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Similar articles for PubMed (Select 17595534)

1.

Studies of otic capsule morphology and gene expression in the Mov13 mouse--an animal model of type I osteogenesis imperfecta.

Stankovic KM, Kristiansen AG, Bizaki A, Lister M, Adams JC, McKenna MJ.

Audiol Neurootol. 2007;12(5):334-43. Epub 2007 Jun 26.

PMID:
17595534
2.

Lack of correlation between the type of COL1A1 or COL1A2 mutation and hearing loss in osteogenesis imperfecta patients.

Hartikka H, Kuurila K, Körkkö J, Kaitila I, Grénman R, Pynnönen S, Hyland JC, Ala-Kokko L.

Hum Mutat. 2004 Aug;24(2):147-54. Erratum in: Hum Mutat. 2004 Nov;24(5):437.

PMID:
15241796
3.

A novel RNA-splicing mutation in COL1A1 gene causing osteogenesis imperfecta type I in a Chinese family.

Xia XY, Cui YX, Huang YF, Pan LJ, Yang B, Wang HY, Li XJ, Shi YC, Lu HY, Zhou YC.

Clin Chim Acta. 2008 Dec;398(1-2):148-51. doi: 10.1016/j.cca.2008.07.030. Epub 2008 Aug 5.

PMID:
18755172
4.

COL1A1 mutation analysis in Lithuanian patients with osteogenesis imperfecta.

Benusiené E, Kucinskas V.

J Appl Genet. 2003;44(1):95-102.

PMID:
12590186
5.

COL1A2 and COL2A1 expression in temporal bone of lethal osteogenesis imperfecta.

Khetarpal U, Morton CC.

Arch Otolaryngol Head Neck Surg. 1993 Dec;119(12):1305-14.

PMID:
17431984
6.

Mutations in type I collagen genes resulting in osteogenesis imperfecta in humans.

Gajko-Galicka A.

Acta Biochim Pol. 2002;49(2):433-41. Review.

7.

OIM and related animal models of osteogenesis imperfecta.

Shapiro JR, Mcbride DJ Jr, Fedarko NS.

Connect Tissue Res. 1995;31(4):265-8. Review.

PMID:
15612365
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.

Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes.

Dimasi DP, Chen JY, Hewitt AW, Klebe S, Davey R, Stirling J, Thompson E, Forbes R, Tan TY, Savarirayan R, Mackey DA, Healey PR, Mitchell P, Burdon KP, Craig JE.

Hum Genet. 2010 Jan;127(1):33-44. doi: 10.1007/s00439-009-0729-3. Epub 2009 Aug 28.

PMID:
19714363
10.

[A new mutation in COL1A1 gene in a family with osteogenesis imperfecta].

Wang Z, Xu DL, Chen Z, Hu JY, Yang Z, Wang LT.

Zhonghua Yi Xue Za Zhi. 2006 Jan 17;86(3):170-3. Chinese.

PMID:
16638323
11.

Osteogenesis imperfecta: prospects for molecular therapeutics.

Forlino A, Marini JC.

Mol Genet Metab. 2000 Sep-Oct;71(1-2):225-32. Review.

PMID:
11001814
12.

Type I collagen mutation alters the strength and fatigue behavior of Mov13 cortical tissue.

Jepsen KJ, Schaffler MB, Kuhn JL, Goulet RW, Bonadio J, Goldstein SA.

J Biomech. 1997 Nov-Dec;30(11-12):1141-7.

PMID:
9456382
13.

Genetic and biochemical analyses of Israeli osteogenesis imperfecta patients.

Ries-Levavi L, Ish-Shalom T, Frydman M, Lev D, Cohen S, Barkai G, Goldman B, Byers P, Friedman E.

Hum Mutat. 2004 Apr;23(4):399-400.

PMID:
15024745
14.

[Genetic basis for skeletal disease. Osteogenesis imperfecta and genetic abnormalities].

Hasegawa K.

Clin Calcium. 2010 Aug;20(8):1190-5. doi: CliCa100811901195. Review. Japanese.

PMID:
20675929
15.

Mutation and polymorphism spectrum in osteogenesis imperfecta type II: implications for genotype-phenotype relationships.

Bodian DL, Chan TF, Poon A, Schwarze U, Yang K, Byers PH, Kwok PY, Klein TE.

Hum Mol Genet. 2009 Feb 1;18(3):463-71. doi: 10.1093/hmg/ddn374. Epub 2008 Nov 7. Erratum in: Hum Mol Genet. 2009 May 15;18(10):1893-5.

16.

Mutational spectrum of type I collagen genes in Korean patients with osteogenesis imperfecta.

Lee KS, Song HR, Cho TJ, Kim HJ, Lee TM, Jin HS, Park HY, Kang S, Jung SC, Koo SK.

Hum Mutat. 2006 Jun;27(6):599.

PMID:
16705691
17.

Association of COL1A1 and otosclerosis: evidence for a shared genetic etiology with mild osteogenesis imperfecta.

McKenna MJ, Kristiansen AG, Bartley ML, Rogus JJ, Haines JL.

Am J Otol. 1998 Sep;19(5):604-10.

PMID:
9752968
18.

Mutations in COL1A1 of type I collagen genes in Chinese patients with osteogenesis imperfecta.

Wang Z, Yang Z, Ke Z, Yang S, Shi H, Wang L.

J Investig Med. 2009 Jun;57(5):662-7. doi: 10.231/JIM.0b013e3181a8d514.

PMID:
19491628
19.

Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2.

Sykes B, Ogilvie D, Wordsworth P, Wallis G, Mathew C, Beighton P, Nicholls A, Pope FM, Thompson E, Tsipouras P, et al.

Am J Hum Genet. 1990 Feb;46(2):293-307.

20.

Pathology of the otic capsule.

Milroy CM, Michaels L.

J Laryngol Otol. 1990 Feb;104(2):83-90.

PMID:
2324629
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