Arindam Maitra

This study identifies an IL-4-SP1-TIMP-2 regulatory axis that contributes to ECM dysregulation in endometriosis and shows the TIMP-2 -418G/C promoter polymorphism affects cytokine-mediated transcription.

The paper investigates IRES-mediated translation of delta160p53 and shows it promotes cancer cell survival and drug resistance by altering cell cycle and apoptosis.

This study maps virus-specific nasal cell states in children using single-cell RNA sequencing and links them to disease severity and asthma risk.

The paper identifies molecular pathways and immune markers in oral cancer, suggesting potential for immune checkpoint therapy in specific patient subtypes.

The paper presents a comprehensive genomic atlas of Indian populations, identifying novel variants and highlighting genetic diversity and pharmacogenomic implications.

The paper investigates RB1 mutations in endometrial cancer, finding higher prevalence in younger patients and linking RB1 mutations to HPV infection pathways.

The paper identifies the TGFβ-ANGPT2-Tie2 axis in cancer-associated fibroblasts that reprograms oral cancer cells to an embryonic-like state, linked to poor prognosis.

This study shows TRF2's non-telomeric function is critical for maintaining neural stem cell identity by repressing differentiation genes through PRC2 recruitment and G4 motif binding.

The paper identifies prognostically relevant co-expression patterns between coding and noncoding RNAs in HPV16-positive cervical cancers and links them to patient survival.

The paper presents AIDA, a diverse single-cell RNA-seq atlas of immune cells, revealing sub-continental diversity impacts on immune cell properties and identifying functional genetic variants.

The paper identifies a novel regulatory axis involving Delta40p53, miR-4671-5p, and SGSH that influences cell cycle progression and cancer outcomes.

The paper identifies novel FLCN mutations in Indian BHDS patients and highlights the role of MTHFR SNPs in disease diagnosis.

The paper identifies non-Spike mutations in Delta variant SARS-CoV-2 that correlate with symptomatic and asymptomatic infections and suggests their potential role in future vaccine-evading variants.

The paper identifies 1296 CpG sites with high temporal variance in DNA methylation associated with preterm birth in the GARBH-Ini cohort.

The paper analyzes whole genome sequences from OSCC-GB patients to detect NUMTs but finds no somatic NUMTs confirmed by PCR and no germline NUMTs specific to OSCC-GB.

The paper sequences 1000 SARS-CoV-2 genomes from India, revealing multiple circulating lineages, predominant A2a haplotype with D614G mutation, and geographic mutation clustering.

The paper identifies crosstalk between nuclear driver gene mutations and mitochondrial DNA mutations in gingivobuccal oral cancer, showing correlations and complementary roles in cancer progression.