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Items: 33

1.

BCAP is a centriolar satellite protein and inhibitor of ciliogenesis.

de Saram P, Iqbal A, Murdoch JN, Wilkinson CJ.

J Cell Sci. 2017 Oct 1;130(19):3360-3373. doi: 10.1242/jcs.196642. Epub 2017 Aug 3.

2.

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.

3.

Scribble is required for normal epithelial cell-cell contacts and lumen morphogenesis in the mammalian lung.

Yates LL, Schnatwinkel C, Hazelwood L, Chessum L, Paudyal A, Hilton H, Romero MR, Wilde J, Bogani D, Sanderson J, Formstone C, Murdoch JN, Niswander LA, Greenfield A, Dean CH.

Dev Biol. 2013 Jan 15;373(2):267-80. doi: 10.1016/j.ydbio.2012.11.012. Epub 2012 Nov 27.

4.

The mouse Wnt/PCP protein Vangl2 is necessary for migration of facial branchiomotor neurons, and functions independently of Dishevelled.

Glasco DM, Sittaramane V, Bryant W, Fritzsch B, Sawant A, Paudyal A, Stewart M, Andre P, Cadete Vilhais-Neto G, Yang Y, Song MR, Murdoch JN, Chandrasekhar A.

Dev Biol. 2012 Sep 15;369(2):211-22. doi: 10.1016/j.ydbio.2012.06.021. Epub 2012 Jul 4.

5.

Brainstem respiratory oscillators develop independently of neuronal migration defects in the Wnt/PCP mouse mutant looptail.

Thoby-Brisson M, Bouvier J, Glasco DM, Stewart ME, Dean C, Murdoch JN, Champagnat J, Fortin G, Chandrasekhar A.

PLoS One. 2012;7(2):e31140. doi: 10.1371/journal.pone.0031140. Epub 2012 Feb 17.

6.

The novel mouse mutant, chuzhoi, has disruption of Ptk7 protein and exhibits defects in neural tube, heart and lung development and abnormal planar cell polarity in the ear.

Paudyal A, Damrau C, Patterson VL, Ermakov A, Formstone C, Lalanne Z, Wells S, Lu X, Norris DP, Dean CH, Henderson DJ, Murdoch JN.

BMC Dev Biol. 2010 Aug 12;10:87. doi: 10.1186/1471-213X-10-87.

7.

Epidermal wound repair is regulated by the planar cell polarity signaling pathway.

Caddy J, Wilanowski T, Darido C, Dworkin S, Ting SB, Zhao Q, Rank G, Auden A, Srivastava S, Papenfuss TA, Murdoch JN, Humbert PO, Parekh V, Boulos N, Weber T, Zuo J, Cunningham JM, Jane SM.

Dev Cell. 2010 Jul 20;19(1):138-47. doi: 10.1016/j.devcel.2010.06.008. Erratum in: Dev Cell. 2010 Aug 17;19(2):353. Parekh, Vishwas [added].

8.

Atypical cadherins Celsr1-3 differentially regulate migration of facial branchiomotor neurons in mice.

Qu Y, Glasco DM, Zhou L, Sawant A, Ravni A, Fritzsch B, Damrau C, Murdoch JN, Evans S, Pfaff SL, Formstone C, Goffinet AM, Chandrasekhar A, Tissir F.

J Neurosci. 2010 Jul 14;30(28):9392-401. doi: 10.1523/JNEUROSCI.0124-10.2010.

9.

The relationship between sonic Hedgehog signaling, cilia, and neural tube defects.

Murdoch JN, Copp AJ.

Birth Defects Res A Clin Mol Teratol. 2010 Aug;88(8):633-52. doi: 10.1002/bdra.20686. Review.

10.

The PCP genes Celsr1 and Vangl2 are required for normal lung branching morphogenesis.

Yates LL, Schnatwinkel C, Murdoch JN, Bogani D, Formstone CJ, Townsend S, Greenfield A, Niswander LA, Dean CH.

