-
1
-
-
0024357992
-
Expression of c-Fos immunoreactivity in transmitter-characterized neurons after stress
-
Ceccatelli S, Villar MJ, Goldstein M, Hokfelt T (1989) Expression of c-Fos immunoreactivity in transmitter-characterized neurons after stress. Proc Natl Acad Sci USA 86:9569-9573.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 9569-9573
-
-
Ceccatelli, S.1
Villar, M.J.2
Goldstein, M.3
Hokfelt, T.4
-
2
-
-
0025311047
-
CENP-B: A major human centromere protein located beneath the kinetochore
-
Cooke CA, Bernat RL, Earnshaw WC (1990) CENP-B: a major human centromere protein located beneath the kinetochore. J Cell Biol 110:1475-1488.
-
(1990)
J Cell Biol
, vol.110
, pp. 1475-1488
-
-
Cooke, C.A.1
Bernat, R.L.2
Earnshaw, W.C.3
-
3
-
-
0026096204
-
Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myodonic epilepsy patients
-
Durner M, Sander T, Greenberg DA, Johnson K, Beck-Mannagetta G, Janz D (1991) Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myodonic epilepsy patients. Neurology 41:1651-1655.
-
(1991)
Neurology
, vol.41
, pp. 1651-1655
-
-
Durner, M.1
Sander, T.2
Greenberg, D.A.3
Johnson, K.4
Beck-Mannagetta, G.5
Janz, D.6
-
4
-
-
0027299118
-
The chromosome 6p epilepsy locus: Exploring mode of inheritance and heterogeneity through linkage analysis
-
Greenberg DA, Delgado-Escueta AV (1993) The chromosome 6p epilepsy locus: exploring mode of inheritance and heterogeneity through linkage analysis. Epilepsia [Suppl]34:pS12-pS18.
-
(1993)
Epilepsia [Suppl]
, vol.34
-
-
Greenberg, D.A.1
Delgado-Escueta, A.V.2
-
5
-
-
0027731681
-
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease
-
Halford S, Wadey R, Roberts C, Daw SC, Whiting JA, O'Donnell H, Dunham I, Bentley D, Lindsay E, Baldini A (1993) Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease. Hum Mol Genet 2:2099-2107.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 2099-2107
-
-
Halford, S.1
Wadey, R.2
Roberts, C.3
Daw, S.C.4
Whiting, J.A.5
O'Donnell, H.6
Dunham, I.7
Bentley, D.8
Lindsay, E.9
Baldini, A.10
-
6
-
-
0027478216
-
A mouse model of Greig cephalopolysyndactyly syndrome: The extra-toesJ mutation contains an intragenic deletion of the Gli3 gene
-
Hui CC, Joyner AL (1993) A mouse model of Greig cephalopolysyndactyly syndrome: the extra-toesJ mutation contains an intragenic deletion of the Gli3 gene. Nat Genet 3:241-246.
-
(1993)
Nat Genet
, vol.3
, pp. 241-246
-
-
Hui, C.C.1
Joyner, A.L.2
-
7
-
-
19144364193
-
Benign adult familial myoclonus epilepsy (BAFME): An autosomal dominant form not linked to the dentatorubral pallidoluysian atrophy (DRPLA) gene
-
Kuwano A, Takakubo F, Morimoto Y, Uyama E, Uchino M, Ando M, Yasuda T, Terao A, Hayayma T, Kobayashi R, Kondo I (1996) Benign adult familial myoclonus epilepsy (BAFME): an autosomal dominant form not linked to the dentatorubral pallidoluysian atrophy (DRPLA) gene. J Med Genet 33:80-81.
-
(1996)
J Med Genet
, vol.33
, pp. 80-81
-
-
Kuwano, A.1
Takakubo, F.2
Morimoto, Y.3
Uyama, E.4
Uchino, M.5
Ando, M.6
Yasuda, T.7
Terao, A.8
Hayayma, T.9
Kobayashi, R.10
Kondo, I.11
-
8
-
-
0024502803
-
Benign familial neonatal convulsions linked to genetic markers on chromosome 20
-
Leppert M, Anderson VE, Quattlebaum T, Stauffer D, O'Connell P, Nakamura Y, Lalouel JM, White R (1989) Benign familial neonatal convulsions linked to genetic markers on chromosome 20. Nature 337:647-648.
-
(1989)
Nature
, vol.337
, pp. 647-648
-
-
Leppert, M.1
Anderson, V.E.2
Quattlebaum, T.3
Stauffer, D.4
O'Connell, P.5
Nakamura, Y.6
Lalouel, J.M.7
White, R.8
-
9
-
-
0029013275
-
Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11: Linkage to convulsions and electroencephalography trait
-
Liu AW, Delgado-Escueta AV, Serratosa JM, Alonso ME, Medina MT, Gee MN, Cordova S, Zhao HZ, Spellman JM, Peek JR (1995) Juvenile myoclonic epilepsy locus in chromosome 6p21.2-p11: linkage to convulsions and electroencephalography trait. Am J Hum Genet 57:368-381.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 368-381
-
-
Liu, A.W.1
Delgado-Escueta, A.V.2
Serratosa, J.M.3
Alonso, M.E.4
Medina, M.T.5
Gee, M.N.6
Cordova, S.7
Zhao, H.Z.8
Spellman, J.M.9
Peek, J.R.10
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