Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 41

1.

Impaired cortico-striatal excitatory transmission triggers epilepsy.

Miyamoto H, Tatsukawa T, Shimohata A, Yamagata T, Suzuki T, Amano K, Mazaki E, Raveau M, Ogiwara I, Oba-Asaka A, Hensch TK, Itohara S, Sakimura K, Kobayashi K, Kobayashi K, Yamakawa K.

Nat Commun. 2019 Apr 23;10(1):1917. doi: 10.1038/s41467-019-09954-9.

2.

Scn2a haploinsufficient mice display a spectrum of phenotypes affecting anxiety, sociability, memory flexibility and ampakine CX516 rescues their hyperactivity.

Tatsukawa T, Raveau M, Ogiwara I, Hattori S, Miyamoto H, Mazaki E, Itohara S, Miyakawa T, Montal M, Yamakawa K.

Mol Autism. 2019 Mar 28;10:15. doi: 10.1186/s13229-019-0265-5. eCollection 2019.

3.

[18F]fluorodeoxyglucose-positron emission tomography study of genetically confirmed patients with Dravet syndrome.

Haginoya K, Togashi N, Kaneta T, Hino-Fukuyo N, Ishitobi M, Kakisaka Y, Uematsu M, Inui T, Okubo Y, Sato R, Miyabayashi T, Arai A, Ogiwara I, Mazaki E, Yamakawa K, Iinuma K, Kure S.

Epilepsy Res. 2018 Nov;147:9-14. doi: 10.1016/j.eplepsyres.2018.08.008. Epub 2018 Aug 27.

PMID:
30176532
4.

Nav1.2 haplodeficiency in excitatory neurons causes absence-like seizures in mice.

Ogiwara I, Miyamoto H, Tatsukawa T, Yamagata T, Nakayama T, Atapour N, Miura E, Mazaki E, Ernst SJ, Cao D, Ohtani H, Itohara S, Yanagawa Y, Montal M, Yuzaki M, Inoue Y, Hensch TK, Noebels JL, Yamakawa K.

Commun Biol. 2018;1. pii: 96. doi: 10.1038/s42003-018-0099-2. Epub 2018 Jul 19.

5.

Altered hippocampal replay is associated with memory impairment in mice heterozygous for the Scn2a gene.

Middleton SJ, Kneller EM, Chen S, Ogiwara I, Montal M, Yamakawa K, McHugh TJ.

Nat Neurosci. 2018 Jul;21(7):996-1003. doi: 10.1038/s41593-018-0163-8. Epub 2018 Jun 4.

PMID:
29867081
6.

Impairments in social novelty recognition and spatial memory in mice with conditional deletion of Scn1a in parvalbumin-expressing cells.

Tatsukawa T, Ogiwara I, Mazaki E, Shimohata A, Yamakawa K.

Neurobiol Dis. 2018 Apr;112:24-34. doi: 10.1016/j.nbd.2018.01.009. Epub 2018 Jan 11.

PMID:
29337050
7.

Nav1.2 is expressed in caudal ganglionic eminence-derived disinhibitory interneurons: Mutually exclusive distributions of Nav1.1 and Nav1.2.

Yamagata T, Ogiwara I, Mazaki E, Yanagawa Y, Yamakawa K.

Biochem Biophys Res Commun. 2017 Sep 30;491(4):1070-1076. doi: 10.1016/j.bbrc.2017.08.013. Epub 2017 Aug 4.

PMID:
28784306
8.

Construction of Models for Nondestructive Prediction of Ingredient Contents in Blueberries by Near-infrared Spectroscopy Based on HPLC Measurements.

Bai W, Yoshimura N, Takayanagi M, Che J, Horiuchi N, Ogiwara I.

J Vis Exp. 2016 Jun 28;(112). doi: 10.3791/53981.

9.

Removal of redundant contigs from de novo RNA-Seq assemblies via homology search improves accurate detection of differentially expressed genes.

