Ali M - Search Results

1

Mutational analysis of MIR184 in sporadic keratoconus and myopia.

Lechner J, Bae HA, Guduric-Fuchs J, Rice A, Govindarajan G, Siddiqui S, Abi Farraj L, Yip SP, Yap M, Das M, Souzeau E, Coster D, Mills RA, Lindsay R, Phillips T, Mitchell P, Ali M, Inglehearn CF, Sundaresan P, Craig JE, Simpson DA, Burdon KP, Willoughby CE. Lechner J, et al. Among authors: ali m. Invest Ophthalmol Vis Sci. 2013 Aug 5;54(8):5266-72. doi: 10.1167/iovs.13-12035. Invest Ophthalmol Vis Sci. 2013. PMID: 23833072 Free article.

2

Mutation in the guanine nucleotide-binding protein beta-3 causes retinal degeneration and embryonic mortality in chickens.

Tummala H, Ali M, Getty P, Hocking PM, Burt DW, Inglehearn CF, Lester DH. Tummala H, et al. Among authors: ali m. Invest Ophthalmol Vis Sci. 2006 Nov;47(11):4714-8. doi: 10.1167/iovs.06-0292. Invest Ophthalmol Vis Sci. 2006. PMID: 17065478

3

Collagen organization in the chicken cornea and structural alterations in the retinopathy, globe enlarged (rge) phenotype--an X-ray diffraction study.

Boote C, Hayes S, Jones S, Quantock AJ, Hocking PM, Inglehearn CF, Ali M, Meek KM. Boote C, et al. Among authors: ali m. J Struct Biol. 2008 Jan;161(1):1-8. doi: 10.1016/j.jsb.2007.08.015. Epub 2007 Sep 7. J Struct Biol. 2008. PMID: 17936639

4

A missense mutation in the nuclear localization signal sequence of CERKL (p.R106S) causes autosomal recessive retinal degeneration.

Ali M, Ramprasad VL, Soumittra N, Mohamed MD, Jafri H, Rashid Y, Danciger M, McKibbin M, Kumaramanickavel G, Inglehearn CF. Ali M, et al. Mol Vis. 2008;14:1960-4. Epub 2008 Oct 30. Mol Vis. 2008. PMID: 18978954 Free PMC article.

5

Genotype-phenotype correlation for leber congenital amaurosis in Northern Pakistan.

McKibbin M, Ali M, Mohamed MD, Booth AP, Bishop F, Pal B, Springell K, Raashid Y, Jafri H, Inglehearn CF. McKibbin M, et al. Among authors: ali m. Arch Ophthalmol. 2010 Jan;128(1):107-13. doi: 10.1001/archophthalmol.2010.309. Arch Ophthalmol. 2010. PMID: 20065226

6

Proteomic profiling of the retinal dysplasia and degeneration chick retina.

Finnegan S, Robson J, Hocking PM, Ali M, Inglehearn CF, Stitt A, Curry WJ. Finnegan S, et al. Among authors: ali m. Mol Vis. 2010 Jan 11;16:7-17. Mol Vis. 2010. PMID: 20069063 Free PMC article.

7

Mutations in TSPAN12 cause autosomal-dominant familial exudative vitreoretinopathy.

Poulter JA, Ali M, Gilmour DF, Rice A, Kondo H, Hayashi K, Mackey DA, Kearns LS, Ruddle JB, Craig JE, Pierce EA, Downey LM, Mohamed MD, Markham AF, Inglehearn CF, Toomes C. Poulter JA, et al. Among authors: ali m. Am J Hum Genet. 2010 Feb 12;86(2):248-53. doi: 10.1016/j.ajhg.2010.01.012. Am J Hum Genet. 2010. PMID: 20159112 Free PMC article.

8

Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma.

Ali M, Buentello-Volante B, McKibbin M, Rocha-Medina JA, Fernandez-Fuentes N, Koga-Nakamura W, Ashiq A, Khan K, Booth AP, Williams G, Raashid Y, Jafri H, Rice A, Inglehearn CF, Zenteno JC. Ali M, et al. Mol Vis. 2010 Jun 23;16:1162-8. Mol Vis. 2010. PMID: 20664696 Free PMC article.

9

The influence of lamellar orientation on corneal material behavior: biomechanical and structural changes in an avian corneal disorder.

Boote C, Elsheikh A, Kassem W, Kamma-Lorger CS, Hocking PM, White N, Inglehearn CF, Ali M, Meek KM. Boote C, et al. Among authors: ali m. Invest Ophthalmol Vis Sci. 2011 Mar 10;52(3):1243-51. doi: 10.1167/iovs.10-5962. Print 2011 Mar. Invest Ophthalmol Vis Sci. 2011. PMID: 21051696 Free PMC article.

10

Familial pattern of Salzmann-type nodular corneal degeneration – a four generation series. Reply to Papanikolaou et al.

Khan K, Ali M, Inglehearn C. Khan K, et al. Among authors: ali m. Br J Ophthalmol. 2011 Jun;95(6):890; author reply 890. doi: 10.1136/bjo.2010.198655. Epub 2010 Dec 16. Br J Ophthalmol. 2011. PMID: 21169267 No abstract available.

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