Resultados da busca - Cutiongco-de la Paz, Eva Maria
- Mostrando 1 - 19 resultados de 19
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The Novel Phosphatase Domain Mutations Q171R and Y65S Switch PTEN from Tumor Suppressor to Oncogene por Garrido, Jose Antonio Ma. G., Alcantara, Krizelle Mae M., Danac, Joshua Miguel C., Serrano, Fidel Emmanuel C., Cutiongco-de la Paz, Eva Maria, Garcia, Reynaldo L.
Publicado em 2021Texto -
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Non-Redundant and Overlapping Oncogenic Readouts of Non-Canonical and Novel Colorectal Cancer KRAS and NRAS Mutants por Alcantara, Krizelle Mae M., Malapit, Joshua Reginald P., Yu, Ryan Timothy D., Garrido, Jose Antonio Ma. G., Rigor, John Paul T., Angeles, Arlou Kristina J., Cutiongco-de la Paz, Eva Maria, Garcia, Reynaldo L.
Publicado em 2019Texto -
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The SLC26A4 c.706C>G (p.Leu236Val) variant is a frequent cause of hearing impairment in Filipino cochlear implantees por Chiong, Charlotte M., Reyes-Quintos, Ma. Rina T., Yarza, Talitha Karisse L., Tobias-Grasso, Celina Ann M., Acharya, Anushree, Leal, Suzanne M., Mohlke, Karen L., Mayol, Nanette L., Cutiongco-de la Paz, Eva Maria, Santos-Cortez, Regie Lyn P.
Publicado em 2018Texto -
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Exome sequencing reveals novel variants and unique allelic spectrum for hearing impairment in Filipino cochlear implantees por Truong, Brittany T., Yarza, Talitha Karisse L., Roberts, Tori Bootpetch, Roberts, Susannah, Xu, Jonathan, Steritz, Matthew J., Tobias-Grasso, Celina Ann M., Azamian, Mahshid, Lalani, Seema R., Mohlke, Karen L., Lee, Nanette R., Cutiongco-de la Paz, Eva Maria, Reyes-Quintos, Maria Rina T., Santos-Cortez, Regie Lyn P., Chiong, Charlotte M.
Publicado em 2019Texto -
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Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone Anomalies por Santos-Cortez, Regie Lyn P., Yarza, Talitha Karisse L., Bootpetch, Tori C., Tantoco, Ma. Leah C., Mohlke, Karen L., Cruz, Teresa Luisa G., Chiong Perez, Mary Ellen, Chan, Abner L., Lee, Nanette R., Tobias-Grasso, Celina Ann M., Reyes-Quintos, Maria Rina T., Cutiongco-de la Paz, Eva Maria, Chiong, Charlotte M.
Publicado em 2021Texto -
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Genetic and Environmental Determinants of Otitis Media in an Indigenous Filipino Population por Santos-Cortez, Regie Lyn P., Reyes-Quintos, Ma. Rina T., Tantoco, Ma. Leah C., Abbe, Izoduwa, Llanes, Erasmo Gonzalo d.V., Ajami, Nadim J., Hutchinson, Diane S., Petrosino, Joseph F., Padilla, Carmencita D., Villarta, Romeo L., Gloria-Cruz, Teresa Luisa, Chan, Abner L., Cutiongco-de la Paz, Eva Maria, Chiong, Charlotte M., Leal, Suzanne M., Abes, Generoso T.
Publicado em 2016Texto -
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Middle ear microbiome differences in indigenous Filipinos with chronic otitis media due to a duplication in the A2ML1 gene por Santos-Cortez, Regie Lyn P., Hutchinson, Diane S., Ajami, Nadim J., Reyes-Quintos, Ma. Rina T., Tantoco, Ma. Leah C., Labra, Patrick John, Lagrana, Sheryl Mae, Pedro, Melquiadesa, Llanes, Erasmo Gonzalo d. V., Gloria-Cruz, Teresa Luisa, Chan, Abner L., Cutiongco-de la Paz, Eva Maria, Belmont, John W., Chonmaitree, Tasnee, Abes, Generoso T., Petrosino, Joseph F., Leal, Suzanne M., Chiong, Charlotte M.
