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Kyu S. Joeng, Ph.D. - Publications

Affiliations: 
2010 Biology & Biomedical Sciences (Developmental Biology) Washington University, Saint Louis, St. Louis, MO 
Area:
Human Development, Molecular Biology
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26 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2022 Lawson LY, Migotsky N, Chermside-Scabbo CJ, Shuster JT, Joeng KS, Civitelli R, Lee B, Silva MJ. Loading-induced bone formation is mediated by Wnt1 induction in osteoblast-lineage cells. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 36: e22502. PMID 35969160 DOI: 10.1096/fj.202200591R  0.391
2022 Zhong L, Yao L, Holdreith N, Yu W, Gui T, Miao Z, Elkaim Y, Li M, Gong Y, Pacifici M, Maity A, Busch TM, Joeng KS, Cengel K, Seale P, et al. Transient expansion and myofibroblast conversion of adipogenic lineage precursors mediate bone marrow repair after radiation. Jci Insight. 7. PMID 35393948 DOI: 10.1172/jci.insight.150323  0.382
2021 Turin CG, Joeng KS, Kallish S, Raper A, Asher S, Campeau PM, Khan AN, Al Mukaddam M. Heterozygous variant in gene in two brothers with early onset osteoporosis. Bone Reports. 15: 101118. PMID 34458510 DOI: 10.1016/j.bonr.2021.101118  0.424
2021 Marom R, Burrage LC, Venditti R, Clément A, Blanco-Sánchez B, Jain M, Scott DA, Rosenfeld JA, Sutton VR, Shinawi M, Mirzaa G, DeVile C, Roberts R, Calder AD, Allgrove J, ... ... Joeng KS, et al. COPB2 loss of function causes a coatopathy with osteoporosis and developmental delay. American Journal of Human Genetics. PMID 34450031 DOI: 10.1016/j.ajhg.2021.08.002  0.327
2018 Alhamdi S, Lee YC, Chowdhury S, Byers PH, Gottschalk M, Taft RJ, Joeng KS, Lee BH, Bird LM. Heterozygous WNT1 variant causing a variable bone phenotype. American Journal of Medical Genetics. Part A. PMID 30246918 DOI: 10.1002/Ajmg.A.40347  0.441
2017 Lim J, Munivez E, Jiang MM, Song IW, Gannon F, Keene DR, Schweitzer R, Lee BH, Joeng KS. mTORC1 Signaling is a Critical Regulator of Postnatal Tendon Development. Scientific Reports. 7: 17175. PMID 29215029 DOI: 10.1038/S41598-017-17384-0  0.452
2017 Joeng KS, Lee YC, Lim J, Chen Y, Jiang MM, Munivez E, Ambrose C, Lee BH. Osteocyte-specific WNT1 regulates osteoblast function during bone homeostasis. The Journal of Clinical Investigation. PMID 28628032 DOI: 10.1172/Jci92617  0.558
2017 Hudson DM, Weis M, Rai J, Joeng KS, Dimori M, Lee BH, Morello R, Eyre DR. P3h3-null and Sc65-null Mice Phenocopy the Collagen Lysine Under-hydroxylation and Cross-linking Abnormality of Ehlers-Danlos Syndrome Type VIA. The Journal of Biological Chemistry. PMID 28115524 DOI: 10.1074/Jbc.M116.762245  0.309
2015 Rajagopal A, Homan EP, Joeng KS, Suzuki M, Bertin T, Cela R, Munivez E, Dawson B, Jiang MM, Gannon F, Crawford S, Lee BH. Restoration of the serum level of SERPINF1 does not correct the bone phenotype in Serpinf1 null mice. Molecular Genetics and Metabolism. PMID 26693895 DOI: 10.1016/J.Ymgme.2015.11.015  0.473
2015 Lu L, Harutyunyan K, Jin W, Wu J, Yang T, Chen Y, Joeng KS, Bae Y, Tao J, Dawson BC, Jiang MM, Lee B, Wang LL. RECQL4 Regulates p53 Function In Vivo During Skeletogenesis. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 30: 1077-89. PMID 25556649 DOI: 10.1002/Jbmr.2436  0.441
2014 Joeng KS, Long F. Wnt7b can replace Ihh to induce hypertrophic cartilage vascularization but not osteoblast differentiation during endochondral bone development. Bone Research. 2: 14004. PMID 26273517 DOI: 10.1038/Boneres.2014.4  0.702
2014 Regan JN, Lim J, Shi Y, Joeng KS, Arbeit JM, Shohet RV, Long F. Up-regulation of glycolytic metabolism is required for HIF1α-driven bone formation. Proceedings of the National Academy of Sciences of the United States of America. 111: 8673-8. PMID 24912186 DOI: 10.1073/Pnas.1324290111  0.672
