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Navaneethakrishnan Krishnamoorthy
Navaneethakrishnan Krishnamoorthy
Sidra Research & Imperial College London
Verified email at sidra.org - Homepage
Title
Cited by
Cited by
Year
The CYP3A4*18 Genotype in the Cytochrome P450 3A4 Gene, a Rapid Metabolizer of Sex Steroids, Is Associated With Low Bone Mineral Density
YS Kang, SY Park, CH Yim, HS Kwak, P Gajendrarao, N Krishnamoorthy, ...
Clinical Pharmacology & Therapeutics 85 (3), 312-318, 2009
832009
A computational modeling approach for enhancing self-assembly and biofunctionalisation of collagen biomimetic peptides
N Krishnamoorthy, MH Yacoub, SN Yaliraki
Biomaterials 32 (30), 7275-7285, 2011
382011
Two patients with Canavan disease and structural modeling of a novel mutation
OK Zaki, N Krishnamoorthy, HS El Abd, SA Harche, RA Mattar, RS Al Disi, ...
Metabolic brain disease 32, 171-177, 2017
372017
Probing possible egress channels for multiple ligands in human CYP3A4: a molecular modeling study
N Krishnamoorthy, P Gajendrarao, S Thangapandian, Y Lee, KW Lee
Journal of molecular modeling 16, 607-614, 2010
352010
Identification of mutation resistance coldspots for targeting the SARS‐CoV2 main protease
N Krishnamoorthy, K Fakhro
IUBMB life 73 (4), 670-675, 2021
302021
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families
MK Alkowari, D Vozzi, S Bhagat, N Krishnamoorthy, A Morgan, Y Hayder, ...
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis 800, 29-36, 2017
272017
Molecular modeling of disease causing mutations in domain C1 of cMyBP-C
P Gajendrarao, N Krishnamoorthy, HS Kassem, S Moharem-Elgamal, ...
PLoS One 8 (3), e59206, 2013
252013
The role of cardiac myosin binding protein C3 in hypertrophic cardiomyopathy‐progress and novel therapeutic opportunities
IA Mohamed, NT Krishnamoorthy, GK Nasrallah, SI Da'as
Journal of cellular physiology 232 (7), 1650-1659, 2017
242017
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss
A Morgan, D Vuckovic, N Krishnamoorthy, E Rubinato, U Ambrosetti, ...
European Journal of Human Genetics 27 (1), 70-79, 2019
232019
Molecular modeling study on orphan human protein CYP4A22 for identification of potential ligand binding site
P Gajendrarao, N Krishnamoorthy, S Sakkiah, P Lazar, KW Lee
Journal of Molecular Graphics and Modelling 28 (6), 524-532, 2010
232010
A neutrophil-driven inflammatory signature characterizes the blood transcriptome fingerprint of psoriasis
A Rawat, D Rinchai, M Toufiq, AK Marr, T Kino, M Garand, ...
Frontiers in immunology 11, 587946, 2020
222020
Pharmacophore mapping and virtual screening for SIRT1 activators
S Sakkiah, N Krishnamoorthy, P Gajendrarao, S Thangapandian, Y Lee, ...
Bull Korean Chem Soc 30 (5), 1153, 2009
222009
An investigation of the molecular mechanism of double cMyBP-C mutation in a patient with end-stage hypertrophic cardiomyopathy
P Gajendrarao, N Krishnamoorthy, S Selvaraj, F Girolami, F Cecchi, ...
Journal of cardiovascular translational research 8, 232-243, 2015
182015
A strategy to enhance secretion of extracellular matrix components by stem cells: relevance to tissue engineering
N Krishnamoorthy, YT Tseng, P Gajendrarao, P Sarathchandra, ...
Tissue Engineering Part A 24 (1-2), 145-156, 2018
172018
Impact of disease-causing mutations on inter-domain interactions in cMyBP-C: a steered molecular dynamics study
N Krishnamoorthy, P Gajendrarao, I Olivotto, M Yacoub
Journal of Biomolecular Structure and Dynamics 35 (9), 1916-1922, 2017
152017
Towards developing a vaccine for rheumatic heart disease
GD Gandhi, N Krishnamoorthy, UMA Motal, M Yacoub
Global Cardiology Science & Practice 2017 (1), 2017
152017
NaNog: A pluripotency homeobox (master) molecule
MH Allouba, AM ElGuindy, N Krishnamoorthy, MH Yacoub, YE Aguib
Global Cardiology Science and Practice 2015 (3), 36, 2015
132015
In silico and in vivo models for Qatari‐specific classical homocystinuria as basis for development of novel therapies
HM Ismail, N Krishnamoorthy, N Al‐Dewik, H Zayed, NA Mohamed, ...
Human mutation 40 (2), 230-240, 2019
122019
Hypertrophic cardiomyopathy-linked variants of cardiac myosin-binding protein C3 display altered molecular properties and actin interaction
SI Da'as, K Fakhro, A Thanassoulas, N Krishnamoorthy, A Saleh, ...
Biochemical Journal 475 (24), 3933-3948, 2018
122018
Next Generation Sequencing and Animal Models Reveal SLC9A3R1 as a New Gene Involved in Human Age-Related Hearing Loss
G Girotto, A Morgan, N Krishnamoorthy, M Cocca, M Brumat, S Bassani, ...
Frontiers in Genetics 10, 142, 2019
112019
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