Results 91 to 100 of about 11,551 (206)

Chromosomal assignment of the ovine hairless (hr) gene by fluorescence in situ hybridization. [PDF]

open access: yes, 2008
Congenital hypotrichosis in mammalian species consists of partial or complete absence of a hair coat at birth. Affected individuals having a partial hair coat at birth may loose it subsequently.The aim of this paper was to physically map the ovine hr
Budelli E   +6 more
core   +1 more source

Comparacao das tecnicas de SSCP, DS-PCR, PCR-RFLP para detecção de mutação no gene mitocondrial 16S RRNA em populacoes de Melipona rufiventris

open access: yesBioscience Journal, 2006
Esse trabalho analisou a região 16S do DNA mitocondrial em populações de Melipona rufiventris do Espírito Santo, comparando a eficiência das técnicas moleculares SSCP (Single Strand Conformation Polymorfism), PCR-RFLP (Restriction Fragment Length ...
Cristina Soares de Sousa   +8 more
doaj  

PCR-SSCP analysis of GH gene in Sarda goats: a high variability and its preliminary effects on dairy performances

open access: yesItalian Journal of Animal Science, 2010
The growth hormone (GH) gene can be utilized as a major gene because in various domestic livestock its polymorphisms have been associated to milk traits.
Giuseppe Massimo Vacca   +4 more
doaj   +1 more source

PCR-SSCP检测急性髓系白血病患者FLT3基因及FLT3/ITD基因突变

open access: yesZhongguo shiyan zhenduanxue, 2009
目的研究急性髓系白血病(AML)患者DNA水平FLT3基因及其内部串联重复(ITD)突变。方法采用多聚酶链反应(PCR)联合单链构象多态性(SSCP)方法检测43例不同免疫分型AML患者DNA水平FLT3基因及FLT3/ITD基因突变。结果43例AML患者经PCR扩增,琼脂糖凝胶电泳FLT3基因检测全部阳性,未发现FLT3/ITD基因突变;SSCP电泳FLT3基因检测全部阳性,43例AML患者中有15例(35%)出现FLT3/ITD基因突变。结论PCR-SSCP适用于检测急性髓系白血病FLT3 ...
黄晶   +4 more
doaj  

Serotyping Dichelobacter nodosus with PCR-SSCP [PDF]

open access: yesJournal of Animal and Veterinary Advances, 2011
Tulay Ifakat Cagatay, Jon Hickford
openaire   +1 more source

结核分支杆菌耐异烟肼分子机制的研究

open access: yesZhongguo shiyan zhenduanxue, 2007
目的探讨耐异烟肼结核分支杆菌KatG基因突变在结核分支杆菌耐异烟肼耐药性测定中的应用价值。方法采用聚合酶链反应——单链构象多态性(PCR-SSCP)分析72株结核分支杆菌KatG基因突变。其中32株为异烟肼(INH)敏感株,40株为INH耐药株,用PCR-SSCP图谱鉴定扩增产物有无突变,H37RV标准株作对照。结果所有INH敏感株SSCP带谱与对照相同;40株INH耐药株中15株与对照相同,25株有不同程度的差异,INH耐药KatG基因突变或缺失的阳性率为62.5 ...
宋阳, 于宏波, 陈晶洁, 韩忠波
doaj  

内視鏡生検検体を用いた食道早期腫瘍形成におけるp53遺伝子変異および蛋白過剰発現の検討 [PDF]

open access: yes, 1997
京都大学0048新制・課程博士博士(医学)甲第6797号医博第1897号新制||医||665(附属図書館)15869UT51-97-H181京都大学大学院医学研究科内科系専攻(主査)教授 野田 亮, 教授 今村 正之, 教授 大熊 稔学位規則第4条第1項該当Doctor of Medical ScienceKyoto ...
金, 義宣
core  

Identificación por PCR-SSCP de genes de cefotaximasas en aislamientos hospitalarios de Enterobacteriaceae

open access: yesRevista Colombiana de Biotecnología, 2009
Las cefotaximasas (CTX-M) son las beta-lactamasas de espectro extendido más ampliamente diseminadas entre especies de la familia Enterobacteriaceae, y son la causa principal de resistencia en aislamientos causantes de infección intrahospitalaria.
José Ramón Mantilla Anaya   +3 more
doaj   +2 more sources

The study of mitochondrial ATP6, ND3 and COX3 gene nucleotide variations in Iranian patients with atherosclerosis by PCR-SSCP [PDF]

open access: yes, 2018
Background and aims: Atherosclerosis is a complex arterial disease that is caused due to the interaction of genetic and environmental factors. Mutations in the mitochondrial genome have probably a direct effect on increased oxidative stress and thereby ...
Hadadzadeh, Mehdi.   +3 more
core  

Studying VSX1 gene mutations in patients with Keratoconus of Chaharmahal and Bakhtiari province, Iran [PDF]

open access: yes, 2013
Background & Aims: Keratoconus (KC) is an eye disorder in which the cornea is swollen, thinned and deformed. Despite extensive studies, the pathophysiological processes and genetic etiology of KC is unknown.
Azadegan-Dehkordi, Fatemeh.   +11 more
core  

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