List of works - Navaneethakrishnan T Krishnamoorthy

Two patients with Canavan disease and structural modeling of a novel mutation

scientific article

Molecular modeling of disease causing mutations in domain C1 of cMyBP-C

scientific article

Probing possible egress channels for multiple ligands in human CYP3A4: a molecular modeling study.

scientific article published on 29 August 2009

Molecular modeling study on orphan human protein CYP4A22 for identification of potential ligand binding site.

scientific article published on 4 December 2009

A computational modeling approach for enhancing self-assembly and biofunctionalisation of collagen biomimetic peptides.

scientific article published on 26 July 2011

An Investigation of the Molecular Mechanism of Double cMyBP-C Mutation in a Patient with End-Stage Hypertrophic Cardiomyopathy

scientific article published on 14 May 2015

A Strategy to Enhance Secretion of Extracellular Matrix Components by Stem Cells: Relevance to Tissue Engineering.

scientific article published on 3 May 2017

Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss.

scientific article

Impact of disease-causing mutations on inter-domain interactions in cMyBP-C: a steered molecular dynamics study.

scientific article published on 8 June 2016

The Role of Cardiac Myosin Binding Protein C3 in Hypertrophic Cardiomyopathy-Progress and Novel Therapeutic Opportunities

scientific article

Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families

scientific article published on 4 May 2017

Structural modeling of p.V31F variant in the aspartoacylase gene

scientific article published on January 21, 2016

NaNog: A pluripotency homeobox (master) molecule.

scientific article

In silico and in vivo models for Qatari-Specific classical homocystinuria as basis for development of novel therapies

article

Molecular modeling study of CodX reveals importance of N-terminal and C-terminal domain in the CodWX complex structure of Bacillus subtilis.

scientific article published on 23 February 2008

Next Generation Sequencing and Animal Models Reveal as a New Gene Involved in Human Age-Related Hearing Loss

article

Functional Characterization of the MYO6 Variant p.E60Q in Non-Syndromic Hearing Loss Patients

scientific article published on 21 March 2022

Genetic modifiers to the PLN L39X mutation in a patient with DCM and sustained ventricular tachycardia?

scientific article

Hypertrophic cardiomyopathy-linked variants of cardiac myosin-binding protein C3 display altered molecular properties and actin interaction

scientific article published on 14 December 2018

List of works by Navaneethakrishnan T Krishnamoorthy

Two patients with Canavan disease and structural modeling of a novel mutation

Molecular modeling of disease causing mutations in domain C1 of cMyBP-C

Probing possible egress channels for multiple ligands in human CYP3A4: a molecular modeling study.

Molecular modeling study on orphan human protein CYP4A22 for identification of potential ligand binding site.

A computational modeling approach for enhancing self-assembly and biofunctionalisation of collagen biomimetic peptides.

An Investigation of the Molecular Mechanism of Double cMyBP-C Mutation in a Patient with End-Stage Hypertrophic Cardiomyopathy

A Strategy to Enhance Secretion of Extracellular Matrix Components by Stem Cells: Relevance to Tissue Engineering.

Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss.

Impact of disease-causing mutations on inter-domain interactions in cMyBP-C: a steered molecular dynamics study.

The Role of Cardiac Myosin Binding Protein C3 in Hypertrophic Cardiomyopathy-Progress and Novel Therapeutic Opportunities

Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families

Structural modeling of p.V31F variant in the aspartoacylase gene

NaNog: A pluripotency homeobox (master) molecule.

In silico and in vivo models for Qatari-Specific classical homocystinuria as basis for development of novel therapies

Molecular modeling study of CodX reveals importance of N-terminal and C-terminal domain in the CodWX complex structure of Bacillus subtilis.

Next Generation Sequencing and Animal Models Reveal as a New Gene Involved in Human Age-Related Hearing Loss

Functional Characterization of the MYO6 Variant p.E60Q in Non-Syndromic Hearing Loss Patients

Genetic modifiers to the PLN L39X mutation in a patient with DCM and sustained ventricular tachycardia?

Hypertrophic cardiomyopathy-linked variants of cardiac myosin-binding protein C3 display altered molecular properties and actin interaction