Hum Mol Genet. 2010 Jun 1;19(11):2251-67. doi: 10.1093/hmg/ddq104. Epub 2010 Mar 10.

11.

Secreted frizzled-related protein disrupts PCP in eye lens fiber cells that have polarised primary cilia.

Sugiyama Y, Stump RJ, Nguyen A, Wen L, Chen Y, Wang Y, Murdoch JN, Lovicu FJ, McAvoy JW.

Dev Biol. 2010 Feb 15;338(2):193-201. doi: 10.1016/j.ydbio.2009.11.033. Epub 2009 Dec 5.

12.

Mouse hitchhiker mutants have spina bifida, dorso-ventral patterning defects and polydactyly: identification of Tulp3 as a novel negative regulator of the Sonic hedgehog pathway.

Patterson VL, Damrau C, Paudyal A, Reeve B, Grimes DT, Stewart ME, Williams DJ, Siggers P, Greenfield A, Murdoch JN.

Hum Mol Genet. 2009 May 15;18(10):1719-39. doi: 10.1093/hmg/ddp075. Epub 2009 Feb 17.

13.

Non-cell-autonomous roles for the planar cell polarity gene Vangl2 in development of the coronary circulation.

Phillips HM, Hildreth V, Peat JD, Murdoch JN, Kobayashi K, Chaudhry B, Henderson DJ.

Circ Res. 2008 Mar 14;102(5):615-23. doi: 10.1161/CIRCRESAHA.107.160861. Epub 2008 Jan 3.

PMID:
18174466
14.

Disruption of planar cell polarity signaling results in congenital heart defects and cardiomyopathy attributable to early cardiomyocyte disorganization.

Phillips HM, Rhee HJ, Murdoch JN, Hildreth V, Peat JD, Anderson RH, Copp AJ, Chaudhry B, Henderson DJ.

Circ Res. 2007 Jul 20;101(2):137-45. Epub 2007 Jun 7.

PMID:
17556662
15.

Disruption of Bardet-Biedl syndrome ciliary proteins perturbs planar cell polarity in vertebrates.

Ross AJ, May-Simera H, Eichers ER, Kai M, Hill J, Jagger DJ, Leitch CC, Chapple JP, Munro PM, Fisher S, Tan PL, Phillips HM, Leroux MR, Henderson DJ, Murdoch JN, Copp AJ, Eliot MM, Lupski JR, Kemp DT, Dollfus H, Tada M, Katsanis N, Forge A, Beales PL.

Nat Genet. 2005 Oct;37(10):1135-40. Epub 2005 Sep 18. Erratum in: Nat Genet. 2005 Dec;37(12):1381.

PMID:
16170314
16.

Vangl2 acts via RhoA signaling to regulate polarized cell movements during development of the proximal outflow tract.

Phillips HM, Murdoch JN, Chaudhry B, Copp AJ, Henderson DJ.

Circ Res. 2005 Feb 18;96(3):292-9. Epub 2005 Jan 6.

PMID:
15637299
17.

The genetic basis of mammalian neurulation.

Copp AJ, Greene ND, Murdoch JN.

Nat Rev Genet. 2003 Oct;4(10):784-93. Review.

PMID:
13679871
18.

Dishevelled: linking convergent extension with neural tube closure.

Copp AJ, Greene ND, Murdoch JN.

Trends Neurosci. 2003 Sep;26(9):453-5. Review.

PMID:
12948650
19.

Mutation of Celsr1 disrupts planar polarity of inner ear hair cells and causes severe neural tube defects in the mouse.

Curtin JA, Quint E, Tsipouri V, Arkell RM, Cattanach B, Copp AJ, Henderson DJ, Spurr N, Stanier P, Fisher EM, Nolan PM, Steel KP, Brown SD, Gray IC, Murdoch JN.

Curr Biol. 2003 Jul 1;13(13):1129-33.

20.

