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Results: 1 to 20 of 84

1.

GDF6, a novel locus for a spectrum of ocular developmental anomalies.

Asai-Coakwell M, French CR, Berry KM, Ye M, Koss R, Somerville M, Mueller R, van Heyningen V, Waskiewicz AJ, Lehmann OJ.

Am J Hum Genet. 2007 Feb;80(2):306-15. Epub 2006 Dec 29.

PMID:
17236135
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Apoptotic and proliferative defects characterize ocular development in a microphthalmic BMP model.

French CR, Stach TR, March LD, Lehmann OJ, Waskiewicz AJ.

Invest Ophthalmol Vis Sci. 2013 Jul 10;54(7):4636-47. doi: 10.1167/iovs.13-11674.

PMID:
23737474
[PubMed - indexed for MEDLINE]
Free Article
3.

Genetic defects of GDF6 in the zebrafish out of sight mutant and in human eye developmental anomalies.

den Hollander AI, Biyanwila J, Kovach P, Bardakjian T, Traboulsi EI, Ragge NK, Schneider A, Malicki J.

BMC Genet. 2010 Nov 11;11:102. doi: 10.1186/1471-2156-11-102.

PMID:
21070663
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Gene-specific differential response to anti-apoptotic therapies in zebrafish models of ocular coloboma.

Gregory-Evans CY, Moosajee M, Shan X, Gregory-Evans K.

Mol Vis. 2011;17:1473-84. Epub 2011 Jun 4.

PMID:
21677791
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Mutation of the bone morphogenetic protein GDF3 causes ocular and skeletal anomalies.

Ye M, Berry-Wynne KM, Asai-Coakwell M, Sundaresan P, Footz T, French CR, Abitbol M, Fleisch VC, Corbett N, Allison WT, Drummond G, Walter MA, Underhill TM, Waskiewicz AJ, Lehmann OJ.

Hum Mol Genet. 2010 Jan 15;19(2):287-98. doi: 10.1093/hmg/ddp496. Epub 2009 Oct 28.

PMID:
19864492
[PubMed - indexed for MEDLINE]
Free Article
6.

Mutational screening of CHX10, GDF6, OTX2, RAX and SOX2 genes in 50 unrelated microphthalmia-anophthalmia-coloboma (MAC) spectrum cases.

Gonzalez-Rodriguez J, Pelcastre EL, Tovilla-Canales JL, Garcia-Ortiz JE, Amato-Almanza M, Villanueva-Mendoza C, Espinosa-Mattar Z, Zenteno JC.

Br J Ophthalmol. 2010 Aug;94(8):1100-4. doi: 10.1136/bjo.2009.173500. Epub 2010 May 21.

PMID:
20494911
[PubMed - indexed for MEDLINE]
7.

Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes.

Asai-Coakwell M, French CR, Ye M, Garcha K, Bigot K, Perera AG, Staehling-Hampton K, Mema SC, Chanda B, Mushegian A, Bamforth S, Doschak MR, Li G, Dobbs MB, Giampietro PF, Brooks BP, Vijayalakshmi P, Sauvé Y, Abitbol M, Sundaresan P, van Heyningen V, Pourquié O, Underhill TM, Waskiewicz AJ, Lehmann OJ.

Hum Mol Genet. 2009 Mar 15;18(6):1110-21. doi: 10.1093/hmg/ddp008. Epub 2009 Jan 6.

PMID:
19129173
[PubMed - indexed for MEDLINE]
Free Article
8.

SNP genome scanning localizes oto-dental syndrome to chromosome 11q13 and microdeletions at this locus implicate FGF3 in dental and inner-ear disease and FADD in ocular coloboma.

Gregory-Evans CY, Moosajee M, Hodges MD, Mackay DS, Game L, Vargesson N, Bloch-Zupan A, Rüschendorf F, Santos-Pinto L, Wackens G, Gregory-Evans K.

