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Items: 8

1.

Analysis of the asymmetrically expressed Ablim1 locus reveals existence of a lateral plate Nodal-independent left sided signal and an early, left-right independent role for nodal flow.

Stevens J, Ermakov A, Braganca J, Hilton H, Underhill P, Bhattacharya S, Brown NA, Norris DP.

BMC Dev Biol. 2010 May 20;10:54. doi: 10.1186/1471-213X-10-54.

2.

Genetic Analysis Reveals a Hierarchy of Interactions between Polycystin-Encoding Genes and Genes Controlling Cilia Function during Left-Right Determination.

Grimes DT, Keynton JL, Buenavista MT, Jin X, Patel SH, Kyosuke S, Vibert J, Williams DJ, Hamada H, Hussain R, Nauli SM, Norris DP.

PLoS Genet. 2016 Jun 6;12(6):e1006070. doi: 10.1371/journal.pgen.1006070. eCollection 2016 Jun.

3.

Paraxial Nodal Expression Reveals a Novel Conserved Structure of the Left-Right Organizer in Four Mammalian Species.

Schröder SS, Tsikolia N, Weizbauer A, Hue I, Viebahn C.

Cells Tissues Organs. 2016;201(2):77-87. doi: 10.1159/000440951. Epub 2016 Jan 8.

4.

Nodal signalling in Xenopus: the role of Xnr5 in left/right asymmetry and heart development.

Tadjuidje E, Kofron M, Mir A, Wylie C, Heasman J, Cha SW.

Open Biol. 2016 Aug;6(8). pii: 150187. doi: 10.1098/rsob.150187.

5.

Cilia are required for asymmetric nodal induction in the sea urchin embryo.

Tisler M, Wetzel F, Mantino S, Kremnyov S, Thumberger T, Schweickert A, Blum M, Vick P.

BMC Dev Biol. 2016 Aug 23;16(1):28. doi: 10.1186/s12861-016-0128-7.

6.

9 + 0 and 9 + 2 cilia are randomly dispersed in the mouse node.

Odate T, Takeda S, Narita K, Kawahara T.

Microscopy (Oxf). 2016 Apr;65(2):119-26. doi: 10.1093/jmicro/dfv352. Epub 2015 Oct 31.

PMID:
26520785
7.

Formin Is Associated with Left-Right Asymmetry in the Pond Snail and the Frog.

Davison A, McDowell GS, Holden JM, Johnson HF, Koutsovoulos GD, Liu MM, Hulpiau P, Van Roy F, Wade CM, Banerjee R, Yang F, Chiba S, Davey JW, Jackson DJ, Levin M, Blaxter ML.

Curr Biol. 2016 Mar 7;26(5):654-60. doi: 10.1016/j.cub.2015.12.071. Epub 2016 Feb 25.

8.

A human laterality disorder caused by a homozygous deleterious mutation in MMP21.

Perles Z, Moon S, Ta-Shma A, Yaacov B, Francescatto L, Edvardson S, Rein AJ, Elpeleg O, Katsanis N.

J Med Genet. 2015 Dec;52(12):840-7. doi: 10.1136/jmedgenet-2015-103336. Epub 2015 Oct 1.

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