A Novel TPM1 Mutation Causes Familial Hypertrophic Cardiomyopathy in an Indian Family: Genetic and Clinical Correlation
Kumar, Prabodh, Paramasivam, Ganesh, Devasia, Tom, Prabhu, Mukund, Rai, Maneesh K., Prakashini, K., Mallya, Sandeep, Reghunathan, Dinesh, Megha, A., Nayak, Krishnananda, Moka, Rajasekhar
Published in Indian journal of clinical biochemistry (2024)
Published in Indian journal of clinical biochemistry (2024)
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Journal Article
Gerbode Ventricular Septal Defect -A Rare Cardiac Anomaly Associated with Genetic Variants in Indian Population- A Case Series
Borkar, Yashvanthi, Nayak, Krishnananda, Shetty, Ranjan K, Bhat, Gopalakrishna, Moka, Rajasekhar
Published in Journal of clinical and diagnostic research (01.03.2017)
Published in Journal of clinical and diagnostic research (01.03.2017)
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Journal Article
Human breast tumor derived endothelial cells exhibit distinct biological properties
Hegde, Mangala, Bhat, Sharath Mohan, Guruprasad, Kanive Parashiva, Moka, Rajasekhar, Ramachandra, Lingadakai, Satyamoorthy, Kapaettu, Joshi, Manjunath B.
Published in Biology of the cell (01.02.2022)
Published in Biology of the cell (01.02.2022)
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Journal Article
ANALYSIS OF GENE COPY NUMBER VARIATIONS IN PATIENTS WITH CARDIAC SEPTAL DEFECTS USING MULTIPLEX LIGATION-DEPENDENT PROBE AMPLIFICATION
YASHVANTHI BORKAR, KRISHNANANDA NAYAK, RANJAN SHETTY K, RAJASEKHAR MOKA
Published in Asian journal of pharmaceutical and clinical research (16.11.2019)
Published in Asian journal of pharmaceutical and clinical research (16.11.2019)
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Journal Article
Primary Cardiac Involvement in the Rare Transthyretin Ile73Val Mutation: A Case Series
Kumar, Prabodh, Paramasivam, Ganesh, Devasia, Tom, K, Prakashini, A, Megha, Nayak, Krishnanada, Joshi, Manjunath B, Moka, Rajasekhar
Published in Circulation. Genomic and precision medicine (01.06.2020)
Published in Circulation. Genomic and precision medicine (01.06.2020)
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Journal Article
Identification of NKX2-5 and GATA4 sequence variations in patients with cardiac septation defects
Borkar, Yashvanthi, Shetty, K Ranjan, Krishnanand, K, Moka, Rajasekhar
Published in Molecular cytogenetics (21.01.2014)
Published in Molecular cytogenetics (21.01.2014)
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Journal Article
MLPA analysis of transcriptional gene(s) variations in patients with congenital heart septation defects
Moka, Rajasekhar, John, Neetha, Borkar, Yashvanthi, Shetty, K Ranjan
Published in Molecular cytogenetics (21.01.2014)
Published in Molecular cytogenetics (21.01.2014)
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Journal Article
A Novel TPM1 Mutation Causes Familial Hypertrophic Cardiomyopathy in an Indian Family: Genetic and Clinical Correlation
Kumar, Prabodh, Paramasivam, Ganesh, Devasia, Tom, Prabhu, Mukund, Rai, Maneesh K, Prakashini, K, Mallya, Sandeep, Reghunathan, Dinesh, Megha, A, Nayak, Krishnananda, Moka, Rajasekhar
Published in Indian journal of clinical biochemistry : IJCB (01.01.2024)
Published in Indian journal of clinical biochemistry : IJCB (01.01.2024)
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