-
1
-
-
0032146571
-
Molecular definition of chromosome translocations involving 10q24 and 19q13 in human malignant glioma cells
-
Chernova O, Cowell JK (1998) Molecular definition of chromosome translocations involving 10q24 and 19q13 in human malignant glioma cells. Cancer Genet Cytogenet 105:60-68
-
(1998)
Cancer Genet Cytogenet
, vol.105
, pp. 60-68
-
-
Chernova, O.1
Cowell, J.K.2
-
2
-
-
0032481137
-
A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors
-
Chernova OB, Somerville RP, Cowell JK (1998) A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors. Oncogene 17:2873-2881
-
(1998)
Oncogene
, vol.17
, pp. 2873-2881
-
-
Chernova, O.B.1
Somerville, R.P.2
Cowell, J.K.3
-
3
-
-
0031817914
-
Apoptosis and apoptosis-related gene products in primary non-Hodgkin's lymphoma of the central nervous system
-
Deckert-Schlüter M, Rang A, Wiestler OD (1998) Apoptosis and apoptosis-related gene products in primary non-Hodgkin's lymphoma of the central nervous system. Acta Neuropathol (Berl) 96:157-162
-
(1998)
Acta Neuropathol (Berl)
, vol.96
, pp. 157-162
-
-
Deckert-Schlüter, M.1
Rang, A.2
Wiestler, O.D.3
-
4
-
-
0033968345
-
Loss of heterozygosity on chromosome 10 is more extensive in primary (de novo) than in secondary glioblastomas
-
Fujisawa H, Reis RM, Nakamura M, Colella S, Yonekawa Y, Kleihues P, Ohgaki H (2000) Loss of heterozygosity on chromosome 10 is more extensive in primary (de novo) than in secondary glioblastomas. Lab Invest 80:65-72
-
(2000)
Lab Invest
, vol.80
, pp. 65-72
-
-
Fujisawa, H.1
Reis, R.M.2
Nakamura, M.3
Colella, S.4
Yonekawa, Y.5
Kleihues, P.6
Ohgaki, H.7
-
5
-
-
0036712759
-
LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures
-
Gu W, Brodtkorb E, Steinlein OK (2002) LGI1 is mutated in familial temporal lobe epilepsy characterized by aphasic seizures. Ann Neurol 52:364-367
-
(2002)
Ann Neurol
, vol.52
, pp. 364-367
-
-
Gu, W.1
Brodtkorb, E.2
Steinlein, O.K.3
-
6
-
-
0037157099
-
The LGI1 gene involved in lateral temporal lobe epilepsy belongs to a new subfamily of leucine-rich repeat proteins
-
Gu W, Wevers A, Schröder H, Grzeschik KH, Derst C, Brodtkorb E, de Vos R, Steinlein OK (2002) The LGI1 gene involved in lateral temporal lobe epilepsy belongs to a new subfamily of leucine-rich repeat proteins. FEBS Lett 519:71-76
-
(2002)
FEBS Lett
, vol.519
, pp. 71-76
-
-
Gu, W.1
Wevers, A.2
Schröder, H.3
Grzeschik, K.H.4
Derst, C.5
Brodtkorb, E.6
De Vos, R.7
Steinlein, O.K.8
-
7
-
-
18544376557
-
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
-
Kalachikov S, Evgrafov O, Ross B, Winawer M, Barker-Cummings C, Martinelli Boneschi F, Choi C, Morozov P, Das K, Teplitskaya E, Yu A, Cayanis E, Penchaszadeh G, Kottmann AH, Pedley TA, Hauser WA, Ottman R, Gilliam TC (2002) Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet 30:335-341
-
(2002)
Nat Genet
, vol.30
, pp. 335-341
-
-
Kalachikov, S.1
Evgrafov, O.2
Ross, B.3
Winawer, M.4
Barker-Cummings, C.5
Martinelli Boneschi, F.6
Choi, C.7
Morozov, P.8
Das, K.9
Teplitskaya, E.10
Yu, A.11
Cayanis, E.12
Penchaszadeh, G.13
Kottmann, A.H.14
Pedley, T.A.15
Hauser, W.A.16
Ottman, R.17
Gilliam, T.C.18
-
8
-
-
0036942140
-
Physical and functional characterization of the human LGI1 gene and its possible role in glioma development
-
Krex D, Hauses M, Appelt H, Mohr B, Ehninger G, Schackert HK, Schackert G (2002) Physical and functional characterization of the human LGI1 gene and its possible role in glioma development. Acta Neuropathol (Berl) 103:255-266
-
(2002)
Acta Neuropathol (Berl)
, vol.103
, pp. 255-266
-
-
Krex, D.1
Hauses, M.2
Appelt, H.3
Mohr, B.4
Ehninger, G.5
Schackert, H.K.6
Schackert, G.7
-
9
-
-
18344363561
-
Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy
-
Morante-Redolat JM, Gorostidi-Pagola A, Piquer-Sirerol S, Saenz A, Poza JJ, Galan J, Gesk S, Sarafidou T, Mautner VF, Binelli S, Staub E, Hinzmann B, French L, Prud'homme JF, Passarelli D, Scannapieco P, Tassinari CA, Avanzini G, Marti-Masso JF, Kluwe L, Deloukas P, Moschonas NK, Michelucci R, Siebert R, Nobile C, Perez-Tur J, Lopez de Munain A (2002) Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy. Hum Mol Genet 11:1119-1128
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1119-1128
-
-
Morante-Redolat, J.M.1
Gorostidi-Pagola, A.2
Piquer-Sirerol, S.3
Saenz, A.4
Poza, J.J.5
Galan, J.6
Gesk, S.7
Sarafidou, T.8
Mautner, V.F.9
Binelli, S.10
Staub, E.11
Hinzmann, B.12
French, L.13
Prud'homme, J.F.14
Passarelli, D.15
Scannapieco, P.16
Tassinari, C.A.17
Avanzini, G.18
Marti-Masso, J.F.19
Kluwe, L.20
Deloukas, P.21
Moschonas, N.K.22
Michelucci, R.23
Siebert, R.24
Nobile, C.25
Perez-Tur, J.26
Lopez De Munain, A.27
more..
-
10
-
-
0038285465
-
Identification of the promoter, genomic structure, and mouse ortholog of LGI1
-
Somerville RP, Chernova O, Liu S, Shoshan Y, Cowell JK (2000) Identification of the promoter, genomic structure, and mouse ortholog of LGI1. Mamm Genome 11:622-627
-
(2000)
Mamm Genome
, vol.11
, pp. 622-627
-
-
Somerville, R.P.1
Chernova, O.2
Liu, S.3
Shoshan, Y.4
Cowell, J.K.5
-
11
-
-
0036709964
-
The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders
-
Staub E, Perez-Tur J, Siebert R, Nobile C, Moschonas NK, Deloukas P, Hinzmann B (2002) The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders. Trends Biochem Sci 27:441-444
-
(2002)
Trends Biochem Sci
, vol.27
, pp. 441-444
-
-
Staub, E.1
Perez-Tur, J.2
Siebert, R.3
Nobile, C.4
Moschonas, N.K.5
Deloukas, P.6
Hinzmann, B.7
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