Lyon MF - Search Results

1

Activating calcium-sensing receptor mutation in the mouse is associated with cataracts and ectopic calcification.

Hough TA, Bogani D, Cheeseman MT, Favor J, Nesbit MA, Thakker RV, Lyon MF. Hough TA, et al. Among authors: lyon mf. Proc Natl Acad Sci U S A. 2004 Sep 14;101(37):13566-71. doi: 10.1073/pnas.0405516101. Epub 2004 Sep 3. Proc Natl Acad Sci U S A. 2004. PMID: 15347804 Free PMC article.

2

A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding.

Lyon MF, Jamieson RV, Perveen R, Glenister PH, Griffiths R, Boyd Y, Glimcher LH, Favor J, Munier FL, Black GC. Lyon MF, et al. Hum Mol Genet. 2003 Mar 15;12(6):585-94. Hum Mol Genet. 2003. PMID: 12620964

3

Two new cataract loci, Ccw and To3, and further mapping of the Npp and Opj cataracts in the mouse.

Kerscher S, Glenister PH, Favor J, Lyon MF. Kerscher S, et al. Among authors: lyon mf. Genomics. 1996 Aug 15;36(1):17-21. doi: 10.1006/geno.1996.0420. Genomics. 1996. PMID: 8812411

4

Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop).

Lyon MF, Bogani D, Boyd Y, Guillot P, Favor J. Lyon MF, et al. Mol Vis. 2000 Oct 31;6:199-203. Mol Vis. 2000. PMID: 11062307 Free article.

5

Mapping of six dominant cataract genes in the mouse.

Everett CA, Glenister PH, Taylor DM, Lyon MF, Kratochvilova-Loester J, Favor J. Everett CA, et al. Among authors: lyon mf. Genomics. 1994 Apr;20(3):429-34. doi: 10.1006/geno.1994.1197. Genomics. 1994. PMID: 8034315

6

Endogenous retroviral insertion in Cryge in the mouse No3 cataract mutant.

Nag N, Peterson K, Wyatt K, Hess S, Ray S, Favor J, Bogani D, Lyon M, Wistow G. Nag N, et al. Genomics. 2007 Apr;89(4):512-20. doi: 10.1016/j.ygeno.2006.12.003. Epub 2007 Jan 12. Genomics. 2007. PMID: 17223009 Free PMC article.

7

A mutation in the connexin 50 (Cx50) gene is a candidate for the No2 mouse cataract.

Steele EC Jr, Lyon MF, Favor J, Guillot PV, Boyd Y, Church RL. Steele EC Jr, et al. Among authors: lyon mf. Curr Eye Res. 1998 Sep;17(9):883-9. doi: 10.1076/ceyr.17.9.883.5144. Curr Eye Res. 1998. PMID: 9746435

8

Identification of a mutation in the MP19 gene, Lim2, in the cataractous mouse mutant To3.

Steele EC Jr, Kerscher S, Lyon MF, Glenister PH, Favor J, Wang J, Church RL. Steele EC Jr, et al. Among authors: lyon mf. Mol Vis. 1997 May 7;3:5. Mol Vis. 1997. PMID: 9238094 Free article.

9

LINE-1 elements and X chromosome inactivation: a function for "junk" DNA?

Lyon MF. Lyon MF. Proc Natl Acad Sci U S A. 2000 Jun 6;97(12):6248-9. doi: 10.1073/pnas.97.12.6248. Proc Natl Acad Sci U S A. 2000. PMID: 10841528 Free PMC article. No abstract available.

10

A gene affecting Wallerian nerve degeneration maps distally on mouse chromosome 4.

Lyon MF, Ogunkolade BW, Brown MC, Atherton DJ, Perry VH. Lyon MF, et al. Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9717-20. doi: 10.1073/pnas.90.20.9717. Proc Natl Acad Sci U S A. 1993. PMID: 8415768 Free PMC article.

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