-
2
-
-
0035660161
-
A case of idiopathic brain calcification associated with dyschromatosis symmetrica hereditaria, aplasia of dental root, and aortic valve sclerosis
-
Tojyo K, Hattori T, Sekijima Y, Yoshida K, Ikeda S. A case of idiopathic brain calcification associated with dyschromatosis symmetrica hereditaria, aplasia of dental root, and aortic valve sclerosis. Rinsho Shinkeigaku 2001;41:299-305.
-
(2001)
Rinsho Shinkeigaku
, vol.41
, pp. 299-305
-
-
Tojyo, K.1
Hattori, T.2
Sekijima, Y.3
Yoshida, K.4
Ikeda, S.5
-
3
-
-
0028208867
-
Dyschromatosis symmetrica hereditaria associated with idiopathic torsion dystonia. A case report
-
Patrizi A, Manneschi V, Pini A, Baioni E, Ghetti P. Dyschromatosis symmetrica hereditaria associated with idiopathic torsion dystonia. A case report. Acta Derm Venereol 1994;74:135-137.
-
(1994)
Acta Derm Venereol
, vol.74
, pp. 135-137
-
-
Patrizi, A.1
Manneschi, V.2
Pini, A.3
Baioni, E.4
Ghetti, P.5
-
4
-
-
0042888576
-
Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria
-
Miyamura Y, Suzuki T, Kono M, Inagaki K, Ito S, Suzuki N, Tomita Y. Mutations of the RNA-specific adenosine deaminase gene (DSRAD) are involved in dyschromatosis symmetrica hereditaria. Am J Hum Genet 2003;73:693-699.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 693-699
-
-
Miyamura, Y.1
Suzuki, T.2
Kono, M.3
Inagaki, K.4
Ito, S.5
Suzuki, N.6
Tomita, Y.7
-
5
-
-
20544455231
-
Mutation analysis of the ADARI gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis
-
Suzuki N, Suzuki T, Inagaki K, et al. Mutation analysis of the ADARI gene in dyschromatosis symmetrica hereditaria and genetic differentiation from both dyschromatosis universalis hereditaria and acropigmentatio reticularis. J Invest Dermatol 2005;124:1186-1192.
-
(2005)
J Invest Dermatol
, vol.124
, pp. 1186-1192
-
-
Suzuki, N.1
Suzuki, T.2
Inagaki, K.3
-
6
-
-
0032912480
-
Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): Report of a Japanese family with the condition and a literature review of 185 cases
-
Oyama M, Shimizu H, Ohata Y, Tajima S, Nishikawa T. Dyschromatosis symmetrica hereditaria (reticulate acropigmentation of Dohi): report of a Japanese family with the condition and a literature review of 185 cases. Br J Dermatol 1999;140:491-496.
-
(1999)
Br J Dermatol
, vol.140
, pp. 491-496
-
-
Oyama, M.1
Shimizu, H.2
Ohata, Y.3
Tajima, S.4
Nishikawa, T.5
-
7
-
-
0028872727
-
Cloning of cDNAs encoding mammalian double-stranded RNA-specific adenosine deaminase
-
O'Connell MA, Krause S, Higuchi M, Hsuan JJ, Totty NF, Jenny A, Keller W. Cloning of cDNAs encoding mammalian double-stranded RNA-specific adenosine deaminase. Mol Cell Biol 1995;15:1389-1397.
-
(1995)
Mol Cell Biol
, vol.15
, pp. 1389-1397
-
-
O'Connell, M.A.1
Krause, S.2
Higuchi, M.3
Hsuan, J.J.4
Totty, N.F.5
Jenny, A.6
Keller, W.7
-
8
-
-
0027772363
-
RNA editing of AMPA receptor subunit GluR-B: A base-paired intron-exon structure determines position and efficiency
-
Higuchi M, Single FN, Kohler M, Sommer B, Sprengel R, Seeburg PH. RNA editing of AMPA receptor subunit GluR-B: a base-paired intron-exon structure determines position and efficiency. Cell 1993;75:1361-1370.
