Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Sravya Thumoju"'
Autor:
Praveen Kumar Neela, Srinivas Reddy Gosla, Akhter Husain, Vasavi Mohan, Sravya Thumoju, Rajeshwari Rajeshwari
Publikováno v:
Indonesian Biomedical Journal, Vol 13, Iss 1, Pp 27-33 (2021)
BACKGROUND: Cleft lip palate is a common congenital anomaly with multifactorial etiology. Many high-risk markers at different loci were reported to be involved in its etiology. Advanced genetic research led to the discovery of evidence of a new linka
Externí odkaz:
https://doaj.org/article/ba2acf341bf44a148b684c385f1dfe5b
Autor:
Praveen Kumar Neela, Gosla Srinivas Reddy, Akhter Husain, Vasavi Mohan, Sravya Thumoju, Rajeshwari BV
Publikováno v:
Global Medical Genetics, Vol 08, Iss 01, Pp 024-031 (2021)
Background Cleft lip palate (CLP) is a common congenital anomaly with multifactorial etiology. Many polymorphisms at different loci on multiple chromosomes were reported to be involved in its etiology. Genetic research on a single multigenerational A
Externí odkaz:
https://doaj.org/article/7334b79f38474544863d72951a75530e
Autor:
Praveen Kumar Neela, Srinivas Reddy Gosla, Akhter Husain, Vasavi Mohan, Sravya Thumoju, Rajeshwari BV
Publikováno v:
Journal of Dental Research, Dental Clinics, Dental Prospects, Vol 14, Iss 2, Pp 93-96 (2020)
Background. Cleft lip and palate (CLP) is a common congenital anomaly. Many genes, like MAPK4 andSOX-1OT, are associated with its etiology in different populations. High-risk markers on these genesreported in other populations were not studied in our
Externí odkaz:
https://doaj.org/article/12fa7ec998e54508b8f5f7062b9f300d
Autor:
Sravya Thumoju, Akhter Husain, Rajeshwari Rajeshwari, Vasavi Mohan, Srinivas Reddy Gosla, Praveen Kumar Neela
Publikováno v:
Indonesian Biomedical Journal, Vol 13, Iss 1, Pp 27-33 (2021)
BACKGROUND: Cleft lip palate is a common congenital anomaly with multifactorial etiology. Many high-risk markers at different loci were reported to be involved in its etiology. Advanced genetic research led to the discovery of evidence of a new linka
Autor:
Sravya Thumoju, Akhter Husain, Gosla Srinivas Reddy, Praveen Kumar Neela, Vasavi Mohan, Rajeshwari Bv
Publikováno v:
Global Medical Genetics
Global Medical Genetics, Vol 08, Iss 01, Pp 024-031 (2021)
Global Medical Genetics, Vol 08, Iss 01, Pp 024-031 (2021)
Background Cleft lip palate (CLP) is a common congenital anomaly with multifactorial etiology. Many polymorphisms at different loci on multiple chromosomes were reported to be involved in its etiology. Genetic research on a single multigenerational A
Autor:
Sravya Thumoju, Srinivas Reddy Gosla, Rajeshwari Bv, Akhter Husain, Praveen Kumar Neela, Vasavi Mohan
Publikováno v:
Journal of Dental Research, Dental Clinics, Dental Prospects
Journal of Dental Research, Dental Clinics, Dental Prospects, Vol 14, Iss 2, Pp 93-96 (2020)
Journal of Dental Research, Dental Clinics, Dental Prospects, Vol 14, Iss 2, Pp 93-96 (2020)
Background. Cleft lip and palate (CLP) is a common congenital anomaly. Many genes, like MAPK4 andSOX-1OT, are associated with its etiology in different populations. High-risk markers on these genesreported in other populations were not studied in our
Autor:
Sireesha Divyakolu, Yog Raj Ahuja, Sravya Thumoju, Vasavi Mohan, Sayeda S Fatima, Triveni Bhopal, Santoshini Gowrishetty
Publikováno v:
International Journal of Medicine and Public Health. 8:112-115
Autor:
Sravya Thumoju, Vasavi Mohan
Scientific research directed at understanding epigenetic aspects of human disease has just begun reaping results with an applicative potential to be used for therapeutic intervention. Epigenetic alterations such as methylation, histone changes, and R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5172edbc8d963f2aad1685ebb31cac17
https://doi.org/10.1016/b978-0-12-812215-0.00018-2
https://doi.org/10.1016/b978-0-12-812215-0.00018-2
Autor:
Mohan Vasavi, Yadavalli Tejaswini, Vemula Ramana Sreekanth, Qurratulain Hasan, Sravya Thumoju, Sireesha Divyakolu, Winnie Thomas, Vallomkonda Nagaratna, Vallomkonda Ramesh OmSai, Yog Raj Ahuja
Publikováno v:
Journal of Neurological Disorders.
Background: Genetic risk factors play an important role in neurological disorders. In this case-control study, we examined the C677T polymorphism (rs1801133) in the Methylenetetrahydrofolate reductase (MTHFR) gene and its association with three neuro