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Items: 8

1.

Interactions of signaling proteins, growth factors and other proteins with heparan sulfate: mechanisms and mysteries.

Billings PC, Pacifici M.

Connect Tissue Res. 2015;56(4):272-80. doi: 10.3109/03008207.2015.1045066. Review.

2.

Hip joint osteochondroma: systematic review of the literature and report of three further cases.

Makhdom AM, Jiang F, Hamdy RC, Benaroch TE, Lavigne M, Saran N.

Adv Orthop. 2014;2014:180254. doi: 10.1155/2014/180254. Epub 2014 May 20. Review.

3.

Stüve-Wiedemann syndrome: LIFR and associated cytokines in clinical course and etiology.

Mikelonis D, Jorcyk CL, Tawara K, Oxford JT.

Orphanet J Rare Dis. 2014 Mar 12;9:34. doi: 10.1186/1750-1172-9-34. Review.

4.

The exostosin family: proteins with many functions.

Busse-Wicher M, Wicher KB, Kusche-Gullberg M.

Matrix Biol. 2014 Apr;35:25-33. doi: 10.1016/j.matbio.2013.10.001. Epub 2013 Oct 12. Review.

5.

Heparan sulfate in skeletal development, growth, and pathology: the case of hereditary multiple exostoses.

Huegel J, Sgariglia F, Enomoto-Iwamoto M, Koyama E, Dormans JP, Pacifici M.

Dev Dyn. 2013 Sep;242(9):1021-32. doi: 10.1002/dvdy.24010. Epub 2013 Jul 29. Review.

6.

Cell biology of osteochondromas: bone morphogenic protein signalling and heparan sulphates.

Cuellar A, Reddi AH.

Int Orthop. 2013 Aug;37(8):1591-6. doi: 10.1007/s00264-013-1906-5. Epub 2013 Jun 15. Review.

7.

The role of microRNAs in the biology of rare diseases.

Salvatore M, Magrelli A, Taruscio D.

Int J Mol Sci. 2011;12(10):6733-42. doi: 10.3390/ijms12106733. Epub 2011 Oct 11. Review.

8.

Hereditary Multiple Osteochondromas.

Wuyts W, Schmale GA, Chansky HA, Raskind WH.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Fong CT, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2016.
2000 Aug 03 [updated 2013 Nov 21].

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