GRAEME MARDON to Female
This is a "connection" page, showing publications GRAEME MARDON has written about Female.
Connection Strength
0.174
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Single cell RNA sequencing of the adult Drosophila eye reveals distinct clusters and novel marker genes for all major cell types. Commun Biol. 2022 12 14; 5(1):1370.
Score: 0.033
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Conditional loss of Kcnj13 in the retinal pigment epithelium causes photoreceptor degeneration. Exp Eye Res. 2018 11; 176:219-226.
Score: 0.025
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Eyes absent tyrosine phosphatase activity is not required for Drosophila development or survival. PLoS One. 2013; 8(3):e58818.
Score: 0.017
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Mouse Dach1 and Dach2 are redundantly required for M?llerian duct development. Genesis. 2008 Apr; 46(4):205-13.
Score: 0.012
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Mouse Dach2 mutants do not exhibit gross defects in eye development or brain function. Genesis. 2006 Feb; 44(2):84-92.
Score: 0.010
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Structure-function analysis of the Drosophila retinal determination protein Dachshund. Dev Biol. 2004 Aug 01; 272(1):231-47.
Score: 0.009
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High-depth African genomes inform human migration and health. Nature. 2020 10; 586(7831):741-748.
Score: 0.007
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The potassium channel KCNJ13 is essential for smooth muscle cytoskeletal organization during mouse tracheal tubulogenesis. Nat Commun. 2018 07 19; 9(1):2815.
Score: 0.006
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NMNAT1 E257K variant, associated with Leber Congenital Amaurosis (LCA9), causes a mild retinal degeneration phenotype. Exp Eye Res. 2018 08; 173:32-43.
Score: 0.006
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POU6f1 Mediates Neuropeptide-Dependent Plasticity in the Adult Brain. J Neurosci. 2018 02 07; 38(6):1443-1461.
Score: 0.006
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The collaborative African genomics network training program: a trainee perspective on training the next generation of African scientists. Genet Med. 2017 07; 19(7):826-833.
Score: 0.006
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Ectopic eye development in Drosophila induced by directed dachshund expression. Development. 1997 Jan; 124(1):45-52.
Score: 0.006
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A Genetic Mechanism for Convergent Skin Lightening during Recent Human Evolution. Mol Biol Evol. 2016 05; 33(5):1177-87.
Score: 0.005
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Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration. Nat Genet. 2012 Sep; 44(9):1035-9.
Score: 0.004
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Exome capture sequencing identifies a novel mutation in BBS4. Mol Vis. 2011; 17:3529-40.
Score: 0.004
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Mouse Zfx protein is similar to Zfy-2: each contains an acidic activating domain and 13 zinc fingers. Mol Cell Biol. 1990 Feb; 10(2):681-8.
Score: 0.003
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The Dachshund gene in development and hormone-responsive tumorigenesis. Trends Endocrinol Metab. 2010 Jan; 21(1):41-9.
Score: 0.003
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Mutation survey of known LCA genes and loci in the Saudi Arabian population. Invest Ophthalmol Vis Sci. 2009 Mar; 50(3):1336-43.
Score: 0.003
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A genetic screen in Drosophila for genes interacting with senseless during neuronal development identifies the importin moleskin. Genetics. 2007 Jan; 175(1):125-41.
Score: 0.003
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Dach1, a vertebrate homologue of Drosophila dachshund, is expressed in the developing eye and ear of both chick and mouse and is regulated independently of Pax and Eya genes. Mech Dev. 2002 Feb; 111(1-2):75-87.
Score: 0.002
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Synergistic regulation of vertebrate muscle development by Dach2, Eya2, and Six1, homologs of genes required for Drosophila eye formation. Genes Dev. 1999 Dec 15; 13(24):3231-43.
Score: 0.002
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Putative transcription activator with alternative isoforms encoded by human ZFX gene. Nature. 1989 Dec 07; 342(6250):708-11.
Score: 0.001
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The sex-determining region of the human Y chromosome encodes a finger protein. Cell. 1987 Dec 24; 51(6):1091-104.
Score: 0.001