Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Avinash M Veerappa"'
Autor:
Uppala Radhakrishna, Samet Albayrak, Rita Zafra, Alosh Baraa, Sangeetha Vishweswaraiah, Avinash M Veerappa, Deepthi Mahishi, Nazia Saiyed, Nitish K Mishra, Chittibabu Guda, Rouba Ali-Fehmi, Ray O Bahado-Singh
Publikováno v:
PLoS ONE, Vol 14, Iss 3, p e0200229 (2019)
Ventricular Septal Defect (VSD), the most common congenital heart defect, is characterized by a hole in the septum between the right and left ventricles. The pathogenesis of VSD is unknown in most clinical cases. There is a paucity of data relevant t
Externí odkaz:
https://doaj.org/article/7c4ef876ecad48a2894b5d2a4a5b7d6f
Autor:
Uppala Radhakrishna, Sangeetha Vishweswaraiah, Avinash M Veerappa, Rita Zafra, Samet Albayrak, Prajna H Sitharam, Nazia M Saiyed, Nitish K Mishra, Chittibabu Guda, Ray Bahado-Singh
Publikováno v:
PLoS ONE, Vol 13, Iss 9, p e0203893 (2018)
Tetralogy of Fallot (TOF) is the most common Critical Congenital Heart Defect (CCHD). The etiology of TOF is unknown in most cases. Preliminary data from our group and others suggest that epigenetic changes may play an important role in CHD. Epidemio
Externí odkaz:
https://doaj.org/article/2dcee422c29642fabbb659704358d1ff
Autor:
Avinash M Veerappa, Sangeetha Vishweswaraiah, Kusuma Lingaiah, Megha Murthy, Raviraj V Suresh, Dinesh S Manjegowda, Nallur B Ramachandra
Publikováno v:
PLoS ONE, Vol 10, Iss 4, p e0121846 (2015)
Global spectrum of CNVs is required to catalog variations to provide a high-resolution on the dynamics of genome-organization and human migration. In this study, we performed genome-wide genotyping using high-resolution arrays and identified 44,109 C
Externí odkaz:
https://doaj.org/article/acc37d796f964be9ae01c7fd06993c8b
Autor:
Avinash M Veerappa, Megha N Murthy, Sangeetha Vishweswaraiah, Kusuma Lingaiah, Raviraj V Suresh, Somanna Ajjamada Nachappa, Nelchi Prashali, Sangeetha Nuggehalli Yadav, Manjula Arsikere Srikanta, Dinesh S Manjegowda, Keshava B Seshachalam, Nallur B Ramachandra
Publikováno v:
PLoS ONE, Vol 9, Iss 2, p e90391 (2014)
MicroRNAs are involved in post-transcriptional down-regulation of gene expression. Variations in miRNA genes can severely affect downstream-regulated genes and their pathways. However, population-specific burden of CNVs on miRNA genes and the complex
Externí odkaz:
https://doaj.org/article/1cfd6cd6ccac4055bb2d01cc13f3e760
Autor:
Avinash M Veerappa, Sangeetha Vishweswaraiah, Kusuma Lingaiah, Megha Murthy, Dinesh S Manjegowda, Radhika Nayaka, Nallur B Ramachandra
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e66843 (2013)
Olfactory receptors (OR), responsible for detection of odor molecules, belong to the largest family of genes and are highly polymorphic in nature having distinct polymorphisms associated with specific regions around the globe. Since there are no repo
Externí odkaz:
https://doaj.org/article/91b178a00b134978b8fe61b344ed9c91
Autor:
Yogita Kattimani, Avinash M. Veerappa
Publikováno v:
Autoimmunity, Vol 51, Iss 4, Pp 147-151 (2018)
Multiple sclerosis (MS) is a demyelinating disease of the central nervous system causing axonal injury, neuronal loss, and atrophy of the central nervous system leading to permanent neurological and clinical disability. Presence of mutations in M9 do
Externí odkaz:
https://doaj.org/article/7c4f72bfb4b94f3d9eb8de926dec97ce
Autor:
Avinash M. Veerappa
Publikováno v:
Ophthalmic genetics. 42(2)
Keratoconus is a progressive thinning, steepening and distortion of the cornea which can lead to loss of vision if left untreated. Keratoconus has a complex multifactorial etiology, with genetic and environmental components contributing to the diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ffd1931966edf6076dc372a8d442fd3
https://pubmed.ncbi.nlm.nih.gov/33554698
https://pubmed.ncbi.nlm.nih.gov/33554698
Publikováno v:
Egyptian Journal of Medical Human Genetics, Vol 21, Iss 1, Pp 1-14 (2020)
Background Autism is a neurodevelopmental condition with genetic heterogeneity. It is characterized by difficulties in reciprocal social interactions with strong repetitive behaviors and stereotyped interests. Copy number variations (CNVs) are genomi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87f9007d12fcbb97b0bb1f1295c27186
https://doi.org/10.1186/s43042-020-00091-3
https://doi.org/10.1186/s43042-020-00091-3
Publikováno v:
Meta Gene. 12:134-137
Discordant phenotypes and diseases in Monozygotic twins (MZ) are always intriguing and genetics is the exclusive reason. Down syndrome is one such disorder, which shows heterogeneity, with occurrences of incidental diseases discordant between cases.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d5f76391a415310ad6d01ea49c0c99ee
https://doi.org/10.1016/j.mgene.2017.03.004
https://doi.org/10.1016/j.mgene.2017.03.004
Autor:
Alosh Baraa, Nitish K. Mishra, Uppala Radhakrishna, Deepthi Mahishi, Chittibabu Guda, Avinash M. Veerappa, Samet Albayrak, Ray O. Bahado-Singh, Sangeetha Vishweswaraiah, Rita Zafra, Rouba Ali-Fehmi, Nazia Saiyed
Publikováno v:
PLoS ONE
PLoS ONE, Vol 14, Iss 3, p e0200229 (2019)
PLoS ONE, Vol 14, Iss 3, p e0200229 (2019)
Ventricular Septal Defect (VSD), the most common congenital heart defect, is characterized by a hole in the septum between the right and left ventricles. The pathogenesis of VSD is unknown in most clinical cases. There is a paucity of data relevant t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5fd411b03055c070b39e76bad50d1fac
http://europepmc.org/articles/PMC6428297
http://europepmc.org/articles/PMC6428297