Ono H, Ishii K, Kozaki T, Ogiwara I, Kanekatsu M, Yamada T.

BMC Genomics. 2015 Dec 4;16:1031. doi: 10.1186/s12864-015-2247-0.

10.

Singular localization of sodium channel β4 subunit in unmyelinated fibres and its role in the striatum.

Miyazaki H, Oyama F, Inoue R, Aosaki T, Abe T, Kiyonari H, Kino Y, Kurosawa M, Shimizu J, Ogiwara I, Yamakawa K, Koshimizu Y, Fujiyama F, Kaneko T, Shimizu H, Nagatomo K, Yamada K, Shimogori T, Hattori N, Miura M, Nukina N.

Nat Commun. 2014 Nov 21;5:5525. doi: 10.1038/ncomms6525.

PMID:
25413837
11.

Expression of an AtNAP gene homolog in senescing morning glory (Ipomoea nil) petals of two cultivars with a different flower life span.

Shinozaki Y, Tanaka T, Ogiwara I, Kanekatsu M, van Doorn WG, Yamada T.

J Plant Physiol. 2014 May 1;171(8):633-8. doi: 10.1016/j.jplph.2014.01.008. Epub 2014 Mar 20.

PMID:
24709156
12.

Length of the dark period affects flower opening and the expression of circadian-clock associated genes as well as xyloglucan endotransglucosylase/hydrolase genes in petals of morning glory (Ipomoea nil).

Shinozaki Y, Tanaka R, Ono H, Ogiwara I, Kanekatsu M, van Doorn WG, Yamada T.

Plant Cell Rep. 2014 Jul;33(7):1121-31. doi: 10.1007/s00299-014-1601-z. Epub 2014 Mar 29.

PMID:
24682460
13.

Tumor suppression effects of bilberry extracts and enzymatically modified isoquercitrin in early preneoplastic liver cell lesions induced by piperonyl butoxide promotion in a two-stage rat hepatocarcinogenesis model.

Hara S, Morita R, Ogawa T, Segawa R, Takimoto N, Suzuki K, Hamadate N, Hayashi SM, Odachi A, Ogiwara I, Shibusawa S, Yoshida T, Shibutani M.

Exp Toxicol Pathol. 2014 Aug;66(5-6):225-34. doi: 10.1016/j.etp.2014.02.002. Epub 2014 Mar 26.

PMID:
24680176
14.

Altered cardiac electrophysiology and SUDEP in a model of Dravet syndrome.

Auerbach DS, Jones J, Clawson BC, Offord J, Lenk GM, Ogiwara I, Yamakawa K, Meisler MH, Parent JM, Isom LL.

PLoS One. 2013 Oct 14;8(10):e77843. doi: 10.1371/journal.pone.0077843. eCollection 2013.

15.

Nav1.1 haploinsufficiency in excitatory neurons ameliorates seizure-associated sudden death in a mouse model of Dravet syndrome.

Ogiwara I, Iwasato T, Miyamoto H, Iwata R, Yamagata T, Mazaki E, Yanagawa Y, Tamamaki N, Hensch TK, Itohara S, Yamakawa K.

Hum Mol Genet. 2013 Dec 1;22(23):4784-804. doi: 10.1093/hmg/ddt331. Epub 2013 Aug 6.

16.

A homozygous mutation of voltage-gated sodium channel β(I) gene SCN1B in a patient with Dravet syndrome.

Ogiwara I, Nakayama T, Yamagata T, Ohtani H, Mazaki E, Tsuchiya S, Inoue Y, Yamakawa K.

Epilepsia. 2012 Dec;53(12):e200-3. doi: 10.1111/epi.12040. Epub 2012 Nov 13.

17.

Mouse with Nav1.1 haploinsufficiency, a model for Dravet syndrome, exhibits lowered sociability and learning impairment.

