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Items: 1 to 20 of 42

1.

Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations.

Schrauwen I, Ealy M, Fransen E, Vanderstraeten K, Thys M, Meyer NC, Cosgarea M, Huber A, Mazzoli M, Pfister M, Smith RJ, Van Camp G.

Hum Genet. 2010 Feb;127(2):155-62. doi: 10.1007/s00439-009-0754-2. Epub 2009 Oct 22.

PMID:
19847460
2.

Overexpression of BMP3 in the developing skeleton alters endochondral bone formation resulting in spontaneous rib fractures.

Gamer LW, Cox K, Carlo JM, Rosen V.

Dev Dyn. 2009 Sep;238(9):2374-81. doi: 10.1002/dvdy.22048.

3.

A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.

Schrauwen I, Ealy M, Huentelman MJ, Thys M, Homer N, Vanderstraeten K, Fransen E, Corneveaux JJ, Craig DW, Claustres M, Cremers CW, Dhooge I, Van de Heyning P, Vincent R, Offeciers E, Smith RJ, Van Camp G.

Am J Hum Genet. 2009 Mar;84(3):328-38. doi: 10.1016/j.ajhg.2009.01.023. Epub 2009 Feb 19.

4.

Detection of rare nonsynonymous variants in TGFB1 in otosclerosis patients.

Thys M, Schrauwen I, Vanderstraeten K, Dieltjens N, Fransen E, Ealy M, Cremers CW, van de Heyning P, Vincent R, Offeciers E, Smith RH, van Camp G.

Ann Hum Genet. 2009 Mar;73(2):171-5. doi: 10.1111/j.1469-1809.2009.00505.x. Epub 2009 Jan 30.

5.

Relation between renin-angiotensin-aldosterone system and otosclerosis: a genetic association and in vitro study.

Imauchi Y, Jeunemaître X, Boussion M, Ferrary E, Sterkers O, Grayeli AB.

Otol Neurotol. 2008 Apr;29(3):295-301.

PMID:
18491423
6.

Association of bone morphogenetic proteins with otosclerosis.

Schrauwen I, Thys M, Vanderstraeten K, Fransen E, Dieltjens N, Huyghe JR, Ealy M, Claustres M, Cremers CR, Dhooge I, Declau F, Van de Heyning P, Vincent R, Somers T, Offeciers E, Smith RJ, Van Camp G.

J Bone Miner Res. 2008 Apr;23(4):507-16.

7.

The coding polymorphism T263I in TGF-beta1 is associated with otosclerosis in two independent populations.

Thys M, Schrauwen I, Vanderstraeten K, Janssens K, Dieltjens N, Van Den Bogaert K, Fransen E, Chen W, Ealy M, Claustres M, Cremers CR, Dhooge I, Declau F, Claes J, Van de Heyning P, Vincent R, Somers T, Offeciers E, Smith RJ, Van Camp G.

Hum Mol Genet. 2007 Sep 1;16(17):2021-30. Epub 2007 Jun 22.

PMID:
17588962
8.

Osteoprotegrin knockout mice demonstrate abnormal remodeling of the otic capsule and progressive hearing loss.

Zehnder AF, Kristiansen AG, Adams JC, Kujawa SG, Merchant SN, McKenna MJ.

Laryngoscope. 2006 Feb;116(2):201-6.

9.

CSF-1, RANKL and OPG regulate osteoclastogenesis during murine tooth eruption.

Heinrich J, Bsoul S, Barnes J, Woodruff K, Abboud S.

Arch Oral Biol. 2005 Oct;50(10):897-908. Epub 2005 Apr 9.

PMID:
16137499
10.

A homozygous BMPR1B mutation causes a new subtype of acromesomelic chondrodysplasia with genital anomalies.

Demirhan O, Türkmen S, Schwabe GC, Soyupak S, Akgül E, Tastemir D, Karahan D, Mundlos S, Lehmann K.

J Med Genet. 2005 Apr;42(4):314-7.

11.

Osteoprotegerin in the inner ear may inhibit bone remodeling in the otic capsule.

Zehnder AF, Kristiansen AG, Adams JC, Merchant SN, McKenna MJ.

Laryngoscope. 2005 Jan;115(1):172-7.

PMID:
15630389
12.

Bone morphogenetic proteins.

Chen D, Zhao M, Mundy GR.

Growth Factors. 2004 Dec;22(4):233-41. Review.

PMID:
15621726
13.

The functional landscape of mouse gene expression.

Zhang W, Morris QD, Chang R, Shai O, Bakowski MA, Mitsakakis N, Mohammad N, Robinson MD, Zirngibl R, Somogyi E, Laurin N, Eftekharpour E, Sat E, Grigull J, Pan Q, Peng WT, Krogan N, Greenblatt J, Fehlings M, van der Kooy D, Aubin J, Bruneau BG, Rossant J, Blencowe BJ, Frey BJ, Hughes TR.

J Biol. 2004;3(5):21. doi: 10.1186/jbiol16. Epub 2004 Dec 6.

14.

Proposed association between the COL1A1 and COL1A2 genes and otosclerosis is not supported by a case-control study in Spain.

Rodríguez L, Rodríguez S, Hermida J, Frade C, Sande E, Visedo G, Martín C, Zapata C.

Am J Med Genet A. 2004 Jul 1;128A(1):19-22.

PMID:
15211650
15.
16.

Inflammatory mediators as essential elements in bone remodeling.

Goldring SR.

Calcif Tissue Int. 2003 Aug;73(2):97-100. Review.

PMID:
14565589
17.

Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2.

Lehmann K, Seemann P, Stricker S, Sammar M, Meyer B, Süring K, Majewski F, Tinschert S, Grzeschik KH, Müller D, Knaus P, Nürnberg P, Mundlos S.

Proc Natl Acad Sci U S A. 2003 Oct 14;100(21):12277-82. Epub 2003 Oct 1.

18.
19.

Bone morphogenetic protein receptor signaling is necessary for normal murine postnatal bone formation.

Zhao M, Harris SE, Horn D, Geng Z, Nishimura R, Mundy GR, Chen D.

J Cell Biol. 2002 Jun 10;157(6):1049-60. Epub 2002 Jun 10.

20.

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