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12,384 results
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Detection of K-ras mutation in sputum by mutant-allele-specific amplification (MASA).
Takeda S, Ichii S, Nakamura Y. Takeda S, et al. Among authors: nakamura y. Hum Mutat. 1993;2(2):112-7. doi: 10.1002/humu.1380020209. Hum Mutat. 1993. PMID: 8318987
Dinucleotide repeat polymorphism on chromosome 9q32.
Toda T, Ikegawa S, Miyake M, Nakahori Y, Nakamura Y. Toda T, et al. Among authors: nakamura y. Jpn J Hum Genet. 1995 Dec;40(4):333-4. doi: 10.1007/BF01900600. Jpn J Hum Genet. 1995. PMID: 8851767
Rapid diagnosis of Miller-Dieker syndrome and isolated lissencephaly sequence by the polymerase chain reaction.
Batanian JR, Ledbetter SA, Wolff RK, Nakamura Y, White R, Dobyns WB, Ledbetter DH. Batanian JR, et al. Among authors: nakamura y. Hum Genet. 1990 Oct;85(5):555-9. doi: 10.1007/BF00194237. Hum Genet. 1990. PMID: 2227942
Accumulation of genetic alterations and progression of primary breast cancer.
Sato T, Akiyama F, Sakamoto G, Kasumi F, Nakamura Y. Sato T, et al. Among authors: nakamura y. Cancer Res. 1991 Nov 1;51(21):5794-9. Cancer Res. 1991. PMID: 1682035
Linkage analysis of hereditary thyroid carcinoma with and without pheochromocytoma.
Narod SA, Sobol H, Nakamura Y, Calmettes C, Baulieu JL, Bigorgne JC, Chabrier G, Couette J, de Gennes JL, Duprey J, et al. Narod SA, et al. Among authors: nakamura y. Hum Genet. 1989 Nov;83(4):353-8. doi: 10.1007/BF00291380. Hum Genet. 1989. PMID: 2572534
Allelotype of breast cancer: cumulative allele losses promote tumor progression in primary breast cancer.
Sato T, Tanigami A, Yamakawa K, Akiyama F, Kasumi F, Sakamoto G, Nakamura Y. Sato T, et al. Among authors: nakamura y. Cancer Res. 1990 Nov 15;50(22):7184-9. Cancer Res. 1990. PMID: 1977515
Association between a single-nucleotide polymorphism in the promoter of the human interleukin-3 gene and rheumatoid arthritis in Japanese patients, and maximum-likelihood estimation of combinatorial effect that two genetic loci have on susceptibility to the disease.
Yamada R, Tanaka T, Unoki M, Nagai T, Sawada T, Ohnishi Y, Tsunoda T, Yukioka M, Maeda A, Suzuki K, Tateishi H, Ochi T, Nakamura Y, Yamamoto K. Yamada R, et al. Among authors: nakamura y. Am J Hum Genet. 2001 Mar;68(3):674-85. doi: 10.1086/318789. Epub 2001 Feb 14. Am J Hum Genet. 2001. PMID: 11179015 Free PMC article.
Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence.
Sakamoto M, Ono J, Okada S, Nakamura Y, Kurahashi H. Sakamoto M, et al. Among authors: nakamura y. J Hum Genet. 2000;45(3):167-70. doi: 10.1007/s100380050204. J Hum Genet. 2000. PMID: 10807542
Novel mutations and genotype-phenotype relationships in 107 families with Fukuyama-type congenital muscular dystrophy (FCMD).
Kondo-Iida E, Kobayashi K, Watanabe M, Sasaki J, Kumagai T, Koide H, Saito K, Osawa M, Nakamura Y, Toda T. Kondo-Iida E, et al. Among authors: nakamura y. Hum Mol Genet. 1999 Nov;8(12):2303-9. doi: 10.1093/hmg/8.12.2303. Hum Mol Genet. 1999. PMID: 10545611
Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome.
Nakagawa H, Koyama K, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Matsuura N, Monden M, Nakamura Y. Nakagawa H, et al. Among authors: nakamura y. Hum Genet. 1998 Aug;103(2):168-72. doi: 10.1007/s004390050801. Hum Genet. 1998. PMID: 9760200
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