Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Juan C Mereb"'
Autor:
Ida Anjomshoaa, Jessica Briseño-Ruiz, Kathleen Deeley, Fernardo A Poletta, Juan C Mereb, Aline L Leite, Priscila A T M Barreta, Thelma L Silva, Piper Dizak, Timothy Ruff, Asli Patir, Mine Koruyucu, Zerrin Abbasoğlu, Priscila L Casado, Andrew Brown, Samer H Zaky, Merve Bayram, Erika C Küchler, Margaret E Cooper, Kai Liu, Mary L Marazita, İlknur Tanboğa, José M Granjeiro, Figen Seymen, Eduardo E Castilla, Iêda M Orioli, Charles Sfeir, Hongjiao Owyang, Marília A R Buzalaf, Alexandre R Vieira
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0143068 (2015)
Aquaporins (AQP) are water channel proteins and the genes coding for AQP2, AQP5, and AQP6 are clustered in 12q13. Since AQP5 is expressed in serous acinar cells of salivary glands, we investigated its involvement in caries. DNA samples from 1,383 ind
Externí odkaz:
https://doaj.org/article/fa8123d599924aa0ac391f8900899508
Autor:
Takehiko Shimizu, Bao Ho, Kathleen Deeley, Jessica Briseño-Ruiz, Italo M Faraco, Brett I Schupack, João A Brancher, Giovana D Pecharki, Erika C Küchler, Patricia N Tannure, Andrea Lips, Thays C S Vieira, Asli Patir, Mine Yildirim, Fernando A Poletta, Juan C Mereb, Judith M Resick, Carla A Brandon, Iêda M Orioli, Eduardo E Castilla, Mary L Marazita, Figen Seymen, Marcelo C Costa, José M Granjeiro, Paula C Trevilatto, Alexandre R Vieira
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e45022 (2012)
There is evidence for a genetic component in caries susceptibility, and studies in humans have suggested that variation in enamel formation genes may contribute to caries. For the present study, we used DNA samples collected from 1,831 individuals fr
Externí odkaz:
https://doaj.org/article/efa7b4edc0da4918b87bf70c99598838
Autor:
Mary L. Marazita, Italo M. Faraco, Clarissa Christina Avelar Fernandez, Maria Arnaudo, Iêda M. Orioli, Eduardo E. Castilla, Flávia Martinez de Carvalho, Alexandre R. Vieira, Juan C. Mereb, Marcelo de Castro Costa, Fernando E. Poletta, Christiane Vasconcellos Cruz Alves Pereira, Ronir Raggio Luiz
Publikováno v:
Archives of Oral Biology. 88:19-23
The identification of clinical patterns of tooth agenesis in individuals born with craniofacial deformities may be a useful tool for risk determination of these defects. We hypothesize that specific craniofacial deformities are associated with third
Autor:
Aditi Jindal, Michelle McMeans, Somnya Narayanan, Erin K. Rose, Shilpa Jain, Mary L. Marazita, Renato Menezes, Ariadne Letra, Flavia M. Carvalho, Carla A. Brandon, Judith M. Resick, Juan C. Mereb, Fernando A. Poletta, Jorge S. Lopez-Camelo, Eduardo E. Castilla, Iêda M. Orioli, Alexandre R. Vieira
Publikováno v:
International Journal of Dentistry, Vol 2011 (2011)
The identification of individuals at a higher risk of developing caries is of great interest. Isolated forms of cleft lip and palate are among the most common craniofacial congenital anomalies in humans. Historically, several reports suggest that ind
Externí odkaz:
https://doaj.org/article/5e018c7df30248a6bbf5bf15decbca67
Autor:
Fernando A. Poletta, Sidney Emanuel Batista dos Santos, Camilla Dutra Vieira-Machado, Alexandre R. Vieira, Luiz Carlos Santana da Silva, Juan C. Mereb, Iêda M. Orioli, Eduardo E. Castilla, Cláudia Maria da Rocha Martins, Flávia Martinez de Carvalho
Publikováno v:
