Hayashi Y - Search Results

1

Hereditary dentatorubral-pallidoluysian atrophy: detection of widespread ubiquitinated neuronal and glial intranuclear inclusions in the brain.

Hayashi Y, Kakita A, Yamada M, Koide R, Igarashi S, Takano H, Ikeuchi T, Wakabayashi K, Egawa S, Tsuji S, Takahashi H. Hayashi Y, et al. Acta Neuropathol. 1998 Dec;96(6):547-52. doi: 10.1007/s004010050933. Acta Neuropathol. 1998. PMID: 9845282

2

Intragenic homozygous deletion of the WT1 gene in Wilms' tumor.

Tadokoro K, Fujii H, Ohshima A, Kakizawa Y, Shimizu K, Sakai A, Sumiyoshi K, Inoue T, Hayashi Y, Yamada M. Tadokoro K, et al. Among authors: hayashi y. Oncogene. 1992 Jun;7(6):1215-21. Oncogene. 1992. PMID: 1350671

3

Establishment of a monoclonal antibody against senile plaques and its application for immunohistological and immunoelectron microscopical studies in the brain of the elderly.

Kawasaki H, Utsuyama M, Takahashi H, Hayashi Y, Kurashima C, Esaki Y, Maruyama N, Hirokawa K. Kawasaki H, et al. Among authors: hayashi y. Acta Neuropathol. 1989;79(1):44-7. doi: 10.1007/BF00308956. Acta Neuropathol. 1989. PMID: 2589024

4

Hayashi Y, Inaba T, Hanada R, Yamada M, Nakagome Y, Yamamoto K. Hayashi Y, et al. Med Pediatr Oncol. 1989;17(2):111-5. doi: 10.1002/mpo.2950170208. Med Pediatr Oncol. 1989. PMID: 2704332

5

Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2A.

Saito M, Hayashi Y, Suzuki T, Tanaka H, Hozumi I, Tsuji S. Saito M, et al. Among authors: hayashi y. Neurology. 1997 Dec;49(6):1630-5. doi: 10.1212/wnl.49.6.1630. Neurology. 1997. PMID: 9409358

6

Suppression of aggregate formation and apoptosis by transglutaminase inhibitors in cells expressing truncated DRPLA protein with an expanded polyglutamine stretch.

Igarashi S, Koide R, Shimohata T, Yamada M, Hayashi Y, Takano H, Date H, Oyake M, Sato T, Sato A, Egawa S, Ikeuchi T, Tanaka H, Nakano R, Tanaka K, Hozumi I, Inuzuka T, Takahashi H, Tsuji S. Igarashi S, et al. Among authors: hayashi y. Nat Genet. 1998 Feb;18(2):111-7. doi: 10.1038/ng0298-111. Nat Genet. 1998. PMID: 9462738

7

Hereditary dentatorubral-pallidoluysian atrophy: ubiquitinated filamentous inclusions in the cerebellar dentate nucleus neurons.

Hayashi Y, Kakita A, Yamada M, Egawa S, Oyanagi S, Naito H, Tsuji S, Takahashi H. Hayashi Y, et al. Acta Neuropathol. 1998 May;95(5):479-82. doi: 10.1007/s004010050828. Acta Neuropathol. 1998. PMID: 9600594

8

Mutations of the p53 gene are involved in Ewing's sarcomas but not in neuroblastomas.

Komuro H, Hayashi Y, Kawamura M, Hayashi K, Kaneko Y, Kamoshita S, Hanada R, Yamamoto K, Hongo T, Yamada M, et al. Komuro H, et al. Among authors: hayashi y, hayashi k. Cancer Res. 1993 Nov 1;53(21):5284-8. Cancer Res. 1993. PMID: 8221663

9

[Random biopsy and recurrence risk in patients with bladder cancer].

Yamada Y, Hayashi Y, Kohri K, Terao E, Hirao N, HoriH, IwaiY, Kato K, Ito T, Tawada T, Asaka H, Andou H, Kawai T, Ikeuchi T, Watanabe H. Yamada Y, et al. Among authors: hayashi y. Nihon Hinyokika Gakkai Zasshi. 1996 Jan;87(1):61-6. doi: 10.5980/jpnjurol1989.87.61. Nihon Hinyokika Gakkai Zasshi. 1996. PMID: 8683895 Free article. Japanese.

10

Molecular analysis for p53 and mdm2 in intracranial germ cell tumors.

Iwato M, Tachibana O, Tohma Y, Nitta H, Hayashi Y, Yamashita J. Iwato M, et al. Among authors: hayashi y. Acta Neuropathol. 2000 Jan;99(1):21-5. doi: 10.1007/pl00007401. Acta Neuropathol. 2000. PMID: 10651023

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