Genomic organization and embryonic expression of Igsf8, an immunoglobulin superfamily member implicated in development of the nervous system and organ epithelia.

Murdoch JN, Doudney K, Gerrelli D, Wortham N, Paternotte C, Stanier P, Copp AJ.

Mol Cell Neurosci. 2003 Jan;22(1):62-74.

PMID:
12595239
21.

Disruption of scribble (Scrb1) causes severe neural tube defects in the circletail mouse.

Murdoch JN, Henderson DJ, Doudney K, Gaston-Massuet C, Phillips HM, Paternotte C, Arkell R, Stanier P, Copp AJ.

Hum Mol Genet. 2003 Jan 15;12(2):87-98.

PMID:
12499390
22.

Cloning and characterization of Igsf9 in mouse and human: a new member of the immunoglobulin superfamily expressed in the developing nervous system.

Doudney K, Murdoch JN, Braybrook C, Paternotte C, Bentley L, Copp AJ, Stanier P.

Genomics. 2002 May;79(5):663-70.

PMID:
11991715
23.

Severe neural tube defects in the loop-tail mouse result from mutation of Lpp1, a novel gene involved in floor plate specification.

Murdoch JN, Doudney K, Paternotte C, Copp AJ, Stanier P.

Hum Mol Genet. 2001 Oct 15;10(22):2593-601.

PMID:
11709546
24.

Circletail, a new mouse mutant with severe neural tube defects: chromosomal localization and interaction with the loop-tail mutation.

Murdoch JN, Rachel RA, Shah S, Beermann F, Stanier P, Mason CA, Copp AJ.

Genomics. 2001 Nov;78(1-2):55-63.

PMID:
11707073
25.

Cardiac malformations, adrenal agenesis, neural crest defects and exencephaly in mice lacking Cited2, a new Tfap2 co-activator.

Bamforth SD, Bragan├ža J, Eloranta JJ, Murdoch JN, Marques FI, Kranc KR, Farza H, Henderson DJ, Hurst HC, Bhattacharya S.

Nat Genet. 2001 Dec;29(4):469-74.

PMID:
11694877
26.

Cardiovascular defects associated with abnormalities in midline development in the Loop-tail mouse mutant.

Henderson DJ, Conway SJ, Greene ND, Gerrelli D, Murdoch JN, Anderson RH, Copp AJ.

Circ Res. 2001 Jul 6;89(1):6-12.

PMID:
11440971
27.
28.

Retinal axon misrouting at the optic chiasm in mice with neural tube closure defects.

Rachel RA, Murdoch JN, Beermann F, Copp AJ, Mason CA.

Genesis. 2000 May;27(1):32-47.

PMID:
10862153
29.

Sequence and expression analysis of Nhlh1: a basic helix-loop-helix gene implicated in neurogenesis.

Murdoch JN, Eddleston J, Leblond-Bourget N, Stanier P, Copp AJ.

Dev Genet. 1999;24(1-2):165-77.

PMID:
10079519
30.
31.

Linkage mapping of Lims1l, the murine homolog of the human LIM domain gene PINCH, to mouse chromosome 10.

Abu-Hayyeh S, Eddleston J, Murdoch JN, Tham M, Copp AJ, Stanier P.

Cytogenet Cell Genet. 1998;82(1-2):46-8.

PMID:
9763658
32.

Paralogous sm22alpha (Tagln) genes map to mouse chromosomes 1 and 9: further evidence for a paralogous relationship.

Stanier P, Abu-Hayyeh S, Murdoch JN, Eddleston J, Copp AJ.

Genomics. 1998 Jul 1;51(1):144-7.

PMID:
9693045
33.

Localization of the mouse gene encoding tyrosine kinase receptor type 10 on distal chromosome 1.

Murdoch JN, Eddleston J, Stanier P, Copp AJ.

Mamm Genome. 1997 Dec;8(12):941-2. No abstract available.

PMID:
9383291

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