Mackey DA - Search Results

1

Key challenges in bringing CRISPR-mediated somatic cell therapy into the clinic.

Nicol D, Eckstein L, Morrison M, Sherkow JS, Otlowski M, Whitton T, Bubela T, Burdon KP, Chalmers D, Chan S, Charlesworth J, Critchley C, Crossley M, de Lacey S, Dickinson JL, Hewitt AW, Kamens J, Kato K, Kleiderman E, Kodama S, Liddicoat J, Mackey DA, Newson AJ, Nielsen J, Wagner JK, McWhirter RE. Nicol D, et al. Among authors: mackey da. Genome Med. 2017 Sep 25;9(1):85. doi: 10.1186/s13073-017-0475-4. Genome Med. 2017. PMID: 28946923 Free PMC article.

2

Laboratory methods in ophthalmic genetics: obtaining DNA from patients.

Dickinson JL, Sale MM, Craig JE, Mackey DA. Dickinson JL, et al. Among authors: mackey da. Ophthalmic Genet. 2001 Mar;22(1):49-60. doi: 10.1076/opge.22.1.49.2240. Ophthalmic Genet. 2001. PMID: 11262650 Review.

3

The Taa1 restriction enzyme provides a simple means to identify the Q368STOP mutation of the myocilin gene in primary open angle glaucoma.

Baird PN, Dickinson J, Craig JE, Mackey DA. Baird PN, et al. Among authors: mackey da. Am J Ophthalmol. 2001 Apr;131(4):510-1. doi: 10.1016/s0002-9394(00)00812-6. Am J Ophthalmol. 2001. PMID: 11292420

4

Retinopathy of prematurity: recent advances in our understanding.

Wheatley CM, Dickinson JL, Mackey DA, Craig JE, Sale MM. Wheatley CM, et al. Among authors: mackey da. Br J Ophthalmol. 2002 Jun;86(6):696-700. doi: 10.1136/bjo.86.6.696. Br J Ophthalmol. 2002. PMID: 12034695 Free PMC article. Review.

5

Retinopathy of prematurity: recent advances in our understanding.

Wheatley CM, Dickinson JL, Mackey DA, Craig JE, Sale MM. Wheatley CM, et al. Among authors: mackey da. Arch Dis Child Fetal Neonatal Ed. 2002 Sep;87(2):F78-82. doi: 10.1136/fn.87.2.f78. Arch Dis Child Fetal Neonatal Ed. 2002. PMID: 12193510 Free PMC article. Review.

6

The apolipoprotein epsilon4 gene is associated with elevated risk of normal tension glaucoma.

Vickers JC, Craig JE, Stankovich J, McCormack GH, West AK, Dickinson JL, McCartney PJ, Coote MA, Healey DL, Mackey DA. Vickers JC, et al. Among authors: mackey da. Mol Vis. 2002 Oct 14;8:389-93. Mol Vis. 2002. PMID: 12379839 Free article.

7

Investigation of crystallin genes in familial cataract, and report of two disease associated mutations.

Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM. Burdon KP, et al. Among authors: mackey da. Br J Ophthalmol. 2004 Jan;88(1):79-83. doi: 10.1136/bjo.88.1.79. Br J Ophthalmol. 2004. PMID: 14693780 Free PMC article.

8

A novel mutation in the Connexin 46 gene causes autosomal dominant congenital cataract with incomplete penetrance.

Burdon KP, Wirth MG, Mackey DA, Russell-Eggitt IM, Craig JE, Elder JE, Dickinson JL, Sale MM. Burdon KP, et al. Among authors: mackey da. J Med Genet. 2004 Aug;41(8):e106. doi: 10.1136/jmg.2004.018333. J Med Genet. 2004. PMID: 15286166 Free PMC article. No abstract available.

9

Genotypic and phenotypic spectrum of X-linked retinoschisis in Australia.

Hewitt AW, FitzGerald LM, Scotter LW, Mulhall LE, McKay JD, Mackey DA. Hewitt AW, et al. Among authors: mackey da. Clin Exp Ophthalmol. 2005 Jun;33(3):233-9. doi: 10.1111/j.1442-9071.2005.01018.x. Clin Exp Ophthalmol. 2005. PMID: 15932525

10

Central corneal thickness is highly heritable: the twin eye studies.

Toh T, Liew SH, MacKinnon JR, Hewitt AW, Poulsen JL, Spector TD, Gilbert CE, Craig JE, Hammond CJ, Mackey DA. Toh T, et al. Among authors: mackey da. Invest Ophthalmol Vis Sci. 2005 Oct;46(10):3718-22. doi: 10.1167/iovs.04-1497. Invest Ophthalmol Vis Sci. 2005. PMID: 16186354 Free article.

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