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Items: 1 to 20 of 312

1.

Novel mutations in Lrp6 orthologs in mouse and human neural tube defects affect a highly dosage-sensitive Wnt non-canonical planar cell polarity pathway.

Allache R, Lachance S, Guyot MC, De Marco P, Merello E, Justice MJ, Capra V, Kibar Z.

Hum Mol Genet. 2014 Apr 1;23(7):1687-99. doi: 10.1093/hmg/ddt558. Epub 2013 Nov 7. Erratum in: Hum Mol Genet. 2014 Aug 1;23(15):4185.

2.

LRP6 exerts non-canonical effects on Wnt signaling during neural tube closure.

Gray JD, Kholmanskikh S, Castaldo BS, Hansler A, Chung H, Klotz B, Singh S, Brown AM, Ross ME.

Hum Mol Genet. 2013 Nov 1;22(21):4267-81. doi: 10.1093/hmg/ddt277. Epub 2013 Jun 16.

3.

Genetic studies of ANKRD6 as a molecular switch between Wnt signaling pathways in human neural tube defects.

Allache R, Wang M, De Marco P, Merello E, Capra V, Kibar Z.

Birth Defects Res A Clin Mol Teratol. 2015 Jan;103(1):20-6. doi: 10.1002/bdra.23273. Epub 2014 Sep 8.

PMID:
25200652
4.

╬▓-catenin regulates Pax3 and Cdx2 for caudal neural tube closure and elongation.

Zhao T, Gan Q, Stokes A, Lassiter RN, Wang Y, Chan J, Han JX, Pleasure DE, Epstein JA, Zhou CJ.

Development. 2014 Jan;141(1):148-57. doi: 10.1242/dev.101550. Epub 2013 Nov 27.

5.

Planar cell polarity gene mutations contribute to the etiology of human neural tube defects in our population.

De Marco P, Merello E, Piatelli G, Cama A, Kibar Z, Capra V.

Birth Defects Res A Clin Mol Teratol. 2014 Aug;100(8):633-41. doi: 10.1002/bdra.23255. Epub 2014 May 17. Review.

PMID:
24838524
6.

Mesenchymal Wnt signaling promotes formation of sternum and thoracic body wall.

Snowball J, Ambalavanan M, Cornett B, Lang R, Whitsett J, Sinner D.

Dev Biol. 2015 May 15;401(2):264-75. doi: 10.1016/j.ydbio.2015.02.014. Epub 2015 Feb 26.

7.

PTK7 modulates Wnt signaling activity via LRP6.

Bin-Nun N, Lichtig H, Malyarova A, Levy M, Elias S, Frank D.

Development. 2014 Jan;141(2):410-21. doi: 10.1242/dev.095984. Epub 2013 Dec 18.

8.

The Wnt receptor Ryk plays a role in mammalian planar cell polarity signaling.

Macheda ML, Sun WW, Kugathasan K, Hogan BM, Bower NI, Halford MM, Zhang YF, Jacques BE, Lieschke GJ, Dabdoub A, Stacker SA.

J Biol Chem. 2012 Aug 24;287(35):29312-23. doi: 10.1074/jbc.M112.362681. Epub 2012 Jul 6.

10.

Rare LRP6 variants identified in spina bifida patients.

Lei Y, Fathe K, McCartney D, Zhu H, Yang W, Ross ME, Shaw GM, Finnell RH.

Hum Mutat. 2015 Mar;36(3):342-9. doi: 10.1002/humu.22750.

11.

Functional interactions between the LRP6 WNT co-receptor and folate supplementation.

Gray JD, Nakouzi G, Slowinska-Castaldo B, Dazard JE, Rao JS, Nadeau JH, Ross ME.

Hum Mol Genet. 2010 Dec 1;19(23):4560-72. doi: 10.1093/hmg/ddq384. Epub 2010 Sep 15.

12.

Lrp6 is required for convergent extension during Xenopus gastrulation.

Tahinci E, Thorne CA, Franklin JL, Salic A, Christian KM, Lee LA, Coffey RJ, Lee E.

Development. 2007 Nov;134(22):4095-106.

13.

Planar cell polarity gene expression correlates with tumor cell viability and prognostic outcome in neuroblastoma.

Dyberg C, Papachristou P, Haug BH, Lagercrantz H, Kogner P, Ringstedt T, Wickstr├Âm M, Johnsen JI.

BMC Cancer. 2016 Mar 31;16:259. doi: 10.1186/s12885-016-2293-2.

14.

Human neural tube defects: genetic causes and prevention.

De Marco P, Merello E, Cama A, Kibar Z, Capra V.

Biofactors. 2011 Jul-Aug;37(4):261-8. doi: 10.1002/biof.170. Epub 2011 Jun 14. Review.

PMID:
21674647
15.

Contribution of VANGL2 mutations to isolated neural tube defects.

Kibar Z, Salem S, Bosoi CM, Pauwels E, De Marco P, Merello E, Bassuk AG, Capra V, Gros P.

Clin Genet. 2011 Jul;80(1):76-82. doi: 10.1111/j.1399-0004.2010.01515.x. Epub 2010 Jul 22.

17.

The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation.

Yates LL, Papakrivopoulou J, Long DA, Goggolidou P, Connolly JO, Woolf AS, Dean CH.

Hum Mol Genet. 2010 Dec 1;19(23):4663-76. doi: 10.1093/hmg/ddq397. Epub 2010 Sep 14.

18.

Genetic interactions between planar cell polarity genes cause diverse neural tube defects in mice.

Murdoch JN, Damrau C, Paudyal A, Bogani D, Wells S, Greene ND, Stanier P, Copp AJ.

Dis Model Mech. 2014 Oct;7(10):1153-63. doi: 10.1242/dmm.016758. Epub 2014 Aug 15.

19.

Mutations in the COPII vesicle component gene SEC24B are associated with human neural tube defects.

Yang XY, Zhou XY, Wang QQ, Li H, Chen Y, Lei YP, Ma XH, Kong P, Shi Y, Jin L, Zhang T, Wang HY.

Hum Mutat. 2013 Aug;34(8):1094-101. doi: 10.1002/humu.22338. Epub 2013 May 13.

PMID:
23592378
20.

The orphan GPCR, Gpr161, regulates the retinoic acid and canonical Wnt pathways during neurulation.

Li BI, Matteson PG, Ababon MF, Nato AQ Jr, Lin Y, Nanda V, Matise TC, Millonig JH.

Dev Biol. 2015 Jun 1;402(1):17-31. doi: 10.1016/j.ydbio.2015.02.007. Epub 2015 Mar 6.

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