Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 44

References for PMC Articles for PubMed (Select 16628246)

1.

The PHD finger, a nuclear protein-interaction domain.

Bienz M.

Trends Biochem Sci. 2006 Jan;31(1):35-40. Epub 2005 Nov 16. Review.

PMID:
16297627
2.

The chromatin-remodeling protein ATRX is critical for neuronal survival during corticogenesis.

Bérubé NG, Mangelsdorf M, Jagla M, Vanderluit J, Garrick D, Gibbons RJ, Higgs DR, Slack RS, Picketts DJ.

J Clin Invest. 2005 Feb;115(2):258-67.

3.
4.

Choroideremia gene product affects trophoblast development and vascularization in mouse extra-embryonic tissues.

Shi W, van den Hurk JA, Alamo-Bethencourt V, Mayer W, Winkens HJ, Ropers HH, Cremers FP, Fundele R.

Dev Biol. 2004 Aug 1;272(1):53-65.

PMID:
15242790
5.

PML nuclear bodies and apoptosis.

Takahashi Y, Lallemand-Breitenbach V, Zhu J, de Thé H.

Oncogene. 2004 Apr 12;23(16):2819-24. Review.

PMID:
15077145
6.

A conserved truncated isoform of the ATR-X syndrome protein lacking the SWI/SNF-homology domain.

Garrick D, Samara V, McDowell TL, Smith AJ, Dobbie L, Higgs DR, Gibbons RJ.

Gene. 2004 Feb 4;326:23-34.

PMID:
14729260
7.

Inheritance of a pre-inactivated paternal X chromosome in early mouse embryos.

Huynh KD, Lee JT.

Nature. 2003 Dec 18;426(6968):857-62. Epub 2003 Dec 7.

PMID:
14661031
8.

The ATRX syndrome protein forms a chromatin-remodeling complex with Daxx and localizes in promyelocytic leukemia nuclear bodies.

Xue Y, Gibbons R, Yan Z, Yang D, McDowell TL, Sechi S, Qin J, Zhou S, Higgs D, Wang W.

Proc Natl Acad Sci U S A. 2003 Sep 16;100(19):10635-40. Epub 2003 Sep 2.

9.

Targeted disruption of Dkc1, the gene mutated in X-linked dyskeratosis congenita, causes embryonic lethality in mice.

He J, Navarrete S, Jasinski M, Vulliamy T, Dokal I, Bessler M, Mason PJ.

Oncogene. 2002 Oct 31;21(50):7740-4.

10.

Maternally transmitted severe glucose 6-phosphate dehydrogenase deficiency is an embryonic lethal.

Longo L, Vanegas OC, Patel M, Rosti V, Li H, Waka J, Merghoub T, Pandolfi PP, Notaro R, Manova K, Luzzatto L.

EMBO J. 2002 Aug 15;21(16):4229-39.

11.
12.

Lsh, a member of the SNF2 family, is required for genome-wide methylation.

Dennis K, Fan T, Geiman T, Yan Q, Muegge K.

Genes Dev. 2001 Nov 15;15(22):2940-4.

13.

Imprinted X inactivation in eutherians: a model of gametic execution and zygotic relaxation.

Huynh KD, Lee JT.

Curr Opin Cell Biol. 2001 Dec;13(6):690-7. Review.

PMID:
11698184
14.

Molecular-clinical spectrum of the ATR-X syndrome.

Gibbons RJ, Higgs DR.

Am J Med Genet. 2000 Fall;97(3):204-12. Review.

PMID:
11449489
15.

Placental development: lessons from mouse mutants.

Rossant J, Cross JC.

Nat Rev Genet. 2001 Jul;2(7):538-48. Review.

PMID:
11433360
16.
17.
18.

Genetic insights into trophoblast differentiation and placental morphogenesis.

Cross JC.

Semin Cell Dev Biol. 2000 Apr;11(2):105-13. Review.

PMID:
10873707
19.

Aberrant cell cycle checkpoint function and early embryonic death in Chk1(-/-) mice.

Takai H, Tominaga K, Motoyama N, Minamishima YA, Nagahama H, Tsukiyama T, Ikeda K, Nakayama K, Nakanishi M, Nakayama K.

Genes Dev. 2000 Jun 15;14(12):1439-47.

20.
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk