Onodera O - Search Results

1

ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19.

Takahashi Y, Fukuda Y, Yoshimura J, Toyoda A, Kurppa K, Moritoyo H, Belzil VV, Dion PA, Higasa K, Doi K, Ishiura H, Mitsui J, Date H, Ahsan B, Matsukawa T, Ichikawa Y, Moritoyo T, Ikoma M, Hashimoto T, Kimura F, Murayama S, Onodera O, Nishizawa M, Yoshida M, Atsuta N, Sobue G; JaCALS; Fifita JA, Williams KL, Blair IP, Nicholson GA, Gonzalez-Perez P, Brown RH Jr, Nomoto M, Elenius K, Rouleau GA, Fujiyama A, Morishita S, Goto J, Tsuji S. Takahashi Y, et al. Among authors: onodera o. Am J Hum Genet. 2013 Nov 7;93(5):900-5. doi: 10.1016/j.ajhg.2013.09.008. Epub 2013 Oct 10. Am J Hum Genet. 2013. PMID: 24119685 Free PMC article.

2

Genomic organization of a cDNA (QM) demonstrating an altered mRNA level in nontumorigenic Wilms' microcell hybrid cells and its localization to Xq28.

Kaneko K, Kobayashi H, Onodera O, Miyatake T, Tsuji S. Kaneko K, et al. Among authors: onodera o. Hum Mol Genet. 1992 Oct;1(7):529-33. doi: 10.1093/hmg/1.7.529. Hum Mol Genet. 1992. PMID: 1339145

3

Rapid diagnosis of tuberculous meningitis by polymerase chain reaction (PCR).

Kaneko K, Onodera O, Miyatake T, Tsuji S. Kaneko K, et al. Among authors: onodera o. Neurology. 1990 Oct;40(10):1617-8. doi: 10.1212/wnl.40.10.1617. Neurology. 1990. PMID: 2120615

4

Molecular cloning of a full-length cDNA for dentatorubral-pallidoluysian atrophy and regional expressions of the expanded alleles in the CNS.

Onodera O, Oyake M, Takano H, Ikeuchi T, Igarashi S, Tsuji S. Onodera O, et al. Am J Hum Genet. 1995 Nov;57(5):1050-60. Am J Hum Genet. 1995. PMID: 7485154 Free PMC article.

5

[Auditory comprehension in transcortical motor aphasia due to a medial lesions of the left frontal lobe].

Otsuki M, Soma Y, Onodera O, Tsuji S, Satoh A, Yamada N. Otsuki M, et al. Among authors: onodera o. No To Shinkei. 1995 Nov;47(11):1081-5. No To Shinkei. 1995. PMID: 7495614 Japanese.

6

Genetic association of the very low density lipoprotein (VLDL) receptor gene with sporadic Alzheimer's disease.

Okuizumi K, Onodera O, Namba Y, Ikeda K, Yamamoto T, Seki K, Ueki A, Nanko S, Tanaka H, Takahashi H, Oyanagi K, Mizusawa H, Kanazawa I, Tsuji S. Okuizumi K, et al. Among authors: onodera o. Nat Genet. 1995 Oct;11(2):207-9. doi: 10.1038/ng1095-207. Nat Genet. 1995. PMID: 7550352

7

Dentatorubral-pallidoluysian atrophy (DRPLA). Molecular basis for wide clinical features of DRPLA.

Ikeuchi T, Koide R, Onodera O, Tanaka H, Oyake M, Takano H, Tsuji S. Ikeuchi T, et al. Among authors: onodera o. Clin Neurosci. 1995;3(1):23-7. Clin Neurosci. 1995. PMID: 7614090

8

Dentatorubral-pallidoluysian atrophy (DRPLA): close correlation of CAG repeat expansions with the wide spectrum of clinical presentations and prominent anticipation.

Ikeuchi T, Onodera O, Oyake M, Koide R, Tanaka H, Tsuji S. Ikeuchi T, et al. Among authors: onodera o. Semin Cell Biol. 1995 Feb;6(1):37-44. doi: 10.1016/1043-4682(95)90013-6. Semin Cell Biol. 1995. PMID: 7620120 Review.

9

Passive transfer and active immunization with the recombinant leucine-zipper (Yo) protein as an attempt to establish an animal model of paraneoplastic cerebellar degeneration.

Tanaka K, Tanaka M, Onodera O, Igarashi S, Miyatake T, Tsuji S. Tanaka K, et al. Among authors: onodera o. J Neurol Sci. 1994 Dec 20;127(2):153-8. doi: 10.1016/0022-510x(94)90067-1. J Neurol Sci. 1994. PMID: 7707074

10

Trial to establish an animal model of paraneoplastic cerebellar degeneration with anti-Yo antibody. 1. Mouse strains bearing different MHC molecules produce antibodies on immunization with recombinant Yo protein, but do not cause Purkinje cell loss.

Tanaka M, Tanaka K, Onodera O, Tsuji S. Tanaka M, et al. Among authors: onodera o. Clin Neurol Neurosurg. 1995 Feb;97(1):95-100. doi: 10.1016/0303-8467(95)00005-5. Clin Neurol Neurosurg. 1995. PMID: 7788981

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