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Detection of <i>β</i>-Hemoglobin Gene and Sickle Cell Disorder from Umbilical Cord Blood
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作者 Sheikh Anika Rahman Md. Shad Ebna Rahaman +6 位作者 shahena aktar shipa Md. Mohosin Rana Rukshana Khan Mohammad Golam Rob Mahmud Jilwatun Noor Firuza Sultana Md. Faruque Miah 《Journal of Biosciences and Medicines》 2017年第10期51-63,共13页
Sickle cell disease (SCD) is one of the most common hemoglobinopathies, which is caused by the replacement of glutamic acid with valine at the sixth position of the beta-globin amino acid chain which sickling of the e... Sickle cell disease (SCD) is one of the most common hemoglobinopathies, which is caused by the replacement of glutamic acid with valine at the sixth position of the beta-globin amino acid chain which sickling of the entire red blood cells in the homozygous (Hb S/S) condition. There are many analyses and screening procedures were developed to detect sickle cell anemia in the early age of birth, especially from heel prick blood, but in case of developing countries, it would be more acceptable to detect sickle cell disorder using umbilical cord blood just after birth rather than using heel prick blood. In this study, umbilical cord blood (UCB) was used to detect β-hemoglobin gene and sickle cell disorder. Polymerase chain reaction (PCR) based analysis was done using two primers (wild-type and mutant type) to detect this disorder. A total number of 22 samples were enrolled in this experiment for PCR amplification among which nineteen samples were identified by amplification of both 267 bp and 517 bp fragments revealing heterozygous sickle cell trait (Hb A/S), whereas three samples were found to amplify of 517 bp only revealing healthy individuals. The result from PCR analysis was then collaborated with the information of the mothers of each sample to analyze the result more conveniently and found that the mothers of all individuals except the three samples had anemia or mild form of anemia, thus it was expected that the newborn might have anemia trait (Hb A/S) the exception was found in case of sample No. 9 and sample No. 15. Both samples showed the bands on 267 bp and 517 bp thus expressed the sickle cell disease trait although the mothers of these samples were not anemic. However, no samples were recorded having sickle cell anemia (9 Hb S/S). The inherent simplicity and low cost of this PCR based analysis with umbilical cord blood will be considered as an effective tool in future newborn screening in Bangladesh. 展开更多
关键词 β-Hemoglobin Gene SICKLE Cell DISORDER UMBILICAL Cord Blood New Born Screening
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Surveillance of Vibrio spp in Penaeus monodon Collected from Shrimp Pond of Satkhira, Bangladesh
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作者 Abdullah-Al-Amin shahena aktar shipa +1 位作者 MNiamul Naser MdFaruque Miah 《Journal of Zoological Research》 2020年第3期1-8,共8页
Vibrio is the most common genera associated with crustaceans and often causing significant economic losses.Many Vibrio species are pathogenic to human and have been implicated in food borne diseases.The present study ... Vibrio is the most common genera associated with crustaceans and often causing significant economic losses.Many Vibrio species are pathogenic to human and have been implicated in food borne diseases.The present study was conducted to identify Vibrio spp.from the tiger shrimp(Penaeus monodon)of shrimp pond at Satkhira,Bangladesh.A total number of 33 Vibrio species isolates were identified from 20 shrimp samples through a series of morphological,physiological and biochemical tests.The work reports the prevalence of Vibrio spp.in the pond environments and the existence of three Vibrio species such as V.alginolyticus,V.parahaemolyticus and V.harveyi were identified.In the study of antibiogram,all isolates were shown 100%sensitive to streptomycin,ciprofloxacin and chloramphenicol.Maximum 41%isolates were shown resistant to co-trimethaxozole whereas 30%and 24%resistant to azithromycin and novobiocin respectively. 展开更多
关键词 Tiger shrimp Morphological Physiological BIOCHEMICAL ANTIBIOGRAM
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