Ito S, Ogiwara I, Yamada K, Miyamoto H, Hensch TK, Osawa M, Yamakawa K.

Neurobiol Dis. 2013 Jan;49:29-40. doi: 10.1016/j.nbd.2012.08.003. Epub 2012 Aug 16.

PMID:
22986304
18.

Efficacy of stiripentol in hyperthermia-induced seizures in a mouse model of Dravet syndrome.

Cao D, Ohtani H, Ogiwara I, Ohtani S, Takahashi Y, Yamakawa K, Inoue Y.

Epilepsia. 2012 Jul;53(7):1140-5. doi: 10.1111/j.1528-1167.2012.03497.x. Epub 2012 May 11.

19.

Different degrees of loss of function between GEFS+ and SMEI Nav 1.1 missense mutants at the same residue induced by rescuable folding defects.

Sugiura Y, Ogiwara I, Hoshi A, Yamakawa K, Ugawa Y.

Epilepsia. 2012 Jun;53(6):e111-4. doi: 10.1111/j.1528-1167.2012.03467.x. Epub 2012 Apr 23.

20.

Acute encephalopathy in a patient with Dravet syndrome.

Tsuji M, Mazaki E, Ogiwara I, Wada T, Iai M, Okumura A, Yamashita S, Yamakawa K, Osaka H.

Neuropediatrics. 2011 Feb;42(2):78-81. doi: 10.1055/s-0031-1279725. Epub 2011 Jun 6.

PMID:
21647847
21.

Deletions of SCN1A 5' genomic region with promoter activity in Dravet syndrome.

Nakayama T, Ogiwara I, Ito K, Kaneda M, Mazaki E, Osaka H, Ohtani H, Inoue Y, Fujiwara T, Uematsu M, Haginoya K, Tsuchiya S, Yamakawa K.

Hum Mutat. 2010 Jul;31(7):820-9. doi: 10.1002/humu.21275.

PMID:
20506560
22.

De novo mutations of voltage-gated sodium channel alphaII gene SCN2A in intractable epilepsies.

Ogiwara I, Ito K, Sawaishi Y, Osaka H, Mazaki E, Inoue I, Montal M, Hashikawa T, Shike T, Fujiwara T, Inoue Y, Kaneda M, Yamakawa K.

Neurology. 2009 Sep 29;73(13):1046-53. doi: 10.1212/WNL.0b013e3181b9cebc.

23.

Nav1.1 localizes to axons of parvalbumin-positive inhibitory interneurons: a circuit basis for epileptic seizures in mice carrying an Scn1a gene mutation.

Ogiwara I, Miyamoto H, Morita N, Atapour N, Mazaki E, Inoue I, Takeuchi T, Itohara S, Yanagawa Y, Obata K, Furuichi T, Hensch TK, Yamakawa K.

J Neurosci. 2007 May 30;27(22):5903-14.

24.

Patients with a sodium channel alpha 1 gene mutation show wide phenotypic variation.

Osaka H, Ogiwara I, Mazaki E, Okamura N, Yamashita S, Iai M, Yamada M, Kurosawa K, Iwamoto H, Yasui-Furukori N, Kaneko S, Fujiwara T, Inoue Y, Yamakawa K.

Epilepsy Res. 2007 Jun;75(1):46-51. Epub 2007 May 15.

PMID:
17507202
25.

Flower color alteration in Lotus japonicus by modification of the carotenoid biosynthetic pathway.

Suzuki S, Nishihara M, Nakatsuka T, Misawa N, Ogiwara I, Yamamura S.

Plant Cell Rep. 2007 Jul;26(7):951-9. Epub 2007 Jan 31.

PMID:
17265153
26.

SCN1A mutation mosaicism in a family with severe myoclonic epilepsy in infancy.

Morimoto M, Mazaki E, Nishimura A, Chiyonobu T, Sawai Y, Murakami A, Nakamura K, Inoue I, Ogiwara I, Sugimoto T, Yamakawa K.

