Genetic epidemiology of coronary artery disease: an Asian Indian perspective [0.03%]
冠心病的遗传流行病学：印度人的视角
Shanker Jayashree,Maitra Arindam,Kakkar V Vijay
Shanker Jayashree
Coronary artery disease (CAD) has emerged as a major cause of morbidity and mortality worldwide. Recent findings on the role of genetic factors in the aetiopathology of CAD have implicated novel genes and variants in addition to those invol...
Sameen Ruqia Imadi,Alvina Gul Kazi,Mohammad Abass Ahanger et al.
Sameen Ruqia Imadi et al.
Different stresses include nutrient deficiency, pathogen attack, exposure to toxic chemicals etc. Transcriptomic studies have been mainly applied to only a few plant species including the model plant, Arabidopsis thaliana. These studies hav...
Upgrade of Castanea sativa (Mill.) genetic resources by sequencing of barcode markers [0.03%]
栗树条形码基因型资源的构建与鉴定研究
Angelo Gismondi,Gabriele Di Marco,Marco Delorenzo et al.
Angelo Gismondi et al.
Characterization and fine mapping of NGP4c(t), a novel gene controlling the number of grains per panicle in rice [0.03%]
控制水稻每穗实粒数的新型基因NGP4c(t)的鉴定与精细定位
Fantao Zhang,Jie Tang,Yi Zhou et al.
Fantao Zhang et al.
Genetic portrait of Lisboa immigrant population from Cabo Verde with mitochondrial DNA analysis [0.03%]
采用线粒体DNA分析手段对来自佛得角的里斯本移民群体进行遗传画像研究
Paulo Morais,António Amorim,Cláudia Vieira da Silva et al.
Paulo Morais et al.
Genetic variants of retinol-binding protein 4 in adolescents are associated with liver function and inflammatory markers but not with obesity and insulin resistance [0.03%]
视黄醇结合蛋白4基因多态性与青少年肝功能和炎症标志物相关但不与肥胖和胰岛素抵抗相关
Chin-Jung Lin,Nain-Feng Chu,Yi-Jen Hung et al.
Chin-Jung Lin et al.
Characterization of low-molecular-weight glutenin subunit genes of Aegilops section Sitopsis and comparative analysis with those of wheat (Triticum aestivum L.) and some Aegilops species [0.03%]
乌鸦草族长穗偃麦草低分子量麦谷蛋白基因的特征及其与普通小麦及某些长穗偃麦草种的关系的比较分析
Zhuo Huang,Hai Long,Xiao-Fnag Yu et al.
Zhuo Huang et al.
Comparative Study
Journal of genetics. 2015 Sep;94(3):497-501. DOI:10.1007/s12041-015-0546-5 2015
Sex-specific asymmetry in eye development in interspecific hybrids in the Drosophila bipectinata species complex [0.03%]
果蝇Drosophila bipectinata种群复杂体间杂种的眼发育性别不对称性研究
Bashisth N Singh,Parul Banerjee
Bashisth N Singh
Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse-Sakati syndrome [0.03%]
印度Woodhouse-Sakati综合征家系中C2orf37基因新的移位杂合突变
Mansoor C Abdulla,Anas M Alazami,Jemshad Alungal et al.
Mansoor C Abdulla et al.
Two novel mutations in ILDR1 gene cause autosomal recessive nonsyndromic hearing loss in consanguineous Iranian families [0.03%]
伊朗近婚配家系中ILDR1基因的两个新突变导致常染色体隐性非综合征型听力损失
Zohreh Mehrjoo,Mojgan Babanejad,Kimia Kahrizi et al.
Zohreh Mehrjoo et al.