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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: brown sd, brown ma. J Bone Miner Res. 2012 Feb;27(2):413-28. doi: 10.1002/jbmr.547. J Bone Miner Res. 2012. PMID: 22028304 Free article.
Suggestive linkage of the parathyroid receptor type 1 to osteoporosis.
Duncan EL, Brown MA, Sinsheimer J, Bell J, Carr AJ, Wordsworth BP, Wass JA. Duncan EL, et al. Among authors: brown ma. J Bone Miner Res. 1999 Dec;14(12):1993-9. doi: 10.1359/jbmr.1999.14.12.1993. J Bone Miner Res. 1999. PMID: 10620056 Free article.
Association of sporadic chondrocalcinosis with a -4-basepair G-to-A transition in the 5'-untranslated region of ANKH that promotes enhanced expression of ANKH protein and excess generation of extracellular inorganic pyrophosphate.
Zhang Y, Johnson K, Russell RG, Wordsworth BP, Carr AJ, Terkeltaub RA, Brown MA. Zhang Y, et al. Among authors: brown ma. Arthritis Rheum. 2005 Apr;52(4):1110-7. doi: 10.1002/art.20978. Arthritis Rheum. 2005. PMID: 15818664 Free article.
Significant deterioration in nanomechanical quality occurs through incomplete extrafibrillar mineralization in rachitic bone: evidence from in-situ synchrotron X-ray scattering and backscattered electron imaging.
Karunaratne A, Esapa CR, Hiller J, Boyde A, Head R, Bassett JH, Terrill NJ, Williams GR, Brown MA, Croucher PI, Brown SD, Cox RD, Barber AH, Thakker RV, Gupta HS. Karunaratne A, et al. Among authors: brown sd, brown ma. J Bone Miner Res. 2012 Apr;27(4):876-90. doi: 10.1002/jbmr.1495. J Bone Miner Res. 2012. PMID: 22161748 Free article.
A mouse with an N-Ethyl-N-nitrosourea (ENU) Induced Trp589Arg Galnt3 mutation represents a model for hyperphosphataemic familial tumoural calcinosis.
Esapa CT, Head RA, Jeyabalan J, Evans H, Hough TA, Cheeseman MT, McNally EG, Carr AJ, Thomas GP, Brown MA, Croucher PI, Brown SD, Cox RD, Thakker RV. Esapa CT, et al. Among authors: brown sd, brown ma. PLoS One. 2012;7(8):e43205. doi: 10.1371/journal.pone.0043205. Epub 2012 Aug 13. PLoS One. 2012. PMID: 22912827 Free PMC article.
An N-ethyl-N-nitrosourea induced corticotropin-releasing hormone promoter mutation provides a mouse model for endogenous glucocorticoid excess.
Bentley L, Esapa CT, Nesbit MA, Head RA, Evans H, Lath D, Scudamore CL, Hough TA, Podrini C, Hannan FM, Fraser WD, Croucher PI, Brown MA, Brown SD, Cox RD, Thakker RV. Bentley L, et al. Among authors: brown sd, brown ma. Endocrinology. 2014 Mar;155(3):908-22. doi: 10.1210/en.2013-1247. Epub 2013 Dec 3. Endocrinology. 2014. PMID: 24302625 Free PMC article.
Mutations in Known Monogenic High Bone Mass Loci Only Explain a Small Proportion of High Bone Mass Cases.
Gregson CL, Wheeler L, Hardcastle SA, Appleton LH, Addison KA, Brugmans M, Clark GR, Ward KA, Paggiosi M, Stone M, Thomas J, Agarwal R, Poole KE, McCloskey E, Fraser WD, Williams E, Bullock AN, Davey Smith G, Brown MA, Tobias JH, Duncan EL. Gregson CL, et al. Among authors: brown ma. J Bone Miner Res. 2016 Mar;31(3):640-9. doi: 10.1002/jbmr.2706. Epub 2015 Oct 6. J Bone Miner Res. 2016. PMID: 26348019 Free PMC article.
1,561 results