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Papers authored by Nanba E

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Inhibition of autophagosome formation restores mitochondrial function in mucolipidosis II and III skin fibroblasts.

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Otomo T, Higaki K, Nanba E, Ozono K, and Sakai N

Molecular genetics and metabolism 98(4):393-9, 2009 Dec - Who cited this? | PubMed ID: 19656701 | Fulltext

Intracerebral cell transplantation therapy for murine GM1 gangliosidosis.

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Sawada T, Tanaka A, Higaki K, Takamura A, Nanba E, Seto T, Maeda M, Yamaguchi E, Matsuda J, and Yamano T

Brain & development 31(10):717-24, 2009 Nov - Who cited this? | PubMed ID: 19118961 | Fulltext

Synthesis of new camptothecin analogs with improved antitumor activities.

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Niizuma S, Tsukazaki M, Suda H, Murata T, Ohwada J, Ozawa S, Fukuda H, Murasaki C, Kohchi M, Morikami K, Yoshinari K, Endo M, Ura M, Tanimura H, Miyazaki Y, Takasuka T,

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Bioorganic & medicinal chemistry letters 19(7):2018-21, 2009 Apr 1 - Who cited this? | PubMed ID: 19254843 | Fulltext

A case of adult onset metachromatic leukodystrophy.

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Ito K, Miura N, Awata S, Nanba E, and Matsuoka H

Psychiatry and clinical neurosciences 63(1):127, 2009 Feb - Who cited this? | PubMed ID: 19154224 | Fulltext

Aberrant promoter methylation and expression of the imprinted PEG3 gene in glioma.

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Otsuka S, Maegawa S, Takamura A, Kamitani H, Watanabe T, Oshimura M, and Nanba E

Proceedings of the Japan Academy. Series B, Physical and biological sciences 85(4):157-65, 2009 - Who cited this? | PubMed ID: 19367087 | Fulltext

Ubiquitin-proteasome system impairment caused by a missense cardiac myosin-binding protein C mutation and associated with cardiac dysfunction in hypertrophic cardiomyopathy.

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Bahrudin U, Morisaki H, Morisaki T, Ninomiya H, Higaki K, Nanba E, Igawa O, Takashima S, Mizuta E, Miake J, Yamamoto Y, Shirayoshi Y, Kitakaze M, Carrier L, and Hisatome I

Journal of molecular biology 384(4):896-907, 2008 Dec 26 - Who cited this? | PubMed ID: 18929575 | Fulltext

A Novel Mutation in the Arylsulfatase A Gene Associated with Adult-Onset Metachromatic Leukodystrophy without Clinical Evidence of Neuropathy.

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Suzuki C, Watanabe M, Tomiyama M, Sugimoto K, Nanba E, Jackson M, Kimura T, Seino Y, Wakasaya Y, Kawarabayashi T, Miki Y, Yamamoto-Watanabe Y, and Shoji M

European neurology 60(6):310-311, 2008 Oct 3 - Who cited this? | PubMed ID: 18832844 | Fulltext

Association of the neuronal cell adhesion molecule (NRCAM) gene variants with autism.

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Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, and Kato N

The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP):1, 2008 Jul 30 - Who cited this? | PubMed ID: 18664314 | Fulltext

Novel beta-galactosidase gene mutation p.W273R in a woman with mucopolysaccharidosis type IVB (Morquio B) and lack of response to in vitro chaperone treatment of her skin fibroblasts.

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Gucev ZS, Tasic V, Jancevska A, Zafirovski G, Kremensky I, Sinigerska I, Nanba E, Higaki K, Gucev F, and Suzuki Y

American journal of medical genetics. Part A 146A(13):1736-40, 2008 Jul 1 - Who cited this? | PubMed ID: 18546276 | Fulltext

No association between the ryanodine receptor 3 gene and autism in a Japanese population.

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Tochigi M, Kato C, Ohashi J, Koishi S, Kawakubo Y, Yamamoto K, Matsumoto H, Hashimoto O, Kim SY, Watanabe K, Kano Y, Nanba E, Kato N, and Sasaki T

Psychiatry and clinical neurosciences 62(3):341, 2008 Jun - Who cited this? | PubMed ID: 18588595 | Fulltext

Association study of the commonly recognized breakpoints in chromosome 15q11-q13 in Japanese autistic patients.

