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Oncotarget
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May 7, 2016
Identification of a novel partner gene, KIAA1217, fused to RET: Functional characterization and inhibitor sensitivity of two isoforms in lung adenocarcinoma
Mi-Sook Lee, Ryong Nam Kim, Hoseok I, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer
|
May 16, 2017
MET Exon 14 Skipping Mutations in Lung Adenocarcinoma: Clinicopathologic Implications and Prognostic Values
Geun Dong Lee, Seung Eun Lee, Doo-Yi Oh, et al.
Human Mutation
|
January 17, 2020
POLD1 variants leading to reduced polymerase activity can cause hearing loss without syndromic features
Doo-Yi Oh, Yoshihiro Matsumoto, Shin-Ichiro Kitajiri, et al.
Journal of Medical Genetics
|
September 2, 2019
Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of human <i>DIAPH1</i>-related cytoskeletopathy
Bong Jik Kim, Takehiko Ueyama, Takushi Miyoshi, et al.
Cancer Research and Treatment
|
January 6, 2017
Patient-Derived Xenograft Models of Epithelial Ovarian Cancer for Preclinical Studies
Eun Jin Heo, Young Jae Cho, William Chi Cho, et al.
Scientific Reports
|
November 30, 2017
ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathy
Kyu-Hee Han, Doo-Yi Oh, Seungmin Lee, et al.
The Journal of Pathology
|
July 26, 2017
Molecular breakdown: a comprehensive view of anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer
Ka-Won Noh, Mi-Sook Lee, Seung Eun Lee, et al.
Eukaryotic Cell
|
January 8, 2008
Requirement for the budding yeast polo kinase Cdc5 in proper microtubule growth and dynamics
Chong J Park, Jung-Eun Park, Tatiana S Karpova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 24, 2020
Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approach
Bong Jik Kim, Doo-Yi Oh, Jin Hee Han, et al.
Experimental & Molecular Medicine
|
July 28, 2021
Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss
Sang-Yeon Lee, Hyun Been Choi, Mina Park, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 51) with videos related to
Sort By:
Page
of 6
Oncotarget
|
May 7, 2016
Identification of a novel partner gene, KIAA1217, fused to RET: Functional characterization and inhibitor sensitivity of two isoforms in lung adenocarcinoma
Mi-Sook Lee, Ryong Nam Kim, Hoseok I, et al.
Journal of Thoracic Oncology : Official Publication of the International Association for the Study of Lung Cancer
|
May 16, 2017
MET Exon 14 Skipping Mutations in Lung Adenocarcinoma: Clinicopathologic Implications and Prognostic Values
Geun Dong Lee, Seung Eun Lee, Doo-Yi Oh, et al.
Human Mutation
|
January 17, 2020
POLD1 variants leading to reduced polymerase activity can cause hearing loss without syndromic features
Doo-Yi Oh, Yoshihiro Matsumoto, Shin-Ichiro Kitajiri, et al.
Journal of Medical Genetics
|
September 2, 2019
Differential disruption of autoinhibition and defect in assembly of cytoskeleton during cell division decide the fate of human <i>DIAPH1</i>-related cytoskeletopathy
Bong Jik Kim, Takehiko Ueyama, Takushi Miyoshi, et al.
Cancer Research and Treatment
|
January 6, 2017
Patient-Derived Xenograft Models of Epithelial Ovarian Cancer for Preclinical Studies
Eun Jin Heo, Young Jae Cho, William Chi Cho, et al.
Scientific Reports
|
November 30, 2017
ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathy
Kyu-Hee Han, Doo-Yi Oh, Seungmin Lee, et al.
The Journal of Pathology
|
July 26, 2017
Molecular breakdown: a comprehensive view of anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer
Ka-Won Noh, Mi-Sook Lee, Seung Eun Lee, et al.
Eukaryotic Cell
|
January 8, 2008
Requirement for the budding yeast polo kinase Cdc5 in proper microtubule growth and dynamics
Chong J Park, Jung-Eun Park, Tatiana S Karpova, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 24, 2020
Significant Mendelian genetic contribution to pediatric mild-to-moderate hearing loss and its comprehensive diagnostic approach
Bong Jik Kim, Doo-Yi Oh, Jin Hee Han, et al.
Experimental & Molecular Medicine
|
July 28, 2021
Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss
Sang-Yeon Lee, Hyun Been Choi, Mina Park, et al.
Page
of 6