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List of works by Arijit Biswas

An in silico and in vitro approach to elucidate the impact of residues flanking the cleavage scissile bonds of FVIII.

scientific article published on 6 July 2017

An update of the mutation profile of Factor 13 A and B genes.

scientific article published on 02 June 2011

Basal cell carcinomas developing independently from BAP1-tumor predisposition syndrome in a patient with bilateral uveal melanoma: Diagnostic challenges to identify patients with BAP1-TPDS

scientific article published on 23 January 2019

Beta2 glycoprotein 1 in Indian patients with SLE

scientific article published on 01 April 2005

Clinicohematologic spectrum in patients with lupus anticoagulant.

scientific article

Coagulation Factor XIIIA Subunit Missense Mutations Affect Structure and Function at the Various Steps of Factor XIII Action

scientific journal article

Coagulation Factor XIIIa Inhibitor Tridegin: On the Role of Disulfide Bonds for Folding, Stability, and Function

scientific article published on 21 March 2019

Coagulation factor XIII deficiency. Diagnosis, prevalence and management of inherited and acquired forms

scientific article published on 07 February 2014

Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A2.

scientific article

Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population

scientific article published on 04 April 2019

Disruption of Structural Disulfides of Coagulation FXIII-B Subunit; Functional Implications for a Rare Bleeding Disorder

scientific article published on 22 April 2019

Eight novel F13A1 gene missense mutations in patients with mild FXIII deficiency: in silico analysis suggests changes in FXIII-A subunit structure/function.

scientific article published on 3 June 2014

Evaluation of role of FV, FVIII and APLAs in the pathogenesis of APCR in FV Leiden negative DVT patients: a study in India.

scientific article

Exploring Diverse Coagulation Factor XIII Subunit Expression Datasets: A Bioinformatic Analysis

scientific article published on 25 April 2022

Exploring the structural similarity yet functional distinction between coagulation factor XIII-B and complement factor H sushi domains

scientific article published on 01 July 2019

Factor V Leiden: is it the chief contributor to activated protein C resistance in Asian-Indian patients with deep vein thrombosis?

scientific article published on 25 February 2008

First report of a FVII-deficient Indian patient carrying double heterozygous mutations in the FVII gene

scientific article published on 24 November 2004

Gene tracking in a family of novel identical twins affected by severe type-III von Willebrand Disease (vWD).

scientific article published on 14 December 2006

Homocystine levels, polymorphisms and the risk of ischemic stroke in young Asian Indians.

scientific article published in March 2009

Human VKORC1 mutations cause variable degrees of 4-hydroxycoumarin resistance and affect putative warfarin binding interfaces.

scientific article published on 27 August 2013

Identification and functional characterization of a novel F5 mutation (Ala512Val, FVB onn ) associated with activated protein C resistance.

scientific article published on 19 April 2016

Identification of Potential Novel Interacting Partners for Coagulation Factor XIII B (FXIII-B) Subunit, a Protein Associated with a Rare Bleeding Disorder

scientific article published on 31 May 2019

Identification of eight novel coagulation factor XIII subunit A mutations: implied consequences for structure and function.

scientific article

Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population.

scientific article

Impact of 789Ala/Ala genotype on quantitative type of von Willebrand disease.

scientific article

Impact of interleukin 6 promoter polymorphisms (-174 G > C, -572 G > C and -597 G > A) on plasma IL-6 levels and their influence on the development of DVT: a study from India

scientific article published on 11 June 2018

Impact of thrombogenic mutations on clinical phenotypes of von Willebrand disease.

scientific article published on 2 December 2009

In silico and in vitro evaluation of the impact of mutations in non-severe haemophilia A patients on assay discrepancies

scientific article published on 17 April 2019

Influence of Interleukin-6 (IL-6) Promoter Gene Polymorphisms (-174G>C, -572G>C, and -597G>A) on IL-6 Plasma Levels and Their Impact in the Development of Acute Ischemic Stroke in Young Indians

scientific article published on 01 January 2019

Inherited warfarin resistance in Indian patients: does it occur?