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Kato C, Tochigi M, Koishi S, Kawakubo Y, Yamamoto K, Matsumoto H, Hashimoto O, Kim SY, Watanabe K, Kano Y, Nanba E, Kato N, and Sasaki T

Psychiatric genetics 18(3):133-6, 2008 Jun - Who cited this? | PubMed ID: 18496211 | Fulltext

A case of galactosialidosis with a homozygous Q49R point mutation.

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Matsumoto N, Gondo K, Kukita J, Higaki K, Paragison RC, and Nanba E

Brain & development, 2008 Apr 4 - Who cited this? | PubMed ID: 18396002 | Fulltext

Enhanced autophagy and mitochondrial aberrations in murine G(M1)-gangliosidosis.

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Takamura A, Higaki K, Kajimaki K, Otsuka S, Ninomiya H, Matsuda J, Ohno K, Suzuki Y, and Nanba E

Biochemical and biophysical research communications 367(3):616, 2008 Mar 14 - Who cited this? | PubMed ID: 18190792 | Fulltext

Mental retardation, spasticity, basal ganglia calcification, cerebral white matter lesions, multiple endocrine defects, telangiectasia and atrophic skin: A new syndrome?.

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Saito Y, Toyoshima M, Oka A, Zhuo L, Moriwaki S, Yamamoto O, Kanzaki S, Hanaki K, Ninomiya H, Nanba E, Kondo A, Maegaki Y, and Ohno K

Brain & development 30(3):221-5, 2008 Mar - Who cited this? | PubMed ID: 17870267 | Fulltext

Association study of the 15q11-q13 maternal expression domain in Japanese autistic patients.

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Kato C, Tochigi M, Ohashi J, Koishi S, Kawakubo Y, Yamamoto K, Matsumoto H, Hashimoto O, Kim SY, Watanabe K, Kano Y, Nanba E, Kato N, and Sasaki T

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics, 2008 Jan 9 - Who cited this? | PubMed ID: 18186074 | Fulltext

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.

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Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, Nicod J,

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Molecular psychiatry 12(12):1129-39, 2007 Dec - Who cited this? | PubMed ID: 17667961 | Fulltext

LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells.

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Francks C, Maegawa S, Laurén J, Abrahams BS, Velayos-Baeza A, Medland SE, Colella S, Groszer M, McAuley EZ, Caffrey TM, Timmusk T, Pruunsild P, Koppel I, Lind PA, Matsumoto-Itaba N, Nicod J,

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Molecular psychiatry 12(12):1057, 2007 Dec - Who cited this? | PubMed ID: 18043708 | Fulltext

Chemical chaperone therapy: clinical effect in murine G(M1)-gangliosidosis.

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Suzuki Y, Ichinomiya S, Kurosawa M, Ohkubo M, Watanabe H, Iwasaki H, Matsuda J, Noguchi Y, Takimoto K, Itoh M, Tabe M, Iida M, Kubo T, Ogawa S, Nanba E, Higaki K,

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Annals of neurology 62(6):671-5, 2007 Dec - Who cited this? | PubMed ID: 17994547 | Fulltext

Tachykinin 1 (TAC1) gene SNPs and haplotypes with autism: a case-control study.

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Marui T, Funatogawa I, Koishi S, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Kato N, and Sasaki T

Brain & development 29(8):510, 2007 Sep - Who cited this? | PubMed ID: 17376622 | Fulltext

Imprinting status of paternally imprinted DLX5 gene in Japanese patients with Rett syndrome.

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Itaba-Matsumoto N, Maegawa S, Yamagata H, Kondo I, Oshimura M, and Nanba E

Brain & development 29(8):491-5, 2007 Sep - Who cited this? | PubMed ID: 17363207 | Fulltext

Antisense suppression of TSC1 gene product, hamartin, enhances neurite outgrowth in NGF-treated PC12h cells.

