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KAZUHIRO YAMAKAWA
KAZUHIRO YAMAKAWA
Nagoya City University Graduate School of Medical Sciences
Verified email at med.nagoya-cu.ac.jp - Homepage
Title
Cited by
Cited by
Year
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
9312007
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
6511990
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
5442001
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
4351993
Mutations in EFHC1 cause juvenile myoclonic epilepsy
T Suzuki, AV Delgado-Escueta, K Aguan, ME Alonso, J Shi, Y Hara, ...
Nature genetics 36 (8), 842-849, 2004
4192004
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
4092003
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
3621992
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
3461998
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
2992002
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
2662004
Targeted disruption of the Epm2a gene causes formation of Lafora inclusion bodies, neurodegeneration, ataxia, myoclonus epilepsy and impaired behavioral …
S Ganesh, AV Delgado-Escueta, T Sakamoto, MR Avila, ...
Human molecular genetics 11 (11), 1251-1262, 2002
2592002
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
2452009
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
2292019
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
2202001
Comparative analyses of copy-number variation in autism spectrum disorder and schizophrenia reveal etiological overlap and biological insights
I Kushima, B Aleksic, M Nakatochi, T Shimamura, T Okada, Y Uno, ...
Cell reports 24 (11), 2838-2856, 2018
2112018
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
1971991
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
1831991
Consensus on diagnosis and management of JME: from founder's observations to current trends
DGAKN Trenité, B Schmitz, D Janz, AV Delgado-Escueta, P Thomas, ...
Epilepsy & Behavior 28, S87-S90, 2013
1822013
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
1782004
Nav1. 1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndrome
I Ogiwara, T Iwasato, H Miyamoto, R Iwata, T Yamagata, E Mazaki, ...
Human molecular genetics 22 (23), 4784-4804, 2013
1772013
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