A. Maiti

发表

Mdr1 Resistance Gene Yb-1-mediated Activation of the Multidrug Ap-endonuclease (ape1/ref-1) in Regulatory Role of Human Supplemental Material

K. Kohno, K. Bhakat, S. Mitra, 2008 .

RIP1/RIP3/MLKL Mediates Myocardial Function Through Necroptosis in Experimental Autoimmune Myocarditis

I. Adini, A. Maiti, A. Adini, 2021, Frontiers in Cardiovascular Medicine.

Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia.

E S Lander, J L Blouin, R M Gardiner, 2001, Genomics.

Emerging Biology of Circulating Tumor Cells (CTCs) in Cancer Detectionand Chemotherapy

A. Maiti, 2013 .

Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations.

L. Looger, P. Gaffney, B. Han, 2014, Human molecular genetics.

ITGAM coding variant (rs1143679) influences the risk of renal disease, discoid rash and immunological manifestations in patients with systemic lupus erythematosus with European ancestry

M. Petri, J. Reveille, G. Alarcón, 2009, Annals of the rheumatic diseases.

Utilization of wetland ecosystem through fish-crop diversification for enhanced productivity and economic stability for fish-farm community of Indian sub-continent

D. Basu, B. Pramanick, Aparna Roy, 2007 .

Genetic determinants of oxidative stress‐mediated sensitization of drug‐resistant cancer cells

A. Maiti, 2012, International journal of cancer.

Identification of G-quadruplex DNA sequences in SARS-CoV2

A. Maiti, 2022, Immunogenetics.

Gene network analysis of oxidative stress-mediated drug sensitivity in resistant ovarian carcinoma cells

A. Maiti, AK Maiti, 2010, The Pharmacogenomics Journal.

Evolutionary shift from purifying selection towards divergent selection of SARS-CoV2 favors its invasion into multiple human organs

A. Maiti, 2021, Virus Research.

Reactive Oxygen Species Reduction is a Key Underlying Mechanism of Drug Resistance in Cancer Chemotherapy

A. Maiti, 2012 .

Development of Biomarkers and Molecular Therapy Based on Inflammatory Genes in Diabetic Nephropathy

A. Maiti, 2021, International journal of molecular sciences.

No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with Primary Ciliary Dyskinesia (PCD)

S. Antonarakis, C. Rossier, C. Gehrig, 2000, Cytogenetic and Genome Research.

Hidradenitis suppurativa (or Acne inversa) with autosomal dominant inheritance is not linked to chromosome 1p21.1‐1q25.3 region

S. Nath, U. Radhakrishna, A. Maiti, 2010, Experimental dermatology.

Poly purine.pyrimidine sequences upstream of the beta-galactosidase gene affect gene expression in Saccharomyces cerevisiae

S. Brahmachari, A. Maiti, 2001, BMC Molecular Biology.

Polypurine/polypyrimidine sequences as cis-acting transcriptional regulators.

S. Brahmachari, A. Maiti, P. Sarkar, 1997, Gene.

Increased risk of lung cancer associated with a functionally impaired polymorphic variant of the human DNA glycosylase NEIL2.

A. Tomkinson, Chen Wu, D. Lin, 2012, DNA repair.

Implications of Gut Microbiota in Complex Human Diseases

W. D. de Vos, A. Maiti, Hao Wu, 2021, International journal of molecular sciences.

Identification, genomic organization, chromosomal mapping and mutation analysis of the human INV gene, the ortholog of a murine gene implicated in left-right axis development and biliary atresia

K. Tsuchiya, S. Takai, T. Mochizuki, 2002, Human Genetics.

Mutations in the DNAH11 (axonemal heavy chain dynein type 11) gene cause one form of situs inversus totalis and most likely primary ciliary dyskinesia

Miguel Armengot, S. Antonarakis, M. Armengot, 2002, Proceedings of the National Academy of Sciences of the United States of America.

Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele

A. Sharp, S. Antonarakis, F. Béna, 2012, Journal of Medical Genetics.

Overcoming Drug Resistance Through Elevation of ROS in Cancer

A. Maiti, 2013 .

Identification, tissue specific expression, and chromosomal localisation of several human dynein heavy chain genes

M. Mattei, A. Maiti, P. Bouvagnet, 2000, European Journal of Human Genetics.

Gene network analysis of small molecules with autoimmune disease associated genes predicts a novel strategy for drug efficacy.

