Similar articles for PMID: 11836356

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1984	1
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1

Identification of a 52 kb deletion downstream of the SOST gene in patients with van Buchem disease.

Balemans W, Patel N, Ebeling M, Van Hul E, Wuyts W, Lacza C, Dioszegi M, Dikkers FG, Hildering P, Willems PJ, Verheij JB, Lindpaintner K, Vickery B, Foernzler D, Van Hul W. Balemans W, et al. J Med Genet. 2002 Feb;39(2):91-7. doi: 10.1136/jmg.39.2.91. J Med Genet. 2002. PMID: 11836356 Free PMC article.

2

Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST).

Balemans W, Ebeling M, Patel N, Van Hul E, Olson P, Dioszegi M, Lacza C, Wuyts W, Van Den Ende J, Willems P, Paes-Alves AF, Hill S, Bueno M, Ramos FJ, Tacconi P, Dikkers FG, Stratakis C, Lindpaintner K, Vickery B, Foernzler D, Van Hul W. Balemans W, et al. Hum Mol Genet. 2001 Mar 1;10(5):537-43. doi: 10.1093/hmg/10.5.537. Hum Mol Genet. 2001. PMID: 11181578

3

A 52-kb deletion in the SOST-MEOX1 intergenic region on 17q12-q21 is associated with van Buchem disease in the Dutch population.

Staehling-Hampton K, Proll S, Paeper BW, Zhao L, Charmley P, Brown A, Gardner JC, Galas D, Schatzman RC, Beighton P, Papapoulos S, Hamersma H, Brunkow ME. Staehling-Hampton K, et al. Am J Med Genet. 2002 Jun 15;110(2):144-52. doi: 10.1002/ajmg.10401. Am J Med Genet. 2002. PMID: 12116252

4

Genetics of Sost/SOST in sclerosteosis and van Buchem disease animal models.

Sebastian A, Loots GG. Sebastian A, et al. Metabolism. 2018 Mar;80:38-47. doi: 10.1016/j.metabol.2017.10.005. Epub 2017 Oct 25. Metabolism. 2018. PMID: 29080811 Free article. Review.

5

SOST-Related Sclerosing Bone Dysplasias.

Appelman-Dijkstra N, Van Lierop A, Papapoulos S. Appelman-Dijkstra N, et al. 2002 Jun 4 [updated 2019 Mar 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2002 Jun 4 [updated 2019 Mar 21]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 36508511 Free Books & Documents. Review.

6

A generalized skeletal hyperostosis in two siblings caused by a novel mutation in the SOST gene.

Balemans W, Cleiren E, Siebers U, Horst J, Van Hul W. Balemans W, et al. Bone. 2005 Jun;36(6):943-7. doi: 10.1016/j.bone.2005.02.019. Bone. 2005. PMID: 15869924

7

Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21.

Balemans W, Van Den Ende J, Freire Paes-Alves A, Dikkers FG, Willems PJ, Vanhoenacker F, de Almeida-Melo N, Alves CF, Stratakis CA, Hill SC, Van Hul W. Balemans W, et al. Am J Hum Genet. 1999 Jun;64(6):1661-9. doi: 10.1086/302416. Am J Hum Genet. 1999. PMID: 10330353 Free PMC article.

8

Polymorphisms in the sclerosteosis/van Buchem disease gene (SOST) region are associated with bone-mineral density in elderly whites.

Uitterlinden AG, Arp PP, Paeper BW, Charmley P, Proll S, Rivadeneira F, Fang Y, van Meurs JB, Britschgi TB, Latham JA, Schatzman RC, Pols HA, Brunkow ME. Uitterlinden AG, et al. Am J Hum Genet. 2004 Dec;75(6):1032-45. doi: 10.1086/426458. Epub 2004 Oct 26. Am J Hum Genet. 2004. PMID: 15514891 Free PMC article.

9

Identification of signal peptide domain SOST mutations in autosomal dominant craniodiaphyseal dysplasia.

Kim SJ, Bieganski T, Sohn YB, Kozlowski K, Semënov M, Okamoto N, Kim CH, Ko AR, Ahn GH, Choi YL, Park SW, Ki CS, Kim OH, Nishimura G, Unger S, Superti-Furga A, Jin DK. Kim SJ, et al. Hum Genet. 2011 May;129(5):497-502. doi: 10.1007/s00439-011-0947-3. Epub 2011 Jan 9. Hum Genet. 2011. PMID: 21221996

10

Control of the SOST bone enhancer by PTH using MEF2 transcription factors.

Leupin O, Kramer I, Collette NM, Loots GG, Natt F, Kneissel M, Keller H. Leupin O, et al. J Bone Miner Res. 2007 Dec;22(12):1957-67. doi: 10.1359/jbmr.070804. J Bone Miner Res. 2007. PMID: 17696759 Free PMC article.

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