Williams LH - Search Results

1

Annexin XI co-localises with calcyclin in proliferating cells of the embryonic mouse testis.

Williams LH, McClive PJ, Van Den Bergen JA, Sinclair AH. Williams LH, et al. Dev Dyn. 2005 Oct;234(2):432-7. doi: 10.1002/dvdy.20548. Dev Dyn. 2005. PMID: 16127703 Free article.

2

Genetic and epigenetic analysis of CHEK2 in sporadic breast, colon, and ovarian cancers.

Williams LH, Choong D, Johnson SA, Campbell IG. Williams LH, et al. Clin Cancer Res. 2006 Dec 1;12(23):6967-72. doi: 10.1158/1078-0432.CCR-06-1770. Clin Cancer Res. 2006. PMID: 17145815

3

Identification of three novel hearing loss mouse strains with mutations in the Tmc1 gene.

Manji SS, Miller KA, Williams LH, Dahl HH. Manji SS, et al. Among authors: williams lh. Am J Pathol. 2012 Apr;180(4):1560-9. doi: 10.1016/j.ajpath.2011.12.034. Epub 2012 Feb 11. Am J Pathol. 2012. PMID: 22330676

4

Identification of candidate growth promoting genes in ovarian cancer through integrated copy number and expression analysis.

Ramakrishna M, Williams LH, Boyle SE, Bearfoot JL, Sridhar A, Speed TP, Gorringe KL, Campbell IG. Ramakrishna M, et al. Among authors: williams lh. PLoS One. 2010 Apr 8;5(4):e9983. doi: 10.1371/journal.pone.0009983. PLoS One. 2010. PMID: 20386695 Free PMC article.

5

Characterization of a novel ENU-generated myosin VI mutant mouse strain with congenital deafness and vestibular dysfunction.

Williams LH, Miller KA, Dahl HH, Manji SS. Williams LH, et al. Hear Res. 2013 May;299:53-62. doi: 10.1016/j.heares.2013.02.006. Epub 2013 Feb 26. Hear Res. 2013. PMID: 23485424

6

Eeyore: a novel mouse model of hereditary deafness.

Miller KA, Williams LH, Dahl HH, Manji SS. Miller KA, et al. Among authors: williams lh. PLoS One. 2013 Sep 23;8(9):e74243. doi: 10.1371/journal.pone.0074243. eCollection 2013. PLoS One. 2013. PMID: 24086324 Free PMC article.

7

An ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in mice.

Manji SS, Miller KA, Williams LH, Andreasen L, Siboe M, Rose E, Bahlo M, Kuiper M, Dahl HH. Manji SS, et al. Among authors: williams lh. Am J Pathol. 2011 Aug;179(2):903-14. doi: 10.1016/j.ajpath.2011.04.002. Epub 2011 Jun 2. Am J Pathol. 2011. PMID: 21689626 Free PMC article.

8

A mutation in synaptojanin 2 causes progressive hearing loss in the ENU-mutagenised mouse strain Mozart.

Manji SS, Williams LH, Miller KA, Ooms LM, Bahlo M, Mitchell CA, Dahl HH. Manji SS, et al. Among authors: williams lh. PLoS One. 2011 Mar 15;6(3):e17607. doi: 10.1371/journal.pone.0017607. PLoS One. 2011. PMID: 21423608 Free PMC article.

9

ST7-mediated suppression of tumorigenicity of prostate cancer cells is characterized by remodeling of the extracellular matrix.

Hooi CF, Blancher C, Qiu W, Revet IM, Williams LH, Ciavarella ML, Anderson RL, Thompson EW, Connor A, Phillips WA, Campbell IG. Hooi CF, et al. Among authors: williams lh. Oncogene. 2006 Jun 29;25(28):3924-33. doi: 10.1038/sj.onc.1209418. Epub 2006 Feb 13. Oncogene. 2006. PMID: 16474848

10

Inner ear morphology is perturbed in two novel mouse models of recessive deafness.

Miller KA, Williams LH, Rose E, Kuiper M, Dahl HH, Manji SS. Miller KA, et al. Among authors: williams lh. PLoS One. 2012;7(12):e51284. doi: 10.1371/journal.pone.0051284. Epub 2012 Dec 12. PLoS One. 2012. PMID: 23251483 Free PMC article.

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