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Floricel F, Higaki K, Maki H, Nanba E, Ninomiya H, and Ohno K

Brain & development 29(8):502-9, 2007 Sep - Who cited this? | PubMed ID: 17376623 | Fulltext

Cyclohexenonic long-chain fatty alcohol has therapeutic effects on diabetes-induced angiopathy in the rat aorta.

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Shinbori C, Saito M, Kinoshita Y, Satoh I, Kono T, Hanada T, Nanba E, Adachi K, Suzuki H, Yamada M, and Satoh K

European journal of pharmacology 567(1-2):139-44, 2007 Jul 12 - Who cited this? | PubMed ID: 17499713 | Fulltext

No association between the neuronal pentraxin II gene polymorphism and autism.

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Marui T, Koishi S, Funatogawa I, Yamamoto K, Matsumoto H, Hashimoto O, Ishijima M, Nanba E, Nishida H, Sugiyama T, Kasai K, Watanabe K, Kano Y, Kato N, and Sasaki T

Progress in neuro-psychopharmacology & biological psychiatry 31(4):940, 2007 May 9 - Who cited this? | PubMed ID: 17408830 | Fulltext

The TSC1 gene product hamartin interacts with NADE.

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Yasui S, Tsuzaki K, Ninomiya H, Floricel F, Asano Y, Maki H, Takamura A, Nanba E, Higaki K, and Ohno K

Molecular and cellular neurosciences 35(1):100-8, 2007 May - Who cited this? | PubMed ID: 17355907 | Fulltext

Variation analysis of beta3-adrenergic receptor and melanocortin-4 receptor genes in childhood obesity.

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Kinoshita T, Hanaki K, Nagaishi J, Kawashima Y, Adachi K, Nanba E, and Kanzaki S

Pediatrics international : official journal of the Japan Pediatric Society 49(2):133-7, 2007 Apr - Who cited this? | PubMed ID: 17445027 | Fulltext

Enhanced autophagic cell death in expanded polyhistidine variants of HOXA1 reduces PBX1-coupled transcriptional activity and inhibits neuronal differentiation.

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Paraguison RC, Higaki K, Yamamoto K, Matsumoto H, Sasaki T, Kato N, and Nanba E

Journal of neuroscience research 85(3):479, 2007 Feb 15 - Who cited this? | PubMed ID: 17131398 | Fulltext

No evidence for significant association between GABA receptor genes in chromosome 15q11-q13 and autism in a Japanese population.

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Tochigi M, Kato C, Koishi S, Kawakubo Y, Yamamoto K, Matsumoto H, Hashimoto O, Kim SY, Watanabe K, Kano Y, Nanba E, Kato N, and Sasaki T

Journal of human genetics 52(12):985-9, 2007 - Who cited this? | PubMed ID: 17957331 | Fulltext

Characteristic findings of auditory brainstem response and otoacoustic emission in the Bronx waltzer mouse.

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Inagaki M, Kon K, Suzuki S, Kobayashi N, Kaga M, and Nanba E

Brain & development 28(10):617-24, 2006 Nov - Who cited this? | PubMed ID: 16730938 | Fulltext

[Biemond syndrome].

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Nanba E

Nippon rinsho. Japanese journal of clinical medicine Suppl 3:401-5, 2006 Sep 28 - Who cited this? | PubMed ID: 17022573 | Fulltext

N-hexacosanol reverses diabetic induced muscarinic hypercontractility of ileum in the rat.

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Shinbori C, Saito M, Kinoshita Y, Satoh I, Kono T, Hanada T, Nanba E, Adachi K, Suzuki H, Yamada M, and Satoh K

European journal of pharmacology 545(2-3):177-84, 2006 Sep 18 - Who cited this? | PubMed ID: 16872599 | Fulltext

Fibroblast screening for chaperone therapy in beta-galactosidosis.

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Iwasaki H, Watanabe H, Iida M, Ogawa S, Tabe M, Higaki K, Nanba E, and Suzuki Y

Brain & development 28(8):482-6, 2006 Sep - Who cited this? | PubMed ID: 16617000 | Fulltext

Serotonin transporter gene promoter polymorphism and autism: a family-based genetic association study in Japanese population.

