These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
286 related items for PubMed ID: 34606641
1. Bone-derived sclerostin and Wnt/β-catenin signaling regulate PDGFRα+ adipoprogenitor cell differentiation. Kim SP, Da H, Wang L, Taketo MM, Wan M, Riddle RC. FASEB J; 2021 Nov; 35(11):e21957. PubMed ID: 34606641 [Abstract] [Full Text] [Related]
2. Wnt/β-catenin signaling regulates adipose tissue lipogenesis and adipocyte-specific loss is rigorously defended by neighboring stromal-vascular cells. Bagchi DP, Nishii A, Li Z, DelProposto JB, Corsa CA, Mori H, Hardij J, Learman BS, Lumeng CN, MacDougald OA. Mol Metab; 2020 Dec; 42():101078. PubMed ID: 32919095 [Abstract] [Full Text] [Related]
3. SOST gene suppression stimulates osteocyte Wnt/β-catenin signaling to prevent bone resorption and attenuates particle-induced osteolysis. Jiao Z, Chai H, Wang S, Sun C, Huang Q, Xu W. J Mol Med (Berl); 2023 May; 101(5):607-620. PubMed ID: 37121919 [Abstract] [Full Text] [Related]
4. GH action influences adipogenesis of mouse adipose tissue-derived mesenchymal stem cells. Olarescu NC, Berryman DE, Householder LA, Lubbers ER, List EO, Benencia F, Kopchick JJ, Bollerslev J. J Endocrinol; 2015 Jul; 226(1):13-23. PubMed ID: 25943560 [Abstract] [Full Text] [Related]
5. Loss of wnt/β-catenin signaling causes cell fate shift of preosteoblasts from osteoblasts to adipocytes. Song L, Liu M, Ono N, Bringhurst FR, Kronenberg HM, Guo J. J Bone Miner Res; 2012 Nov; 27(11):2344-58. PubMed ID: 22729939 [Abstract] [Full Text] [Related]
6. Enhanced prostacyclin formation and Wnt signaling in sclerostin deficient osteocytes and bone. Ryan ZC, Craig TA, Salisbury JL, Carpio LR, McGee-Lawrence M, Westendorf JJ, Kumar R. Biochem Biophys Res Commun; 2014 May 23; 448(1):83-8. PubMed ID: 24780398 [Abstract] [Full Text] [Related]
7. The skeletal cell-derived molecule sclerostin drives bone marrow adipogenesis. Fairfield H, Falank C, Harris E, Demambro V, McDonald M, Pettitt JA, Mohanty ST, Croucher P, Kramer I, Kneissel M, Rosen CJ, Reagan MR. J Cell Physiol; 2018 Feb 23; 233(2):1156-1167. PubMed ID: 28460416 [Abstract] [Full Text] [Related]
14. Heavy Metal Ion Regulation of Gene Expression: MECHANISMS BY WHICH LEAD INHIBITS OSTEOBLASTIC BONE-FORMING ACTIVITY THROUGH MODULATION OF THE Wnt/β-CATENIN SIGNALING PATHWAY. Beier EE, Sheu TJ, Dang D, Holz JD, Ubayawardena R, Babij P, Puzas JE. J Biol Chem; 2015 Jul 17; 290(29):18216-18226. PubMed ID: 25975268 [Abstract] [Full Text] [Related]
15. Inducible brown adipose tissue, or beige fat, is anabolic for the skeleton. Rahman S, Lu Y, Czernik PJ, Rosen CJ, Enerback S, Lecka-Czernik B. Endocrinology; 2013 Aug 17; 154(8):2687-701. PubMed ID: 23696565 [Abstract] [Full Text] [Related]
16. Sclerostin mediates bone response to mechanical unloading through antagonizing Wnt/beta-catenin signaling. Lin C, Jiang X, Dai Z, Guo X, Weng T, Wang J, Li Y, Feng G, Gao X, He L. J Bone Miner Res; 2009 Oct 17; 24(10):1651-61. PubMed ID: 19419300 [Abstract] [Full Text] [Related]
18. Lrp4 expression by adipocytes and osteoblasts differentially impacts sclerostin's endocrine effects on body composition and glucose metabolism. Kim SP, Da H, Li Z, Kushwaha P, Beil C, Mei L, Xiong WC, Wolfgang MJ, Clemens TL, Riddle RC. J Biol Chem; 2019 Apr 26; 294(17):6899-6911. PubMed ID: 30842262 [Abstract] [Full Text] [Related]