Development of feline microsatellites and SNPs for evaluating primary cataract candidate genes as cause for cataract in Angolan lions (Panthera leo bleyenberghi).
暂无分享,去创建一个
[1] R. Agarwala,et al. A high-resolution cat radiation hybrid and integrated FISH mapping resource for phylogenomic studies across Felidae. , 2009, Genomics.
[2] C. Kannabiran,et al. A missense mutation in LIM2 causes autosomal recessive congenital cataract , 2008, Molecular vision.
[3] J. Hejtmancik. Congenital cataracts and their molecular genetics. , 2008, Seminars in cell & developmental biology.
[4] Yanhua Qi,et al. A substitution of arginine to lysine at the COOH-terminus of MIP caused a different binocular phenotype in a congenital cataract family. , 2007, Molecular vision.
[5] K. Sperling,et al. A novel mutation in the connexin 46 (GJA3) gene associated with autosomal dominant congenital cataract in an Indian family. , 2007, Molecular vision.
[6] S. O’Brien,et al. Genome Annotation Resource Fields--GARFIELD: a genome browser for Felis catus. , 2007, The Journal of heredity.
[7] Qingjiong Zhang,et al. Insights into the beaded filament of the eye lens. , 2007, Experimental cell research.
[8] V. Vanita,et al. A novel "pearl box" cataract associated with a mutation in the connexin 46 (GJA3) gene , 2007, Molecular vision.
[9] A. Bernhard,et al. Lens-Anomalies and Other Ophthalmic Findings in a Group of Closely-Related Angola Lions (Panthera leo bleyenberghi) , 2006 .
[10] Colin A. Johnson,et al. Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutations , 2005, Human Genetics.
[11] D. Hunt,et al. A novel GJA8 mutation is associated with autosomal dominant lamellar pulverulent cataract: further evidence for gap junction dysfunction in human cataract , 2005, Journal of Medical Genetics.
[12] J. Graw. Congenital hereditary cataracts. , 2004, The International journal of developmental biology.
[13] S. Bhattacharya,et al. Functional impairment of lens aquaporin in two families with dominantly inherited cataracts. , 2000, Human molecular genetics.
[14] S. Bhattacharya,et al. The genetics of childhood cataract , 2000, Journal of medical genetics.
[15] D. Weeks,et al. A juvenile-onset, progressive cataract locus on chromosome 3q21-q22 is associated with a missense mutation in the beaded filament structural protein-2. , 2000, American journal of human genetics.
[16] S. Bhattacharya,et al. Connexin46 mutations in autosomal dominant congenital cataract. , 1999, American journal of human genetics.
[17] R. Ferrell,et al. A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMD , 1998, Nature Genetics.
[18] S. Bhattacharya,et al. A missense mutation in the human connexin50 gene (GJA8) underlies autosomal dominant "zonular pulverulent" cataract, on chromosome 1q. , 1998, American journal of human genetics.
[19] N J Cox,et al. Allele-sharing models: LOD scores and accurate linkage tests. , 1997, American journal of human genetics.
[20] Richard L. Maas,et al. PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects , 1994, Nature Genetics.
[21] A. Whittemore,et al. A class of tests for linkage using affected pedigree members. , 1994, Biometrics.
[22] C D Thatcher,et al. Comparison of kittens fed queen's milk with those fed milk replacers. , 1993, American journal of veterinary research.
[23] I. Weisse,et al. Operation einer kongenitalen Katarakt bei einem Sibirischen Tiger , 1979 .
[24] Gelatt Kn,et al. Congenital cataracts in a Persian kitten (a case report). , 1975 .
[25] G. Abecasis,et al. Merlin—rapid analysis of dense genetic maps using sparse gene flow trees , 2002, Nature Genetics.
[26] I. Weisse,et al. [Operation on a congenital cataract in a Siberian Tiger]. , 1979, Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift fur Augenheilkunde.