Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Pradeep Kumar Vegi"'
Autor:
Nagarjuna Sivaraj, K Vijaya Rachel, Tarun Kumar Suvvari, Shilaja Prasad, Sriharsha Boppana, Vineetha Naidu, Pradeep Kumar Vegi, Youssef Aboufandi, L V Simhachalam Kutikuppala
Publikováno v:
Journal of the Scientific Society, Vol 49, Iss 3, Pp 272-276 (2022)
Background: Several research have looked at the significance of SNPs in inflammatory mediator genes and their link to preeclamptic pregnancies, but the results have not been conclusive enough to explain why SNPs in inflammatory mediator genes may inc
Externí odkaz:
https://doaj.org/article/dc0e42ac6c61471f974a759ceaa83e0b
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 2, Pp BC15-BC18 (2015)
Introduction: Recurrent spontaneous abortion (RSA) is a multifactorial clinical obstetrics complication commonly occurring in pregnancy. Many research studies have noted the mutations such as C677T in N5, N10 - Methylenetetrahydrofolate reductase
Externí odkaz:
https://doaj.org/article/8784cebef51047f3b7639457077ab18c
Publikováno v:
Case Reports in Pediatrics, Vol 2013 (2013)
Goldenhar syndrome is a rare developmental disorder characterised by hemifacial microsomia, epibulbar tumours, ear malformation, and vertebral anomalies. As monozygotic (MZ) twins are believed to be genetically identical, discordance for disease phen
Externí odkaz:
https://doaj.org/article/0c2bf0b1ce3b4ad79dd2cd4c4c6c02a2
Autor:
Nagarjuna Sivaraj, Vijaya Rachel K, Tarun Kumar Suvvari, Shilaja Prasad, Boppana Sri Harsha, Vineetha Majji, Pradeep Kumar Vegi, Papa Kusuma Bunga
Publikováno v:
Cureus.
Introduction Many studies have gone into single nucleotide polymorphisms (SNPs) in inflammatory-associated genes and preeclampsia risk; still, the findings are inconclusive. The current study aims to evaluate the association of SNP rs2229238 in the i
Publikováno v:
MedPulse International Journal of Biochemistry. 11:111-115
Publikováno v:
Case Reports in Pediatrics
Case Reports in Pediatrics, Vol 2013 (2013)
Case Reports in Pediatrics, Vol 2013 (2013)
Goldenhar syndrome is a rare developmental disorder characterised by hemifacial microsomia, epibulbar tumours, ear malformation, and vertebral anomalies. As monozygotic (MZ) twins are believed to be genetically identical, discordance for disease phen
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 9, Iss 2, Pp BC15-BC18 (2015)
Introduction: Recurrent spontaneous abortion (RSA) is a multifactorial clinical obstetrics complication commonly occurring in pregnancy. Many research studies have noted the mutations such as C677T in N5, N10 - Methylenetetrahydrofolate reductase (MT
Publikováno v:
International Journal of Advances in Medicine. 1:1
Background: Fluoride in cellular respiratory processes and its association in free radical generation are extensively studied. Cell permeability generates the oxidative stress through free radical species entry that sequentially affects the cellular
Publikováno v:
Nigerian Journal of Experimental and Clinical Biosciences. 1:53
Organophosphates (OPs) are widely used as insecticides. Accidental OP poisoning is reported world over. These compounds inhibit the enzyme acetylcholinesterase within the peripheral and central nervous system by phosphorylation of its esteratic site.