Semina EV - Search Results

1

Mutations in laminin alpha 1 result in complex, lens-independent ocular phenotypes in zebrafish.

Semina EV, Bosenko DV, Zinkevich NC, Soules KA, Hyde DR, Vihtelic TS, Willer GB, Gregg RG, Link BA. Semina EV, et al. Dev Biol. 2006 Nov 1;299(1):63-77. doi: 10.1016/j.ydbio.2006.07.005. Epub 2006 Jul 12. Dev Biol. 2006. PMID: 16973147 Free article.

2

Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts.

Semina EV, Brownell I, Mintz-Hittner HA, Murray JC, Jamrich M. Semina EV, et al. Hum Mol Genet. 2001 Feb 1;10(3):231-6. doi: 10.1093/hmg/10.3.231. Hum Mol Genet. 2001. PMID: 11159941

3

Using zebrafish to study the complex genetics of glaucoma.

McMahon C, Semina EV, Link BA. McMahon C, et al. Among authors: semina ev. Comp Biochem Physiol C Toxicol Pharmacol. 2004 Jul;138(3):343-50. doi: 10.1016/j.cca.2004.03.003. Comp Biochem Physiol C Toxicol Pharmacol. 2004. PMID: 15533792 Review.

4

Zebrafish pitx3 is necessary for normal lens and retinal development.

Shi X, Bosenko DV, Zinkevich NS, Foley S, Hyde DR, Semina EV, Vihtelic TS. Shi X, et al. Among authors: semina ev. Mech Dev. 2005 Apr;122(4):513-27. doi: 10.1016/j.mod.2004.11.012. Epub 2004 Dec 10. Mech Dev. 2005. PMID: 15804565 Free article.

5

laminin alpha 1 gene is essential for normal lens development in zebrafish.

Zinkevich NS, Bosenko DV, Link BA, Semina EV. Zinkevich NS, et al. Among authors: semina ev. BMC Dev Biol. 2006 Mar 7;6:13. doi: 10.1186/1471-213X-6-13. BMC Dev Biol. 2006. PMID: 16522196 Free PMC article.

6

Functional analysis of human mutations in homeodomain transcription factor PITX3.

Sakazume S, Sorokina E, Iwamoto Y, Semina EV. Sakazume S, et al. Among authors: semina ev. BMC Mol Biol. 2007 Sep 21;8:84. doi: 10.1186/1471-2199-8-84. BMC Mol Biol. 2007. PMID: 17888164 Free PMC article.

7

Examination of SOX2 in variable ocular conditions identifies a recurrent deletion in microphthalmia and lack of mutations in other phenotypes.

Reis LM, Tyler RC, Schneider A, Bardakjian T, Semina EV. Reis LM, et al. Among authors: semina ev. Mol Vis. 2010 Apr 28;16:768-73. Mol Vis. 2010. PMID: 20454695 Free PMC article.

8

Potential novel mechanism for Axenfeld-Rieger syndrome: deletion of a distant region containing regulatory elements of PITX2.

Volkmann BA, Zinkevich NS, Mustonen A, Schilter KF, Bosenko DV, Reis LM, Broeckel U, Link BA, Semina EV. Volkmann BA, et al. Among authors: semina ev. Invest Ophthalmol Vis Sci. 2011 Mar 18;52(3):1450-9. doi: 10.1167/iovs.10-6060. Print 2011 Mar. Invest Ophthalmol Vis Sci. 2011. PMID: 20881290 Free PMC article.

9

Genetics of anterior segment dysgenesis disorders.

Reis LM, Semina EV. Reis LM, et al. Among authors: semina ev. Curr Opin Ophthalmol. 2011 Sep;22(5):314-24. doi: 10.1097/ICU.0b013e328349412b. Curr Opin Ophthalmol. 2011. PMID: 21730847 Free PMC article. Review.

10

pitx2 Deficiency results in abnormal ocular and craniofacial development in zebrafish.

Liu Y, Semina EV. Liu Y, et al. Among authors: semina ev. PLoS One. 2012;7(1):e30896. doi: 10.1371/journal.pone.0030896. Epub 2012 Jan 27. PLoS One. 2012. PMID: 22303467 Free PMC article.

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