Yamamoto M - Search Results

1

Loss of heterozygosity on the long arm of chromosome 22 in pheochromocytoma.

Tanaka N, Nishisho I, Yamamoto M, Miya A, Shin E, Karakawa K, Fujita S, Kobayashi T, Rouleau GA, Mori T, et al. Tanaka N, et al. Among authors: yamamoto m. Genes Chromosomes Cancer. 1992 Nov;5(4):399-403. doi: 10.1002/gcc.2870050416. Genes Chromosomes Cancer. 1992. PMID: 1283329

2

Preclinical detection of MEN 2A gene carrier using linked DNA markers.

Tanaka N, Yamamoto M, Miki T, Okazaki M, Sakita I, Shimotake T, Kobayashi T, Miyauchi A, Mori T, Takai S. Tanaka N, et al. Among authors: yamamoto m. Jinrui Idengaku Zasshi. 1991 Jun;36(2):165-70. doi: 10.1007/BF01876580. Jinrui Idengaku Zasshi. 1991. PMID: 1681126

3

Tight linkage of the ret proto-oncogene with the multiple endocrine neoplasia type 2A locus.

Yamamoto M, Miki T, Tanaka N, Miya A, Shin E, Karakawa K, Kobayashi T, Tahira T, Ishizaka Y, Itoh F, et al. Yamamoto M, et al. Jpn J Clin Oncol. 1991 Jun;21(3):149-52. Jpn J Clin Oncol. 1991. PMID: 1682518

4

Identification and analysis of the ret proto-oncogene promoter region in neuroblastoma cell lines and medullary thyroid carcinomas from MEN2A patients.

Itoh F, Ishizaka Y, Tahira T, Yamamoto M, Miya A, Imai K, Yachi A, Takai S, Sugimura T, Nagao M. Itoh F, et al. Among authors: yamamoto m. Oncogene. 1992 Jun;7(6):1201-6. Oncogene. 1992. PMID: 1350670

5

Activated sialidase activity in transformed lymphocytes by Epstein-Barr (EB) virus of sialidosis type I (cherry-red spot-myoclonus syndrome).

Yamamoto M, Yamauchi T, Yamamoto K, Kobayashi T. Yamamoto M, et al. Among authors: yamamoto k. J Neurol Sci. 1995 Jul;131(1):105-7. doi: 10.1016/0022-510x(95)00102-8. J Neurol Sci. 1995. PMID: 7561940

6

Simple and rapid detection of large mitochondrial DNA deletions in mitochondrial encephalomyopathy by long PCR.

Yamamoto M, Hamada K, Shimokawa M, Kobayashi T. Yamamoto M, et al. Muscle Nerve. 1996 Jul;19(7):928-9. Muscle Nerve. 1996. PMID: 8965858 No abstract available.

7

Long-term follow-up of radiosurgically treated arteriovenous malformations in children: report of nine cases.

Yamamoto M, Jimbo M, Ide M, Tanaka N, Lindquist C, Steiner L. Yamamoto M, et al. Surg Neurol. 1992 Aug;38(2):95-100. doi: 10.1016/0090-3019(92)90084-z. Surg Neurol. 1992. PMID: 1509353

8

[A case of Wegener's granulomatosis with pachymeningitis].

Niimi T, Sugiura Y, Sato S, Yoshinouchi T, Yamada Y, Akita K, Maeda H, Mori T, Kawaguchi H, Morishita M, Yamamoto M, Ueda R. Niimi T, et al. Among authors: yamamoto m. Nihon Kokyuki Gakkai Zasshi. 2000 Jul;38(7):561-5. Nihon Kokyuki Gakkai Zasshi. 2000. PMID: 11019573 Japanese.

9

Molecular cloning, nucleotide sequence, and expression of the structural gene for alkaline serine protease from alkaliphilic Bacillus sp. 221.

Takami H, Kobayashi T, Kobayashi M, Yamamoto M, Nakamura S, Aono R, Horikoshi K. Takami H, et al. Among authors: yamamoto m. Biosci Biotechnol Biochem. 1992 Sep;56(9):1455-60. doi: 10.1271/bbb.56.1455. Biosci Biotechnol Biochem. 1992. PMID: 1368952 Free article.

10

Long-term results of radiosurgery for arteriovenous malformation: neurodiagnostic imaging and histological studies of angiographically confirmed nidus obliteration.

Yamamoto M, Jimbo M, Kobayashi M, Toyoda C, Ide M, Tanaka N, Lindquist C, Steiner L. Yamamoto M, et al. Surg Neurol. 1992 Mar;37(3):219-30. doi: 10.1016/0090-3019(92)90235-f. Surg Neurol. 1992. PMID: 1536028

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