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Doo-Yi Oh

Showing results (31-40 of 51) with videos related to

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Human Mutation|August 26, 2020
Novel genotype-phenotype correlation of functionally characterized LMX1A variants linked to sensorineural hearing lossSang-Yeon Lee, Jin Hee Han, Marge Carandang, et al.
Cancer Research and Treatment|October 20, 2022
Cancer-Specific Sequences in the Diagnosis and Treatment of NUT CarcinomaMi-Sook Lee, Sungbin An, Ji-Young Song, et al.
Journal of Translational Medicine|November 29, 2018
Mutational and phenotypic spectrum of OTOF-related auditory neuropathy in Koreans: eliciting reciprocal interaction between bench and clinicsBong Jik Kim, Jeong Hun Jang, Jin Hee Han, et al.
Oncotarget|October 6, 2015
HER2 as a novel therapeutic target for cervical cancerDoo-Yi Oh, Seokhwi Kim, Yoon-La Choi, et al.
Human Mutation|February 12, 2019
Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafnessBong Jik Kim, Dong-Kyu Kim, Jin Hee Han, et al.
Journal of Medical Genetics|March 23, 2021
Rising of <i>LOXHD1</i> as a signature causative gene of down-sloping hearing loss in people in their teens and 20sBong Jik Kim, Hyoung Won Jeon, Woosung Jeon, et al.
Scientific Reports|October 1, 2021
Powerful use of automated prioritization of candidate variants in genetic hearing loss with extreme etiologic heterogeneitySo Young Kim, Seungmin Lee, Go Hun Seo, et al.
American Journal of Human Genetics|May 7, 2016
Analyzing Somatic Genome Rearrangements in Human Cancers by Using Whole-Exome SequencingLixing Yang, Mi-Sook Lee, Hengyu Lu, et al.
Cancer Research and Treatment|September 25, 2020
TM4SF4 and LRRK2 Are Potential Therapeutic Targets in Lung and Breast Cancers through Outlier AnalysisKyungsoo Jung, Joon-Seok Choi, Beom-Mo Koo, et al.
Scientific Reports|February 9, 2019
Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric populationJae Joon Han, Pham Dinh Nguyen, Doo-Yi Oh, et al.
Pageof 6

Showing results (31-40 of 51) with videos related to

Sort By:
Pageof 6
Human Mutation|August 26, 2020
Novel genotype-phenotype correlation of functionally characterized LMX1A variants linked to sensorineural hearing lossSang-Yeon Lee, Jin Hee Han, Marge Carandang, et al.
Cancer Research and Treatment|October 20, 2022
Cancer-Specific Sequences in the Diagnosis and Treatment of NUT CarcinomaMi-Sook Lee, Sungbin An, Ji-Young Song, et al.
Journal of Translational Medicine|November 29, 2018
Mutational and phenotypic spectrum of OTOF-related auditory neuropathy in Koreans: eliciting reciprocal interaction between bench and clinicsBong Jik Kim, Jeong Hun Jang, Jin Hee Han, et al.
Oncotarget|October 6, 2015
HER2 as a novel therapeutic target for cervical cancerDoo-Yi Oh, Seokhwi Kim, Yoon-La Choi, et al.
Human Mutation|February 12, 2019
Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafnessBong Jik Kim, Dong-Kyu Kim, Jin Hee Han, et al.
Journal of Medical Genetics|March 23, 2021
Rising of <i>LOXHD1</i> as a signature causative gene of down-sloping hearing loss in people in their teens and 20sBong Jik Kim, Hyoung Won Jeon, Woosung Jeon, et al.
Scientific Reports|October 1, 2021
Powerful use of automated prioritization of candidate variants in genetic hearing loss with extreme etiologic heterogeneitySo Young Kim, Seungmin Lee, Go Hun Seo, et al.
American Journal of Human Genetics|May 7, 2016
Analyzing Somatic Genome Rearrangements in Human Cancers by Using Whole-Exome SequencingLixing Yang, Mi-Sook Lee, Hengyu Lu, et al.
Cancer Research and Treatment|September 25, 2020
TM4SF4 and LRRK2 Are Potential Therapeutic Targets in Lung and Breast Cancers through Outlier AnalysisKyungsoo Jung, Joon-Seok Choi, Beom-Mo Koo, et al.
Scientific Reports|February 9, 2019
Elucidation of the unique mutation spectrum of severe hearing loss in a Vietnamese pediatric populationJae Joon Han, Pham Dinh Nguyen, Doo-Yi Oh, et al.
Pageof 6