RIKEN Center for Brain Science (previously RIKEN Brain Science Institute)
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TitoloCitata daAnno
Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer
T Sato, A Tanigami, K Yamakawa, F Akiyama, F Kasumi, G Sakamoto, ...
Cancer research 50 (22), 7184-7189, 1990
Nav1. 1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation
I Ogiwara, H Miyamoto, N Morita, N Atapour, E Mazaki, I Inoue, ...
Journal of Neuroscience 27 (22), 5903-5914, 2007
A missense mutation of the Na+ channel αII subunit gene Nav1. 2 in a patient with febrile and afebrile seizures causes channel dysfunction
T Sugawara, Y Tsurubuchi, KL Agarwala, M Ito, G Fukuma, ...
Proceedings of the National Academy of Sciences 98 (11), 6384-6389, 2001
Prognostic significance of p53 mutations and 3p deletions in primary resected non-small cell lung cancer
Y Horio, T Takahashi, T Kuroishi, K Hibi, M Suyama, T Niimi, K Shimokata, ...
Cancer research 53 (1), 1-4, 1993
Mutations in EFHC1 cause juvenile myoclonic epilepsy
T Suzuki, AV Delgado-Escueta, K Aguan, ME Alonso, J Shi, Y Hara, ...
Nature genetics 36 (8), 842, 2004
Mutations of sodium channel α subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic–clonic seizures
T Fujiwara, T Sugawara, E Mazaki‐Miyazaki, Y Takahashi, K Fukushima, ...
Brain 126 (3), 531-546, 2003
Three distinct regions involved in 3p deletion in human lung cancer.
K Hibi, T Takahashi, K Yamakawa, R Ueda, Y Sekido, Y Ariyoshi, ...
Oncogene 7 (3), 445-449, 1992
DSCAM: a novel member of the immunoglobulin superfamily maps in a Down syndrome region and is involved in the development of the nervous system
K Yamakawa, YK Huo, MA Haendel, R Hubert, XN Chen, GE Lyons, ...
Human molecular genetics 7 (2), 227-237, 1998
Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy
T Sugawara, E Mazaki–Miyazaki, K Fukushima, J Shimomura, T Fujiwara, ...
Neurology 58 (7), 1122-1124, 2002
A nonsense mutation of the sodium channel gene SCN2A in a patient with intractable epilepsy and mental decline
K Kamiya, M Kaneda, T Sugawara, E Mazaki, N Okamura, M Montal, ...
Journal of Neuroscience 24 (11), 2690-2698, 2004
Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioralá…
S Ganesh, AV Delgado-Escueta, T Sakamoto, MR Avila, ...
Human molecular genetics 11 (11), 1251-1262, 2002
Nav1. 1 mutations cause febrile seizures associated with afebrile partial seizures
T Sugawara, E Mazaki–Miyazaki, M Ito, H Nagafuji, G Fukuma, ...
Neurology 57 (4), 703-705, 2001
Common regions of deletion on chromosomes 5q, 6q, and 10q in renal cell carcinoma
R Morita, S Saito, J Ishikawa, O Ogawa, O Yoshida, K Yamakawa, ...
Cancer research 51 (21), 5817-5820, 1991
A detailed deletion mapping of the short arm of chromosome 3 in sporadic renal cell carcinoma
K Yamakawa, R Morita, E Takahashi, T Hori, J Ishikawa, Y Nakamura
Cancer research 51 (17), 4707-4711, 1991
De novo mutations of voltage-gated sodium channel αII gene SCN2A in intractable epilepsies
I Ogiwara, K Ito, Y Sawaishi, H Osaka, E Mazaki, I Inoue, M Montal, ...
Neurology 73 (13), 1046-1053, 2009
Dosage-dependent over-expression of genes in the trisomic region of Ts1Cje mouse model for Down syndrome
K Amano, H Sago, C Uchikawa, T Suzuki, SE Kotliarova, N Nukina, ...
Human Molecular Genetics 13 (13), 1333-1340, 2004
Laforin, defective in the progressive myoclonus epilepsy of Lafora type, is a dual-specificity phosphatase associated with polyribosomes
S Ganesh, KL Agarwala, K Ueda, T Akagi, K Shoda, T Usui, T Hashikawa, ...
Human molecular genetics 9 (15), 2251-2261, 2000
A Kv4. 2 truncation mutation in a patient with temporal lobe epilepsy
B Singh, I Ogiwara, M Kaneda, N Tokonami, E Mazaki, K Baba, ...
Neurobiology of disease 24 (2), 245-253, 2006
Isolation and characterization of 19 dinucleotide repeat polymorphisms on chromosome 3p
MH Jones, K Yamakawa, Y Nakamura
Human molecular genetics 1 (2), 131-133, 1992
Mitochondrial dysfunction and tau hyperphosphorylation in Ts1Cje, a mouse model for Down syndrome
EA Shukkur, A Shimohata, T Akagi, W Yu, M Yamaguchi, M Murayama, ...
Human molecular genetics 15 (18), 2752-2762, 2006
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