Brandenburg SA - Search Results

1

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. Among authors: brandenburg sa. 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.

2

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. Among authors: brandenburg sa. 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.

3

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

4

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. Hum Mol Genet. 1999 Apr;8(4):683-90. doi: 10.1093/hmg/8.4.683. Hum Mol Genet. 1999. PMID: 10072438

5

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. 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.

6

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. Cancer Res. 2002 Nov 15;62(22):6442-6. Cancer Res. 2002. PMID: 12438232

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. Cancer Res. 1998 Sep 15;58(18):4155-9. Cancer Res. 1998. PMID: 9751628

8

Comprehensive high-throughput arrays for relative methylation (CHARM).

Irizarry RA, Ladd-Acosta C, Carvalho B, Wu H, Brandenburg SA, Jeddeloh JA, Wen B, Feinberg AP. Irizarry RA, et al. Among authors: brandenburg sa. Genome Res. 2008 May;18(5):780-90. doi: 10.1101/gr.7301508. Epub 2008 Mar 3. Genome Res. 2008. PMID: 18316654 Free PMC article.

9

Targeted disruption of the Kvlqt1 gene causes deafness and gastric hyperplasia in mice.

Lee MP, Ravenel JD, Hu RJ, Lustig LR, Tomaselli G, Berger RD, Brandenburg SA, Litzi TJ, Bunton TE, Limb C, Francis H, Gorelikow M, Gu H, Washington K, Argani P, Goldenring JR, Coffey RJ, Feinberg AP. Lee MP, et al. Among authors: brandenburg sa. J Clin Invest. 2000 Dec;106(12):1447-55. doi: 10.1172/JCI10897. J Clin Invest. 2000. PMID: 11120752 Free PMC article.

10

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. Science. 2003 Mar 14;299(5613):1753-5. doi: 10.1126/science.1080902. Science. 2003. PMID: 12637750

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