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Items: 8

1.

Loss of function of Colgalt1 disrupts collagen post-translational modification and causes musculoskeletal defects.

Geister KA, Lopez-Jimenez AJ, Houghtaling S, Ho TH, Vanacore R, Beier DR.

Dis Model Mech. 2019 Jun 17;12(6). pii: dmm037176. doi: 10.1242/dmm.037176.

2.

The SWI/SNF ATP-dependent nucleosome remodeler promotes resection initiation at a DNA double-strand break in yeast.

Wiest NE, Houghtaling S, Sanchez JC, Tomkinson AE, Osley MA.

Nucleic Acids Res. 2017 Jun 2;45(10):5887-5900. doi: 10.1093/nar/gkx221.

3.

Molecular assays to investigate chromatin changes during DNA double-strand break repair in yeast.

Houghtaling S, Tsukuda T, Osley MA.

Methods Mol Biol. 2011;745:79-97. doi: 10.1007/978-1-61779-129-1_6.

PMID:
21660690
4.

Tempol protects against oxidative damage and delays epithelial tumor onset in Fanconi anemia mice.

Zhang QS, Eaton L, Snyder ER, Houghtaling S, Mitchell JB, Finegold M, Van Waes C, Grompe M.

Cancer Res. 2008 Mar 1;68(5):1601-8. doi: 10.1158/0008-5472.CAN-07-5186.

5.

Fancd2 functions in a double strand break repair pathway that is distinct from non-homologous end joining.

Houghtaling S, Newell A, Akkari Y, Taniguchi T, Olson S, Grompe M.

Hum Mol Genet. 2005 Oct 15;14(20):3027-33. Epub 2005 Aug 31.

PMID:
16135554
6.

Heterozygosity for p53 (Trp53+/-) accelerates epithelial tumor formation in fanconi anemia complementation group D2 (Fancd2) knockout mice.

Houghtaling S, Granville L, Akkari Y, Torimaru Y, Olson S, Finegold M, Grompe M.

Cancer Res. 2005 Jan 1;65(1):85-91.

7.

Regulated interaction of the Fanconi anemia protein, FANCD2, with chromatin.

Montes de Oca R, Andreassen PR, Margossian SP, Gregory RC, Taniguchi T, Wang X, Houghtaling S, Grompe M, D'Andrea AD.

Blood. 2005 Feb 1;105(3):1003-9. Epub 2004 Sep 28.

PMID:
15454491
8.

Epithelial cancer in Fanconi anemia complementation group D2 (Fancd2) knockout mice.

Houghtaling S, Timmers C, Noll M, Finegold MJ, Jones SN, Meyn MS, Grompe M.

Genes Dev. 2003 Aug 15;17(16):2021-35. Epub 2003 Jul 31.

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