Zobrazeno 1 - 10
of 35
pro vyhledávání: '"Lina M, Moreno Uribe"'
Autor:
Ronilo Ragodos, Tong Wang, Carmencita Padilla, Jacqueline T. Hecht, Fernando A. Poletta, Iêda M. Orioli, Carmen J. Buxó, Azeez Butali, Consuelo Valencia-Ramirez, Claudia Restrepo Muñeton, George L. Wehby, Seth M. Weinberg, Mary L. Marazita, Lina M. Moreno Uribe, Brian J. Howe
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-8 (2022)
Abstract Children with orofacial clefting (OFC) present with a wide range of dental anomalies. Identifying these anomalies is vital to understand their etiology and to discern the complex phenotypic spectrum of OFC. Such anomalies are currently ident
Externí odkaz:
https://doaj.org/article/3800fcecdedd481ebcf9fe8c511f1042
Autor:
Rasha N. Alotaibi, Brian J. Howe, Jonathan M. Chernus, Nandita Mukhopadhyay, Carla Sanchez, Frederic W. B. Deleyiannis, Katherine Neiswanger, Carmencita Padilla, Fernando A. Poletta, Ieda M. Orioli, Carmen J. Buxó, Jacqueline T. Hecht, George L. Wehby, Ross E. Long, Alexandre R. Vieira, Seth M. Weinberg, John R. Shaffer, Lina M. Moreno Uribe, Mary L. Marazita
Publikováno v:
BMC Oral Health, Vol 21, Iss 1, Pp 1-11 (2021)
Abstract Background Dental caries is one of the most common chronic diseases and is influenced by a complex interplay of genetic and environmental factors. Most previous genetic studies of caries have focused on identifying genes that contribute to d
Externí odkaz:
https://doaj.org/article/7e1cb49b8d3c4ae58f9dc61b99d267ba
Autor:
Rasha N. Alotaibi, Brian J. Howe, Lina M. Moreno Uribe, Consuelo Valencia Ramirez, Claudia Restrepo, Frederic W. B. Deleyiannis, Carmencita Padilla, Ieda M. Orioli, Carmen J. Buxó, Jacqueline T. Hecht, George L. Wehby, Katherine Neiswanger, Jeffrey C. Murray, John R. Shaffer, Seth M. Weinberg, Mary L. Marazita
Publikováno v:
Frontiers in Dental Medicine, Vol 2 (2022)
Odontogenesis is a complex process, where disruption can result in dental anomalies and/or increase the risk of developing dental caries. Based on previous studies, certain dental anomalies tend to co-occur in patients, suggesting that these traits m
Externí odkaz:
https://doaj.org/article/c38559fa829e4202a54842f1ed2b3eec
Autor:
Ronilo Ragodos, Tong Wang, Carmencita Padilla, Jacqueline T. Hecht, Fernando A. Poletta, Iêda M. Orioli, Carmen J. Buxó, Azeez Butali, Consuelo Valencia-Ramirez, Claudia Restrepo Muñeton, George L. Wehby, Seth M. Weinberg, Mary L. Marazita, Lina M. Moreno Uribe, Brian J. Howe
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/63f57458558b42f78b2802c5a0743553
Autor:
Brian J. Howe, Chandler Pendleton, Miyuraj Harishchandra Hikkaduwa Withanage, Christopher A. Childs, Erliang Zeng, Arjen van Wijk, Ruurd Hermus, Carmencita Padilla, Jacqueline T. Hecht, Fernando A. Poletta, Iêda M. Orioli, Carmen J. Buxó-Martínez, Frederic Deleyiannis, Alexandre R. Vieira, Azeez Butali, Consuelo Valencia-Ramirez, Claudia Restrepo Muñeton, George L. Wehby, Seth M. Weinberg, Mary L. Marazita, Lina M. Moreno Uribe, Xian-Jin Xie
Publikováno v:
Dentistry Journal, Vol 10, Iss 7, p 128 (2022)