Publicado em 2016Texto -
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The rs1458038 variant near FGF5 is associated with poor response to calcium channel blockers among Filipinos por Punzalan, Felix Eduardo R., Cutiongco – de la Paz, Eva Maria C., Nevado, Jose Jr. B., Magno, Jose Donato A., Ona, Deborah Ignacia D., Aman, Aimee Yvonne Criselle L., Tiongson, Marc Denver A., Llanes, Elmer Jasper B., Reganit, Paul Ferdinand M., Tiongco, Richard Henry P., Santos, Lourdes Ella G., Aherrera, Jaime Alfonso M., Abrahan, Lauro L., Agustin, Charlene F., Bejarin, Adrian John P., Sy, Rody G.
Publicado em 2022Texto -
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Rare A2ML1 variants confer susceptibility to otitis media por Santos-Cortez, Regie Lyn P., Chiong, Charlotte M., Reyes-Quintos, Ma. Rina T., Tantoco, Ma. Leah C., Wang, Xin, Acharya, Anushree, Abbe, Izoduwa, Giese, Arnaud P., Smith, Joshua D., Allen, E. Kaitlynn, Li, Biao, Cutiongco-de la Paz, Eva Maria, Garcia, Marieflor Cristy, Llanes, Erasmo Gonzalo D.V., Labra, Patrick John, Gloria-Cruz, Teresa Luisa I., Chan, Abner L., Wang, Gao T., Daly, Kathleen A., Shendure, Jay, Bamshad, Michael J., Nickerson, Deborah A., Patel, Janak A., Riazuddin, Saima, Sale, Michele M., Chonmaitree, Tasnee, Ahmed, Zubair M., Abes, Generoso T., Leal, Suzanne M.
Publicado em 2015Texto -
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Variants of SLC2A10 may be Linked to Poor Response to Metformin por Paz-Pacheco, Elizabeth, Nevado, Jose B, Cutiongco-de la Paz, Eva Maria C, Jasul, Gabriel V, Aman, Aimee Yvonne Criselle L, Ribaya, Elizabeth Laurize A, Francisco, Mark David G, Guanzon, Ma Luz Vicenta V, Uyking-Naranjo, May L, Añonuevo-Cruz, Ma Cecille S, Maningat, Maria Patricia Deanna D, Jaring, Cristina V, Nacpil-Dominguez, Paulette D, Pala-Mohamad, Aniza B, Canto, Abigail U, Quisumbing, John Paul M, Lat, Annabelle Marie M, Bernardo, Diane Carla C, Mansibang, Noemie Marie M, Calpito, Karell Jo Angelique C, Ribaya, Vincent Sean D, Ferrer, Julius Patrick Y, Biwang, Jessica H, Melegrito, Jodelyn B, Deguit, Christian Deo T, Panerio, Carlos Emmanuel G
Publicado em 2022Texto -
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Detection and Genome Sequencing of SARS-CoV-2 Variants Belonging to the B.1.1.7 Lineage in the Philippines por Tablizo, Francis A., Saloma, Cynthia P., Castro, Marc Jerrone R., Kim, Kenneth M., Yangzon, Maria Sofia L., Lapid, Carlo M., Maralit, Benedict A., Ayes, Marc Edsel C., Yap, Jan Michael C., Llames, Jo-Hannah S., Araiza, Shiela Mae M., Punayan, Kris P., Asin, Irish Coleen A., Tambaoan, Candice Francheska B., Chong, Asia Louisa U., Padilla, Karol Sophia Agape R., Cruz, Rianna Patricia S., Morado, El King D., Dizon, Joshua Gregor A., Cutiongco-de la Paz, Eva Maria, de Guzman, Alethea R., Hao, Razel Nikka M., Zamora, Arianne A., Pacial, Devon Ray, Magalang, Juan Antonio R., Alejandria, Marissa, Carlos, Celia, Ong-Lim, Anna, Salvaña, Edsel Maurice, Wong, John Q., Montoya, Jaime C., Singh-Vergeire, Maria Rosario
Publicado em 2021Texto -
