Yuqing Chen

B. Dawson, Brendan H. Lee, Yuqing Chen, 2016, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay.

David R. Murdock, Lisa T. Emrick, Alyssa A. Tran, 2021, American journal of human genetics.

A Global Slc7a7 Knockout Mouse Model Demonstrates Characteristic Phenotypes of Human Lysinuric Protein Intolerance.

Denise G. Lanza, Jennie R. Green, Jason D. Heaney, 2020, Human molecular genetics.

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.

Arginase overexpression in neurons and its effect on traumatic brain injury.

R. Ratan, C. Robertson, Philippe M. Campeau, 2018, Molecular genetics and metabolism.

Nitric oxide modulates bone anabolism through regulation of osteoblast glycolysis and differentiation.

B. Dawson, L. Burrage, Brendan H. Lee, 2020, The Journal of clinical investigation.

A Transgenic Mouse Model of OI Type V Supports a Neomorphic Mechanism of the IFITM5 Mutation

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

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.

Mice Expressing Mutant Trpv4 Recapitulate the Human TRPV4 Disorders

Brendan H. Lee, Yuqing Chen, D. Cohn, 2014, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Connective tissue alterations in Fkbp10 2 / 2 mice

Brendan H. Lee, D. Eyre, Yuqing Chen, 2014 .

E-selectin ligand-1 regulates growth plate homeostasis in mice by inhibiting the intracellular processing and secretion of mature TGF-beta.

A. Beaudet, D. Rifkin, B. Keller, 2010, The Journal of clinical investigation.

Nitric-oxide supplementation for treatment of long-term complications in argininosuccinic aciduria.

N. Brunetti‐Pierri, D. Harrison, N. Bryan, 2012, American journal of human genetics.

Runx2 contributes to murine Col10a1 gene regulation through direct interaction with its cis-enhancer

Brendan H. Lee, Q. Zheng, Yuqing Chen, 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1.

M. Dickinson, D. Tibboel, Brendan H. Lee, 2012, Human molecular genetics.

Disease‐Modifying Osteoarthritis Treatment With Interleukin‐1 Receptor Antagonist Gene Therapy in Small and Large Animal Models

B. Dawson, Brendan H. Lee, Yuqing Chen, 2018, Arthritis & rheumatology.

COPB2 haploinsufficiency causes a coatopathy with osteoporosis and developmental delay

David R. Murdock, Lisa T. Emrick, Alyssa A. Tran, 2020, bioRxiv.

Whole‐Exome Sequencing Identifies an Intronic Cryptic Splice Site in SERPINF1 Causing Osteogenesis Imperfecta Type VI

Alyssa A. Tran, R. Gibbs, S. Jhangiani, 2018, JBMR plus.

Dimorphic effects of Notch signaling in bone homeostasis

Brendan H. Lee, Guang Zhou, Yuqing Chen, 2008, Nature Medicine.

Brachy–syndactyly caused by loss of Sfrp2 function

Chad A Shaw, Bernhard Zabel, C. Shaw, 2008, Journal of cellular physiology.

Dominance of SOX9 function over RUNX2 during skeletogenesis

Brendan H. Lee, Q. Zheng, E. Sebald, 2006, Proceedings of the National Academy of Sciences.

Type X collagen gene regulation by Runx2 contributes directly to its hypertrophic chondrocyte–specific expression in vivo

Brendan H. Lee, Q. Zheng, Guang Zhou, 2003, The Journal of cell biology.

Targeted Deletion of MicroRNA-22 Promotes Stress-Induced Cardiac Dilation and Contractile Dysfunction

Anton J. Enright, A. Enright, A. Bradley, 2012, Circulation.

Sc65 Is a Novel Endoplasmic Reticulum Protein That Regulates Bone Mass Homeostasis

L. Suva, Frances L. Swain, D. Eyre, 2014, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

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.

Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasis

C. Ambrose, Brendan H. Lee, Yuqing Chen, 2017, The Journal of clinical investigation.

The Crucial p53-Dependent Oncogenic Role of JAB1 in Osteosarcoma in vivo

Brendan H. Lee, Guang Zhou, Yuqing Chen, 2020, Oncogene.

Interaction of TGFβ and BMP Signaling Pathways during Chondrogenesis

B. Keller, Brendan H. Lee, Yuqing Chen, 2011, PloS one.

The transcriptional cofactor Jab1/Cops5 is crucial for BMP‐mediated mouse chondrocyte differentiation by repressing p53 activity

Brendan H. Lee, Guang Zhou, Yuqing Chen, 2021, Journal of cellular physiology.

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.

Localization of the Cis‐Enhancer Element for Mouse Type X Collagen Expression in Hypertrophic Chondrocytes In Vivo

B. Keller, A. Parker, Brendan H. Lee, 2009, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

CRTAP Is Required for Prolyl 3- Hydroxylation and Mutations Cause Recessive Osteogenesis Imperfecta

F. Glorieux, P. Byers, Brendan H. Lee, 2006, Cell.

Fkbp10 Deletion in Osteoblasts Leads to Qualitative Defects in Bone

C. Ambrose, P. Fratzl, Brendan H. Lee, 2017, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Requirement of argininosuccinate lyase for systemic nitric oxide production

Marshall Summar, William E O'Brien, Philippe M Campeau, 2011, Nature Medicine.

ADAMTS-7 forms a positive feedback loop with TNF-α in the pathogenesis of osteoarthritis

Brendan H. Lee, Yuqing Chen, Chuan-ju Liu, 2013, Annals of the rheumatic diseases.

Specificity and efficiency of reporter expression in adult neural progenitors vary substantially among nestin‐CreERT2 lines

Michael J. Yetman, Yuqing Chen, J. Jankowsky, 2014, The Journal of comparative neurology.

A novel mouse model for SNP in Steroid Receptor Co-activator-1 reveals role in bone density and breast cancer metastasis.

Adrian V. Lee, G. Tseng, S. Oesterreich, 2021, Endocrinology.

Corner fracture type spondylometaphyseal dysplasia: Overlap with type II collagenopathies

Alyssa A. Tran, R. Gibbs, Mahim Jain, 2016, American journal of medical genetics. Part A.

CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia.

Lei Zhou, B. Gelb, D. Chitayat, 1999, Human molecular genetics.