原创力文档de-novo assembly and analysis of the heterozygous triploid genome of the wine spoilage yeast dekkera bruxellensis awri1499新创的装配和分析杂合的三倍体基因组的葡萄酒败坏酵母dekkera bruxellensis awri1499.pdfVIP
- 3
- 0
- 约6.79万字
- 约 10页
- 2017-09-12 发布于上海
- 举报
de-novo assembly and analysis of the heterozygous triploid genome of the wine spoilage yeast dekkera bruxellensis awri1499新创的装配和分析杂合的三倍体基因组的葡萄酒败坏酵母dekkera bruxellensis awri1499
De-Novo Assembly and Analysis of the Heterozygous
Triploid Genome of the Wine Spoilage Yeast Dekkera
bruxellensis AWRI1499
1 . 1. 1 1,2
Chris D. Curtin * , Anthony R. Borneman , Paul J. Chambers , Isak S. Pretorius
1The Australian Wine Research Institute, Adelaide, Australia, 2 The University of South Australia, Adelaide, Australia
Abstract
Despite its industrial importance, the yeast species Dekkera (Brettanomyces) bruxellen
您可能关注的文档
- defective lamin a-rb signaling in hutchinson-gilford progeria syndrome and reversal by farnesyltransferase inhibition有缺陷的核纤层蛋白a-rb信号hutchinson-gilford早衰症综合征治疗抑制和逆转.pdf
- deficiency of antinociception and excessive grooming induced by acute immobilization stress in per1 mutant mice镇痛效应不足和过度修饰引起的急性固定压力per1突变小鼠.pdf
- deficiency in nucleotide excision repair family gene activity, especially ercc3, is associated with non-pigmented hair fiber growth基因的核苷酸切除修复缺陷的家庭活动,尤其是ercc3 non-pigmented头发纤维增长相关联.pdf
- deficiencies in jasmonate-mediated plant defense reveal quantitative variation in botrytis cinerea pathogenesis不足jasmonate-mediated植物防御揭示量变葡萄孢菌发病机理.pdf
- deficiency of the mitochondrial electron transport chain in muscle does not cause insulin resistance缺乏线粒体电子传递链的肌肉不会导致胰岛素抵抗.pdf
- deficient liver biosynthesis of docosahexaenoic acid correlates with cognitive impairment in alzheimer's disease缺乏肝二十二碳六烯酸的生物合成与认知障碍的阿尔茨海默氏症.pdf
- deficiency of interleukin-15 enhances susceptibility to acetaminophen-induced liver injury in mice缺乏interleukin-15增强敏感性在对乙酰氨基酚诱导性肝损伤小鼠.pdf
- deficient spindle assembly checkpoint in multiple myeloma缺乏纺锤体组装在多发性骨髓瘤检查点.pdf
- deficient plakophilin-1 expression due to a mutation in pkp1 causes ectodermal dysplasia-skin fragility syndrome in chesapeake bay retriever dogspkp1 plakophilin-1不足表达由于基因突变导致外胚层的dysplasia-skin脆弱性综合症在切萨皮克海湾寻回犬狗.pdf
- deficiency of c-c chemokine receptor 5 suppresses tumor development via inactivation of nf-κb and upregulation of il-1ra in melanoma model缺乏碳碳趋化因子受体5抑制肿瘤的发展通过失活nf-κb和il-1ra upregulation黑色素瘤模型.pdf
文档评论（0）