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OTITIS MEDIA SUSCEPTIBILITY AND SHIFTS IN THE HEAD AND NECK MICROBIOME DUE TO SPINK5 VARIANTS por Frank, Daniel N., Giese, Arnaud P.J., Hafrén, Lena, Bootpetch, Tori C., Yarza, Talitha Karisse L., Steritz, Matthew J., Pedro, Melquiadesa, Labra, Patrick John, Daly, Kathleen A., Tantoco, Ma. Leah C., Szeremeta, Wasyl, Reyes-Quintos, Maria Rina T., Ahankoob, Niaz, Llanes, Erasmo Gonzalo d.V., Pine, Harold S., Yousaf, Sairah, Ir, Diana, Einarsdottir, Elisabet, de la Cruz, Rhodieleen Anne R., Lee, Nanette R., Nonato, Rachelle Marie A., Robertson, Charles E., Ong, Kimberly Mae C., Magno, Jose Pedrito M., Chiong, Alessandra Nadine E., Espiritu-Chiong, Ma. Carmina, Agustin, Ma. Luz San, Cruz, Teresa Luisa G., Abes, Generoso T., Bamshad, Michael J., Cutiongco-de la Paz, Eva Maria, Kere, Juha, Nickerson, Deborah A., Mohlke, Karen L., Riazuddin, Saima, Chan, Abner L., Mattila, Petri S., Leal, Suzanne M., Ryan, Allen F., Ahmed, Zubair M., Chonmaitree, Tasnee, Sale, Michele M., Chiong, Charlotte M., Santos-Cortez, Regie Lyn P.
Publicado em 2020Texto -
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A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13 por Leslie, Elizabeth J., Carlson, Jenna C., Shaffer, John R., Feingold, Eleanor, Wehby, George, Laurie, Cecelia A., Jain, Deepti, Laurie, Cathy C., Doheny, Kimberly F., McHenry, Toby, Resick, Judith, Sanchez, Carla, Jacobs, Jennifer, Emanuele, Beth, Vieira, Alexandre R., Neiswanger, Katherine, Lidral, Andrew C., Valencia-Ramirez, Luz Consuelo, Lopez-Palacio, Ana Maria, Valencia, Dora Rivera, Arcos-Burgos, Mauricio, Czeizel, Andrew E., Field, L. Leigh, Padilla, Carmencita D., Cutiongco-de la Paz, Eva Maria, C., Deleyiannis, Frederic, Christensen, Kaare, Munger, Ronald G., Lie, Rolv T., Wilcox, Allen, Romitti, Paul A., Castilla, Eduardo E., Mereb, Juan C., Poletta, Fernando A., Orioli, Iêda M., Carvalho, Flavia M., Hecht, Jacqueline T., Blanton, Susan H., Buxó, Carmen J., Butali, Azeez, Mossey, Peter A., Adeyemo, Wasiu L., James, Olutayo, Braimah, Ramat O., Aregbesola, Babatunde S., Eshete, Mekonen A., Abate, Fikre, Koruyucu, Mine, Seymen, Figen, Ma, Lian, de Salamanca, Javier Enríquez, Weinberg, Seth M., Moreno, Lina, Murray, Jeffrey C., Marazita, Mary L.
Publicado em 2016Texto -
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A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3 por Leslie, Elizabeth J., Liu, Huan, Carlson, Jenna C., Shaffer, John R., Feingold, Eleanor, Wehby, George, Laurie, Cecelia A., Jain, Deepti, Laurie, Cathy C., Doheny, Kimberly F., McHenry, Toby, Resick, Judith, Sanchez, Carla, Jacobs, Jennifer, Emanuele, Beth, Vieira, Alexandre R., Neiswanger, Katherine, Standley, Jennifer, Czeizel, Andrew E., Deleyiannis, Frederic, Christensen, Kaare, Munger, Ronald G., Lie, Rolv T., Wilcox, Allen, Romitti, Paul A., Field, L. Leigh, Padilla, Carmencita D., Cutiongco-de la Paz, Eva Maria C., Lidral, Andrew C., Valencia-Ramirez, Luz Consuelo, Lopez-Palacio, Ana Maria, Valencia, Dora Rivera, Arcos-Burgos, Mauricio, Castilla, Eduardo E., Mereb, Juan C., Poletta, Fernando A., Orioli, Iêda M., Carvalho, Flavia M., Hecht, Jacqueline T., Blanton, Susan H., Buxó, Carmen J., Butali, Azeez, Mossey, Peter A., Adeyemo, Wasiu L., James, Olutayo, Braimah, Ramat O., Aregbesola, Babatunde S., Eshete, Mekonen A., Deribew, Milliard, Koruyucu, Mine, Seymen, Figen, Ma, Lian, de Salamanca, Javier Enríquez, Weinberg, Seth M., Moreno, Lina, Cornell, Robert A., Murray, Jeffrey C., Marazita, Mary L.
