Ralston SH - Search Results

1

TIA1 variant drives myodegeneration in multisystem proteinopathy with SQSTM1 mutations.

Lee Y, Jonson PH, Sarparanta J, Palmio J, Sarkar M, Vihola A, Evilä A, Suominen T, Penttilä S, Savarese M, Johari M, Minot MC, Hilton-Jones D, Maddison P, Chinnery P, Reimann J, Kornblum C, Kraya T, Zierz S, Sue C, Goebel H, Azfer A, Ralston SH, Hackman P, Bucelli RC, Taylor JP, Weihl CC, Udd B. Lee Y, et al. Among authors: ralston sh. J Clin Invest. 2018 Mar 1;128(3):1164-1177. doi: 10.1172/JCI97103. Epub 2018 Feb 19. J Clin Invest. 2018. PMID: 29457785 Free PMC article.

2

Loss of ubiquitin-binding associated with Paget's disease of bone p62 (SQSTM1) mutations.

Cavey JR, Ralston SH, Hocking LJ, Sheppard PW, Ciani B, Searle MS, Layfield R. Cavey JR, et al. Among authors: ralston sh. J Bone Miner Res. 2005 Apr;20(4):619-24. doi: 10.1359/JBMR.041205. Epub 2004 Dec 6. J Bone Miner Res. 2005. PMID: 15765181 Free article.

3

Mutations of SQSTM1 are associated with severity and clinical outcome in paget disease of bone.

Visconti MR, Langston AL, Alonso N, Goodman K, Selby PL, Fraser WD, Ralston SH. Visconti MR, et al. Among authors: ralston sh. J Bone Miner Res. 2010 Nov;25(11):2368-73. doi: 10.1002/jbmr.132. J Bone Miner Res. 2010. PMID: 20499339 Free article. Clinical Trial.

4

Optineurin Negatively Regulates Osteoclast Differentiation by Modulating NF-κB and Interferon Signaling: Implications for Paget's Disease.

Obaid R, Wani SE, Azfer A, Hurd T, Jones R, Cohen P, Ralston SH, Albagha OME. Obaid R, et al. Among authors: ralston sh. Cell Rep. 2015 Nov 10;13(6):1096-1102. doi: 10.1016/j.celrep.2015.09.071. Epub 2015 Oct 29. Cell Rep. 2015. PMID: 26527009 Free PMC article.

5

Analysis of Transcriptional Regulation in Bone Cells.

Jin H, Sophocleous A, Azfer A, Ralston SH. Jin H, et al. Among authors: ralston sh. Methods Mol Biol. 2019;1914:145-167. doi: 10.1007/978-1-4939-8997-3_8. Methods Mol Biol. 2019. PMID: 30729464

6

Rare Inherited forms of Paget's Disease and Related Syndromes.

Ralston SH, Taylor JP. Ralston SH, et al. Calcif Tissue Int. 2019 May;104(5):501-516. doi: 10.1007/s00223-019-00520-5. Epub 2019 Feb 13. Calcif Tissue Int. 2019. PMID: 30756140 Free PMC article. Review.

7

A New Gene for Susceptibility to Paget's Disease of Bone and for Multisystem Proteinopathy.

Ralston SH. Ralston SH. J Bone Miner Res. 2020 Aug;35(8):1385-1386. doi: 10.1002/jbmr.4090. Epub 2020 Jun 26. J Bone Miner Res. 2020. PMID: 32589291 Free article. No abstract available.

8

Targeted Inactivation of Rin3 Increases Trabecular Bone Mass by Reducing Bone Resorption and Favouring Bone Formation.

Vallet M, Sophocleous A, Törnqvist AE, Azfer A, Hof RV, Albagha OM, Ralston SH. Vallet M, et al. Among authors: ralston sh. Calcif Tissue Int. 2021 Jul;109(1):92-102. doi: 10.1007/s00223-021-00827-2. Epub 2021 Mar 16. Calcif Tissue Int. 2021. PMID: 33725152 Free PMC article.

9

Correction to: Rare Inherited forms of Paget's Disease and Related Syndromes.

Ralston SH, Taylor JP. Ralston SH, et al. Calcif Tissue Int. 2021 Jun;108(6):827. doi: 10.1007/s00223-021-00850-3. Calcif Tissue Int. 2021. PMID: 33876254 No abstract available.

10

Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy.

Korb M, Peck A, Alfano LN, Berger KI, James MK, Ghoshal N, Healzer E, Henchcliffe C, Khan S, Mammen PPA, Patel S, Pfeffer G, Ralston SH, Roy B, Seeley WW, Swenson A, Mozaffar T, Weihl C, Kimonis V; VCP Standards of Care Working Group. Korb M, et al. Among authors: ralston sh. Orphanet J Rare Dis. 2022 Jan 29;17(1):23. doi: 10.1186/s13023-022-02172-5. Orphanet J Rare Dis. 2022. PMID: 35093159 Free PMC article. Review.

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