scientific article published in October 2007

Inherited warfarin resistance in Indian patients: does it occur?

scientific article published on 01 July 2007

Insights into the Folding of Disulfide-Rich μ-Conotoxins

scientific article published on 01 October 2018

Inter-locus as well as intra-locus heterogeneity in LINE-1 promoter methylation in common human cancers suggests selective demethylation pressure at specific CpGs.

scientific article

Intron retention resulting from a silent mutation in the VWF gene that structurally influences the 5' splice site

scientific article published on 19 August 2016

Mutation distribution in the von Willebrand factor gene related to the different von Willebrand disease (VWD) types in a cohort of VWD patients

scientific article published on 07 August 2012

NLRP7 inter-domain interactions: the NACHT-associated domain is the physical mediator for oligomeric assembly

scientific article

NLRP7, Involved in Hydatidiform Molar Pregnancy (HYDM1), Interacts with the Transcriptional Repressor ZBTB16.

scientific article published on 29 June 2015

Novel insights into structure and function of factor XIIIa-inhibitor tridegin.

scientific article published on 5 December 2014

Prenatal diagnosis of haemophilia A by chorionic villus sampling and cordocentesis: all India Institute of Medical Science experience.

scientific article published in January 2007

Prevalence of Factor V Genetic Variants Associated With Indian APCR Contributing to Thrombotic Risk.

scientific article published on 23 December 2015

Protein C and Protein S: causative factor for developing a hemorrhagic infarct in a HbE/Beta thalassemia child.

scientific article

Prothrombotic factors and the risk of acute onset non-cardioembolic stroke in young Asian Indians.

scientific article

Prothrombotic polymorphisms, mutations, and their association with pediatric non-cardioembolic stroke in Asian-Indian patients.

scientific article published on 4 October 2008

Recurrent abortions in Asian Indians: no role of factor V Leiden Hong Kong/Cambridge mutation and MTHFR polymorphism.

scientific article published on 26 December 2007

Revisiting the mechanism of coagulation factor XIII activation and regulation from a structure/functional perspective ⬇️

scientific article published on 25 July 2016

Screening of the GPX3 gene identifies the "T" allele of the SNP -861A/T as a risk for ischemic stroke in young Asian Indians

scientific article published on 8 August 2014

Screening of the NOS3 gene identifies the variants 894G/T, 1998C/G and 2479G/A to be associated with acute onset ischemic stroke in young Asian Indians

scientific article published on 20 June 2014

Structural and functional influences of coagulation factor XIII subunit B heterozygous missense mutants

scientific article published on 10 April 2015

The Arg98Trp mutation in human VKORC1 causing VKCFD2 disrupts a di-arginine-based ER retention motif

scientific article

The Plasma Factor XIII Heterotetrameric Complex Structure: Unexpected Unequal Pairing within a Symmetric Complex

scientific article published on 21 November 2019

The Role of PAI-1 4G/5G Promoter Polymorphism and Its Levels in the Development of Ischemic Stroke in Young Indian Population.

scientific article published in May 2017

The nitric oxide synthase 3 gene polymorphisms and their association with deep vein thrombosis in Asian Indian patients.

scientific article published on 28 January 2010

Thrombin activatable fibrinolysis inhibitor gene polymorphisms are associated with antigenic levels in the Asian-Indian population but may not be a risk for stroke

scientific article published on 01 November 2008

Type-3 von Willebrand disease in India-Clinical spectrum and molecular profile

scientific article published on 08 July 2018

Use of Intron 1 and 22 inversions and linkage analysis in carrier detection of hemophilia A in Indians.

scientific article

VKORC1 and VKORC1L1 have distinctly different oral anticoagulant dose-response characteristics and binding sites

scientific article published on 01 March 2018

Warfarin and vitamin K compete for binding to Phe55 in human VKOR.

scientific article published on 12 December 2016

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