214 related articles for article (PubMed ID: 32969478)
1. FKBP8 variants are risk factors for spina bifida.
Tian T; Cao X; Kim SE; Lin YL; Steele JW; Cabrera RM; Karki M; Yang W; Marini NJ; Hoffman EN; Han X; Hu C; Wang L; Wlodarczyk BJ; Shaw GM; Ren A; Finnell RH; Lei Y
Hum Mol Genet; 2020 Nov; 29(18):3132-3144. PubMed ID: 32969478
[TBL] [Abstract][Full Text] [Related]
2. Mouse Fkbp8 activity is required to inhibit cell death and establish dorso-ventral patterning in the posterior neural tube.
Wong RL; Wlodarczyk BJ; Min KS; Scott ML; Kartiko S; Yu W; Merriweather MY; Vogel P; Zambrowicz BP; Finnell RH
Hum Mol Genet; 2008 Feb; 17(4):587-601. PubMed ID: 18003640
[TBL] [Abstract][Full Text] [Related]
3. Genome-wide association mapping in dogs enables identification of the homeobox gene, NKX2-8, as a genetic component of neural tube defects in humans.
Safra N; Bassuk AG; Ferguson PJ; Aguilar M; Coulson RL; Thomas N; Hitchens PL; Dickinson PJ; Vernau KM; Wolf ZT; Bannasch DL
PLoS Genet; 2013; 9(7):e1003646. PubMed ID: 23874236
[TBL] [Abstract][Full Text] [Related]
4. Overexpression of Grainyhead-like 3 causes spina bifida and interacts genetically with mutant alleles of Grhl2 and Vangl2 in mice.
De Castro SCP; Gustavsson P; Marshall AR; Gordon WM; Galea G; Nikolopoulou E; Savery D; Rolo A; Stanier P; Andersen B; Copp AJ; Greene NDE
Hum Mol Genet; 2018 Dec; 27(24):4218-4230. PubMed ID: 30189017
[TBL] [Abstract][Full Text] [Related]
5. Neural tube closure depends on expression of Grainyhead-like 3 in multiple tissues.
De Castro SCP; Hirst CS; Savery D; Rolo A; Lickert H; Andersen B; Copp AJ; Greene NDE
Dev Biol; 2018 Mar; 435(2):130-137. PubMed ID: 29397878
[TBL] [Abstract][Full Text] [Related]
6. β-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. PubMed ID: 24284205
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Dominant negative GPR161 rare variants are risk factors of human spina bifida.
Kim SE; Lei Y; Hwang SH; Wlodarczyk BJ; Mukhopadhyay S; Shaw GM; Ross ME; Finnell RH
Hum Mol Genet; 2019 Jan; 28(2):200-208. PubMed ID: 30256984
[TBL] [Abstract][Full Text] [Related]
10. A critical role of noggin in developing folate-nonresponsive NTD in Fkbp8 -/- embryos.
Tsurubuchi T; Allender EV; Siddiqui MR; Shim KW; Ichi S; Boshnjaku V; Mania-Farnell B; Xi G; Finnell RH; McLone DG; Tomita T; Mayanil CS
Childs Nerv Syst; 2014 Aug; 30(8):1343-53. PubMed ID: 24817375
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Untargeted metabolite profiling of murine embryos to reveal metabolic perturbations associated with neural tube closure defects.
Hansler A; Chen Q; Gray JD; Ross ME; Finnell RH; Gross SS
Birth Defects Res A Clin Mol Teratol; 2014 Aug; 100(8):623-32. PubMed ID: 25115437
[TBL] [Abstract][Full Text] [Related]
14. Genetic and functional analysis of SHROOM1-4 in a Chinese neural tube defect cohort.
Chen Z; Kuang L; Finnell RH; Wang H
Hum Genet; 2018 Mar; 137(3):195-202. PubMed ID: 29423651
[TBL] [Abstract][Full Text] [Related]
15. Spina bifida and other neural tube defects.
Northrup H; Volcik KA
Curr Probl Pediatr; 2000; 30(10):313-32. PubMed ID: 11147289
[TBL] [Abstract][Full Text] [Related]
16. Pathobiology and genetics of neural tube defects.
Finnell RH; Gould A; Spiegelstein O
Epilepsia; 2003; 44 Suppl 3():14-23. PubMed ID: 12790882
[TBL] [Abstract][Full Text] [Related]
17. Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model.
Gustavsson P; Greene ND; Lad D; Pauws E; de Castro SC; Stanier P; Copp AJ
Hum Mol Genet; 2007 Nov; 16(21):2640-6. PubMed ID: 17720888
[TBL] [Abstract][Full Text] [Related]
18. Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida.
Cao X; Tian T; Steele JW; Cabrera RM; Aguiar-Pulido V; Wadhwa S; Bhavani N; Bi P; Gargurevich NH; Hoffman EN; Cai CQ; Marini NJ; Yang W; Shaw GM; Ross ME; Finnell RH; Lei Y
Hum Mutat; 2020 Apr; 41(4):786-799. PubMed ID: 31898828
[TBL] [Abstract][Full Text] [Related]
19. A Shared Pathogenic Mechanism for Valproic Acid and
Takla TN; Luo J; Sudyk R; Huang J; Walker JC; Vora NL; Sexton JZ; Parent JM; Tidball AM
Cells; 2023 Jun; 12(13):. PubMed ID: 37443734
[TBL] [Abstract][Full Text] [Related]
20. Mutations in planar cell polarity gene SCRIB are associated with spina bifida.
Lei Y; Zhu H; Duhon C; Yang W; Ross ME; Shaw GM; Finnell RH
PLoS One; 2013; 8(7):e69262. PubMed ID: 23922697
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
