.9
Ohno, K.10
Misugi, N.11
Sasaki, Y.12
Takeda, K.13
Kawai, M.14
Otani, K.15
Murakami, T.16
Saito, K.17
Fukuyama, Y.18
Shimizu, T.19
Kanazawa, I.20
Nakamura, Y.21
more..
-
23
-
-
0021165870
-
Duchenne dystrophy: Reduced density of orthogonal array subunit particles in muscle plasma membrane
-
Wakayama Y, Okayasu H, Shibuya S, Kumagai T (1984) Duchenne dystrophy: reduced density of orthogonal array subunit particles in muscle plasma membrane. Neurology 34:1313-1317
-
(1984)
Neurology
, vol.34
, pp. 1313-1317
-
-
Wakayama, Y.1
Okayasu, H.2
Shibuya, S.3
Kumagai, T.4
-
24
-
-
0022194593
-
Freeze-fracture studies of muscle plasma membrane in Fukuyama-type congenital muscular dystrophy
-
Wakayama Y, Kumagai T, Shibuya S (1985) Freeze-fracture studies of muscle plasma membrane in Fukuyama-type congenital muscular dystrophy. Neurology 35:1587-1593
-
(1985)
Neurology
, vol.35
, pp. 1587-1593
-
-
Wakayama, Y.1
Kumagai, T.2
Shibuya, S.3
-
25
-
-
0022911109
-
Small size of orthogonal array in muscle plasma membrane of Fukuyama type congenital muscular dystrophy
-
Berl
-
Wakayama Y, Kumagai T, Jimi T (1986) Small size of orthogonal array in muscle plasma membrane of Fukuyama type congenital muscular dystrophy. Acta Neuropathol (Berl) 72:130-133
-
(1986)
Acta Neuropathol
, vol.72
, pp. 130-133
-
-
Wakayama, Y.1
Kumagai, T.2
Jimi, T.3
-
26
-
-
0025295467
-
Immunoreactivity of antibodies raised against synthetic peptide fragments predicted from mid portions of dystrophin cDNA
-
Wakayama Y, Jimi T, Takeda A, Misugi N, Kumagai T, Miyake S, Shibuya S (1990) Immunoreactivity of antibodies raised against synthetic peptide fragments predicted from mid portions of dystrophin cDNA. J Neurol Sci 97:241-250
-
(1990)
J Neurol Sci
, vol.97
, pp. 241-250
-
-
Wakayama, Y.1
Jimi, T.2
Takeda, A.3
Misugi, N.4
Kumagai, T.5
Miyake, S.6
Shibuya, S.7
-
27
-
-
0028887768
-
Ultrastructural localization of the C-terminus of the 43-kd dystrophin-associated glycoprotein and its relation to dystrophin in normal murine skeletal myofiber
-
Wakayama Y, Shibuya S, Takeda A, Jimi T, Nakamura Y, Oniki H (1995) Ultrastructural localization of the C-terminus of the 43-kd dystrophin- associated glycoprotein and its relation to dystrophin in normal murine skeletal myofiber. Am J Pathol 146:189-196
-
(1995)
Am J Pathol
, vol.146
, pp. 189-196
-
-
Wakayama, Y.1
Shibuya, S.2
Takeda, A.3
Jimi, T.4
Nakamura, Y.5
Oniki, H.6
-
28
-
-
0030641481
-
Immunogold and freeze etch electron microscopic studies of merosin localization in basal lamina of human skeletal muscle fibers
-
Berl
-
Wakayama Y, Murahashi M, Jimi T, Kojima H, Shibuya S, Oniki H (1997) Immunogold and freeze etch electron microscopic studies of merosin localization in basal lamina of human skeletal muscle fibers. Acta Neuropathol (Berl) 93:34-42
-
(1997)
Acta Neuropathol
, vol.93
, pp. 34-42
-
-
Wakayama, Y.1
Murahashi, M.2
Jimi, T.3
Kojima, H.4
Shibuya, S.5
Oniki, H.6
-
29
-
-
9144252841
-
Ultrastructural alterations of the muscle plasma membrane and related structures in Fukuyama muscular dystrophy: Comparative study with other types of muscular dystrophies
-
Fukuyama Y, Osawa M, Saito K (eds). Elsevier, Amsterdam
-
Wakayama Y, Shibuya S, Kumagai T, Kobayashi T, Yamashita S, Misugi N, Miyake S, Murahashi M, Jimi T, Oniki H (1997) Ultrastructural alterations of the muscle plasma membrane and related structures in Fukuyama muscular dystrophy: comparative study with other types of muscular dystrophies. In: Fukuyama Y, Osawa M, Saito K (eds) Congenital muscular dystrophies. Elsevier, Amsterdam, pp 213-230
