Publications

The following are recent publications from the members of this lab. Click on the title of a publication to read its abstract, or follow the Pubmed ID link to view the Pubmed entry.

CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype.

Burnight ER, Wiley LA, Drack AV, Braun TA, Anfinson KR, Kaalberg EE, Halder JA, Affatigato LM, Mullins RF, Stone EM, Tucker BA.

Gene Therapy May 8 2014
Pubmed ID: 24807808
RNA interference-based therapy for spinocerebellar ataxia type 7 retinal degeneration.

Ramachandran PS, Bhattarai S, Singh P, Boudreau RL, Thompson S, Laspada AR, Drack AV, Davidson BL.

PLoS One. Apr 23 2014
Pubmed ID: 24759684
Is age-related macular degeneration a microvascular disease?

Mullins RF, Khanna A, Schoo DP, Tucker BA, Sohn EH, Drack AV, Stone EM.

Advances in experimental medicine and biology. Mar 25 2014
Pubmed ID: 24664709
Office probing for treatment of nasolacrimal duct obstruction in infants.

Miller AM, Chandler DL, Repka MX, Hoover DL, Lee KA, Melia M, Rychwalski PJ, Silbert DI; Pediatric Eye Disease Investigator Group, Beck RW, Crouch ER 3rd, Donahue S, Holmes JM, Quinn GE, Sala NA, Schloff S, Wallace DK, Foster NC, Frick KD, Golden RP, Lamb

Journal of AAPOS Feb 22 2014
Pubmed ID: 24568978
Strabismus surgery in patients receiving warfarin anticoagulation

Kemp PS, Larson SA, Drack AV.

Journal of AAPOS Feb 22 2014
Pubmed ID: 24568993
Immunosuppressive Treatment for Retinal Degeneration in Juvenile Neuronal Ceroid Lipofuscinosis (Juvenile Batten Disease).

Drack AV, Mullins RF, Pfeifer WL, Augustine EF, Stasheff SF, Hong SD.

Ophthalmic Genetics Feb 19 2014
Pubmed ID: 24547931
TRIP8b is required for maximal expression of HCN1 in the mouse retina.

Pan Y, Bhattarai S, Modestou M, Drack AV, Chetkovich DM, Baker SA.

PLoS one Jan 7 2014
Pubmed ID: 24409334
BBS mutations modify phenotypic expression of CEP290-related ciliopathies.

Zhang Y, Seo S, Bhattarai S, Bugge K, Searby CC, Zhang Q, Drack AV, Stone EM, Sheffield VC.

Human Molecular Genetics Jan 1 2014
Pubmed ID: 23943788
Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1.

Seo S, Mullins RF, Dumitrescu AV, Bhattarai S, Gratie D, Wang K, Stone EM, Sheffield V, Drack AV

Investigative Ophthalmology & Visual Science Sep 11 2013
Pubmed ID: 23900607
Subretinal gene therapy of mice with Bardet-Biedl syndrome type 1.

Seo S, Mullins RF, Dumitrescu AV, Bhattarai S, Gratie D, Wang K, Stone EM, Sheffield V, Drack AV.

Investigative Ophthalmology & Visual Science Sep 1 2013
Pubmed ID: 23900607

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