Lista de obras - Navaneethakrishnan T Krishnamoorthy

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

artículo científico publicado en 2017

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

artículo científico publicado en 2011

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

artículo científico publicado en 2015

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

artículo científico publicado en 2022

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

artículo científico publicado en 2015

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

scientific article published on 14 December 2018

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

artículo científico publicado en 2016

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

article

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

artículo científico publicado en 2013

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

artículo científico publicado en 2008

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

artículo científico publicado en 2009

NaNog: A pluripotency homeobox (master) molecule.

artículo científico publicado en 2015

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

article

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

artículo científico publicado en 2018

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

artículo científico publicado en 2009

Structural modeling of p.V31F variant in the aspartoacylase gene

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2016

Lista de obras de Navaneethakrishnan T Krishnamoorthy

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

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

Functional Characterization of the <i>MYO6</i> 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

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

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

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

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

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

NaNog: A pluripotency homeobox (master) molecule.

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

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

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

Structural modeling of p.V31F variant in the aspartoacylase gene

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

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

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