Yangjin Bae

发表

Notch Signaling in Skeletal Stem Cells

Brendan H. Lee, Shan Chen, Yangjin Bae, 2013, Calcified Tissue International.

Notch Signaling in Skeletal Development, Homeostasis and Pathogenesis

Brendan H. Lee, J. Zieba, Yangjin Bae, 2020, Biomolecules.

Intra-iliac Artery Injection for Efficient and Selective Modeling of Microscopic Bone Metastasis.

X. Zhang, Brendan H. Lee, Yangjin Bae, 2016, Journal of visualized experiments : JoVE.

Losartan increases bone mass and accelerates chondrocyte hypertrophy in developing skeleton.

B. Dawson, Brendan H. Lee, Yuqing Chen, 2015, Molecular genetics and metabolism.

Loss of DDRGK1 modulates SOX9 ubiquitination in spondyloepimetaphyseal dysplasia

R. Gibbs, Philippe M. Campeau, James T. Lu, 2017, The Journal of clinical investigation.

E-selectin ligand 1 regulates bone remodeling by limiting bioactive TGF-β in the bone microenvironment

C. Ambrose, Brendan H. Lee, Yuqing Chen, 2013, Proceedings of the National Academy of Sciences.

SHP Repression of Bile Acid Biosynthesis by Remodeling Complex in the Feedback Role of an mSin 3 A-Swi / Snf Chromatin

Ji Miao, J. Kemper, Hwajin Kim, 2004 .

Repression of CAR-mediated transactivation of CYP2B genes by the orphan nuclear receptor, short heterodimer partner (SHP).

J. Kemper, B. Kemper, Yangjin Bae, 2004, DNA and cell biology.

miRNA‐34c Suppresses Osteosarcoma Progression In Vivo by Targeting Notch and E2F

S. Ketkar, Brendan H. Lee, F. Gannon, 2022, JBMR plus.

Notch gain of function inhibits chondrocyte differentiation via Rbpj-dependent suppression of Sox9

Jianning Tao, Brendan H. Lee, Yuqing Chen, 2013, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Yunis-Varón syndrome is caused by mutations in FIG4, encoding a phosphoinositide phosphatase.

A. V. Vulto-van Silfhout, E. Haan, R. Gibbs, 2013, American journal of human genetics.

Notch Signaling in Skeletal Stem Cells

Brendan H. Lee, Shan Chen, Yangjin Bae, 2013, Calcified Tissue International.

Therapeutic Antibody Targeting Tumor- and Osteoblastic Niche-Derived Jagged1 Sensitizes Bone Metastasis to Chemotherapy.

Yibin Kang, K. Pantel, A. Coxon, 2017, Cancer cell.

ATRAID regulates the action of nitrogen-containing bisphosphonates on bone

Jonathan C. Baker, M. Gardner, D. Sabatini, 2020, Science Translational Medicine.

Heterozygous variants in ACTL6A, encoding a component of the BAF complex, are associated with intellectual disability

Alyssa A. Tran, J. Rosenfeld, B. D. de Vries, 2017, Human mutation.

miRNA-34c regulates Notch signaling during bone development.

B. Dawson, Jianning Tao, Philippe M. Campeau, 2012, Human molecular genetics.

The transcriptional repressor JHDM3A demethylates trimethyl histone H3 lysine 9 and lysine 36

Paul Tempst, Yi Zhang, Hediye Erdjument-Bromage, 2006, Nature.

85. Osteogenic Osteosarcoma

Jianning Tao, Yangjin Bae, Brendan H. Lee, 2013 .

Inhibitory Cross-talk between Estrogen Receptor (ER) and Constitutively Activated Androstane Receptor (CAR)

J. Kemper, L. N. Petz, Hwajin Kim, 2002, The Journal of Biological Chemistry.

Functional Inhibitory Cross-talk between Constitutive Androstane Receptor and Hepatic Nuclear Factor-4 in Hepatic Lipid/Glucose Metabolism Is Mediated by Competition for Binding to the DR1 Motif and to the Common Coactivators, GRIP-1 and PGC-1α*

Ji Miao, J. Kemper, Yangjin Bae, 2006, Journal of Biological Chemistry.

RECQL4 Regulates p53 Function In Vivo During Skeletogenesis

B. Dawson, Jianning Tao, Brendan H. Lee, 2015, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

MicroRNA miR-23a cluster promotes osteocyte differentiation by regulating TGF-β signalling in osteoblasts

Rui Chen, Philippe M Campeau, B. Dawson, 2017, Nature Communications.

RUNX2 and Cleidocranial Dysplasia

L. Burrage, Yangjin Bae, D. Napierala, 2016 .

Analysis of multiple nuclear receptor binding sites for CAR/RXR in the phenobarbital responsive unit of CYP2B2.

J. Kemper, B. Kemper, Yangjin Bae, 2006, Archives of biochemistry and biophysics.

Whole-exome sequencing identifies mutations in the nucleoside transporter gene SLC29A3 in dysosteosclerosis, a form of osteopetrosis.

R. Gibbs, Philippe M. Campeau, James T. Lu, 2012, Human molecular genetics.

ATRAID, a genetic factor that regulates the clinical action of nitrogen-containing bisphosphonates on bone

Jonathan C. Baker, M. Gardner, D. Sabatini, 2018, bioRxiv.

miRNA‐34c Suppresses Osteosarcoma Progression In Vivo by Targeting Notch and E2F

S. Ketkar, Brendan H. Lee, F. Gannon, 2021, bioRxiv.