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Meera Purushottam

Showing results (31-40 of 89) with videos related to

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Scientific Reports|October 27, 2021
Analysis of whole exome sequencing in severe mental illness hints at selection of brain development and immune related genesJayant Mahadevan, Ajai Kumar Pathak, Alekhya Vemula, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|May 9, 2022
Clinical, Radiological, and Genetic Profile of Spinocerebellar Ataxia 12: A Hospital-Based Cohort AnalysisValakunja Harikrishna Ganaraja, Vikram V Holla, Albert Stezin, et al.
Asian Journal of Psychiatry|July 22, 2014
An exploratory association study of the influence of dysbindin and neuregulin polymorphisms on brain morphometry in patients with schizophrenia and healthy subjects from South IndiaPriyadarshini Thirunavukkarasu, Anupa A Vijayakumari, John P John, et al.
Annals of Indian Academy of Neurology|May 16, 2024
Revisiting Friedreich's Ataxia: Phenotypic and Imaging CharacteristicsRohan Mahale, Meera Purushottam, Raviprakash Singh, et al.
Bioinformation|October 9, 2008
Evolutionary analysis of PHLPP1 gene in humans and non-human primatesPadmanabhan Anbazhagan, Meera Purushottam, H B Kiran Kumar, et al.
Neurobiology of Aging|January 14, 2018
Mutation burden profile in familial Alzheimer's disease cases from IndiaAdhikarla Syama, Somdatta Sen, Lakshmi Narayanan Kota, et al.
Asian Journal of Psychiatry|June 1, 2017
Effect of CLU and PICALM polymorphisms on AD risk: A study from south IndiaBhagyalakshmi Mallapura Shankarappa, Lakshmi Narayanan Kota, Meera Purushottam, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|December 27, 2014
Reduced telomere length in neurodegenerative disorders may suggest shared biologyLakshmi Narayanan Kota, Srikala Bharath, Meera Purushottam, et al.
Journal of Clinical Neurology (Seoul, Korea)|January 13, 2017
Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large CohortSeena Vengalil, Veeramani Preethish-Kumar, Kiran Polavarapu, et al.
Stem Cell Research|November 20, 2022
Generation of a new human induced pluripotent stem cell (hiPSC) line from a South Asian Indian with a MYBPC3<sup>Δ</sup><sup>25bp</sup> variantPrasanth Chimata, Deepak K Kashyap, Thiagarajan Sairam, et al.
Pageof 9

Showing results (31-40 of 89) with videos related to

Sort By:
Pageof 9
Scientific Reports|October 27, 2021
Analysis of whole exome sequencing in severe mental illness hints at selection of brain development and immune related genesJayant Mahadevan, Ajai Kumar Pathak, Alekhya Vemula, et al.
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|May 9, 2022
Clinical, Radiological, and Genetic Profile of Spinocerebellar Ataxia 12: A Hospital-Based Cohort AnalysisValakunja Harikrishna Ganaraja, Vikram V Holla, Albert Stezin, et al.
Asian Journal of Psychiatry|July 22, 2014
An exploratory association study of the influence of dysbindin and neuregulin polymorphisms on brain morphometry in patients with schizophrenia and healthy subjects from South IndiaPriyadarshini Thirunavukkarasu, Anupa A Vijayakumari, John P John, et al.
Annals of Indian Academy of Neurology|May 16, 2024
Revisiting Friedreich's Ataxia: Phenotypic and Imaging CharacteristicsRohan Mahale, Meera Purushottam, Raviprakash Singh, et al.
Bioinformation|October 9, 2008
Evolutionary analysis of PHLPP1 gene in humans and non-human primatesPadmanabhan Anbazhagan, Meera Purushottam, H B Kiran Kumar, et al.
Neurobiology of Aging|January 14, 2018
Mutation burden profile in familial Alzheimer's disease cases from IndiaAdhikarla Syama, Somdatta Sen, Lakshmi Narayanan Kota, et al.
Asian Journal of Psychiatry|June 1, 2017
Effect of CLU and PICALM polymorphisms on AD risk: A study from south IndiaBhagyalakshmi Mallapura Shankarappa, Lakshmi Narayanan Kota, Meera Purushottam, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|December 27, 2014
Reduced telomere length in neurodegenerative disorders may suggest shared biologyLakshmi Narayanan Kota, Srikala Bharath, Meera Purushottam, et al.
Journal of Clinical Neurology (Seoul, Korea)|January 13, 2017
Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Confirmed by Multiplex Ligation-Dependent Probe Amplification: Genotype-Phenotype Correlation in a Large CohortSeena Vengalil, Veeramani Preethish-Kumar, Kiran Polavarapu, et al.
Stem Cell Research|November 20, 2022
Generation of a new human induced pluripotent stem cell (hiPSC) line from a South Asian Indian with a MYBPC3<sup>Δ</sup><sup>25bp</sup> variantPrasanth Chimata, Deepak K Kashyap, Thiagarajan Sairam, et al.
Pageof 9