Zobrazeno 1 - 10
of 11
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:
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, 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:
Akhter Husain, Srinivas Reddy Gosla, Sravya Thumoju, Praveen Kumar Neela, Rajeshwari Bv, Vasavi Mohan
Publikováno v:
Contemporary Clinical Dentistry
Background: Several genes are associated with the etiology of cleft lip and palate (CLP) in different populations. Many nucleotide variants on genes such as GRHL3, IRF6, NAT2, SDC2, BCL3, and PVRL1 were reported in different populations, but not stud
Autor:
Neha Aggarwal, Yasuto Araki, Erfan Aref-Eshghi, Takahiro Arima, Yunfeng Bai, Bahar Barani, Megan Beetch, Georgina E.T. Blake, Graham C. Burdge, Deanna Alexis Carere, Pearl Chang, Pao-Yang Chen, Mariano Colón-Caraballo, Fabio Coppedè, Buddhadeb Dawn, Pierre-Antoine Dugué, Sarah El-Heis, Eliana Portilla Fernandez, Idhaliz Flores-Caldera, Oscar H. Franco, Andrea Fuso, Mohsen Ghanbari, Asish K. Ghosh, Peter D. Gluckman, Keith M. Godfrey, Moloya Gohain, Steven G. Gray, Mark A. Hanson, Hiromitsu Hattori, Christian M. Hedrich, Hitoshi Hiura, John L. Hopper, Amir Hosseini, Cathrine Hoyo, Fei-Man Hsu, Wilfried Karmaus, Norio Kobayashi, Jannet Kocerha, Alexander K. Koliada, Leila Larijani, Sophie A. Lelièvre, Shuai Li, Karen A. Lillycrop, Jui-Hsien Lu, Katarzyna Lubecka, Oleh V. Lushchak, Masato Maekawa, Amanda H. Mahnke, Giuseppina Mastrototaro, Roger L. Milne, Toshihide Mimura, Janos Minarovits, Saverio Minucci, Rajesh C. Miranda, Vasavi Mohan, Taulant Muka, Nandini Mukherjee, Apiwat Mutirangura, Jana Nano, Khue Vu Nguyen, Hans Helmut Niller, Hiroaki Okae, Sarah S. Park, Kamthorn Pruksananonda, Sheeja Rajasingh, Johnson Rajasingh, Joanna Rakoczy, Derrick E. Rancourt, David I. Rodenhiser, Bekim Sadikovic, Sabita N. Saldanha, Nihal A. Salem, Saheli Samanta, Laila C. Schenkel, Alessandro Sessa, David A. Skaar, Patricia Sorrow, Barbara Stefanska, Souta Takahashi, Sravya Thumoju, Trygve O. Tollefsbol, Jenna Troup, Alexander M. Tseng, Alexander M. Vaiserman, Douglas E. Vaughan, Sumei Wang, Ruilan Wang, Artisa Wasinarom, Yoshihisa Watanabe, Erica D. Watson, Wanyin Wu, Zhigang Zhou, Ali H. Ziyab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4affac6b3e3aa49d1eb3752b63567349
https://doi.org/10.1016/b978-0-12-812215-0.01002-5
https://doi.org/10.1016/b978-0-12-812215-0.01002-5
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