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See also: EFHC2 EF-hand domain containing 2 in the Gene database

efhc2 in Homo sapiensMus musculusRattus norvegicusAll 239 Gene records

Search results

Items: 12

1.

EF-hand domain containing 2 (Efhc2) is crucial for distal segmentation of pronephros in zebrafish.

Barrodia P, Patra C, Swain RK.

Cell Biosci. 2018 Oct 16;8:53. doi: 10.1186/s13578-018-0253-z. eCollection 2018.

2.

A novel contiguous deletion involving NDP, MAOB and EFHC2 gene in a patient with familial Norrie disease: bilateral blindness and leucocoria without other deficits.

Jia B, Huang L, Chen Y, Liu S, Chen C, Xiong K, Song L, Zhou Y, Yang X, Zhong M.

J Genet. 2017 Dec;96(6):1015-1020.

3.

No relation between EFHC2 gene polymorphism and Idiopathic generalized epilepsy.

Berrin T, Hikmet Y, Gülşen V, Ferda B, Erdal B, Ece O.

Afr Health Sci. 2015 Dec;15(4):1204-10. doi: 10.4314/ahs.v15i4.20.

4.

Variation in the X-linked EFHC2 gene is associated with social cognitive abilities in males.

Startin CM, Fiorentini C, de Haan M, Skuse DH.

PLoS One. 2015 Jun 24;10(6):e0131604. doi: 10.1371/journal.pone.0131604. eCollection 2015.

5.

Influence of sex and genetic variability on expression of X-linked genes in human monocytes.

Castagné R, Zeller T, Rotival M, Szymczak S, Truong V, Schillert A, Trégouët DA, Münzel T, Ziegler A, Cambien F, Blankenberg S, Tiret L.

Genomics. 2011 Nov;98(5):320-6. doi: 10.1016/j.ygeno.2011.06.009. Epub 2011 Jul 6.

6.

Preliminary evidence of association between EFHC2, a gene implicated in fear recognition, and harm avoidance.

Blaya C, Moorjani P, Salum GA, Gonçalves L, Weiss LA, Leistner-Segal S, Manfro GG, Smoller JW.

Neurosci Lett. 2009 Mar 6;452(1):84-6. doi: 10.1016/j.neulet.2009.01.036. Epub 2009 Jan 19.

PMID:
19429002
7.

EFHC2 SNP rs7055196 is not associated with fear recognition in 45,X Turner syndrome.

Zinn AR, Kushner H, Ross JL.

Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):507-9.

PMID:
17948898
8.

Genetic polymorphisms and idiopathic generalized epilepsies.

Lucarini N, Verrotti A, Napolioni V, Bosco G, Curatolo P.

Pediatr Neurol. 2007 Sep;37(3):157-64. Review.

PMID:
17765802
9.

Contiguous deletion of the NDP, MAOA, MAOB, and EFHC2 genes in a patient with Norrie disease, severe psychomotor retardation and myoclonic epilepsy.

Rodriguez-Revenga L, Madrigal I, Alkhalidi LS, Armengol L, González E, Badenas C, Estivill X, Milà M.

Am J Med Genet A. 2007 May 1;143A(9):916-20.

PMID:
17431911
10.

Identification of EFHC2 as a quantitative trait locus for fear recognition in Turner syndrome.

Weiss LA, Purcell S, Waggoner S, Lawrence K, Spektor D, Daly MJ, Sklar P, Skuse D.

Hum Mol Genet. 2007 Jan 1;16(1):107-13. Epub 2006 Dec 12.

PMID:
17164267
11.

Tektin interactions and a model for molecular functions.

Setter PW, Malvey-Dorn E, Steffen W, Stephens RE, Linck RW.

Exp Cell Res. 2006 Sep 10;312(15):2880-96. Epub 2006 Jun 6.

PMID:
16831421
12.

A new EF-hand containing gene EFHC2 on Xp11.4: tentative evidence for association with juvenile myoclonic epilepsy.

Gu W, Sander T, Heils A, Lenzen KP, Steinlein OK.

Epilepsy Res. 2005 Aug-Sep;66(1-3):91-8.

PMID:
16112844

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