European Journal of Oral Sciences. 124:406-411
Increased susceptibility to cleft lip, with or without cleft palate (CL±P) has been observed in South America, as related to Amerindian ancestry, using epidemiological data, uniparental markers, and blood groups. In this study, it was evaluated whet
Autor:
Eduardo E. Castilla, Takehiko Shimizu, José Mauro Granjeiro, Juan C. Mereb, Alexandre R. Vieira, Ariadne Letra, Renato Menezes Silva, Fernando A. Poletta, Iêda M. Orioli
Publikováno v:
The Journal of craniofacial surgery. 29(2)
The 19q13 locus has been linked to cleft lip and palate by our group and independently by others. Here we fine mapped the region in an attempt to identify an etiological variant that can explain cleft lip and palate occurrence. A total of 2739 indivi
Autor:
Erika Calvano Küchler, M. Yildirim, José Mauro Granjeiro, Margaret E. Cooper, João Armando Brancher, Jessica Briseño-Ruiz, E. E. Castilla, Iêda M. Orioli, Mary L. Marazita, Italo M. Faraco, Juan C. Mereb, Giovana Daniela Pecharki, Figen Seymen, Patricia Nivoloni Tannure, Alexandre R. Vieira, Asli Patir, Paula Cristina Trevilatto, Takehiko Shimizu, T.C.S. Vieira, Andrea Lips, Marcelo de Castro Costa, Carla A. Brandon, Fernando A. Poletta, Judith M. Resick, Kathleen Deeley
Publikováno v:
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Caries is a multifactorial disease and little is still known about the host genetic factors influencing susceptibility. Our previous genome-wide linkage scan has identified the interval 5q12.1–5q13.3 as linked to low caries susceptibility in Filipi
Autor:
Carmen J. Buxó, Katherine Neiswanger, Ana Maria Lopez-Palacio, Lian Ma, Mauricio Arcos-Burgos, Luz Consuelo Valencia-Ramirez, Seth M. Weinberg, Jacqueline T. Hecht, Dora Rivera Valencia, Eva Maria Cutiongco-de la Paz, Eduardo E. Castilla, Robert A. Cornell, Toby Goldstein McHenry, Babatunde S. Aregbesola, Mary L. Marazita, Elizabeth J. Leslie, Flávia Martinez de Carvalho, Lina M. Moreno, Andrew E. Czeizel, Mekonen Eshete, Cecelia A. Laurie, John R. Shaffer, Carmencita Padilla, Rolv T. Lie, Carla A. Sanchez, Ramat Oyebunmi Braimah, Jennifer Standley, Peter A. Mossey, Susan H. Blanton, Iêda M. Orioli, Kaare Christensen, Olutayo James, Frederic W.-B. Deleyiannis, Javier Enríquez de Salamanca, Alexandre R. Vieira, Wasiu Lanre Adeyemo, Huan Liu, Allen J. Wilcox, Jenna C. Carlson, George L. Wehby, Paul A. Romitti, Ronald G. Munger, Fernando A. Poletta, L. Leigh Field, Judith M. Resick, Cathy C. Laurie, Figen Seymen, Mine Koruyucu, Azeez Butali, Andrew C. Lidral, Kimberly F. Doheny, Milliard Deribew, Deepti Jain, Eleanor Feingold, Juan C. Mereb, Jeffrey C. Murray, Beth Emanuele, Jennifer Jacobs
Publikováno v:
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Leslie, E J, Liu, H, Carlson, J C, Shaffer, J R, Feingold, E, Wehby, G, Laurie, C A, Jain, D, Laurie, C C, Doheny, K F, McHenry, T, Resick, J, Sanchez, C, Jacobs, J, Emanuele, B, Vieira, A R, Neiswanger, K, Standley, J, Czeizel, A E, Deleyiannis, F, Christensen, K, Munger, R G, Lie, R T, Wilcox, A, Romitti, P A, Field, L L, Padilla, C D, Cutiongco-de la Paz, E M C, Lidral, A C, Valencia-Ramirez, L C, Lopez-Palacio, A M, Valencia, D R, Arcos-Burgos, M, Castilla, E E, Mereb, J C, Poletta, F A, Orioli, I M, Carvalho, F M, Hecht, J T, Blanton, S H, Buxó, C J, Butali, A, Mossey, P A, Adeyemo, W L, James, O, Braimah, R O, Aregbesola, B S, Eshete, M A, Deribew, M, Koruyucu, M, Seymen, F, Ma, L, de Salamanca, J E, Weinberg, S M, Moreno, L, Cornell, R A, Murray, J C & Marazita, M L 2016, ' A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3 ', American Journal of Human Genetics, vol. 98, no. 4, pp. 744-754 . https://doi.org/10.1016/j.ajhg.2016.02.014
