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 |
0.383 |
|
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 |
0.442 |
|
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 |
|
Show low-probability matches. |