146 related articles for article (PubMed ID: 29205322)
1. A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly.
Ishida M; Cullup T; Boustred C; James C; Docker J; English C; ; Lench N; Copp AJ; Moore GE; Greene NDE; Stanier P
Clin Genet; 2018 Apr; 93(4):870-879. PubMed ID: 29205322
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. The search for genetic determinants of human neural tube defects.
Wolujewicz P; Ross ME
Curr Opin Pediatr; 2019 Dec; 31(6):739-746. PubMed ID: 31693581
[TBL] [Abstract][Full Text] [Related]
4. Modeling anterior development in mice: diet as modulator of risk for neural tube defects.
Kappen C
Am J Med Genet C Semin Med Genet; 2013 Nov; 163C(4):333-56. PubMed ID: 24124024
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A detailed musculoskeletal study of a fetus with anencephaly and spina bifida (craniorachischisis), and comparison with other cases of human congenital malformations.
Alghamdi MA; Ziermann JM; Gregg L; Diogo R
J Anat; 2017 Jun; 230(6):842-858. PubMed ID: 28266009
[TBL] [Abstract][Full Text] [Related]
7. Variants identified in PTK7 associated with neural tube defects.
Lei Y; Kim SE; Chen Z; Cao X; Zhu H; Yang W; Shaw GM; Zheng Y; Zhang T; Wang HY; Finnell RH
Mol Genet Genomic Med; 2019 Apr; 7(4):e00584. PubMed ID: 30689296
[TBL] [Abstract][Full Text] [Related]
8. Association between weight gain during pregnancy and neural tube defects and gastroschisis in offspring.
Yang W; Carmichael SL; Tinker SC; Shaw GM;
Birth Defects Res A Clin Mol Teratol; 2012 Dec; 94(12):1019-25. PubMed ID: 22847944
[TBL] [Abstract][Full Text] [Related]
9. Mutations in genes encoding the glycine cleavage system predispose to neural tube defects in mice and humans.
Narisawa A; Komatsuzaki S; Kikuchi A; Niihori T; Aoki Y; Fujiwara K; Tanemura M; Hata A; Suzuki Y; Relton CL; Grinham J; Leung KY; Partridge D; Robinson A; Stone V; Gustavsson P; Stanier P; Copp AJ; Greene ND; Tominaga T; Matsubara Y; Kure S
Hum Mol Genet; 2012 Apr; 21(7):1496-503. PubMed ID: 22171071
[TBL] [Abstract][Full Text] [Related]
10. Human neural tube defects: developmental biology, epidemiology, and genetics.
Detrait ER; George TM; Etchevers HC; Gilbert JR; Vekemans M; Speer MC
Neurotoxicol Teratol; 2005; 27(3):515-24. PubMed ID: 15939212
[TBL] [Abstract][Full Text] [Related]
11. CIC missense variants contribute to susceptibility for spina bifida.
Han X; Cao X; Aguiar-Pulido V; Yang W; Karki M; Ramirez PAP; Cabrera RM; Lin YL; Wlodarczyk BJ; Shaw GM; Ross ME; Zhang C; Finnell RH; Lei Y
Hum Mutat; 2022 Dec; 43(12):2021-2032. PubMed ID: 36054333
[TBL] [Abstract][Full Text] [Related]
12. Whole-Exome Sequencing Identifies Damaging
Wang L; Ren A; Tian T; Li N; Cao X; Zhang P; Jin L; Li Z; Shen Y; Zhang B; Finnell RH; Lei Y
Front Neurosci; 2019; 13():1285. PubMed ID: 31849593
[TBL] [Abstract][Full Text] [Related]
13. ARMC5 controls the degradation of most Pol II subunits, and ARMC5 mutation increases neural tube defect risks in mice and humans.
Luo H; Lao L; Au KS; Northrup H; He X; Forget D; Gauthier MS; Coulombe B; Bourdeau I; Shi W; Gagliardi L; Fragoso MCBV; Peng J; Wu J
Genome Biol; 2024 Jan; 25(1):19. PubMed ID: 38225631
[TBL] [Abstract][Full Text] [Related]
14. The surface ectoderm exhibits spatially heterogenous tension that correlates with YAP localisation during spinal neural tube closure in mouse embryos.
Marshall AR; Galea GL; Copp AJ; Greene NDE
Cells Dev; 2023 Jun; 174():203840. PubMed ID: 37068590
[TBL] [Abstract][Full Text] [Related]
15. A Shared Pathogenic Mechanism for Valproic Acid and SHROOM3 Knockout in a Brain Organoid Model of Neural Tube Defects.
Takla TN; Luo J; Sudyk R; Huang J; Walker JC; Vora NL; Sexton JZ; Parent JM; Tidball AM
bioRxiv; 2023 Apr; ():. PubMed ID: 37090564
[TBL] [Abstract][Full Text] [Related]
16. Genome-wide analysis of spina bifida risk variants in a case-control study from Bangladesh.
Tindula G; Issac B; Mukherjee SK; Ekramullah SM; Arman DM; Islam J; Suchanda HS; Sun L; Rockowitz S; Christiani DC; Warf BC; Mazumdar M
Birth Defects Res; 2024 Mar; 116(3):e2331. PubMed ID: 38526198
[TBL] [Abstract][Full Text] [Related]
17. Identification and functional analysis of rare HECTD1 missense variants in human neural tube defects.
Oxman E; Li H; Wang HY; Zohn IE
Hum Genet; 2024 Mar; 143(3):263-277. PubMed ID: 38451291
[TBL] [Abstract][Full Text] [Related]
18. Exencephaly-Anencephaly Sequence Associated with Maxillary Brachygnathia, Spinal Defects, and Palatoschisis in a Male Domestic Cat.
Marc S; Savici J; Sicoe B; Boldura OM; Paul C; Otavă G
Animals (Basel); 2023 Dec; 13(24):. PubMed ID: 38136919
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of craniorachischisis totalis.
Costa P; Fontoura Oliveira A; Baptista Vilaça A
BMJ Case Rep; 2022 Apr; 15(4):. PubMed ID: 35470163
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
