Detalhe da pesquisa
1.
Erythrocyte miRNA-92a-3p interactions with PfEMP1 as determinants of clinical malaria.
Funct Integr Genomics
; 23(2): 93, 2023 Mar 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-36941394
2.
A pilot randomized controlled trial to compare the effectiveness of two 14-day primaquine regimens for the radical cure of vivax malaria in South India.
Malar J
; 17(1): 321, 2018 Sep 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30176897
3.
Therapeutics through glycobiology: an approach for targeted elimination of malaria.
Biologia (Bratisl)
; : 1-5, 2023 Jan 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-36643690
4.
Transcriptomic approaches for identifying potential transmission blocking vaccine candidates in Plasmodium falciparum: a review of current knowledge and future directions.
3 Biotech
; 13(10): 344, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37711230
5.
Genome-wide DNA methylation profiling after Ayurveda intervention to bronchial asthmatics identifies differential methylation in several transcription factors with immune process related function.
J Ayurveda Integr Med
; 14(2): 100692, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37018893
6.
Malaria Epidemiology and COVID-19 Pandemic: Are They Interrelated?
OMICS
; 26(4): 179-188, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35404686
7.
Erythrocyte miRNA regulators and malarial pathophysiology.
Infect Genet Evol
; 93: 105000, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34252617
8.
Categorical complexities of Plasmodium falciparum malaria in individuals is associated with genetic variations in ADORA2A and GRK5 genes.
Infect Genet Evol
; 34: 188-99, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26066465
9.
Single nucleotide polymorphisms of ADRB2 gene and their association with susceptibility for Plasmodium falciparum malaria and asthma in an Indian population.
Infect Genet Evol
; 20: 140-7, 2013 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-24012958
10.
Allele, genotype, and composite genotype effects of IL-1A +4845 and IL-1B +3954 polymorphisms for chronic periodontitis in an Indian population.
Indian J Dent Res
; 22(4): 612, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-22124068
11.
Hypoplasia/aplasia of pelvis, femora, fibulae, ulna, digits and nails: Fuhrmann syndrome without WNT7A mutations.
Clin Dysmorphol
; 20(4): 205-209, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21716096
12.
Allele, genotype, and composite genotype effects of IL-1A +4845 and IL-1B +3954 polymorphisms for chronic periodontitis in an Indian population.
Artigo
em Inglês
| IMSEAR | ID: sea-140088
13.
Novel deletions in MYH7 and MYBPC3 identified in Indian families with familial hypertrophic cardiomyopathy.
J Mol Cell Cardiol
; 35(6): 623-36, 2003 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-12788380