S. Takai

发表

The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.

C Eng, P Komminoth, D. Clayton, 1996, JAMA.

Loss of alleles at loci on chromosome 13 in human primary gastric cancers.

T. Honjo, I. Nishisho, T. Miki, 1988, Genomics.

Amylase Isozymes in Human Thyroid Tissues α Expression of Updated Version

Masahiko, A. Horii, K. Matsubara, 2006 .

D10S20, a previously unmapped RFLP (OS-3), is located on 10q near D10S4.

J. Kidd, A. Pakstis, Y. Chen, 1988, Genomics.

Analysis of steroid 21-hydroxylase gene in five unrelated Japanese patients with 21-hydroxylase deficiency.

T. Honjo, J. Nakura, P. White, 1987, Endocrinologia japonica.

Genotype‐phenotype correlation in multiple endocrine neoplasia type 2: report of the International RET Mutation Consortium

B. Ponder, S. Thibodeau, L. Mulligan, 1995, Journal of internal medicine.

Allele loss on chromosome 10 and point mutation of ras oncogenes are infrequent in tumors of MEN 2A.

A. Miyauchi, A. Miya, T. Miki, 1989, Henry Ford Hospital medical journal.

Loss of genes on chromosome 22 in medullary thyroid carcinoma and pheochromocytoma.

A. Miyauchi, I. Nishisho, T. Miki, 1987, Japanese journal of cancer research : Gann.

Involvement of the retinoblastoma gene in primary osteosarcomas and other bone and soft-tissue tumors.

H. Yoshikawa, N. Araki, A. Uchida, 1991, Clinical orthopaedics and related research.

Multiple endocrine neoplasia type 2 syndromes in Japan.

A. Miyauchi, T. Miki, S. Takai, 1984, Henry Ford Hospital medical journal.

Immunohistochemical analysis of amylase isoenzymes in thyroid cancer.

M. Higashiyama, N. Tomita, T. Monden, 1991, Journal of Clinical Pathology.

Studies of multiple endocrine neoplasia type 2A syndrome: linkage analyses and comparison of constitutional and tumor genotypes.

A. Miyauchi, I. Nishisho, T. Miki, 1987, Henry Ford Hospital medical journal.

An anonymous single copy chromosome 18 probe associated with a frequent RFLP (D18S5).

T. Honjo, I. Nishisho, T. Miki, 1986, Nucleic acids research.

Prediction of affected MEN2A gene carriers by DNA linkage analysis for early total thyroidectomy: a progress in clinical screening program for children with hereditary cancer syndrome.

S. Takai, T. Shimotake, N. Iwai, 1992, Journal of pediatric surgery.

Expression of α-Amylase Isozymes in Human Thyroid Tissues

N. Tomita, A. Horii, K. Matsubara, 1991 .