Bell PA - Search Results

1

Genotype to phenotype correlations in cartilage oligomeric matrix protein associated chondrodysplasias.

Briggs MD, Brock J, Ramsden SC, Bell PA. Briggs MD, et al. Among authors: bell pa. Eur J Hum Genet. 2014 Nov;22(11):1278-82. doi: 10.1038/ejhg.2014.30. Epub 2014 Mar 5. Eur J Hum Genet. 2014. PMID: 24595329 Free PMC article.

2

The utility of mouse models to provide information regarding the pathomolecular mechanisms in human genetic skeletal diseases: The emerging role of endoplasmic reticulum stress (Review).

Briggs MD, Bell PA, Pirog KA. Briggs MD, et al. Among authors: bell pa. Int J Mol Med. 2015 Jun;35(6):1483-92. doi: 10.3892/ijmm.2015.2158. Epub 2015 Mar 30. Int J Mol Med. 2015. PMID: 25824717 Free PMC article. Review.

3

Mesencephalic astrocyte-derived neurotropic factor is an important factor in chondrocyte ER homeostasis.

Bell PA, Dennis EP, Hartley CL, Jackson RM, Porter A, Boot-Handford RP, Pirog KA, Briggs MD. Bell PA, et al. Cell Stress Chaperones. 2019 Jan;24(1):159-173. doi: 10.1007/s12192-018-0953-7. Epub 2018 Dec 12. Cell Stress Chaperones. 2019. PMID: 30543055 Free PMC article.

4

An unfolded protein response is the initial cellular response to the expression of mutant matrilin-3 in a mouse model of multiple epiphyseal dysplasia.

Nundlall S, Rajpar MH, Bell PA, Clowes C, Zeeff LA, Gardner B, Thornton DJ, Boot-Handford RP, Briggs MD. Nundlall S, et al. Among authors: bell pa. Cell Stress Chaperones. 2010 Nov;15(6):835-49. doi: 10.1007/s12192-010-0193-y. Epub 2010 Apr 30. Cell Stress Chaperones. 2010. PMID: 20428984 Free PMC article.

5

Loss of matrilin 1 does not exacerbate the skeletal phenotype in a mouse model of multiple epiphyseal dysplasia caused by a Matn3 V194D mutation.

Bell PA, Piróg KA, Fresquet M, Thornton DJ, Boot-Handford RP, Briggs MD. Bell PA, et al. Arthritis Rheum. 2012 May;64(5):1529-39. doi: 10.1002/art.33486. Arthritis Rheum. 2012. PMID: 22083516 Free PMC article.

6

Analysis of the cartilage proteome from three different mouse models of genetic skeletal diseases reveals common and discrete disease signatures.

Bell PA, Wagener R, Zaucke F, Koch M, Selley J, Warwood S, Knight D, Boot-Handford RP, Thornton DJ, Briggs MD. Bell PA, et al. Biol Open. 2013 Jun 18;2(8):802-11. doi: 10.1242/bio.20135280. eCollection 2013 Aug 15. Biol Open. 2013. PMID: 23951406 Free PMC article.

7

Armet/Manf and Creld2 are components of a specialized ER stress response provoked by inappropriate formation of disulphide bonds: implications for genetic skeletal diseases.

Hartley CL, Edwards S, Mullan L, Bell PA, Fresquet M, Boot-Handford RP, Briggs MD. Hartley CL, et al. Among authors: bell pa. Hum Mol Genet. 2013 Dec 20;22(25):5262-75. doi: 10.1093/hmg/ddt383. Epub 2013 Aug 15. Hum Mol Genet. 2013. PMID: 23956175 Free PMC article.

8

Abnormal chondrocyte apoptosis in the cartilage growth plate is influenced by genetic background and deletion of CHOP in a targeted mouse model of pseudoachondroplasia.

Piróg KA, Irman A, Young S, Halai P, Bell PA, Boot-Handford RP, Briggs MD. Piróg KA, et al. Among authors: bell pa. PLoS One. 2014 Feb 18;9(2):e85145. doi: 10.1371/journal.pone.0085145. eCollection 2014. PLoS One. 2014. PMID: 24558358 Free PMC article.

9

A novel transgenic mouse model of growth plate dysplasia reveals that decreased chondrocyte proliferation due to chronic ER stress is a key factor in reduced bone growth.

Gualeni B, Rajpar MH, Kellogg A, Bell PA, Arvan P, Boot-Handford RP, Briggs MD. Gualeni B, et al. Among authors: bell pa. Dis Model Mech. 2013 Nov;6(6):1414-25. doi: 10.1242/dmm.013342. Epub 2013 Sep 12. Dis Model Mech. 2013. PMID: 24046357 Free PMC article.

10

New therapeutic targets in rare genetic skeletal diseases.

Briggs MD, Bell PA, Wright MJ, Pirog KA. Briggs MD, et al. Among authors: bell pa. Expert Opin Orphan Drugs. 2015 Oct 3;3(10):1137-1154. doi: 10.1517/21678707.2015.1083853. Epub 2015 Sep 24. Expert Opin Orphan Drugs. 2015. PMID: 26635999 Free PMC article.

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