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Koishi S, Yamamoto K, Matsumoto H, Koishi S, Enseki Y, Oya A, Asakura A, Aoki Y, Atsumi M, Iga T, Inomata J, Inoko H, Sasaki T, Nanba E, Kato N, Ishii T,

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Brain & development 28(4):257-60, 2006 May - Who cited this? | PubMed ID: 16481140 | Fulltext

Evidence for proteasomal degradation of Kv1.5 channel protein.

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Kato M, Ogura K, Miake J, Sasaki N, Taniguchi S, Igawa O, Yoshida A, Hoshikawa Y, Murata M, Nanba E, Kurata Y, Kawata Y, Ninomiya H, Morisaki T, Kitakaze M, and Hisatome I

Biochemical and biophysical research communications 337(1):343-8, 2005 Nov 11 - Who cited this? | PubMed ID: 16185660 | Fulltext

Polyhistidine tract expansions in HOXA1 result in intranuclear aggregation and increased cell death.

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Paraguison RC, Higaki K, Sakamoto Y, Hashimoto O, Miyake N, Matsumoto H, Yamamoto K, Sasaki T, Kato N, and Nanba E

Biochemical and biophysical research communications 336(4):1033-9, 2005 Nov 4 - Who cited this? | PubMed ID: 16168961 | Fulltext

Subtype switching of T-type Ca 2+ channels from Cav3.2 to Cav3.1 during differentiation of embryonic stem cells to cardiac cell lineage.

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Mizuta E, Miake J, Yano S, Furuichi H, Manabe K, Sasaki N, Igawa O, Hoshikawa Y, Shigemasa C, Nanba E, Ninomiya H, Hidaka K, Morisaki T, Tajima F, and Hisatome I

Circulation journal : official journal of the Japanese Circulation Society 69(10):1284-9, 2005 Oct - Who cited this? | PubMed ID: 16195632 | Fulltext

No association of FOXP2 and PTPRZ1 on 7q31 with autism from the Japanese population.

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Marui T, Koishi S, Funatogawa I, Yamamoto K, Matsumoto H, Hashimoto O, Nanba E, Kato C, Ishijima M, Watanabe K, Kasai K, Kato N, and Sasaki T

Neuroscience research 53(1):91-4, 2005 Sep - Who cited this? | PubMed ID: 15998549 | Fulltext

Mutation at cleavage site of insulin-like growth factor receptor in a short-stature child born with intrauterine growth retardation.

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Kawashima Y, Kanzaki S, Yang F, Kinoshita T, Hanaki K, Nagaishi J, Ohtsuka Y, Hisatome I, Ninomoya H, Nanba E, Fukushima T, and Takahashi S

The Journal of clinical endocrinology and metabolism 90(8):4679-87, 2005 Aug - Who cited this? | PubMed ID: 15928254 | Fulltext

Proteasomal degradation of Kir6.2 channel protein and its inhibition by a Na+ channel blocker aprindine.

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Tanaka H, Miake J, Notsu T, Sonyama K, Sasaki N, Iitsuka K, Kato M, Taniguchi S, Igawa O, Yoshida A, Shigemasa C, Hoshikawa Y, Kurata Y, Kuniyasu A, Nakayama H, Inagaki N,

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Biochemical and biophysical research communications 331(4):1001-6, 2005 Jun 17 - Who cited this? | PubMed ID: 15882977 | Fulltext

[Myotonic dystrophy].

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Nanba E

Nippon rinsho. Japanese journal of clinical medicine 63(3):429-33, 2005 Mar - Who cited this? | PubMed ID: 15773341 | Fulltext

Functional assessment of ABCG2 (BCRP) gene polymorphisms to protein expression in human placenta.

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Kobayashi D, Ieiri I, Hirota T, Takane H, Maegawa S, Kigawa J, Suzuki H, Nanba E, Oshimura M, Terakawa N, Otsubo K, Mine K, and Sugiyama Y

Drug metabolism and disposition: the biological fate of chemicals 33(1):94-101, 2005 Jan - Who cited this? | PubMed ID: 15475413 | Fulltext

Allelic expression imbalance of the human CYP3A4 gene and individual phenotypic status.

