DDA Property sale Deeds & Agreements Registration Procedure. DDA Property Legal Due diligence Assistance Stamp Duty & Registration Charges of property in Delhi
Drug resistance detection and mutation patterns of multidrug resistant tuberculosis strains from children in Delhidoi:10.1016/j.jegh.2016.12.003DrugresistanceLineprobeassayRetreatmentcasesSmearpositiveTuberculosisA total of 312 sputum samples from pediatric patients presumptive of multidrug resistant tuberculosis ...
Towards deciphering the mechanism underlying the attenuation of Comp1, a whole genome sequencing approach was undertaken. Eight Single Nucleotide Polymorphisms (SNPs) unique to the Comp1 strain were identified. Of these, 5 SNPs were non-synonymous and included a G➞A mutation resulting in a W159...
Correlations between the physiological status of plants and their radio sensitivity are often correlated to water content of the tissue, since the most frequent primary target of ionizing radiation is the water molecule.30 Chemical mutagen dose is determined in account of the properties of the ...
Daman SalujaIndian Journal of Medical MicrobiologyMutation pattern in the genome of Neisseria gonorrhoeae and its association with multidrug-resistant isolates from Delhi, India. Sachdev D,Kumari I,Bala M,et al. Indian J Med Microbiol . 2017
This study was aimed to assess the diagnostic utility of IHC on formalin fixed bone marrow biopsies in comparison with the reference molecular method (allele specific oligonucleotide-polymerase chain reaction; ASO-PCR) to predict NPM1 mutation status in AML patients.Chopra, AnitaSoni, SushantPati, ...
Herein we report a novel missense mutation at the nucleotide position 30829-T > A in the exon 8 of factor IX gene. This transversion leads to the substitution of histidine 236 to glutamine. This resulting abnormal protein has been named factor IXDelhi. Molecular modelling was performed to...
The pathogenesis includes RET proto-oncogene mutation; the most frequently observed mutation is in exon 11 codon 634. We report pedigree of a large Indian family involving three generations including 21 members with MEN2A, in whom RET mutation status was determined. We then analyzed their clinical...
Mohammad ShahidaVarinderpal S. DhillonbHesham Saleh KhalilaShameemul HaquecBhadur Shah Zafar MargNew DelhiDr Varinderpal S DhillonSwaraj BatradSyed Akhtar Husainc
Probing the effect of the non-active-site mutation Y229W in New Delhi metallo-beta-lactamase-1 by site-directed mutagenesis,kinetic studies,and molecular dynamics simulations. Chen J,Chen H,Shi Y,et al. PLoS One . 2013J. Chen, H. Chen, Y. Shi et al., "Probing the effect of the ...