-
(1997)
Congenital Muscular Dystrophies
, pp. 213-230
-
-
Wakayama, Y.1
Shibuya, S.2
Kumagai, T.3
Kobayashi, T.4
Yamashita, S.5
Misugi, N.6
Miyake, S.7
Murahashi, M.8
Jimi, T.9
Oniki, H.10
-
30
-
-
0348168471
-
Analytical studies on the mechanism of the depletion of the aquaporin 4 molecule in the muscle plasma membrane with Duchenne muscular dystrophy
-
Wakayama Y, Jimi T, Inoue M, Kojima H, Murahashi M, Kumagai T, Yamashita S, Hara H, Shibuya S (2000) Analytical studies on the mechanism of the depletion of the aquaporin 4 molecule in the muscle plasma membrane with Duchenne muscular dystrophy (abstract). Ann Neurol 48:471-472
-
(2000)
Ann Neurol
, vol.48
, pp. 471-472
-
-
Wakayama, Y.1
Jimi, T.2
Inoue, M.3
Kojima, H.4
Murahashi, M.5
Kumagai, T.6
Yamashita, S.7
Hara, H.8
Shibuya, S.9
-
31
-
-
0036192032
-
Reduced aquaporin 4 expression in the muscle plasma membrane of patients with Duchenne muscular dystrophy
-
Wakayama Y, Jimi T, Inoue M, Kojima H, Murahashi M, Kumagai T, Yamashita S, Hara H, Shibuya S (2002) Reduced aquaporin 4 expression in the muscle plasma membrane of patients with Duchenne muscular dystrophy. Arch Neurol 59:431-437
-
(2002)
Arch Neurol
, vol.59
, pp. 431-437
-
-
Wakayama, Y.1
Jimi, T.2
Inoue, M.3
Kojima, H.4
Murahashi, M.5
Kumagai, T.6
Yamashita, S.7
Hara, H.8
Shibuya, S.9
-
32
-
-
0030944752
-
Early ultrastructural changes in the central nervous system in Fukuyama congenital muscular dystrophy
-
Yamamoto T, Shibata N, Kanazawa M, Kobayashi M, Komori T, Kondo E, Saito K, Osawa M (1997) Early ultrastructural changes in the central nervous system in Fukuyama congenital muscular dystrophy. Ultrastruct Pathol 21:355-360
-
(1997)
Ultrastruct Pathol
, vol.21
, pp. 355-360
-
-
Yamamoto, T.1
Shibata, N.2
Kanazawa, M.3
Kobayashi, M.4
Komori, T.5
Kondo, E.6
Saito, K.7
Osawa, M.8
-
33
-
-
0029086229
-
DNA cloning, gene organization, and chromosomal localization of a human mercurial insensitive water channel: Evidence for distinct transcriptional units
-
Yang B, Ma T, Verkman AS (1995) cDNA cloning, gene organization, and chromosomal localization of a human mercurial insensitive water channel: evidence for distinct transcriptional units. J Biol Chem 270:22907-22913
-
(1995)
J Biol Chem
, vol.270
, pp. 22907-22913
-
-
Yang, B.1
Ma, T.2
Verkman, A.S.3
-
34
-
-
0029926097
-
The mercurial insensitive water channel (AQP-4) forms orthogonal arrays in stably transfected Chinese hamster ovary cells
-
Yang B, Brown D, Verkman AS (1996) The mercurial insensitive water channel (AQP-4) forms orthogonal arrays in stably transfected Chinese hamster ovary cells. J Biol Chem 271:4577-4580
-
(1996)
J Biol Chem
, vol.271
, pp. 4577-4580
-
-
Yang, B.1
Brown, D.2
Verkman, A.S.3
-
35
-
-
23044519703
-
Aquaporin 4 is absent at the sarcolemma and at perivascular astrocyte endfeet in alpha1-syntrophin knockout mice
-
Yokota T, Miyagoe Y, Hosaka Y, Tsukita K, Kameya S, Shibuya S, Matsuda R, Wakayama Y, Takeda S (2000) Aquaporin 4 is absent at the sarcolemma and at perivascular astrocyte endfeet in alpha1-syntrophin knockout mice. Proc Jpn Acad 76(B):22-27
-
(2000)
Proc Jpn Acad
, vol.76
, Issue.B
, pp. 22-27
-
-
Yokota, T.1
Miyagoe, Y.2
Hosaka, Y.3
Tsukita, K.4
Kameya, S.5
Shibuya, S.6
Matsuda, R.7
Wakayama, Y.8
Takeda, S.9
|