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Navaneethakrishnan Krishnamoorthy

Showing results (11-20 of 25) with videos related to

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Journal of Molecular Graphics & Modelling|April 11, 2008
Molecular modeling study of CodX reveals importance of N-terminal and C-terminal domain in the CodWX complex structure of Bacillus subtilisNavaneethakrishnan Krishnamoorthy, Poornima Gajendrarao, Soo Hyun Eom, et al.
Plos One|March 26, 2013
Molecular modeling of disease causing mutations in domain C1 of cMyBP-CPoornima Gajendrarao, Navaneethakrishnan Krishnamoorthy, Heba Sh Kassem, et al.
Frontiers in Genetics|March 14, 2019
Next Generation Sequencing and Animal Models Reveal <i>SLC9A3R1</i> as a New Gene Involved in Human Age-Related Hearing LossGiorgia Girotto, Anna Morgan, Navaneethakrishnan Krishnamoorthy, et al.
Tissue Engineering. Part A|May 4, 2017
A Strategy to Enhance Secretion of Extracellular Matrix Components by Stem Cells: Relevance to Tissue EngineeringNavaneethakrishnan Krishnamoorthy, Yuan-Tsan Tseng, Poornima Gajendrarao, et al.
The Biochemical Journal|November 18, 2018
Hypertrophic cardiomyopathy-linked variants of cardiac myosin-binding protein C3 display altered molecular properties and actin interactionSahar I Da'as, Khalid Fakhro, Angelos Thanassoulas, et al.
European Journal of Medical Genetics|February 19, 2022
A recessive variant in SIM2 in a child with complex craniofacial anomalies and global developmental delayAlya A Al-Kurbi, Sahar Isa Da'as, Waleed Aamer, et al.
Mutation Research|May 15, 2017
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari familiesMoza K Alkowari, Diego Vozzi, Shruti Bhagat, et al.
European Journal of Human Genetics : EJHG|September 5, 2018
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing lossAnna Morgan, Dragana Vuckovic, Navaneethakrishnan Krishnamoorthy, et al.
International Journal of Molecular Sciences|March 25, 2022
Functional Characterization of the <i>MYO6</i> Variant p.E60Q in Non-Syndromic Hearing Loss PatientsMoza Alkowari, Meritxell Espino-Guarch, Sahar Daas, et al.
Journal of Translational Medicine|November 4, 2022
Assessing the genetic burden of familial hypercholesterolemia in a large middle eastern biobankGeethanjali Devadoss Gandhi, Waleed Aamer, Navaneethakrishnan Krishnamoorthy, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Journal of Molecular Graphics & Modelling|April 11, 2008
Molecular modeling study of CodX reveals importance of N-terminal and C-terminal domain in the CodWX complex structure of Bacillus subtilisNavaneethakrishnan Krishnamoorthy, Poornima Gajendrarao, Soo Hyun Eom, et al.
Plos One|March 26, 2013
Molecular modeling of disease causing mutations in domain C1 of cMyBP-CPoornima Gajendrarao, Navaneethakrishnan Krishnamoorthy, Heba Sh Kassem, et al.
Frontiers in Genetics|March 14, 2019
Next Generation Sequencing and Animal Models Reveal <i>SLC9A3R1</i> as a New Gene Involved in Human Age-Related Hearing LossGiorgia Girotto, Anna Morgan, Navaneethakrishnan Krishnamoorthy, et al.
Tissue Engineering. Part A|May 4, 2017
A Strategy to Enhance Secretion of Extracellular Matrix Components by Stem Cells: Relevance to Tissue EngineeringNavaneethakrishnan Krishnamoorthy, Yuan-Tsan Tseng, Poornima Gajendrarao, et al.
The Biochemical Journal|November 18, 2018
Hypertrophic cardiomyopathy-linked variants of cardiac myosin-binding protein C3 display altered molecular properties and actin interactionSahar I Da'as, Khalid Fakhro, Angelos Thanassoulas, et al.
European Journal of Medical Genetics|February 19, 2022
A recessive variant in SIM2 in a child with complex craniofacial anomalies and global developmental delayAlya A Al-Kurbi, Sahar Isa Da'as, Waleed Aamer, et al.
Mutation Research|May 15, 2017
Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari familiesMoza K Alkowari, Diego Vozzi, Shruti Bhagat, et al.
European Journal of Human Genetics : EJHG|September 5, 2018
Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing lossAnna Morgan, Dragana Vuckovic, Navaneethakrishnan Krishnamoorthy, et al.
International Journal of Molecular Sciences|March 25, 2022
Functional Characterization of the <i>MYO6</i> Variant p.E60Q in Non-Syndromic Hearing Loss PatientsMoza Alkowari, Meritxell Espino-Guarch, Sahar Daas, et al.
Journal of Translational Medicine|November 4, 2022
Assessing the genetic burden of familial hypercholesterolemia in a large middle eastern biobankGeethanjali Devadoss Gandhi, Waleed Aamer, Navaneethakrishnan Krishnamoorthy, et al.
Pageof 3