Oliver PL - Search Results

1

The mixed-lineage leukemia fusion partner AF4 stimulates RNA polymerase II transcriptional elongation and mediates coordinated chromatin remodeling.

Bitoun E, Oliver PL, Davies KE. Bitoun E, et al. Among authors: oliver pl. Hum Mol Genet. 2007 Jan 1;16(1):92-106. doi: 10.1093/hmg/ddl444. Epub 2006 Nov 29. Hum Mol Genet. 2007. PMID: 17135274

2

Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy.

Isaacs AM, Jeans A, Oliver PL, Vizor L, Brown SD, Hunter AJ, Davies KE. Isaacs AM, et al. Among authors: oliver pl. Mol Cell Neurosci. 2002 Sep;21(1):114-25. doi: 10.1006/mcne.2002.1158. Mol Cell Neurosci. 2002. PMID: 12359155

3

A mutation in Af4 is predicted to cause cerebellar ataxia and cataracts in the robotic mouse.

Isaacs AM, Oliver PL, Jones EL, Jeans A, Potter A, Hovik BH, Nolan PM, Vizor L, Glenister P, Simon AK, Gray IC, Spurr NK, Brown SD, Hunter AJ, Davies KE. Isaacs AM, et al. Among authors: oliver pl. J Neurosci. 2003 Mar 1;23(5):1631-7. doi: 10.1523/JNEUROSCI.23-05-01631.2003. J Neurosci. 2003. PMID: 12629167 Free PMC article.

4

Mediation of Af4 protein function in the cerebellum by Siah proteins.

Oliver PL, Bitoun E, Clark J, Jones EL, Davies KE. Oliver PL, et al. Proc Natl Acad Sci U S A. 2004 Oct 12;101(41):14901-6. doi: 10.1073/pnas.0406196101. Epub 2004 Sep 30. Proc Natl Acad Sci U S A. 2004. PMID: 15459319 Free PMC article.

5

Expression profiling in spinal muscular atrophy reveals an RNA binding protein deficit.

Anderson KN, Baban D, Oliver PL, Potter A, Davies KE. Anderson KN, et al. Among authors: oliver pl. Neuromuscul Disord. 2004 Nov;14(11):711-22. doi: 10.1016/j.nmd.2004.08.009. Neuromuscul Disord. 2004. PMID: 15482955

6

Analysis of human neurological disorders using mutagenesis in the mouse.

Oliver PL, Davies KE. Oliver PL, et al. Clin Sci (Lond). 2005 May;108(5):385-97. doi: 10.1042/CS20050041. Clin Sci (Lond). 2005. PMID: 15831088 Review.

7

Identification and characterization of murine SCARA5, a novel class A scavenger receptor that is expressed by populations of epithelial cells.

Jiang Y, Oliver P, Davies KE, Platt N. Jiang Y, et al. J Biol Chem. 2006 Apr 28;281(17):11834-45. doi: 10.1074/jbc.M507599200. Epub 2006 Jan 6. J Biol Chem. 2006. PMID: 16407294 Free article.

8

Mutations in alpha-tubulin cause abnormal neuronal migration in mice and lissencephaly in humans.

Keays DA, Tian G, Poirier K, Huang GJ, Siebold C, Cleak J, Oliver PL, Fray M, Harvey RJ, Molnár Z, Piñon MC, Dear N, Valdar W, Brown SD, Davies KE, Rawlins JN, Cowan NJ, Nolan P, Chelly J, Flint J. Keays DA, et al. Among authors: oliver pl. Cell. 2007 Jan 12;128(1):45-57. doi: 10.1016/j.cell.2006.12.017. Cell. 2007. PMID: 17218254 Free PMC article.

9

A dominant mutation in Snap25 causes impaired vesicle trafficking, sensorimotor gating, and ataxia in the blind-drunk mouse.

Jeans AF, Oliver PL, Johnson R, Capogna M, Vikman J, Molnár Z, Babbs A, Partridge CJ, Salehi A, Bengtsson M, Eliasson L, Rorsman P, Davies KE. Jeans AF, et al. Among authors: oliver pl. Proc Natl Acad Sci U S A. 2007 Feb 13;104(7):2431-6. doi: 10.1073/pnas.0610222104. Epub 2007 Feb 5. Proc Natl Acad Sci U S A. 2007. PMID: 17283335 Free PMC article.

10

Comparative genetic analysis: the utility of mouse genetic systems for studying human monogenic disease.

Oliver PL, Bitoun E, Davies KE. Oliver PL, et al. Mamm Genome. 2007 Jul;18(6-7):412-24. doi: 10.1007/s00335-007-9014-8. Epub 2007 May 21. Mamm Genome. 2007. PMID: 17514509 Free PMC article. Review.

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