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Page 1
Structural and molecular hair abnormalities in trichothiodystrophy.
Liang C, Morris A, Schlücker S, Imoto K, Price VH, Menefee E, Wincovitch SM, Levin IW, Tamura D, Strehle KR, Kraemer KH, DiGiovanna JJ. Liang C, et al. Among authors: imoto k. J Invest Dermatol. 2006 Oct;126(10):2210-6. doi: 10.1038/sj.jid.5700384. Epub 2006 May 25. J Invest Dermatol. 2006. PMID: 16728971 Free article.
XPC initiation codon mutation in xeroderma pigmentosum patients with and without neurological symptoms.
Khan SG, Oh KS, Emmert S, Imoto K, Tamura D, Digiovanna JJ, Shahlavi T, Armstrong N, Baker CC, Neuburg M, Zalewski C, Brewer C, Wiggs E, Schiffmann R, Kraemer KH. Khan SG, et al. Among authors: imoto k. DNA Repair (Amst). 2009 Jan 1;8(1):114-25. doi: 10.1016/j.dnarep.2008.09.007. Epub 2008 Nov 14. DNA Repair (Amst). 2009. PMID: 18955168 Free PMC article.
Unexpected occurrence of xeroderma pigmentosum in an uncle and nephew.
Christen-Zaech S, Imoto K, Khan SG, Oh KS, Tamura D, Digiovanna JJ, Boyle J, Patronas NJ, Schiffmann R, Kraemer KH, Paller AS. Christen-Zaech S, et al. Among authors: imoto k. Arch Dermatol. 2009 Nov;145(11):1285-91. doi: 10.1001/archdermatol.2009.279. Arch Dermatol. 2009. PMID: 19917958 Free PMC article.
Cancer and neurologic degeneration in xeroderma pigmentosum: long term follow-up characterises the role of DNA repair.
Bradford PT, Goldstein AM, Tamura D, Khan SG, Ueda T, Boyle J, Oh KS, Imoto K, Inui H, Moriwaki S, Emmert S, Pike KM, Raziuddin A, Plona TM, DiGiovanna JJ, Tucker MA, Kraemer KH. Bradford PT, et al. Among authors: imoto k. J Med Genet. 2011 Mar;48(3):168-76. doi: 10.1136/jmg.2010.083022. Epub 2010 Nov 19. J Med Genet. 2011. PMID: 21097776 Free PMC article.
508 results