-
(1993)
Cell
, vol.75
, pp. 1361-1370
-
-
Higuchi, M.1
Single, F.N.2
Kohler, M.3
Sommer, B.4
Sprengel, R.5
Seeburg, P.H.6
-
9
-
-
0031039834
-
Spatial distribution of kainate receptor subunit mRNA in the mouse basal ganglia and ventral mesencephalon
-
Bischoff S, Barhanin J, Bettler B, Mulle C, Heinemann S. Spatial distribution of kainate receptor subunit mRNA in the mouse basal ganglia and ventral mesencephalon. J Comp Neurol 1997;379:541-562.
-
(1997)
J Comp Neurol
, vol.379
, pp. 541-562
-
-
Bischoff, S.1
Barhanin, J.2
Bettler, B.3
Mulle, C.4
Heinemann, S.5
-
10
-
-
0036400936
-
Changes in AMPA receptor binding in an animal model of inborn paroxysmal dystonia
-
Nobrega JN, Raymond R, Barlow K, Hamann M, Richter A. Changes in AMPA receptor binding in an animal model of inborn paroxysmal dystonia. Exp Neurol 2002;176:371-376.
-
(2002)
Exp Neurol
, vol.176
, pp. 371-376
-
-
Nobrega, J.N.1
Raymond, R.2
Barlow, K.3
Hamann, M.4
Richter, A.5
-
11
-
-
0027418964
-
The AMPA receptor antagonist NBQX exerts antidystonic effects in an animal model of idiopathic dystonia
-
Richter A, Loscher W, Loschmann PA. The AMPA receptor antagonist NBQX exerts antidystonic effects in an animal model of idiopathic dystonia. Eur J Pharmacol 1993;231:287-291.
-
(1993)
Eur J Pharmacol
, vol.231
, pp. 287-291
-
-
Richter, A.1
Loscher, W.2
Loschmann, P.A.3
-
12
-
-
0034535312
-
Requirement of the RNA editing deaminase ADARI gene for embryonic erythropoiesis
-
Wang Q, Khillan J, Gaude P, Nishikura K. Requirement of the RNA editing deaminase ADARI gene for embryonic erythropoiesis. Science 2000;290:1765-1768.
-
(2000)
Science
, vol.290
, pp. 1765-1768
-
-
Wang, Q.1
Khillan, J.2
Gaude, P.3
Nishikura, K.4
-
13
-
-
15044346521
-
Deficient RNA editing of GluR2 and neuronal death in amyotrophic lateral sclerosis
-
Kwak S, Kawahara Y. Deficient RNA editing of GluR2 and neuronal death in amyotrophic lateral sclerosis. J Mol Med 2005;83:110-120.
-
(2005)
J Mol Med
, vol.83
, pp. 110-120
-
-
Kwak, S.1
Kawahara, Y.2
-
14
-
-
0033037008
-
Role of glutaraldehyde in calcification of porcine aortic valve fibroblasts
-
Kim KM, Herrera GA, Battarbee HD. Role of glutaraldehyde in calcification of porcine aortic valve fibroblasts. Am J Pathol 1999;154:843-852.
-
(1999)
Am J Pathol
, vol.154
, pp. 843-852
-
-
Kim, K.M.1
Herrera, G.A.2
Battarbee, H.D.3
-
15
-
-
0035297147
-
Bilateral striopallidodentate calcinosis: Clinical characteristics of patients seen in a registry
-
Manyam BV, Walters AS, Narla KR. Bilateral striopallidodentate calcinosis: clinical characteristics of patients seen in a registry. Mov Disord 2001;16:258-264.
-
(2001)
Mov Disord
, vol.16
, pp. 258-264
-
-
Manyam, B.V.1
Walters, A.S.2
Narla, K.R.3
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