1.
Inheritance of Two Mutants of Fiber and SSR Analysis of Lint Gene and Fuzz Gene in Upland Cotton;
陆地棉两个纤维突变体的遗传以及纤维和短绒基因SSR标记分析
2.
Cloning and Analysis of Cotton Fiber Development-associated Genes in Diverse Fiber Mutant
几个棉花纤维突变体及纤维发育相关基因的初步分析
3.
Analysis of Different Proteins of Fuzz Mutant in Gossypium.arboreum;
亚洲棉短纤维发育突变体蛋白质差异分析
4.
Effects of Plant Hormones on Elongation and Development of Fiber in Cotton Mutant Li-1;
植物激素对棉花突变体Li-1纤维伸长发育的影响
5.
SSR Marker Location and Analysis of Genetic Similarity of Fiber Development Mutants in Cotton;
棉纤维发育突变体SSR标记定位和遗传相似性分析
6.
Developmental and Gene Expression Analysis of a Fuzzless Mutant of Gossypium Hirsutum;
陆地棉无短绒突变体GZnn的纤维发育及其基因表达分析
7.
The relationship between FGFR3 mutation and urothelial carcinoma of bladder
成纤维细胞生长因子受体突变与膀胱尿路上皮癌的关系
8.
Rheological Characteristics of Short Cellulose Fiber Filled Elastomer
纤维素短纤维填充弹性体的流变特性
9.
Tn4351 Insertional Mutagenesis of Cytophaga Hutchinsonii and Identification of the Mutants;
哈氏噬纤维菌的Tn4351插入突变及突变子筛选与分析
10.
The usually long process of a nerve fiber that generally conducts impulses away from the body of the nerve cell.
轴突一般传导远离神经细胞体的冲动的神经纤维突，通常为长突
11.
Cell Biology and Molecular Pharmacology of Pig Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) and △F508-pCFTR;
猪囊性纤维化跨膜电导调节因子及其△F508突变体的细胞生物学和分子药理学研究
12.
Detecting and Analyzing on Mutation of Fibroblost Growth Factor Recepter 3 Gene in A Congenital Achondroplasia Family
先天性软骨发育不全家系成纤维细胞生长因子受体3基因突变检测与分析
13.
The thrombolytic effect of reteplase in treating rabbit retinal vein occlusion
组织型纤维蛋白溶解酶原激活剂缺失突变体治疗兔视网膜静脉阻塞的疗效
14.
Study on rheological property of cellulose/ionic liquids
纤维素/离子液体溶液流变行为的研究
15.
Inherited Dysfibrinogenemia Caused by Arg19Gly in theαChain of Fibrinogen
一个纤维蛋白原α链Arg 19 Gly突变导致的遗传性异常纤维蛋白原血症家系
16.
Glial fibrillary acidic protein mutation in a Chinese girl with infantile Alexander disease
一例婴儿型亚历山大病胶质细胞原纤维酸性蛋白基因突变研究
17.
Congenital Fibrosis of the Extraocular Muscles in Chinese Families: Clinical Phenotype, Linkage Mapping, and Mutation Identification of KIF21A;
先天性眼外肌纤维化家系连锁分析及KIF21A基因的突变检测
18.
Linkage Analysis in Two Chinese Family with Congenital Fibrosis of Extraocular Muscles and Mutation Screening of Kif21A;
两个先天性广泛眼外肌纤维化家系的连锁分析及Kif21A基因突变研究