Consejería de Sanidad de la Comunidad de Madrid
Leslie, E J, Liu, H, Carlson, J C, Shaffer, J R, Feingold, E, Wehby, G, Laurie, C A, Jain, D, Laurie, C C, Doheny, K F, McHenry, T, Resick, J, Sanchez, C, Jacobs, J, Emanuele, B, Vieira, A R, Neiswanger, K, Standley, J, Czeizel, A E, Deleyiannis, F, Christensen, K, Munger, R G, Lie, R T, Wilcox, A, Romitti, P A, Field, L L, Padilla, C D, Cutiongco-de la Paz, E M C, Lidral, A C, Valencia-Ramirez, L C, Lopez-Palacio, A M, Valencia, D R, Arcos-Burgos, M, Castilla, E E, Mereb, J C, Poletta, F A, Orioli, I M, Carvalho, F M, Hecht, J T, Blanton, S H, Buxó, C J, Butali, A, Mossey, P A, Adeyemo, W L, James, O, Braimah, R O, Aregbesola, B S, Eshete, M A, Deribew, M, Koruyucu, M, Seymen, F, Ma, L, de Salamanca, J E, Weinberg, S M, Moreno, L, Cornell, R A, Murray, J C & Marazita, M L 2016, ' A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3 ', American Journal of Human Genetics, vol. 98, no. 4, pp. 744-754 . https://doi.org/10.1016/j.ajhg.2016.02.014
Cleft palate (CP) is a common birth defect occurring in 1 in 2,500 live births. Approximately half of infants with CP have a syndromic form, exhibiting other physical and cognitive disabilities. The other half have nonsyndromic CP, and to date, few g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7467c71ba3adfcf20201b467fc5062b
https://hdl.handle.net/20.500.12530/27047
https://hdl.handle.net/20.500.12530/27047
Autor:
Renato Menezes, Ariadne Letra, Robert J. Weyant, Eduardo E. Castilla, Daniel W. McNeil, Louise P. Schulhof, Steven Wendell, Carla A. Brandon, Alexandre R. Vieira, Fernando A. Poletta, Judith M. Resick, Rebecca S. DeSensi, Kathleen Deeley, Asli Patir, M. Yildirim, Jacqueline Noel, Adriana Modesto, Ida Anjomshoaa, Christopher Rozhon, Jorge S. Lopez-Camelo, Iêda M. Orioli, Juan C. Mereb, Mary L. Marazita, Wendy M. Carricato, Nicholas Callahan, Richard J. Crout, Pooja Gandhi, Figen Seymen
Publikováno v:
ISRN Dentistry
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Caries is a multifactorial disease, and studies aiming to unravel the factors modulating its etiology must consider all known predisposing factors. One major factor is bacterial colonization, and Streptococcus mutans is the main microorganism associa
Autor:
Iêda M. Orioli, Eduardo E. Castilla, Joaquín Dopazo, Miguel A. M. Moreira, Héctor N. Seuánez, Renata F. Fonseca, Flávia M. de Carvalho, Alexandre R. Vieira, Juan C. Mereb, Fernando A. Poletta, David Montaner
Publikováno v:
EUROPEAN JOURNAL OF ORAL SCIENCES
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
r-CIPF. Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
instname
r-CIPF: Repositorio Institucional Producción Científica del Centro de Investigación Principe Felipe (CIPF)
Centro de Investigación Principe Felipe (CIPF)
The etiology of cleft lip with or without cleft palate (CL±P) is complex and heterogeneous, and multiple genetic and environmental factors are involved. Some candidate genes reported to be associated with oral clefts are located on the X chromosome.