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Hirota T, Ieiri I, Takane H, Maegawa S, Hosokawa M, Kobayashi K, Chiba K, Nanba E, Oshimura M, Sato T, Higuchi S, and Otsubo K

Human molecular genetics 13(23):2959-69, 2004 Dec 1 - Who cited this? | PubMed ID: 15459178 | Fulltext

Association between the neurofibromatosis-1 (NF1) locus and autism in the Japanese population.

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Marui T, Hashimoto O, Nanba E, Kato C, Tochigi M, Umekage T, Ishijima M, Kohda K, Kato N, and Sasaki T

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 131(1):43-7, 2004 Nov 15 - Who cited this? | PubMed ID: 15389774 | Fulltext

Expression of HSP 70 and its mRNAS during ischemia-reperfusion in the rat bladder.

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Saito M, Tominaga L, Nanba E, Kinoshita Y, Housi D, Miyagawa I, and Satoh K

Life sciences 75(15):1879-86, 2004 Aug 27 - Who cited this? | PubMed ID: 15302231 | Fulltext

N-octyl-beta-valienamine up-regulates activity of F213I mutant beta-glucosidase in cultured cells: a potential chemical chaperone therapy for Gaucher disease.

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Lin H, Sugimoto Y, Ohsaki Y, Ninomiya H, Oka A, Taniguchi M, Ida H, Eto Y, Ogawa S, Matsuzaki Y, Sawa M, Inoue T, Higaki K, Nanba E, Ohno K, and Suzuki Y

Biochimica et biophysica acta 1689(3):219-28, 2004 Aug 4 - Who cited this? | PubMed ID: 15276648 | Fulltext

[A case of middle-aged onset sialidosis type I].

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Sakazume Y, Tanaka M, Isobe I, Tominaga R, Nanba E, and Okamoto K

Rinsho shinkeigaku = Clinical neurology 44(8):541-4, 2004 Aug - Who cited this? | PubMed ID: 15471091 | Fulltext

State-dependent blocking actions of azimilide dihydrochlo-ride (NE-10064) on human cardiac Na(+) channels.

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Miake J, Kurata Y, Iizuka K, Furuichi H, Manabe K, Sasaki N, Yamamoto Y, Hoshikawa Y, Taniguchi S, Yoshida A, Igawa O, Makita N, Shiota G, Nanba E, Ohgi S, Narahashi T,

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Circulation journal : official journal of the Japanese Circulation Society 68(7):703-11, 2004 Jul - Who cited this? | PubMed ID: 15226638 | Fulltext

Developmental changes of Ni(2+) sensitivity and automaticity in Nkx2.5-positive cardiac precursor cells from murine embryonic stem cell.

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Manabe K, Miake J, Sasaki N, Furuichi H, Yano S, Mizuta E, Yamamoto Y, Hoshikawa Y, Yamazaki H, Tajima F, Shiota G, Nanba E, Ohgi S, Hidaka K, Morisaki T, Kurata Y,

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Circulation journal : official journal of the Japanese Circulation Society 68(7):724-6, 2004 Jul - Who cited this? | PubMed ID: 15226643 | Fulltext

Increased NPC1 mRNA in skin fibroblasts from Niemann-Pick disease type C patients.

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Yamamoto T, Feng JH, Higaki K, Taniguchi M, Nanba E, Ninomiya H, and Ohno K

Brain & development 26(4):245-50, 2004 Jun - Who cited this? | PubMed ID: 15130691 | Fulltext

Novel TSC2 mutations and decreased expression of tuberin in cultured tumor cells with an insertion mutation.

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Feng JH, Yamamoto T, Nanba E, Ninomiya H, Oka A, and Ohno K

Human mutation 23(4):397, 2004 Apr - Who cited this? | PubMed ID: 15024740 | Fulltext

Expression of heat shock protein 70 and its mRNAs during ischemia-reperfusion in the rat prostate.

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Saito M, Tominaga L, Nanba E, and Miyagawa I

European journal of pharmacology 487(1-3):199-203, 2004 Mar 8 - Who cited this? | PubMed ID: 15033392 | Fulltext

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