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Results: 15

1.

Concordance analysis for QTL detection in dairy cattle: a case study of leg morphology.

van den Berg I, Fritz S, Rodriguez S, Rocha D, Boussaha M, Lund MS, Boichard D.

Genet Sel Evol. 2014 May 19;46(1):31. doi: 10.1186/1297-9686-46-31.

PMID:
24884971
[PubMed - in process]
Free PMC Article
2.

Influence of ranibizumab treatment on the extracellular matrix in patients with neovascular age-related macular degeneration.

Nita M, Michalska-Małecka K, Mazurek U, Kimsa M, Strzałka-Mrozik B, Grzybowski A, Romaniuk D.

Med Sci Monit. 2014 May 28;20:875-83. doi: 10.12659/MSM.890031.

PMID:
24866589
[PubMed - in process]
Free PMC Article
3.

Genomic patterns of homozygosity in worldwide human populations.

Pemberton TJ, Absher D, Feldman MW, Myers RM, Rosenberg NA, Li JZ.

Am J Hum Genet. 2012 Aug 10;91(2):275-92. doi: 10.1016/j.ajhg.2012.06.014.

PMID:
22883143
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Proteomic analysis of Col11a1-associated protein complexes.

Brown RJ, Mallory C, McDougal OM, Oxford JT.

Proteomics. 2011 Dec;11(24):4660-76. doi: 10.1002/pmic.201100058. Epub 2011 Nov 23.

PMID:
22038862
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Organ-, inflammation- and cancer specific transcriptional fingerprints of pancreatic and hepatic stellate cells.

Erkan M, Weis N, Pan Z, Schwager C, Samkharadze T, Jiang X, Wirkner U, Giese NA, Ansorge W, Debus J, Huber PE, Friess H, Abdollahi A, Kleeff J.

Mol Cancer. 2010 Apr 23;9:88. doi: 10.1186/1476-4598-9-88.

PMID:
20416094
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Significant ophthalmoarthropathy associated with ectodermal dysplasia in a child with Marshall-Stickler overlap: a case report.

Al Kaissi A, Ganger R, Klaushofer K, Grill F.

Cases J. 2008 Oct 24;1(1):270. doi: 10.1186/1757-1626-1-270.

PMID:
18950500
[PubMed]
Free PMC Article
7.

Collagen 11a1 is indirectly activated by lymphocyte enhancer-binding factor 1 (Lef1) and negatively regulates osteoblast maturation.

Kahler RA, Yingst SM, Hoeppner LH, Jensen ED, Krawczak D, Oxford JT, Westendorf JJ.

Matrix Biol. 2008 May;27(4):330-8. doi: 10.1016/j.matbio.2008.01.002. Epub 2008 Jan 16.

PMID:
18280717
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Global control of aberrant splice-site activation by auxiliary splicing sequences: evidence for a gradient in exon and intron definition.

Královicová J, Vorechovsky I.

Nucleic Acids Res. 2007;35(19):6399-413. Epub 2007 Sep 18.

PMID:
17881373
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

A male-specific quantitative trait locus on 1p21 controlling human stature.

Sammalisto S, Hiekkalinna T, Suviolahti E, Sood K, Metzidis A, Pajukanta P, Lilja HE, Soro-Paavonen A, Taskinen MR, Tuomi T, Almgren P, Orho-Melander M, Groop L, Peltonen L, Perola M.

J Med Genet. 2005 Dec;42(12):932-9. Epub 2005 Apr 12.

PMID:
15827092
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

A novel retinoic acid-response element requires an enhancer element mediator for transcriptional activation.

Harris LR, Kamarainen OP, Sevakivi M, Miller GC, Clarke JW, Potter JL, Bridgewater LC.

Biochem J. 2004 Oct 1;383(Pt 1):37-43.

PMID:
15206905
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

The role of structural genes in the pathogenesis of osteoarthritic disorders.

Reginato AM, Olsen BR.

Arthritis Res. 2002;4(6):337-45. Epub 2002 Aug 30. Review.

PMID:
12453309
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Collagen of articular cartilage.

Eyre D.

Arthritis Res. 2002;4(1):30-5. Epub 2001 Oct 5. Review.

PMID:
11879535
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Autosomal recessive disorder otospondylomegaepiphyseal dysplasia is associated with loss-of-function mutations in the COL11A2 gene.

Melkoniemi M, Brunner HG, Manouvrier S, Hennekam R, Superti-Furga A, Kääriäinen H, Pauli RM, van Essen T, Warman ML, Bonaventure J, Miny P, Ala-Kokko L.

Am J Hum Genet. 2000 Feb;66(2):368-77.

PMID:
10677296
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes.

Annunen S, Körkkö J, Czarny M, Warman ML, Brunner HG, Kääriäinen H, Mulliken JB, Tranebjaerg L, Brooks DG, Cox GF, Cruysberg JR, Curtis MA, Davenport SL, Friedrich CA, Kaitila I, Krawczynski MR, Latos-Bielenska A, Mukai S, Olsen BR, Shinno N, Somer M, Vikkula M, Zlotogora J, Prockop DJ, Ala-Kokko L.

Am J Hum Genet. 1999 Oct;65(4):974-83.

PMID:
10486316
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Clinical and Molecular genetics of Stickler syndrome.

Snead MP, Yates JR.

J Med Genet. 1999 May;36(5):353-9. Review.

PMID:
10353778
[PubMed - indexed for MEDLINE]
Free PMC Article

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