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2011
C. Y. Pan, Lan, X. Y., Zhao, H. Y., Hu, S. R., Huai, Y. T., Lei, C. Z., and Chen, H., A novel genetic variant of the goat Six6 gene and its association with production traits in Chinese goat breeds, vol. 10, pp. 3888-3900, 2011.
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Dyn. 234: 718-725. http://dx.doi.org/10.1002/dvdy.20463 PMid:15973738   Diaczok D, Romero C, Zunich J, Marshall I, et al. (2008). A novel dominant negative mutation of OTX2 associated with combined pituitary hormone deficiency. J. Clin. Endocr. Metab. 93: 4351-4359. http://dx.doi.org/10.1210/jc.2008-1189 PMid:18728160 PMCid:2582563   Eller A, Branch DW, Nelson L and Silver R (2008). 247: The -634GC polymorphism in the regulatory 5ꞌ untranslated region (5' UTR) of the vascular endothelial growth factor (VEGF) gene is associated with unexplained recurrent pregnancy loss (RPL). Am. J. Obstet. Gynecol. 199 (Suppl 1): S81. http://dx.doi.org/10.1016/j.ajog.2008.09.275   Greenwood TA and Kelsoe JR (2003). Promoter and intronic variants affect the transcriptional regulation of the human dopamine transporter gene. Genomics 82: 511-520. http://dx.doi.org/10.1016/S0888-7543(03)00142-3   Gupta N, Ahlawat SPS, Kumar D, Gupta SC, et al. (2007). Single nucleotide polymorphism in growth hormone gene exon-4 and exon-5 using PCR-SSCP in Black Bengal goats - a prolific meat breed of India. Meat Sci. 76: 658-665. http://dx.doi.org/10.1016/j.meatsci.2007.02.005 PMid:22061242   Hu S, Mamedova A and Hegde RS (2008). DNA-binding and regulation mechanisms of the SIX family of retinal determination proteins. Biochemistry 47: 3586-3594. http://dx.doi.org/10.1021/bi702186s PMid:18293925   Huai YT, Lan XY, Ma L, Wang J, et al. (2011). Novel mutation in TGA stop-codon of bovine SIX6 gene. Mol. Biol. 45: 218-224. http://dx.doi.org/10.1134/S0026893310061093   Jean D, Bernier G and Gruss P (1999). Six6 (Optx2) is a novel murine Six3-related homeobox gene that demarcates the presumptive pituitary/hypothalamic axis and the ventral optic stalk. Mech. Dev. 84: 31-40. http://dx.doi.org/10.1016/S0925-4773(99)00068-4   Kim DJ, Park BL, Yoon S, Lee HK, et al. (2007). 5' UTR polymorphism of dopamine receptor D1 (DRD1) associated with severity and temperament of alcoholism. Biochem. Biophys. Res. Commun. 357: 1135-1141. http://dx.doi.org/10.1016/j.bbrc.2007.04.074 PMid:17466946   Kumar JP (2009). The sine oculis homeobox (SIX) family of transcription factors as regulators of development and disease. Cell Mol. Life Sci. 66: 565-583. http://dx.doi.org/10.1007/s00018-008-8335-4 PMid:18989625 PMCid:2716997   Lai X, Lan X, Chen H, Wang X, et al. (2009). A novel SNP of the Hesx1 gene in bovine and its associations with average daily gain. Mol. Biol. Rep. 36: 1677-1681. http://dx.doi.org/10.1007/s11033-008-9368-3 PMid:18853282   Lan XY, Pan CY, Chen H, Zhang CL, et al. (2007). An AluI PCR-RFLP detecting a silent allele at the goat POU1F1 locus and its association with production traits. Small Rumin. Res. 73: 12. http://dx.doi.org/10.1016/j.smallrumres.2006.10.009   Lan XY, Pan CY, Li JY, Guo YW, et al. (2009a). Twelve novel SNPs of the goat POU1F1 gene and their associations with cashmere traits. Small Rumin. Res. 85: 116-121. http://dx.doi.org/10.1016/j.smallrumres.2009.08.002   Lan X, Pan C, Zhang L, Zhao M, et al. (2009b). A novel missense (A79V) mutation of goat PROP1 gene and its association with production traits. Mol. Biol. Rep. 36: 2069-2073. http://dx.doi.org/10.1007/s11033-008-9418-x PMid:19031010   Lan XY, Lai X, Li ZJ, Wang J, et al. (2010) Effects of genetic variability of the caprine homeobox transcription factor HESX1 gene on performance traits. Mol. Biol. Rep. 37: 441-449. http://dx.doi.org/10.1007/s11033-009-9625-0 PMid:19629745   Lasky-Su J and Lange C (2010). Statistical challenges for genome-wide association studies of suicidality using family data. Eur. Psychiatry 25: 307-309. http://dx.doi.org/10.1016/j.eurpsy.2009.12.019 PMid:20447807 PMCid:2925169   Lawson MJ and Zhang L (2008). Housekeeping and tissue-specific genes differ in simple sequence repeats in the 5'-UTR region. Gene 407: 54-62. http://dx.doi.org/10.1016/j.gene.2007.09.017 PMid:17964742   Li MJ, Lan XY, Chen H, Zhang LZ, et al. (2008). The novel missense mutation of goat LHX4 gene. Small Rumin. Res. 79: 109-112. http://dx.doi.org/10.1016/j.smallrumres.2008.06.005   Li S, Crenshaw EB, Rawson EJ, Simmons DM, et al. (1990). Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene Pit-1. Nature 347: 528-533. http://dx.doi.org/10.1038/347528a0 PMid:1977085   Liang Y, Cui J, Yang G, Leung FC, et al. (2006). Polymorphisms of 5' flanking region of chicken prolactin gene. Domest. Anim. Endocrinol. 30: 1-16. http://dx.doi.org/10.1016/j.domaniend.2005.05.006 PMid:15970423   Medeiros-Neto G, de Lacerda L and Wondisford FE (1997). Familial Congenital Hypothyroidism Caused by Abnormal and Bioinactive TSH due to Mutations in the beta-Subunit Gene. Trends Endocrinol. Metab. 8: 15-20. http://dx.doi.org/10.1016/S1043-2760(96)00203-2   Nei M and Li WH (1979). Mathematical model for studying genetic variation in terms of restriction endonucleases. Proc. Natl. Acad. Sci. U. S. A. 76: 5269-5273. http://dx.doi.org/10.1073/pnas.76.10.5269 PMid:291943 PMCid:413122   Pedersen LD, Sorensen AC and Berg P (2009). Marker-assisted selection can reduce true as well as pedigree-estimated inbreeding. J. Dairy Sci. 92: 2214-2223. http://dx.doi.org/10.3168/jds.2008-1616 PMid:19389980   Petrie JR, Pearson ER and Sutherland C (2011). Implications of genome wide association studies for the understanding of type 2 diabetes pathophysiology. Biochem. Pharmacol. 81: 471-477. http://dx.doi.org/10.1016/j.bcp.2010.11.010 PMid:21111713   Pfäffle R and Klammt J (2011). Pituitary transcription factors in the aetiology of combined pituitary hormone deficiency. Best. Pract. Res. Clin. Endocrinol. Metab. 25: 43-60. http://dx.doi.org/10.1016/j.beem.2010.10.014 PMid:21396574   Rachel L, Daniel DC, Nichol LGM and Mellon PL (2011). Hypothalamic dysregulation and infertility in mice lacking the homeodomain protein Six6. J. Neurosci. 31: 426-438. http://dx.doi.org/10.1523/JNEUROSCI.1688-10.2011 PMid:21228153 PMCid:3103738   Sahana G, Guldbrandtsen B and Lund MS (2011). Genome-wide association study for calving traits in Danish and Swedish Holstein cattle. J. Dairy Sci. 94: 479-486. http://dx.doi.org/10.3168/jds.2010-3381 PMid:21183059   Sambrook J and Russell DW (2001). Molecular Cloning: A Laboratory Manual. 3rd edn. Cold Spring Harbor Laboratory Press, New York.   Sham P, Bader JS, Craig I, O'Donovan M, et al. (2002). DNA Pooling: a tool for large-scale association studies. Nat. Rev. Genet. 3: 862-871. http://dx.doi.org/10.1038/nrg930 PMid:12415316   Sobrier ML, Maghnie M, Vie-Luton MP, Secco A, et al. (2006). Novel HESX1 mutations associated with a life-threatening neonatal phenotype, pituitary aplasia, but normally located posterior pituitary and no optic nerve abnormalities. Clin. Endocrinol. Metab. 91: 4528-4536. http://dx.doi.org/10.1210/jc.2006-0426 PMid:16940453   Tétreault N, Champagne MP and Bernier G (2009). The LIM homeobox transcription factor Lhx2 is required to specify the retina field and synergistically cooperates with Pax6 for Six6 trans-activation. Dev. Biol. 327: 541-550. http://dx.doi.org/10.1016/j.ydbio.2008.12.022 PMid:19146846   Thomas MG, Enns RM, Shirley KL, Garcia MD, et al. (2007). Associations of DNA polymorphisms in growth hormone and its transcriptional regulators with growth and carcass traits in two populations of Brangus bulls. Genet. Mol. Res. 6: 222-237. PMid:17469072   Wang DY, Zhang YJ, Liu YQ and Yang YZ (2009). Karyotype and single nucleotide polymorphism of the prolactin gene in milking bucks. Small Rumin. Res. 87: 96-101. http://dx.doi.org/10.1016/j.smallrumres.2009.09.032   Wang GB, Li CR, Yang J, Wen PQ, et al. (2011). A regulatory polymorphism in promoter region of TNFR1 gene is associated with Kawasaki disease in Chinese individuals. Hum. Immunol. 72: 451-457. http://dx.doi.org/10.1016/j.humimm.2011.02.004 PMid:21315128   Weasner BP and Kumar JP (2009). The non-conserved C-terminal segments of Sine Oculis Homeobox (SIX) proteins confer functional specificity. Genesis 47: 514-523. http://dx.doi.org/10.1002/dvg.20517 PMid:19422020 PMCid:2738589   Weller JI and Ron M (2011). Invited review: quantitative trait nucleotide determination in the era of genomic selection. J. Dairy Sci. 94: 1082-1090. http://dx.doi.org/10.3168/jds.2010-3793 PMid:21338774