220 related articles for article (PubMed ID: 35741713)
1.
Mohd-Zin SW; Tan ACW; Atroosh WM; Thong MK; Azizi AB; Greene NDE; Abdul-Aziz NM
Genes (Basel); 2022 May; 13(6):. PubMed ID: 35741713
[TBL] [Abstract][Full Text] [Related]
2. Mapping the Universe of Eph Receptor and Ephrin Ligand Transcripts in Epithelial and Fiber Cells of the Eye Lens.
Vu MP; Cheng C
Cells; 2022 Oct; 11(20):. PubMed ID: 36291158
[TBL] [Abstract][Full Text] [Related]
3. Expression profiling of the ephrin (EFN) and Eph receptor (EPH) family of genes in atherosclerosis-related human cells.
Sakamoto A; Sugamoto Y; Tokunaga Y; Yoshimuta T; Hayashi K; Konno T; Kawashiri MA; Takeda Y; Yamagishi M
J Int Med Res; 2011; 39(2):522-7. PubMed ID: 21672356
[TBL] [Abstract][Full Text] [Related]
4. Rare deleterious variants in GRHL3 are associated with human spina bifida.
Lemay P; De Marco P; Emond A; Spiegelman D; Dionne-Laporte A; Laurent S; Merello E; Accogli A; Rouleau GA; Capra V; Kibar Z
Hum Mutat; 2017 Jun; 38(6):716-724. PubMed ID: 28276201
[TBL] [Abstract][Full Text] [Related]
5. Attenuation of eph receptor kinase activation in cancer cells by coexpressed ephrin ligands.
Falivelli G; Lisabeth EM; Rubio de la Torre E; Perez-Tenorio G; Tosato G; Salvucci O; Pasquale EB
PLoS One; 2013; 8(11):e81445. PubMed ID: 24348920
[TBL] [Abstract][Full Text] [Related]
6. Genetic variants in GRHL3 and risk for neural tube defects: A case-control and case-parent triad/control study.
Yang W; Xiao Y; Tian T; Jin L; Wang L; Ren A
Birth Defects Res; 2019 Nov; 111(19):1468-1478. PubMed ID: 31332962
[TBL] [Abstract][Full Text] [Related]
7. Disruption of ephrin B/Eph B interaction results in abnormal cochlear innervation patterns.
Zhou CQ; Lee J; Henkemeyer MJ; Lee KH
Laryngoscope; 2011 Jul; 121(7):1541-7. PubMed ID: 21647913
[TBL] [Abstract][Full Text] [Related]
8. The impact of CFNS-causing EFNB1 mutations on ephrin-B1 function.
Makarov R; Steiner B; Gucev Z; Tasic V; Wieacker P; Wieland I
BMC Med Genet; 2010 Jun; 11():98. PubMed ID: 20565770
[TBL] [Abstract][Full Text] [Related]
9. Identification of new candidate genes for spina bifida through exome sequencing.
Azzarà A; Rendeli C; Crivello AM; Brugnoletti F; Rumore R; Ausili E; Sangiorgi E; Gurrieri F
Childs Nerv Syst; 2021 Aug; 37(8):2589-2596. PubMed ID: 33855610
[TBL] [Abstract][Full Text] [Related]
10. Methylmercury alters Eph and ephrin expression during neuronal differentiation of P19 embryonal carcinoma cells.
Wilson DT; Polunas MA; Zhou R; Halladay AK; Lowndes HE; Reuhl KR
Neurotoxicology; 2005 Aug; 26(4):661-74. PubMed ID: 15990172
[TBL] [Abstract][Full Text] [Related]
11. Testing for genetic associations in a spina bifida population: analysis of the HOX gene family and human candidate gene regions implicated by mouse models of neural tube defects.
Volcik KA; Blanton SH; Kruzel MC; Townsend IT; Tyerman GH; Mier RJ; Northrup H
Am J Med Genet; 2002 Jul; 110(3):203-7. PubMed ID: 12116226
[TBL] [Abstract][Full Text] [Related]
12. A Novel Occulta-Type Spina Bifida Mediated by Murine Double Heterozygotes
Abdullah NL; Mohd-Zin SW; Ahmad-Annuar A; Abdul-Aziz NM
Front Cell Dev Biol; 2017; 5():105. PubMed ID: 29312933
[TBL] [Abstract][Full Text] [Related]
13. Ephrin/ephrin receptor expression during early stages of mouse inner ear development.
Saeger BM; Suhm M; Neubüser A
Dev Dyn; 2011 Jun; 240(6):1578-85. PubMed ID: 21465626
[TBL] [Abstract][Full Text] [Related]
14. EPH/ephrin profile and EPHB2 expression predicts patient survival in breast cancer.
Husa AM; Magić Ž; Larsson M; Fornander T; Pérez-Tenorio G
Oncotarget; 2016 Apr; 7(16):21362-80. PubMed ID: 26870995
[TBL] [Abstract][Full Text] [Related]
15. Eph and ephrin expression in normal placental development and preeclampsia.
Goldman-Wohl D; Greenfield C; Haimov-Kochman R; Ariel I; Anteby EY; Hochner-Celnikier D; Farhat M; Yagel S
Placenta; 2004 Aug; 25(7):623-30. PubMed ID: 15193868
[TBL] [Abstract][Full Text] [Related]
16. Mini-review: toward understanding mechanisms of genetic neural tube defects in mice.
Harris MJ; Juriloff DM
Teratology; 1999 Nov; 60(5):292-305. PubMed ID: 10525207
[TBL] [Abstract][Full Text] [Related]
17. The Evolutionary History of Ephs and Ephrins: Toward Multicellular Organisms.
Arcas A; Wilkinson DG; Nieto MÁ
Mol Biol Evol; 2020 Feb; 37(2):379-394. PubMed ID: 31589243
[TBL] [Abstract][Full Text] [Related]
18. DNA methylation aberrations rather than polymorphisms of FZD3 gene increase the risk of spina bifida in a high-risk region for neural tube defects.
Shangguan S; Wang L; Chang S; Lu X; Wang Z; Wu L; Wang J; Wang X; Guan Z; Bao Y; Zhao H; Zou J; Niu B; Zhang T
Birth Defects Res A Clin Mol Teratol; 2015 Jan; 103(1):37-44. PubMed ID: 25131656
[TBL] [Abstract][Full Text] [Related]
19. Epidemiologic and genetic aspects of spina bifida and other neural tube defects.
Au KS; Ashley-Koch A; Northrup H
Dev Disabil Res Rev; 2010; 16(1):6-15. PubMed ID: 20419766
[TBL] [Abstract][Full Text] [Related]
20. Viewing the Eph receptors with a focus on breast cancer heterogeneity.
Nikas I; Ryu HS; Theocharis S
Cancer Lett; 2018 Oct; 434():160-171. PubMed ID: 30055288
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]