Ehrlich M - Search Results

1

Satellite DNA hypomethylation in karyotyped Wilms tumors.

Ehrlich M, Hopkins NE, Jiang G, Dome JS, Yu MC, Woods CB, Tomlinson GE, Chintagumpala M, Champagne M, Dillerg L, Parham DM, Sawyer J. Ehrlich M, et al. Cancer Genet Cytogenet. 2003 Mar;141(2):97-105. doi: 10.1016/s0165-4608(02)00668-4. Cancer Genet Cytogenet. 2003. PMID: 12606126

2

Preferential induction of chromosome 1 multibranched figures and whole-arm deletions in a human pro-B cell line treated with 5-azacytidine or 5-azadeoxycytidine.

Hernandez R, Frady A, Zhang XY, Varela M, Ehrlich M. Hernandez R, et al. Among authors: ehrlich m. Cytogenet Cell Genet. 1997;76(3-4):196-201. doi: 10.1159/000134548. Cytogenet Cell Genet. 1997. PMID: 9186523

3

DNA demethylation and pericentromeric rearrangements of chromosome 1.

Ji W, Hernandez R, Zhang XY, Qu GZ, Frady A, Varela M, Ehrlich M. Ji W, et al. Among authors: ehrlich m. Mutat Res. 1997 Sep 5;379(1):33-41. doi: 10.1016/s0027-5107(97)00088-2. Mutat Res. 1997. PMID: 9330620

4

Hypomethylation of pericentromeric DNA in breast adenocarcinomas.

Narayan A, Ji W, Zhang XY, Marrogi A, Graff JR, Baylin SB, Ehrlich M. Narayan A, et al. Among authors: ehrlich m. Int J Cancer. 1998 Sep 11;77(6):833-8. doi: 10.1002/(sici)1097-0215(19980911)77:6<833::aid-ijc6>3.0.co;2-v. Int J Cancer. 1998. PMID: 9714050

5

Frequent hypomethylation in Wilms tumors of pericentromeric DNA in chromosomes 1 and 16.

Qu GZ, Grundy PE, Narayan A, Ehrlich M. Qu GZ, et al. Among authors: ehrlich m. Cancer Genet Cytogenet. 1999 Feb;109(1):34-9. doi: 10.1016/s0165-4608(98)00143-5. Cancer Genet Cytogenet. 1999. PMID: 9973957

6

Satellite DNA hypomethylation vs. overall genomic hypomethylation in ovarian epithelial tumors of different malignant potential.

Qu G, Dubeau L, Narayan A, Yu MC, Ehrlich M. Qu G, et al. Among authors: ehrlich m. Mutat Res. 1999 Jan 25;423(1-2):91-101. doi: 10.1016/s0027-5107(98)00229-2. Mutat Res. 1999. PMID: 10029684

7

DNA hypomethylation and unusual chromosome instability in cell lines from ICF syndrome patients.

Tuck-Muller CM, Narayan A, Tsien F, Smeets DF, Sawyer J, Fiala ES, Sohn OS, Ehrlich M. Tuck-Muller CM, et al. Among authors: ehrlich m. Cytogenet Cell Genet. 2000;89(1-2):121-8. doi: 10.1159/000015590. Cytogenet Cell Genet. 2000. PMID: 10894953

8

ABL1 promoter methylation can exist independently of BCR-ABL transcription in chronic myeloid leukemia hematopoietic progenitors.

Sun B, Jiang G, Zaydan MA, La Russa VF, Safah H, Ehrlich M. Sun B, et al. Among authors: ehrlich m. Cancer Res. 2001 Sep 15;61(18):6931-7. Cancer Res. 2001. PMID: 11559572

9

Methylation of the FSHD syndrome-linked subtelomeric repeat in normal and FSHD cell cultures and tissues.

Tsien F, Sun B, Hopkins NE, Vedanarayanan V, Figlewicz D, Winokur S, Ehrlich M. Tsien F, et al. Among authors: ehrlich m. Mol Genet Metab. 2001 Nov;74(3):322-31. doi: 10.1006/mgme.2001.3219. Mol Genet Metab. 2001. PMID: 11708861

10

DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes.

Ehrlich M, Buchanan KL, Tsien F, Jiang G, Sun B, Uicker W, Weemaes CM, Smeets D, Sperling K, Belohradsky BH, Tommerup N, Misek DE, Rouillard JM, Kuick R, Hanash SM. Ehrlich M, et al. Hum Mol Genet. 2001 Dec 1;10(25):2917-31. doi: 10.1093/hmg/10.25.2917. Hum Mol Genet. 2001. PMID: 11741835

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