K. Lim

发表

Core Binding Factor β of Osteoblasts Maintains Cortical Bone Mass via Stabilization of Runx2 in Mice

G. Stein, J. Lian, J. Stein, 2015, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Core Binding Factor β of Osteoblasts Maintains Cortical Bone Mass via Stabilization of Runx2 in Mice

G. Stein, J. Lian, J. Stein, 2015, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

The cleidocranial dysplasia‐related R131G mutation in the Runt‐related transcription factor RUNX2 disrupts binding to DNA but not CBF‐β

G. Stein, J. Lian, A. V. van Wijnen, 2010, Journal of cellular biochemistry.

Physcion‐8‐O‐β‐D‐glucopyranoside enhances the commitment of mouse mesenchymal progenitors into osteoblasts and their differentiation: Possible involvement of signaling pathways to activate BMP gene expression

Sang-Joon Park, K. Lim, Je-Yong Choi, 2010, Journal of cellular biochemistry.

Sclerostin neutralization unleashes the osteoanabolic effects of Dkk1 inhibition.

G. Loots, A. Robling, K. Lim, 2018, JCI insight.

Osteoblast-Specific Overexpression of Human WNT16 Increases Both Cortical and Trabecular Bone Mass and Structure in Mice.

M. Econs, A. Robling, K. Lim, 2016, Endocrinology.

Topically administered Risedronate shows powerful anti-osteoporosis effect in ovariectomized mouse model.

Jong-sang Park, K. Lim, Xiangguo Che, 2012, Bone.

Vascular expression of the chemokine CX3CL1 promotes osteoclast recruitment and exacerbates bone resorption in an irradiated murine model.

K. Lim, Je-Yong Choi, C. Hwang, 2014, Bone.

Functional Cooperation between Vitamin D Receptor and Runx2 in Vitamin D-Induced Vascular Calcification

S. Kato, In-kyu Lee, K. Lim, 2013, PloS one.

Co-deletion of Lrp5 and Lrp6 in the skeleton severely diminishes bone gain from sclerostin antibody administration.

A. Robling, M. Warman, B. Williams, 2020, Bone.

Combination therapy in the Col2a1G610C mouse model of Osteogenesis Imperfecta reveals an additive effect of enhancing LRP5 signaling and inhibiting TGFβ signaling on trabecular bone but not on cortical bone.

A. Robling, M. Warman, K. Lim, 2020, Bone.

Pten deletion in Dmp1‐expressing cells does not rescue the osteopenic effects of Wnt/β‐catenin suppression

A. Robling, H. Yokota, K. Lim, 2020, Journal of cellular physiology.

Adult-Onset Deletion of β-Catenin in (10kb)Dmp1-Expressing Cells Prevents Intermittent PTH-Induced Bone Gain.

A. Robling, J. Hong, K. Lim, 2016, Endocrinology.

Induction of Lrp5 HBM-causing mutations in Cathepsin-K expressing cells alters bone metabolism.

A. Robling, J. Hong, M. Warman, 2019, Bone.

Enhanced Wnt signaling improves bone mass and strength, but not brittleness, in the Col1a1(+/mov13) mouse model of type I Osteogenesis Imperfecta.

A. Boskey, A. Robling, D. Zurakowski, 2016, Bone.

Clcn7F318L/+ as a new mouse model of Albers-Schönberg disease.

R. Baron, A. Robling, J. Caetano-Lopes, 2017, Bone.

Core Binding Factor β Plays a Critical Role During Chondrocyte Differentiation

K. Lim, Na-Rae Park, Xiangguo Che, 2016, Journal of cellular physiology.

An osteocalcin-deficient mouse strain without endocrine abnormalities

Cassandra R Diegel, Jennifer C W Hu, Gabrielle E Foxa, 2019, bioRxiv.

Bone Mass and Strength are Significantly Improved in Mice Overexpressing Human WNT16 in Osteocytes

M. Econs, A. Robling, K. Lim, 2017, Calcified Tissue International.

Independent validation of experimental results requires timely and unrestricted access to animal models and reagents

Cassandra R Diegel, Steven Hann, Ugur M Ayturk, 2020, PLoS genetics.

Sclerostin neutralization unleashes the osteoanabolic effects of Dkk1 inhibition.

G. Loots, A. Robling, K. Lim, 2018, JCI insight.

The cleidocranial dysplasia‐related R131G mutation in the Runt‐related transcription factor RUNX2 disrupts binding to DNA but not CBF‐β

G. Stein, J. Lian, A. V. van Wijnen, 2010, Journal of cellular biochemistry.