S. Nath, A. Maiti, 2013, Autoimmunity reviews.

Non-synonymous variant (Gly307Ser) in CD226 is associated with susceptibility to multiple autoimmune diseases.

J. Anaya, A. Rojas-Villarraga, G. Tobón, 2010, Rheumatology.

Combined protein- and nucleic acid-level effects of rs1143679 (R77H), a lupus-predisposing variant within ITGAM.

L. Looger, K. Chua, J. Harley, 2014, Human molecular genetics.

Admixture Mapping in Lupus Identifies Multiple Functional Variants within IFIH1 Associated with Apoptosis, Inflammation, and Autoantibody Production

Scott M. Williams, L. Looger, P. Gaffney, 2013, PLoS genetics.

Confirmation of an association between rs6822844 at the Il2-Il21 region and multiple autoimmune diseases: evidence of a general susceptibility locus.

J. Anaya, A. Rojas-Villarraga, X. Kim-Howard, 2010, Arthritis and rheumatism.

The African-American population with a low allele frequency of SNP rs1990760 (T allele) in IFIH1 predicts less IFN-beta expression and potential vulnerability to COVID-19 infection

A. Maiti, 2020, Immunogenetics.

Evaluation of 19 Autoimmune Disease-associated Loci with Rheumatoid Arthritis in a Colombian Population: Evidence for Replication and Gene-Gene Interaction

Juan-Manuel Anaya, Adriana Rojas-Villarraga, J. Anaya, 2011, The Journal of Rheumatology.

Interaction Arthritis in a Colombian Population : Evidence for Replication and Gene-Gene Evaluation of 19 Autoimmune Disease-associated Loci with Rheumatoid

J. Anaya, J. Guthridge, X. Kim-Howard, 2011 .

Mutator phenotype of mammalian cells due to deficiency of NEIL1 DNA glycosylase, an oxidized base-specific repair enzyme.

S. Mitra, H. Spratt, I. Boldogh, 2008, DNA repair.

Expression Signatures of Long Noncoding RNAs in Left Ventricular Noncompaction

A. Maiti, Na Ta, Dingyang Liu, 2021, Frontiers in Cardiovascular Medicine.

Analysis of marketing efficiency of water chestnut (Trapa natansL.) in 24 – Parganas (North) of West Bengal

A. Maiti, S. Kundu, 2015 .

Isolation, in silico characterization and chromosomal localization of a group of cDNAs from ciliated epithelial cells after in vitro ciliogenesis

A. Maiti, P. Bouvagnet, M. Jorissen, 2001, Genome Biology.

Urinary Cytokines as Potential Biomarkers of Mild Cognitive Impairment and Alzheimer’s Disease: A Pilot Study

A. Yilmaz, S. Bartolone, M. Maddens, 2023, Journal of Alzheimer's disease reports.

Genome-wide Association Study of Long COVID

Patrick J. Short, Y. Okada, M. Mangino, 2023, medRxiv.

Evolutionary shift from purifying selection towards divergent selection of SARS-CoV2 favors its invasion into multiple human organs

A. Maiti, 2021, Virus Research.

Regulatory Role of Human AP-Endonuclease (APE1/Ref-1) in YB-1-Mediated Activation of the Multidrug Resistance Gene MDR1

K. Kohno, K. Bhakat, S. Mitra, 2008, Molecular and Cellular Biology.

Genetic determinants of oxidative stress‐mediated sensitization of drug‐resistant cancer cells

A. Maiti, 2012, International journal of cancer.

Hidradenitis suppurativa (or Acne inversa) with autosomal dominant inheritance is not linked to chromosome 1p21.1‐1q25.3 region

S. Nath, U. Radhakrishna, A. Maiti, 2010, Experimental dermatology.

On The Origin of SARS-COV2 Virus

A. Maiti, 2020, SSRN Electronic Journal.

Elevate the ROS Level to Kill Cancer Cells during Chemotherapy

A. Maiti, 2012 .