Tsien F - Search Results

1

IL-7Rα deficiency in p53null mice exacerbates thymocyte telomere erosion and lymphomagenesis.

Kibe R, Zhang S, Guo D, Marrero L, Tsien F, Rodriguez P, Khan S, Zieske A, Huang J, Li W, Durum SK, Iwakuma T, Cui Y. Kibe R, et al. Among authors: tsien f. Cell Death Differ. 2012 Jul;19(7):1139-51. doi: 10.1038/cdd.2011.203. Epub 2012 Jan 27. Cell Death Differ. 2012. PMID: 22281704 Free PMC article.

2

Characterization of multipotent mesenchymal stem cells from the bone marrow of rhesus macaques.

Izadpanah R, Joswig T, Tsien F, Dufour J, Kirijan JC, Bunnell BA. Izadpanah R, et al. Among authors: tsien f. Stem Cells Dev. 2005 Aug;14(4):440-51. doi: 10.1089/scd.2005.14.440. Stem Cells Dev. 2005. PMID: 16137233

3

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. Mol Genet Metab. 2001 Nov;74(3):322-31. doi: 10.1006/mgme.2001.3219. Mol Genet Metab. 2001. PMID: 11708861

4

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. Among authors: tsien f. Hum Mol Genet. 2001 Dec 1;10(25):2917-31. doi: 10.1093/hmg/10.25.2917. Hum Mol Genet. 2001. PMID: 11741835

5

Chromosome preparation from cultured cells.

Howe B, Umrigar A, Tsien F. Howe B, et al. Among authors: tsien f. J Vis Exp. 2014 Jan 28;(83):e50203. doi: 10.3791/50203. J Vis Exp. 2014. PMID: 24513647 Free PMC article.

6

Long-term in vitro expansion alters the biology of adult mesenchymal stem cells.

Izadpanah R, Kaushal D, Kriedt C, Tsien F, Patel B, Dufour J, Bunnell BA. Izadpanah R, et al. Among authors: tsien f. Cancer Res. 2008 Jun 1;68(11):4229-38. doi: 10.1158/0008-5472.CAN-07-5272. Cancer Res. 2008. PMID: 18519682 Free PMC article.

7

Phenotypic features of a boy with trisomy of 16q22-->qter due to paternal Y; 16 translocation.

Tsien F, Morava E, Talarski A, Marble M. Tsien F, et al. Clin Dysmorphol. 2005 Oct;14(4):177-181. Clin Dysmorphol. 2005. PMID: 16155418

8

Prolonged culture of normal chorionic villus cells yields ICF syndrome-like chromatin decondensation and rearrangements.

Tsien F, Fiala ES, Youn B, Long TI, Laird PW, Weissbecker K, Ehrlich M. Tsien F, et al. Cytogenet Genome Res. 2002;98(1):13-21. doi: 10.1159/000068543. Cytogenet Genome Res. 2002. PMID: 12584436

9

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: tsien f. Cytogenet Cell Genet. 2000;89(1-2):121-8. doi: 10.1159/000015590. Cytogenet Cell Genet. 2000. PMID: 10894953

10

High frequencies of ICF syndrome-like pericentromeric heterochromatin decondensation and breakage in chromosome 1 in a chorionic villus sample.

Ehrlich M, Tsien F, Herrera D, Blackman V, Roggenbuck J, Tuck-Muller CM. Ehrlich M, et al. Among authors: tsien f. J Med Genet. 2001 Dec;38(12):882-4. doi: 10.1136/jmg.38.12.882. J Med Genet. 2001. PMID: 11768395 Free PMC article. No abstract available.

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