Publicado em 2016Texto -
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A2ML1 and otitis media: novel variants, differential expression and relevant pathways por Larson, Eric D., Magno, Jose Pedrito M., Steritz, Matthew J., Llanes, Erasmo Gonzalo d.V., Cardwell, Jonathan, Pedro, Melquiadesa, Roberts, Tori Bootpetch, Einarsdottir, Elisabet, Rosanes, Rose Anne Q., Greenlee, Christopher, Santos, Rachel Ann P., Yousaf, Ayesha, Streubel, Sven-Olrik, Santos, Aileen Trinidad R., Ruiz, Amanda G., Lagrana-Villagracia, Sheryl Mae, Ray, Dylan, Yarza, Talitha Karisse L., Scholes, Melissa A., Anderson, Catherine B., Acharya, Anushree, Gubbels, Samuel P., Bamshad, Michael J., Cass, Stephen P., Lee, Nanette R., Shaikh, Rehan S., Nickerson, Deborah A., Mohlke, Karen L., Prager, Jeremy D., Cruz, Teresa Luisa G., Yoon, Patricia J., Abes, Generoso T., Schwartz, David A., Chan, Abner L., Wine, Todd M., Cutiongco-de la Paz, Eva Maria, Friedman, Norman, Kechris, Katerina, Kere, Juha, Leal, Suzanne M., Yang, Ivana V., Patel, Janak A., Tantoco, Ma. Leah C., Riazuddin, Saima, Chan, Kenny H., Mattila, Petri S., Reyes-Quintos, Maria Rina T., Ahmed, Zubair M., Jenkins, Herman A., Chonmaitree, Tasnee, Hafrén, Lena, Chiong, Charlotte M., Santos-Cortez, Regie Lyn P.
Publicado em 2019Texto -
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FUT2 Variants Confer Susceptibility to Familial Otitis Media por Santos-Cortez, Regie Lyn P., Chiong, Charlotte M., Frank, Daniel N., Ryan, Allen F., Giese, Arnaud P.J., Bootpetch Roberts, Tori, Daly, Kathleen A., Steritz, Matthew J., Szeremeta, Wasyl, Pedro, Melquiadesa, Pine, Harold, Yarza, Talitha Karisse L., Scholes, Melissa A., Llanes, Erasmo Gonzalo d.V., Yousaf, Saira, Friedman, Norman, Tantoco, Ma. Leah C., Wine, Todd M., Labra, Patrick John, Benoit, Jeanne, Ruiz, Amanda G., de la Cruz, Rhodieleen Anne R., Greenlee, Christopher, Yousaf, Ayesha, Cardwell, Jonathan, Nonato, Rachelle Marie A., Ray, Dylan, Ong, Kimberly Mae C., So, Edward, Robertson, Charles E., Dinwiddie, Jordyn, Lagrana-Villagracia, Sheryl Mae, Gubbels, Samuel P., Shaikh, Rehan S., Cass, Stephen P., Einarsdottir, Elisabet, Lee, Nanette R., Schwartz, David A., Gloria-Cruz, Teresa Luisa I., Bamshad, Michael J., Yang, Ivana V., Kere, Juha, Abes, Generoso T., Prager, Jeremy D., Riazuddin, Saima, Chan, Abner L., Yoon, Patricia J., Nickerson, Deborah A., Cutiongco-de la Paz, Eva Maria, Streubel, Sven-Olrik, Reyes-Quintos, Maria Rina T., Jenkins, Herman A., Mattila, Petri, Chan, Kenny H., Mohlke, Karen L., Leal, Suzanne M., Hafrén, Lena, Chonmaitree, Tasnee, Sale, Michele M., Ahmed, Zubair M.
Publicado em 2018Texto