Leder P - Search Results

1

A maternal-zygotic effect gene, Zfp57, maintains both maternal and paternal imprints.

Li X, Ito M, Zhou F, Youngson N, Zuo X, Leder P, Ferguson-Smith AC. Li X, et al. Among authors: leder p. Dev Cell. 2008 Oct;15(4):547-57. doi: 10.1016/j.devcel.2008.08.014. Dev Cell. 2008. PMID: 18854139 Free PMC article.

2

Formin-1 protein associates with microtubules through a peptide domain encoded by exon-2.

Zhou F, Leder P, Martin SS. Zhou F, et al. Among authors: leder p. Exp Cell Res. 2006 Apr 15;312(7):1119-26. doi: 10.1016/j.yexcr.2005.12.035. Epub 2006 Feb 9. Exp Cell Res. 2006. PMID: 16480715

3

Identifying genes preferentially expressed in undifferentiated embryonic stem cells.

Li X, Leder P. Li X, et al. Among authors: leder p. BMC Cell Biol. 2007 Aug 28;8:37. doi: 10.1186/1471-2121-8-37. BMC Cell Biol. 2007. PMID: 17725840 Free PMC article.

4

Fibroblast growth factor receptor 3 is a negative regulator of bone growth.

Deng C, Wynshaw-Boris A, Zhou F, Kuo A, Leder P. Deng C, et al. Among authors: leder p. Cell. 1996 Mar 22;84(6):911-21. doi: 10.1016/s0092-8674(00)81069-7. Cell. 1996. PMID: 8601314 Free article.

5

Formin 1-isoform IV deficient cells exhibit defects in cell spreading and focal adhesion formation.

Dettenhofer M, Zhou F, Leder P. Dettenhofer M, et al. Among authors: leder p. PLoS One. 2008 Jun 18;3(6):e2497. doi: 10.1371/journal.pone.0002497. PLoS One. 2008. PMID: 18560567 Free PMC article.

6

Formin1 disruption confers oligodactylism and alters Bmp signaling.

Zhou F, Leder P, Zuniga A, Dettenhofer M. Zhou F, et al. Among authors: leder p. Hum Mol Genet. 2009 Jul 1;18(13):2472-82. doi: 10.1093/hmg/ddp185. Epub 2009 Apr 20. Hum Mol Genet. 2009. PMID: 19383632 Free PMC article.

7

Pleiotropic defects in ataxia-telangiectasia protein-deficient mice.

Elson A, Wang Y, Daugherty CJ, Morton CC, Zhou F, Campos-Torres J, Leder P. Elson A, et al. Among authors: leder p. Proc Natl Acad Sci U S A. 1996 Nov 12;93(23):13084-9. doi: 10.1073/pnas.93.23.13084. Proc Natl Acad Sci U S A. 1996. PMID: 8917548 Free PMC article.

8

Genome-wide SNP analysis of Tg.AC transgenic mice reveals an oncogenic collaboration between v-Ha-ras and Ink4a, which is absent in p53 deficiency.

Leder A, McMenamin J, Zhou F, Moran JL, Beier DR, Leder P. Leder A, et al. Among authors: leder p. Oncogene. 2008 Apr 10;27(17):2456-65. doi: 10.1038/sj.onc.1210866. Epub 2007 Oct 22. Oncogene. 2008. PMID: 17952114

9

Genetic interaction between the unstable v-Ha-RAS transgene (Tg.AC) and the murine Werner syndrome gene: transgene instability and tumorigenesis.

Leder A, Lebel M, Zhou F, Fontaine K, Bishop A, Leder P. Leder A, et al. Among authors: leder p. Oncogene. 2002 Sep 26;21(43):6657-68. doi: 10.1038/sj.onc.1205795. Oncogene. 2002. PMID: 12242664

10

Parental-specific methylation of an imprinted transgene is established during gametogenesis and progressively changes during embryogenesis.

Chaillet JR, Vogt TF, Beier DR, Leder P. Chaillet JR, et al. Among authors: leder p. Cell. 1991 Jul 12;66(1):77-83. doi: 10.1016/0092-8674(91)90140-t. Cell. 1991. PMID: 1649008

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