Hum Mol Genet. 2007 Oct 15;16(20):2482-93. Epub 2007 Jul 25.

PMID:
17656375
[PubMed - indexed for MEDLINE]
Free Article
9.

Comparative sequence analysis of the Gdf6 locus reveals a duplicon-mediated chromosomal rearrangement in rodents and rapidly diverging coding and regulatory sequences.

Mortlock DP, Portnoy ME, Chandler RL; NISC Comparative Sequencing Program, Green ED.

Genomics. 2004 Nov;84(5):814-23.

PMID:
15475260
[PubMed - indexed for MEDLINE]
10.

Pathways in blood and vessel development revealed through zebrafish genetics.

Crosier PS, Kalev-Zylinska ML, Hall CJ, Flores MV, Horsfield JA, Crosier KE.

Int J Dev Biol. 2002;46(4):493-502. Review.

PMID:
12141436
[PubMed - indexed for MEDLINE]
Free Article
11.

Eye and neural defects associated with loss of GDF6.

Hanel ML, Hensey C.

BMC Dev Biol. 2006 Sep 29;6:43.

PMID:
17010201
[PubMed - indexed for MEDLINE]
Free PMC Article
12.
13.

Morpholino phenocopies of the bmp2b/swirl and bmp7/snailhouse mutations.

Imai Y, Talbot WS.

Genesis. 2001 Jul;30(3):160-3. No abstract available.

PMID:
11477698
[PubMed - indexed for MEDLINE]
14.

Molecular mechanisms regulating ocular apoptosis in zebrafish gdf6a mutants.

Pant SD, March LD, Famulski JK, French CR, Lehmann OJ, Waskiewicz AJ.

Invest Ophthalmol Vis Sci. 2013 Aug 28;54(8):5871-9. doi: 10.1167/iovs.12-11315.

PMID:
23847306
[PubMed - indexed for MEDLINE]
Free Article
15.

pitx2 Deficiency results in abnormal ocular and craniofacial development in zebrafish.

Liu Y, Semina EV.

PLoS One. 2012;7(1):e30896. doi: 10.1371/journal.pone.0030896. Epub 2012 Jan 27.

PMID:
22303467
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

A complex chromosome translocation resulting in deletion 11p and associated with uveal colobomata.

Friling R, Yassur Y, Abeliovich D, Biedner B, Galil A, Dagan J, Carmi R.

Ophthalmic Genet. 1995 Jun;16(2):71-4.

PMID:
7493159
[PubMed - indexed for MEDLINE]
17.

Optic disc coloboma and localized chorioretinal defects in constitutional partial trisomy 8 mosaicism.

Taban M, Marcotty A, Traboulsi EI.

Ophthalmic Genet. 2006 Sep;27(3):103-5.

PMID:
17050287
[PubMed - indexed for MEDLINE]
18.

bozozok directly represses bmp2b transcription and mediates the earliest dorsoventral asymmetry of bmp2b expression in zebrafish.

Leung T, Bischof J, Söll I, Niessing D, Zhang D, Ma J, Jäckle H, Driever W.

Development. 2003 Aug;130(16):3639-49.

PMID:
12835381
[PubMed - indexed for MEDLINE]
Free Article
19.

Germ cell aneuploidy in zebrafish with mutations in the mitotic checkpoint gene mps1.

Poss KD, Nechiporuk A, Stringer KF, Lee C, Keating MT.

Genes Dev. 2004 Jul 1;18(13):1527-32.

PMID:
15231734
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

The ventral to dorsal BMP activity gradient in the early zebrafish embryo is determined by graded expression of BMP ligands.

Ramel MC, Hill CS.

Dev Biol. 2013 Jun 15;378(2):170-82. doi: 10.1016/j.ydbio.2013.03.003. Epub 2013 Mar 13.

PMID:
23499658
[PubMed - indexed for MEDLINE]
Free PMC Article

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