Epilepsia. 2006 Oct;47(10):1732-6.

27.

A Kv4.2 truncation mutation in a patient with temporal lobe epilepsy.

Singh B, Ogiwara I, Kaneda M, Tokonami N, Mazaki E, Baba K, Matsuda K, Inoue Y, Yamakawa K.

Neurobiol Dis. 2006 Nov;24(2):245-53. Epub 2006 Aug 24.

PMID:
16934482
28.

Physiological changes in gentian axillary buds during two-step preculturing with sucrose that conferred high levels of tolerance to desiccation and cryopreservation.

Suzuki M, Ishikawa M, Okuda H, Noda K, Kishimoto T, Nakamura T, Ogiwara I, Shimura I, Akihama T.

Ann Bot. 2006 Jun;97(6):1073-81. Epub 2006 Mar 24.

29.

Sodium channel dysfunction in intractable childhood epilepsy with generalized tonic-clonic seizures.

Rhodes TH, Vanoye CG, Ohmori I, Ogiwara I, Yamakawa K, George AL Jr.

J Physiol. 2005 Dec 1;569(Pt 2):433-45. Epub 2005 Oct 6.

30.

Role of the C-terminal domain of RNA polymerase II in U2 snRNA transcription and 3' processing.

Jacobs EY, Ogiwara I, Weiner AM.

Mol Cell Biol. 2004 Jan;24(2):846-55.

32.

Retropositional parasitism of SINEs on LINEs: identification of SINEs and LINEs in elasmobranchs.

Ogiwara I, Miya M, Ohshima K, Okada N.

Mol Biol Evol. 1999 Sep;16(9):1238-50.

PMID:
10486979
33.

SINEs and LINEs share common 3' sequences: a review.

Okada N, Hamada M, Ogiwara I, Ohshima K.

Gene. 1997 Dec 31;205(1-2):229-43. Review.

PMID:
9461397
34.

Effect of ooplast activation on the development of oocytes following nucleus transfer in cattle.

Kono T, Sotomaru Y, Aono F, Takahasi T, Ogiwara I, Sekizawa F, Arai T, Nakahara T.

Theriogenology. 1994;41(7):1463-71.

PMID:
16727500
35.

[Morphological studies of Japanese mandibular third molars].

Ogiwara I.

Shikwa Gakuho. 1985 Apr;85(4):453-83. Japanese. No abstract available.

PMID:
3862240
36.

[Morphological characteristics of Japanese mandibular third molars- roots number and accessory root (author's transl)].

Ogiwara I, Adachi M, Morita T.

Shikwa Gakuho. 1981 May;81(5):889-98. Japanese. No abstract available.

PMID:
6944804
37.

[A study in two cases of maxillary prismaticher molar (hypertaurodont) (author's transl)].

Ogiwara I.

Shikwa Gakuho. 1978 Oct;78(10):1583-6. Japanese. No abstract available.

PMID:
297307
38.

[4 cases of the upper canine erupting in the palate].

Ogiwara I.

Shikwa Gakuho. 1967 Mar;67(3):419-22. Japanese. No abstract available.

PMID:
5234656
39.

[Rare case of fusion of the upper incisor and lateral incisor associated with abnormal labial cusp].

Ogiwara I.

Shikwa Gakuho. 1966 Jul;66(7):653-6. Japanese. No abstract available.

PMID:
5229508
40.

[Supernumerary teeth appearing on the labial or buccal surface. With special reference to unusual cases].

Ogiwara I.

Shikwa Gakuho. 1966 Mar;66(3):48-52. Japanese. No abstract available.

PMID:
5220545
41.

[A case report of partial anodontia with visceral inversion].

Ogiwara I.

Shikwa Gakuho. 1965 Nov;65(11):41-5. Japanese. No abstract available.

PMID:
5216032

Supplemental Content

Loading ...
Support Center