Individuals with orofacial clefting (OFC) have a higher prevalence of tooth agenesis (TA) overall. Neither the precise etiology of TA, nor whether TA occurs in patterns that differ by gender or cleft type is yet known. This meta-analysis aims to iden
Externí odkaz:
https://doaj.org/article/91b389eb162e410caba2b94f455fc1fd
Autor:
Karlijne Indencleef, Hanne Hoskens, Myoung Keun Lee, Julie D. White, Chenxing Liu, Ryan J. Eller, Sahin Naqvi, George L. Wehby, Lina M. Moreno Uribe, Jacqueline T. Hecht, Ross E. Long, Kaare Christensen, Frederic W. Deleyiannis, Susan Walsh, Mark D. Shriver, Stephen Richmond, Joanna Wysocka, Hilde Peeters, John R. Shaffer, Mary L. Marazita, Greet Hens, Seth M. Weinberg, Peter Claes
Publikováno v:
Frontiers in Genetics, Vol 12 (2021)
Unaffected relatives of individuals with non-syndromic cleft lip with or without cleft palate (NSCL/P) show distinctive facial features. The presence of this facial endophenotype is potentially an expression of underlying genetic susceptibility to NS
Externí odkaz:
https://doaj.org/article/b44ba2f0b8b04c2ab9758cb8e66b3391
Autor:
Lina M. Moreno Uribe, Mary L. Marazita
Publikováno v:
Cleft and Craniofacial Orthodontics. :39-60
Autor:
Rasha N. Alotaibi, Brian J. Howe, Lina M. Moreno Uribe, Carla Sanchez, Frederic W.B. Deleyiannis, Carmencita Padilla, Fernando A. Poletta, Ieda M. Orioli, Carmen J. Buxó, George L. Wehby, Alexandre R. Vieira, Jeffrey Murray, Consuelo Valencia-Ramírez, Claudia P. Restrepo Muñeton, Ross E. Long, John R. Shaffer, Steven E. Reis, Seth M. Weinberg, Katherine Neiswanger, Daniel W. McNeil, Mary L. Marazita
Publikováno v:
Human Heredity. 87:34-50
Introduction: Enamel hypoplasia causes a reduction in the thickness of affected enamel and is one of the most common dental anomalies. This defect is caused by environmental and/or genetic factors that interfere with tooth formation, emphasizing the
Autor:
Jacqueline T. Hecht, Carmencita D. Padilla, Lina M. Moreno Uribe, Consuelo Valencia-Ramirez, Tong Wang, Iêda M. Orioli, Seth M. Weinberg, Carmen J. Buxó, Azeez Butali, Fernando A. Poletta, B.J. Howe, George L. Wehby, Mary L. Marazita, Ronilo Ragodos, Claudia P. Restrepo Muñeton
Children with orofacial clefting (OFC) present with a wide range of dental anomalies. Identifying these anomalies is vital to understand their etiology and to discern the complex phenotypic spectrum of OFC. Such anomalies are currently identified usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c64bb247e93ba4ba06b4aac6d67cb7b
https://doi.org/10.21203/rs.3.rs-1061414/v1
https://doi.org/10.21203/rs.3.rs-1061414/v1
Autor:
Ronilo, Ragodos, Tong, Wang, Carmencita, Padilla, Jacqueline T, Hecht, Fernando A, Poletta, Iêda M, Orioli, Carmen J, Buxó, Azeez, Butali, Consuelo, Valencia-Ramirez, Claudia, Restrepo Muñeton, George L, Wehby, Seth M, Weinberg, Mary L, Marazita, Lina M, Moreno Uribe, Brian J, Howe
Publikováno v:
Scientific reports. 12(1)
Children with orofacial clefting (OFC) present with a wide range of dental anomalies. Identifying these anomalies is vital to understand their etiology and to discern the complex phenotypic spectrum of OFC. Such anomalies are currently identified usi