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Yangjin Bae

Showing results (21-30 of 26) with videos related to

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American Journal of Human Genetics|April 30, 2013
Yunis-Varón syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatasePhilippe M Campeau, Guy M Lenk, James T Lu, et al.
Cancer Cell|December 13, 2017
Therapeutic Antibody Targeting Tumor- and Osteoblastic Niche-Derived Jagged1 Sensitizes Bone Metastasis to ChemotherapyHanqiu Zheng, Yangjin Bae, Sabine Kasimir-Bauer, et al.
The Journal of Clinical Investigation|March 7, 2017
Loss of DDRGK1 modulates SOX9 ubiquitination in spondyloepimetaphyseal dysplasiaAdetutu T Egunsola, Yangjin Bae, Ming-Ming Jiang, et al.
The Journal of Clinical Investigation|January 2, 2025
ATRX silences Cartpt expression in osteoblastic cells during skeletal developmentYi-Ting Chen, Ming-Ming Jiang, Carolina Leynes, et al.
Human Mutation|June 27, 2017
Heterozygous variants in ACTL6A, encoding a component of the BAF complex, are associated with intellectual disabilityRonit Marom, Mahim Jain, Lindsay C Burrage, et al.
Science Translational Medicine|May 22, 2020
<i>ATRAID</i> regulates the action of nitrogen-containing bisphosphonates on boneLauren E Surface, Damon T Burrow, Jinmei Li, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
American Journal of Human Genetics|April 30, 2013
Yunis-Varón syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatasePhilippe M Campeau, Guy M Lenk, James T Lu, et al.
Cancer Cell|December 13, 2017
Therapeutic Antibody Targeting Tumor- and Osteoblastic Niche-Derived Jagged1 Sensitizes Bone Metastasis to ChemotherapyHanqiu Zheng, Yangjin Bae, Sabine Kasimir-Bauer, et al.
The Journal of Clinical Investigation|March 7, 2017
Loss of DDRGK1 modulates SOX9 ubiquitination in spondyloepimetaphyseal dysplasiaAdetutu T Egunsola, Yangjin Bae, Ming-Ming Jiang, et al.
The Journal of Clinical Investigation|January 2, 2025
ATRX silences Cartpt expression in osteoblastic cells during skeletal developmentYi-Ting Chen, Ming-Ming Jiang, Carolina Leynes, et al.
Human Mutation|June 27, 2017
Heterozygous variants in ACTL6A, encoding a component of the BAF complex, are associated with intellectual disabilityRonit Marom, Mahim Jain, Lindsay C Burrage, et al.
Science Translational Medicine|May 22, 2020
<i>ATRAID</i> regulates the action of nitrogen-containing bisphosphonates on boneLauren E Surface, Damon T Burrow, Jinmei Li, et al.
Pageof 3