Results 71 to 80 of about 6,961 (161)
目的探讨采用直接检测结核病人痰标本中rpoB基因和KatG基因突变。评价该方法检测结核分支杆菌对利福平(RFP)和异烟肼(INH)耐药性。方法用PCR-SSCP技术分析,对35例耐INH(或含耐异烟肼)、63例耐RFP(或含耐RFP)的肺结核病人痰标本和20例非结核性肺部疾病组痰标本进行rpoB和KatG基因突变的检测。结果以结核分支杆菌H37RV为对照,63例耐RFP痰标本中57例PCR扩增阳性,其中46例SSCP图谱与H37Rv标准株有差异,rpoB突变率为65.2 ...
包洪 +4 more
doaj
PCR-SSCP genotipizacija polimorfizma 4G/5G inhibitora-1 aktivatora plazminogena [PDF]
Inhibitor plazminogen aktivatora-1 (PAI-1) važan je regulator fibrinolize. U promotorskoj regiji gena za PAI-1 utvrđen je insercijsko-delecijski 4G/5G polimorfizam koji utječe na razinu plazmatskog PAI-1. Cilj rada bio je optimirati novu i jednostavnu PCR-SSCP metodu genotipizacije ovog polimorfizma, te utvrditi distribuciju genotipova i alela u ...
Šimundić, Ana-Maria +3 more
openaire +1 more source
Fish species identification in canned tuna by DNA analysis (PCR-SSCP)
Peer ...
Rehbein, Hartmut +6 more
openaire +4 more sources
Detection of Epidermal Growth Factor Receptor (EGFR) Gene Mutation in Formalin Fixed Paraffin Embedded Tissue by Polymerase Chain Reaction-Single Strand Conformational Polymorphism (PCR-SSCP) in Non-Small Cell Lung Cancer in the Northeastern Region of Thailand [PDF]
Saiyaros K +3 more
europepmc +1 more source
Genetic Identification of Trichomonas vaginalis by Using the Actin Gene and Molecular Based Methods
Background: Trichomonas vaginalis is the agent of urogenital tract infection that causes human trichomoniasis with some serious health complications.
Mohammad Matini +6 more
doaj
El síndrome de estrés porcino (PSS) es una enfermedad hereditaria monogénica recesiva relacionada con el gen receptor ryanodina (Ryr1). Utilizando PCR-SSCP y PCR-RFLP se tipificaron genéticamente 14 individuos de cerdos comerciales con el rasgo ...
Darwin Y Hernández +2 more
doaj
目的探讨用PCR-SSCP方法检测淋球菌氟喹诺酮耐药基因突变的研究。方法自行设计gyrA基因特异性扩增引物,运用PCR-SSCP银染色方法检测基因突变。结果在30例淋球菌临床分离株中选取13例,对其gyrA基因342 bp扩增产物进行DNA序列测定,其91位和95位位点发生突变。结论通过本研究所使用PCR-SSCP的方法检测临床分离出的淋球菌是否对氟喹诺酮耐药,并通过序列分析了解到淋球菌耐药基因突变以gyrA基因编码91位及95位点的氨基酸的碱基突变为主。通过此方法可以早期、准确 ...
刘铁梅 +3 more
doaj
Hereditary non-polyposis colorectal cancer (HNPCC) is the most frequent autosomal dominant predisposition for development of colorectal cancer (CRC) caused by germline defects in mismatch repair (MMR) genes.
Shadi Javan +5 more
doaj
Introducción de la técnica PCR-RFLP para el diagnóstico de dos mutaciones en el gen VHL
Fundamento: La enfermedad de Von Hippel-Lindau es un trastorno neoplásico hereditario. Se debe a mutaciones germinales en el gen VHL. En Cuba se realiza el diagnóstico molecular por el método de análisis de polimorfismo conformacional de simple cadena de
Antonio Alejandro Esperón +2 more
doaj
Identification of novel single nucleotide polymorphisms in the DGAT1 gene of buffaloes by PCR-SSCP. [PDF]
Raut AA +9 more
europepmc +1 more source

