Brandenburg S - Search Results

1

Loss of imprinting in colorectal cancer linked to hypomethylation of H19 and IGF2.

Cui H, Onyango P, Brandenburg S, Wu Y, Hsieh CL, Feinberg AP. Cui H, et al. Among authors: brandenburg s. Cancer Res. 2002 Nov 15;62(22):6442-6. Cancer Res. 2002. PMID: 12438232

2

Loss of IGF2 imprinting: a potential marker of colorectal cancer risk.

Cui H, Cruz-Correa M, Giardiello FM, Hutcheon DF, Kafonek DR, Brandenburg S, Wu Y, He X, Powe NR, Feinberg AP. Cui H, et al. Among authors: brandenburg s. Science. 2003 Mar 14;299(5613):1753-5. doi: 10.1126/science.1080902. Science. 2003. PMID: 12637750

3

Loss of imprinting of insulin growth factor II gene: a potential heritable biomarker for colon neoplasia predisposition.

Cruz-Correa M, Cui H, Giardiello FM, Powe NR, Hylind L, Robinson A, Hutcheon DF, Kafonek DR, Brandenburg S, Wu Y, He X, Feinberg AP. Cruz-Correa M, et al. Among authors: brandenburg s. Gastroenterology. 2004 Apr;126(4):964-70. doi: 10.1053/j.gastro.2003.12.051. Gastroenterology. 2004. PMID: 15057734

4

Loss of imprinting of insulin-like growth factor-II in Wilms' tumor commonly involves altered methylation but not mutations of CTCF or its binding site.

Cui H, Niemitz EL, Ravenel JD, Onyango P, Brandenburg SA, Lobanenkov VV, Feinberg AP. Cui H, et al. Among authors: brandenburg sa. Cancer Res. 2001 Jul 1;61(13):4947-50. Cancer Res. 2001. PMID: 11431321

5

Distinct effects on gene expression of chemical and genetic manipulation of the cancer epigenome revealed by a multimodality approach.

Gius D, Cui H, Bradbury CM, Cook J, Smart DK, Zhao S, Young L, Brandenburg SA, Hu Y, Bisht KS, Ho AS, Mattson D, Sun L, Munson PJ, Chuang EY, Mitchell JB, Feinberg AP. Gius D, et al. Among authors: brandenburg sa. Cancer Cell. 2004 Oct;6(4):361-71. doi: 10.1016/j.ccr.2004.08.029. Cancer Cell. 2004. PMID: 15488759 Free article.

6

Children with idiopathic hemihypertrophy and beckwith-wiedemann syndrome have different constitutional epigenotypes associated with wilms tumor.

Niemitz EL, Feinberg AP, Brandenburg SA, Grundy PE, DeBaun MR. Niemitz EL, et al. Am J Hum Genet. 2005 Nov;77(5):887-91. doi: 10.1086/497540. Epub 2005 Oct 3. Am J Hum Genet. 2005. PMID: 16252245 Free PMC article.

7

Somatic mutation of TSSC5, a novel imprinted gene from human chromosome 11p15.5.

Lee MP, Reeves C, Schmitt A, Su K, Connors TD, Hu RJ, Brandenburg S, Lee MJ, Miller G, Feinberg AP. Lee MP, et al. Among authors: brandenburg s. Cancer Res. 1998 Sep 15;58(18):4155-9. Cancer Res. 1998. PMID: 9751628

8

Two novel genes in the center of the 11p15 imprinted domain escape genomic imprinting.

Lee MP, Brandenburg S, Landes GM, Adams M, Miller G, Feinberg AP. Lee MP, et al. Among authors: brandenburg s. Hum Mol Genet. 1999 Apr;8(4):683-90. doi: 10.1093/hmg/8.4.683. Hum Mol Genet. 1999. PMID: 10072438

9

Loss of imprinting of a paternally expressed transcript, with antisense orientation to KVLQT1, occurs frequently in Beckwith-Wiedemann syndrome and is independent of insulin-like growth factor II imprinting.

Lee MP, DeBaun MR, Mitsuya K, Galonek HL, Brandenburg S, Oshimura M, Feinberg AP. Lee MP, et al. Among authors: brandenburg s. Proc Natl Acad Sci U S A. 1999 Apr 27;96(9):5203-8. doi: 10.1073/pnas.96.9.5203. Proc Natl Acad Sci U S A. 1999. PMID: 10220444 Free PMC article.

10

Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects.

DeBaun MR, Niemitz EL, McNeil DE, Brandenburg SA, Lee MP, Feinberg AP. DeBaun MR, et al. Am J Hum Genet. 2002 Mar;70(3):604-11. doi: 10.1086/338934. Epub 2002 Jan 28. Am J Hum Genet. 2002. PMID: 11813134 Free PMC article.

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