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“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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Betty P, Nathalie I and Jean B (2004). Efficient screening for expressed sequence tag polymorphisms (ESTPs) by DNA pool sequencing and denaturing gradient gel electrophoresis (DGGE) in spruces. Mol. Breed. 13: 263-279.
http://dx.doi.org/10.1023/B:MOLB.0000022528.01656.c8
Bhattacharya TK, Chatterjee RN, Sharma RP, Niranjan M, et al. (2011). Associations between novel polymorphisms at the 5'-UTR region of the prolactin gene and egg production and quality in chickens. Theriogenology 75: 655-661.
http://dx.doi.org/10.1016/j.theriogenology.2010.10.005
PMid:21111467
Cheyette BN, Green PJ, Martin K, Garren H, et al. (1994). The Drosophila sine oculis locus encodes a homeodomain-containing protein required for the development of the entire visual system. Neuron 12: 977-996.
http://dx.doi.org/10.1016/0896-6273(94)90308-5
Conte I, Morcillo J and Bovolenta P (2005). Comparative analysis of Six 3 and Six 6 distribution in the developing and adult mouse brain. Dev. 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