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Xeroderma pigmentosum-variant patients from America, Europe, and Asia.
Inui H, Oh KS, Nadem C, Ueda T, Khan SG, Metin A, Gozukara E, Emmert S, Slor H, Busch DB, Baker CC, DiGiovanna JJ, Tamura D, Seitz CS, Gratchev A, Wu WH, Chung KY, Chung HJ, Azizi E, Woodgate R, Schneider TD, Kraemer KH. Inui H, et al. Among authors: busch db. J Invest Dermatol. 2008 Aug;128(8):2055-68. doi: 10.1038/jid.2008.48. Epub 2008 Mar 27. J Invest Dermatol. 2008. PMID: 18368133 Free PMC article.
Reduced XPC DNA repair gene mRNA levels in clinically normal parents of xeroderma pigmentosum patients.
Khan SG, Oh KS, Shahlavi T, Ueda T, Busch DB, Inui H, Emmert S, Imoto K, Muniz-Medina V, Baker CC, DiGiovanna JJ, Schmidt D, Khadavi A, Metin A, Gozukara E, Slor H, Sarasin A, Kraemer KH. Khan SG, et al. Among authors: busch db. Carcinogenesis. 2006 Jan;27(1):84-94. doi: 10.1093/carcin/bgi204. Epub 2005 Aug 4. Carcinogenesis. 2006. PMID: 16081512
Relationship of neurologic degeneration to genotype in three xeroderma pigmentosum group G patients.
Emmert S, Slor H, Busch DB, Batko S, Albert RB, Coleman D, Khan SG, Abu-Libdeh B, DiGiovanna JJ, Cunningham BB, Lee MM, Crollick J, Inui H, Ueda T, Hedayati M, Grossman L, Shahlavi T, Cleaver JE, Kraemer KH. Emmert S, et al. Among authors: busch db. J Invest Dermatol. 2002 Jun;118(6):972-82. doi: 10.1046/j.1523-1747.2002.01782.x. J Invest Dermatol. 2002. PMID: 12060391 Free article.
A stop codon in xeroderma pigmentosum group C families in Turkey and Italy: molecular genetic evidence for a common ancestor.
Gozukara EM, Khan SG, Metin A, Emmert S, Busch DB, Shahlavi T, Coleman DM, Miller M, Chinsomboon N, Stefanini M, Kraemer KH. Gozukara EM, et al. Among authors: busch db. J Invest Dermatol. 2001 Aug;117(2):197-204. doi: 10.1046/j.1523-1747.2001.01424.x. J Invest Dermatol. 2001. PMID: 11511294 Free article.
Clinical, cellular, and molecular features of an Israeli xeroderma pigmentosum family with a frameshift mutation in the XPC gene: sun protection prolongs life.
Slor H, Batko S, Khan SG, Sobe T, Emmert S, Khadavi A, Frumkin A, Busch DB, Albert RB, Kraemer KH. Slor H, et al. Among authors: busch db. J Invest Dermatol. 2000 Dec;115(6):974-80. doi: 10.1046/j.1523-1747.2000.00190.x. J Invest Dermatol. 2000. PMID: 11121128 Free article.
Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.
Meira LB, Graham JM Jr, Greenberg CR, Busch DB, Doughty AT, Ziffer DW, Coleman DM, Savre-Train I, Friedberg EC. Meira LB, et al. Among authors: busch db. Am J Hum Genet. 2000 Apr;66(4):1221-8. doi: 10.1086/302867. Epub 2000 Mar 15. Am J Hum Genet. 2000. PMID: 10739753 Free PMC article.
Increased ultraviolet sensitivity and chromosomal instability related to P53 function in the xeroderma pigmentosum variant.
Cleaver JE, Afzal V, Feeney L, McDowell M, Sadinski W, Volpe JP, Busch DB, Coleman DM, Ziffer DW, Yu Y, Nagasawa H, Little JB. Cleaver JE, et al. Among authors: busch db. Cancer Res. 1999 Mar 1;59(5):1102-8. Cancer Res. 1999. PMID: 10070969 Free article.
The human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cells.
Liu N, Lamerdin JE, Tucker JD, Zhou ZQ, Walter CA, Albala JS, Busch DB, Thompson LH. Liu N, et al. Among authors: busch db. Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9232-7. doi: 10.1073/pnas.94.17.9232. Proc Natl Acad Sci U S A. 1997. PMID: 9256465 Free PMC article.
Phenotypic heterogeneity in nucleotide excision repair mutants of rodent complementation groups 1 and 4.
Busch DB, van Vuuren H, de Wit J, Collins A, Zdzienicka MZ, Mitchell DL, Brookman KW, Stefanini M, Riboni R, Thompson LH, Albert RB, van Gool AJ, Hoeijmakers J. Busch DB, et al. Mutat Res. 1997 Mar 12;383(2):91-106. doi: 10.1016/s0921-8777(96)00048-1. Mutat Res. 1997. PMID: 9088342
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