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Page 1
A novel role for thyroid hormone receptor beta in cellular radiosensitivity.
Matsuse M, Saenko V, Sedliarou I, Rogounovitch T, Nakazawa Y, Mitsutake N, Akulevich N, Namba H, Yamashita S. Matsuse M, et al. Among authors: nakazawa y. J Radiat Res. 2008 Jan;49(1):17-27. doi: 10.1269/jrr.07065. Epub 2007 Oct 25. J Radiat Res. 2008. PMID: 17965546 Free article.
Oncogenic role of miR-17-92 cluster in anaplastic thyroid cancer cells.
Takakura S, Mitsutake N, Nakashima M, Namba H, Saenko VA, Rogounovitch TI, Nakazawa Y, Hayashi T, Ohtsuru A, Yamashita S. Takakura S, et al. Among authors: nakazawa y. Cancer Sci. 2008 Jun;99(6):1147-54. doi: 10.1111/j.1349-7006.2008.00800.x. Epub 2008 Apr 21. Cancer Sci. 2008. PMID: 18429962 Free PMC article.
Mutation analysis of RAP1 gene in papillary thyroid carcinomas.
Matsuse M, Mitsutake N, Rogounovitch T, Saenko V, Nakazawa Y, Rumyantsev P, Lushnikov E, Suzuki K, Yamashita S. Matsuse M, et al. Among authors: nakazawa y. Endocr J. 2009;56(1):161-4. doi: 10.1507/endocrj.k08e-244. Epub 2008 Oct 24. Endocr J. 2009. PMID: 18948674 Free article.
Induction of micronuclei in germinating onion seed root tip cells irradiated with high energy heavy ions.
Takatsuji T, Takayanagi H, Morishita K, Nojima K, Furusawa Y, Nakazawa Y, Matsuse M, Akamatsu S, Hirano N, Hirashima N, Hotokezaka S, Ijichi T, Kakimoto C, Kanemaru T, Koshitake M, Moriuchi A, Yamamoto K, Yoshikawa I. Takatsuji T, et al. Among authors: nakazawa y. J Radiat Res. 2010;51(3):315-23. doi: 10.1269/jrr.09028. J Radiat Res. 2010. PMID: 20505265 Free article.
Mutations in UVSSA cause UV-sensitive syndrome and impair RNA polymerase IIo processing in transcription-coupled nucleotide-excision repair.
Nakazawa Y, Sasaki K, Mitsutake N, Matsuse M, Shimada M, Nardo T, Takahashi Y, Ohyama K, Ito K, Mishima H, Nomura M, Kinoshita A, Ono S, Takenaka K, Masuyama R, Kudo T, Slor H, Utani A, Tateishi S, Yamashita S, Stefanini M, Lehmann AR, Yoshiura K, Ogi T. Nakazawa Y, et al. Nat Genet. 2012 May;44(5):586-92. doi: 10.1038/ng.2229. Nat Genet. 2012. PMID: 22466610 Free article.
Identification of the first ATRIP-deficient patient and novel mutations in ATR define a clinical spectrum for ATR-ATRIP Seckel Syndrome.
Ogi T, Walker S, Stiff T, Hobson E, Limsirichaikul S, Carpenter G, Prescott K, Suri M, Byrd PJ, Matsuse M, Mitsutake N, Nakazawa Y, Vasudevan P, Barrow M, Stewart GS, Taylor AM, O'Driscoll M, Jeggo PA. Ogi T, et al. Among authors: nakazawa y. PLoS Genet. 2012;8(11):e1002945. doi: 10.1371/journal.pgen.1002945. Epub 2012 Nov 8. PLoS Genet. 2012. PMID: 23144622 Free PMC article.
1,113 results