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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1997 | 2 |
1998 | 2 |
2000 | 1 |
2024 | 0 |
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Page 1
Identical mutations in the CSB gene associated with either Cockayne syndrome or the DeSanctis-cacchione variant of xeroderma pigmentosum.
Hum Mol Genet. 2000 May 1;9(8):1171-5. doi: 10.1093/hmg/9.8.1171.
Hum Mol Genet. 2000.
PMID: 10767341
Mutations in the XPD helicase gene result in XP and TTD phenotypes, preventing interaction between XPD and the p44 subunit of TFIIH.
Coin F, Marinoni JC, Rodolfo C, Fribourg S, Pedrini AM, Egly JM.
Coin F, et al.
Nat Genet. 1998 Oct;20(2):184-8. doi: 10.1038/2491.
Nat Genet. 1998.
PMID: 9771713
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Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndrome.
Mallery DL, Tanganelli B, Colella S, Steingrimsdottir H, van Gool AJ, Troelstra C, Stefanini M, Lehmann AR.
Mallery DL, et al.
Am J Hum Genet. 1998 Jan;62(1):77-85. doi: 10.1086/301686.
Am J Hum Genet. 1998.
PMID: 9443879
Free PMC article.
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Poly(ADP-ribose) synthesis: a useful parameter for identifying apoptotic cells.
Donzelli M, Negri C, Mandarino A, Rossi L, Prosperi E, Frouin I, Bernardi R, Bürkle A, Scovassi AI.
Donzelli M, et al.
Histochem J. 1997 Nov-Dec;29(11-12):831-7. doi: 10.1023/a:1026485622824.
Histochem J. 1997.
PMID: 9466150
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Multiparametric staining to identify apoptotic human cells.
Negri C, Donzelli M, Bernardi R, Rossi L, Bürkle A, Scovassi AI.
Negri C, et al.
Exp Cell Res. 1997 Jul 10;234(1):174-7. doi: 10.1006/excr.1997.3591.
Exp Cell Res. 1997.
PMID: 9223383
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