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Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans.

机译：犬的全基因组关联作图可以鉴定同源盒基因NKX2-8，它是人类神经管缺陷的遗传组成部分。

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Noa Safra; Alexander G Bassuk; Polly J Ferguson; Miriam Aguilar; Rochelle L Coulson; Nicholas Thomas; Peta L Hitchens; Peter J Dickinson; Karen M Vernau; Zena T Wolf; Danika L Bannasch;
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1. Genome-Wide Association Mapping in Dogs Enables Identification of the Homeobox Gene, NKX2-8, as a Genetic Component of Neural Tube Defects in Humans [J] . Noa Safra, Alexander G. Bassuk, Polly J. Ferguson, PLoS Genetics . 2013,第7期

机译：狗的全基因组关联映射使得能够鉴定同源盒基因 NKX2-8 作为人类神经管缺陷的遗传成分。
2. Identification of retinal homeobox retinal homeobox ( rax rax ) gene gene –dependent genes by a microarray approach: The DNA endoglycosylase neil3 neil3 is a major downstream component of the rax rax genetic pathway [J] . Pan Yi, Kelly Lisa E., El‐Hodiri Heithem M. Developmental dynamics: an official publication of the American Association of Anatomists . 2018,第11期

机译：通过微阵列方法鉴定视网膜Homeobox视网膜homeobox（rax rax）基因基因依赖性基因：DNA内皮糖基酶Neil3 neil3是rax rax遗传途径的主要下游成分
3. Comment on changes in sex ratio in neural tube defects since food fortification with folic acid: Re "hypothesis: The female excess in cranial neural tube defects reflects an epigenetic drag of the inactivating X chromosome on the molecular mechanisms of neural tube fold elevation" [J] . EvansJ.A. Birth defects research, Part A. Clinical and molecular teratology . 2012,第11期

机译：自从用叶酸强化食物后，神经管缺陷的性别比例变化评论：关于“假说：颅神经管缺陷的女性过多反映了失活的X染色体对神经管皱折抬高的分子机制的表观遗传阻力”
4. Genome-Wide Association Mapping Reveals Genetic Architecture of DurAble Spot Blotch Resistance in US Barley Breeding Germplasm [C] . Hao Zhou, Brian J. Steffenson Advance in barley sciences : proceedings of 11th international barley genetics symposium . 2012

机译：全基因组关联图谱揭示了美国大麦育种种种对持久性斑点病的抗性遗传结构
5. Mutations in the Planar Cell Polarity gene, Fuzzy, are associated with neural tube defects in humans. [D] . Seo, Jung Hwa. 2012

机译：平面细胞极性基因Fuzzy的突变与人类的神经管缺陷有关。
6. Genome-Wide Association Mapping in Dogs Enables Identification of the Homeobox Gene NKX2-8 as a Genetic Component of Neural Tube Defects in Humans [O] . Noa Safra, Alexander G. Bassuk, Polly J. Ferguson, 2013

机译：在狗中的全基因组关联映射使得能够鉴定同源盒基因NKX2-8作为人类神经管缺陷的遗传成分。
7. Genetic Association Analyses of Nitric Oxide Synthase Genes and Neural Tube Defects Vary by Phenotype [O] . Karen L. Soldano, Melanie E. Garrett, Heidi L. Cope, 2013

机译：一氧化氮合酶基因和神经管缺陷的遗传关联分析因表型而变化
8. Genome-Wide Association Mapping for Intelligence in Military Working Dogs: Canine Cohort, Canine Intelligence Assessment Regimen, Genome-Wide Single Nucleotide Polymorphism (SNP) Typing, and Unsupervised Classification Algorithm for Genome-Wide Association Data Analysis [R] . Chan, V. T., Mauzy, C. A., Soto, A., 2011

机译：军事工作犬智力的全基因组关联图谱：犬群，犬智力评估方案，全基因组单核苷酸多态性（sNp）分型和无监督分类算法的全基因组关联数据分析

Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans.

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