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A lack of thyroid hormones rather than excess thyrotropin causes abnormal skeletal development in hypothyroidism.
Bassett JH, Williams AJ, Murphy E, Boyde A, Howell PG, Swinhoe R, Archanco M, Flamant F, Samarut J, Costagliola S, Vassart G, Weiss RE, Refetoff S, Williams GR. Bassett JH, et al. Among authors: howell pg. Mol Endocrinol. 2008 Feb;22(2):501-12. doi: 10.1210/me.2007-0221. Epub 2007 Oct 11. Mol Endocrinol. 2008. PMID: 17932107 Free PMC article.
Activated invariant NKT cells regulate osteoclast development and function.
Hu M, Bassett JH, Danks L, Howell PG, Xu K, Spanoudakis E, Kotsianidis I, Boyde A, Williams GR, Horwood N, Roberts IA, Karadimitris A. Hu M, et al. Among authors: howell pg. J Immunol. 2011 Mar 1;186(5):2910-7. doi: 10.4049/jimmunol.1002353. Epub 2011 Jan 28. J Immunol. 2011. PMID: 21278350
Analysis of skeletal phenotypes in thyroid hormone receptor mutant mice.
Bassett JH, O'Shea PJ, Chassande O, Samarut J, Cheng SY, Vennstrom B, Howell PG, Boyde A, Williams GR. Bassett JH, et al. Among authors: howell pg. Scanning. 2006 Apr 1;28(2):91-93. doi: 10.1002/sca.4950280201. Scanning. 2006. PMID: 19584945 Free PMC article. No abstract available.
A mouse model for spondyloepiphyseal dysplasia congenita with secondary osteoarthritis due to a Col2a1 mutation.
Esapa CT, Hough TA, Testori S, Head RA, Crane EA, Chan CP, Evans H, Bassett JH, Tylzanowski P, McNally EG, Carr AJ, Boyde A, Howell PG, Clark A, Williams GR, Brown MA, Croucher PI, Nesbit MA, Brown SD, Cox RD, Cheeseman MT, Thakker RV. Esapa CT, et al. Among authors: howell pg. J Bone Miner Res. 2012 Feb;27(2):413-28. doi: 10.1002/jbmr.547. J Bone Miner Res. 2012. PMID: 22028304 Free article.
65 results