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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2008 | 1 |
2009 | 1 |
2010 | 1 |
2011 | 1 |
2012 | 1 |
2024 | 0 |
Search Results
5 results
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Page 1
Proteomic profiling of the retinal dysplasia and degeneration chick retina.
Mol Vis. 2010 Jan 11;16:7-17.
Mol Vis. 2010.
PMID: 20069063
Free PMC article.
Null mutations in LTBP2 cause primary congenital glaucoma.
Ali M, McKibbin M, Booth A, Parry DA, Jain P, Riazuddin SA, Hejtmancik JF, Khan SN, Firasat S, Shires M, Gilmour DF, Towns K, Murphy AL, Azmanov D, Tournev I, Cherninkova S, Jafri H, Raashid Y, Toomes C, Craig J, Mackey DA, Kalaydjieva L, Riazuddin S, Inglehearn CF.
Ali M, et al.
Am J Hum Genet. 2009 May;84(5):664-71. doi: 10.1016/j.ajhg.2009.03.017. Epub 2009 Apr 9.
Am J Hum Genet. 2009.
PMID: 19361779
Free PMC article.
Item in Clipboard
Profiling retinal biochemistry in the MPDZ mutant retinal dysplasia and degeneration chick: a model of human RP and LCA.
Beattie JR, Finnegan S, Hamilton RW, Ali M, Inglehearn CF, Stitt AW, McGarvey JJ, Hocking PM, Curry WJ.
Beattie JR, et al.
Invest Ophthalmol Vis Sci. 2012 Jan 25;53(1):413-20. doi: 10.1167/iovs.11-8591.
Invest Ophthalmol Vis Sci. 2012.
PMID: 22159006
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The D153del mutation in GNB3 gene causes tissue specific signalling patterns and an abnormal renal morphology in Rge chickens.
Tummala H, Fleming S, Hocking PM, Wehner D, Naseem Z, Ali M, Inglehearn CF, Zhelev N, Lester DH.
Tummala H, et al.
PLoS One. 2011;6(8):e21156. doi: 10.1371/journal.pone.0021156. Epub 2011 Aug 22.
PLoS One. 2011.
PMID: 21887213
Free PMC article.
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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.
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