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Eva Maria Cutiongco de la Paz

Showing results (1-10 of 23) with videos related to

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Molecular Genetics & Genomic Medicine|September 22, 2016
Genetics and genomic medicine in the PhilippinesCarmencita D Padilla, Eva Maria Cutiongco-de la Paz
Oncology Letters|July 11, 2019
Phenotypic characterization of the novel, non-hotspot oncogenic KRAS mutants E31D and E63KArlou Kristina J Angeles, Ryan Timothy D Yu, Eva Maria Cutiongco-De La Paz, et al.
Cells|December 24, 2021
The Novel Phosphatase Domain Mutations Q171R and Y65S Switch PTEN from Tumor Suppressor to OncogeneJose Antonio Ma G Garrido, Krizelle Mae M Alcantara, Joshua Miguel C Danac, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 1, 2019
Training in clinical genetics and genetic counseling in AsiaEva Maria Cutiongco-de la Paz, Brian Hon-Yin Chung, Sultana M H Faradz, et al.
Cells|December 11, 2019
Non-Redundant and Overlapping Oncogenic Readouts of Non-Canonical and Novel Colorectal Cancer KRAS and NRAS MutantsKrizelle Mae M Alcantara, Joshua Reginald P Malapit, Ryan Timothy D Yu, et al.
Journal of Community Genetics|June 28, 2018
Genetic counseling in an indigenous Filipino community with a high prevalence of A2ML1-related otitis mediaEva Maria Cutiongco-de la Paz, Melquiadesa Pedro, Talitha Karisse L Yarza, et al.
Journal of Genetic Counseling|September 20, 2013
Genetic counseling/consultation in South-East Asia: a report from the workshop at the 10th Asia pacific conference on human geneticsOlga Zayts, Srikant Sarangi, Meow-Keong Thong, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 17, 2018
The SLC26A4 c.706C>G (p.Leu236Val) Variant is a Frequent Cause of Hearing Impairment in Filipino Cochlear ImplanteesCharlotte M Chiong, Ma Rina T Reyes-Quintos, Talitha Karisse L Yarza, et al.
Human Molecular Genetics|November 7, 2019
Methylation changes in the peripheral blood of Filipinos with type 2 diabetes suggest spurious transcription initiation at TXNIPDominic S Albao, Eva Maria Cutiongco-de la Paz, Maria Elizabeth Mercado, et al.
Genes|April 30, 2021
Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone AnomaliesRegie Lyn P Santos-Cortez, Talitha Karisse L Yarza, Tori C Bootpetch, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
Molecular Genetics & Genomic Medicine|September 22, 2016
Genetics and genomic medicine in the PhilippinesCarmencita D Padilla, Eva Maria Cutiongco-de la Paz
Oncology Letters|July 11, 2019
Phenotypic characterization of the novel, non-hotspot oncogenic KRAS mutants E31D and E63KArlou Kristina J Angeles, Ryan Timothy D Yu, Eva Maria Cutiongco-De La Paz, et al.
Cells|December 24, 2021
The Novel Phosphatase Domain Mutations Q171R and Y65S Switch PTEN from Tumor Suppressor to OncogeneJose Antonio Ma G Garrido, Krizelle Mae M Alcantara, Joshua Miguel C Danac, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|May 1, 2019
Training in clinical genetics and genetic counseling in AsiaEva Maria Cutiongco-de la Paz, Brian Hon-Yin Chung, Sultana M H Faradz, et al.
Cells|December 11, 2019
Non-Redundant and Overlapping Oncogenic Readouts of Non-Canonical and Novel Colorectal Cancer KRAS and NRAS MutantsKrizelle Mae M Alcantara, Joshua Reginald P Malapit, Ryan Timothy D Yu, et al.
Journal of Community Genetics|June 28, 2018
Genetic counseling in an indigenous Filipino community with a high prevalence of A2ML1-related otitis mediaEva Maria Cutiongco-de la Paz, Melquiadesa Pedro, Talitha Karisse L Yarza, et al.
Journal of Genetic Counseling|September 20, 2013
Genetic counseling/consultation in South-East Asia: a report from the workshop at the 10th Asia pacific conference on human geneticsOlga Zayts, Srikant Sarangi, Meow-Keong Thong, et al.
Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|August 17, 2018
The SLC26A4 c.706C>G (p.Leu236Val) Variant is a Frequent Cause of Hearing Impairment in Filipino Cochlear ImplanteesCharlotte M Chiong, Ma Rina T Reyes-Quintos, Talitha Karisse L Yarza, et al.
Human Molecular Genetics|November 7, 2019
Methylation changes in the peripheral blood of Filipinos with type 2 diabetes suggest spurious transcription initiation at TXNIPDominic S Albao, Eva Maria Cutiongco-de la Paz, Maria Elizabeth Mercado, et al.
Genes|April 30, 2021
Identification of Novel Candidate Genes and Variants for Hearing Loss and Temporal Bone AnomaliesRegie Lyn P Santos-Cortez, Talitha Karisse L Yarza, Tori C Bootpetch, et al.
Pageof 3