2014 Joeng KS, Lee YC, Jiang MM, Bertin TK, Chen Y, Abraham AM, Ding H, Bi X, Ambrose CG, Lee BH. The swaying mouse as a model of osteogenesis imperfecta caused by WNT1 mutations. Human Molecular Genetics. 23: 4035-42. PMID 24634143 DOI: 10.1093/Hmg/Ddu117  0.525
2014 Chen J, Tu X, Esen E, Joeng KS, Lin C, Arbeit JM, Rüegg MA, Hall MN, Ma L, Long F. WNT7B promotes bone formation in part through mTORC1. Plos Genetics. 10: e1004145. PMID 24497849 DOI: 10.1371/Journal.Pgen.1004145  0.717
2014 Joeng KS, Regan J, Long F. Radioactive in situ hybridization to detect gene expression in skeletal tissue sections. Methods in Molecular Biology (Clifton, N.J.). 1130: 217-32. PMID 24482176 DOI: 10.1007/978-1-62703-989-5_16  0.544
2013 Laine CM, Joeng KS, Campeau PM, Kiviranta R, Tarkkonen K, Grover M, Lu JT, Pekkinen M, Wessman M, Heino TJ, Nieminen-Pihala V, Aronen M, Laine T, Kröger H, Cole WG, et al. WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta. The New England Journal of Medicine. 368: 1809-16. PMID 23656646 DOI: 10.1056/Nejmoa1215458  0.462
2013 Joeng KS, Long F. Constitutive activation of Gli2 impairs bone formation in postnatal growing mice. Plos One. 8: e55134. PMID 23383082 DOI: 10.1371/Journal.Pone.0055134  0.72
2013 Laine C, Joeng KS, Campeau P, Kiviranta R, Tarkkonen K, Grover M, Lu J, Pekkinen M, Wessman M, Heino T, Nieminen-Pihala V, Laine T, Kroger H, Cole W, Lehesjoki A, et al. WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta identify a key WNT ligand regulating bone mass Bone Abstracts. DOI: 10.1530/Boneabs.2.Lb2  0.466
2012 Choi SW, Jeong DU, Kim JA, Lee B, Joeng KS, Long F, Kim DW. Indian Hedgehog signalling triggers Nkx3.2 protein degradation during chondrocyte maturation Biochemical Journal. 443: 789-798. PMID 22507129 DOI: 10.1042/Bj20112062  0.673
2012 Heller E, Hurchla MA, Xiang J, Su X, Chen S, Schneider J, Joeng KS, Vidal M, Goldberg L, Deng H, Hornick MC, Prior JL, Piwnica-Worms D, Long F, Cagan R, et al. Hedgehog signaling inhibition blocks growth of resistant tumors through effects on tumor microenvironment. Cancer Research. 72: 897-907. PMID 22186138 DOI: 10.1158/0008-5472.Can-11-2681  0.615
2012 Tu X, Joeng KS, Long F. Indian hedgehog requires additional effectors besides Runx2 to induce osteoblast differentiation. Developmental Biology. 362: 76-82. PMID 22155527 DOI: 10.1016/J.Ydbio.2011.11.013  0.675
2011 Joeng KS, Schumacher CA, Zylstra-Diegel CR, Long F, Williams BO. Lrp5 and Lrp6 redundantly control skeletal development in the mouse embryo. Developmental Biology. 359: 222-9. PMID 21924256 DOI: 10.1016/J.Ydbio.2011.08.020  0.653
2009 Joeng KS, Long F. The Gli2 transcriptional activator is a crucial effector for Ihh signaling in osteoblast development and cartilage vascularization. Development (Cambridge, England). 136: 4177-85. PMID 19906844 DOI: 10.1242/Dev.041624  0.668
2008 Wu X, Tu X, Joeng KS, Hilton MJ, Williams DA, Long F. Rac1 activation controls nuclear localization of beta-catenin during canonical Wnt signaling. Cell. 133: 340-53. PMID 18423204 DOI: 10.1016/J.Cell.2008.01.052  0.66
2007 Tu X, Joeng KS, Nakayama KI, Nakayama K, Rajagopal J, Carroll TJ, McMahon AP, Long F. Noncanonical Wnt signaling through G protein-linked PKCdelta activation promotes bone formation. Developmental Cell. 12: 113-27. PMID 17199045 DOI: 10.1016/J.Devcel.2006.11.003  0.722
2006 Long F, Joeng KS, Xuan S, Efstratiadis A, McMahon AP. Independent regulation of skeletal growth by Ihh and IGF signaling. Developmental Biology. 298: 327-33. PMID 16905129 DOI: 10.1016/J.Ydbio.2006.06.042  0.559
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