TAHİR OLGUN'UN MANZUM BATI EDEBİYATI TARİHİ
نویسندگان
چکیده
منابع مشابه
Arogya Vardhii Bati and Anand Bhairava Ras, Two Amoebicidal Ayurvedic Drugs
Two ayurvedic preparations Arogya Vardhini Bati (AVB) and Anand Bhairava Ras (ABR) were found to cure intestinal amoebiasis of rat and hepatic amoebiasis of golden hamster. Both AVB and ABR were found to be amoebicidal against trophozoites of Entamoeba histolytic at 500 μg/ml in vitro and cured caecal amoebiasis of rat at 200 mg/kg/dose/5 dyas, in vivo.
متن کاملMultiplex SNP typing by bioluminometric assay coupled with terminator incorporation (BATI)
A multiplex single-nucleotide polymorphism (SNP) typing platform using 'bioluminometric assay coupled with terminator [2',3'-dideoxynucleoside triphosphates (ddNTPs)] incorporation' (named 'BATI' for short) was developed. All of the reactions are carried out in a single reaction chamber containing target DNAs, DNA polymerase, reagents necessary for converting PPi into ATP and reagents for lucif...
متن کاملExploring new pharmacology and toxicological screening and safety evaluation of one widely used formulation of Nidrakar Bati from South Asia region
BACKGROUND Nidrakar Bati (NKB) is an herbal remedy consisted with seven medicinal herbs widely used to cure Somnifacient (sleeping aid) in South Asia as Ayurvedic medicinal system. In the present study, pharmacological and toxicological effects of this medicine was investigated in mice to validate the safety and efficacy of the herb. METHODS Organic solvent extracts NKB were prepared using ma...
متن کاملAntenatal Diagnosis of a Case of Pentalogy of Cantrell Associated with Phocomelia Cantrell Pentaloji ve Fokomelia Birlikteliği Saptanan Olgunun Antenatal Tanısı
Melek Çiçek, Kafkas Üniversitesi Tıp Fakültesi, Kadın Hastalıkları ve Doğum Anabilim Dalı, Tel. 0506 8609381 Email. [email protected] Geliş Tarihi: 05.12.2011 • Kabul Tarihi: 16.12.2011 ABSTRACT Pentalogy of Cantrell is a rare congenital syndrome; described as the association of partial or complete ectopia cordis, a supraumbilical abdominal wall defect, congenital heart defects, defects ...
متن کاملRare Structural Chromosomal Abnormalities in Prenatal Diagnosis; Clinical and Cytogenetic Findings on 10125 Prenatal Cases Prenatal Tanıda Nadir Yapısal Kromozom Anomaliler; 10125 Prenatal Olgunun Klinik ve Sitogenetik Bulguları
Results: A structural chromosomal abnormality was observed in 95 cases. The most frequently observed structural abnormalities were balanced translocations with a frequency of 53.7% (51 cases) followed by unbalanced translocations (16.8%), inversions (11.6%), supernumerary marker chromosomes (8.4%), duplications (4.2%), deletions and ring chromosomes (2.1%) and complex translocation (1.1%). rare...
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ژورنال
عنوان ژورنال: International Journal Of Turkish Literature Culture Education
سال: 2017
ISSN: 2147-0146
DOI: 10.7884/teke.4094