193 related articles for article (PubMed ID: 34490995)
21. Deciphering the function of canonical Wnt signals in development and disease: conditional loss- and gain-of-function mutations of beta-catenin in mice.
Grigoryan T; Wend P; Klaus A; Birchmeier W
Genes Dev; 2008 Sep; 22(17):2308-41. PubMed ID: 18765787
[TBL] [Abstract][Full Text] [Related]
22. Effect of arsenite, maternal age, and embryonic sex on spina bifida, exencephaly, and resorption rates in the splotch mouse.
Martin LJ; Machado AF; Loza MA; Mao GE; Lee GS; Hovland DN; Cantor RM; Collins MD
Birth Defects Res A Clin Mol Teratol; 2003 Apr; 67(4):231-9. PubMed ID: 12854658
[TBL] [Abstract][Full Text] [Related]
23. A spontaneous and novel Pax3 mutant mouse that models Waardenburg syndrome and neural tube defects.
Ohnishi T; Miura I; Ohba H; Shimamoto C; Iwayama Y; Wakana S; Yoshikawa T
Gene; 2017 Apr; 607():16-22. PubMed ID: 28043919
[TBL] [Abstract][Full Text] [Related]
24. Spina bifida-predisposing heterozygous mutations in Planar Cell Polarity genes and Zic2 reduce bone mass in young mice.
Orriss IR; Lanham S; Savery D; Greene NDE; Stanier P; Oreffo R; Copp AJ; Galea GL
Sci Rep; 2018 Feb; 8(1):3325. PubMed ID: 29463853
[TBL] [Abstract][Full Text] [Related]
25. LRP6 exerts non-canonical effects on Wnt signaling during neural tube closure.
Gray JD; Kholmanskikh S; Castaldo BS; Hansler A; Chung H; Klotz B; Singh S; Brown AM; Ross ME
Hum Mol Genet; 2013 Nov; 22(21):4267-81. PubMed ID: 23773994
[TBL] [Abstract][Full Text] [Related]
26. Rescue of neural tube defects in Pax-3-deficient embryos by p53 loss of function: implications for Pax-3- dependent development and tumorigenesis.
Pani L; Horal M; Loeken MR
Genes Dev; 2002 Mar; 16(6):676-80. PubMed ID: 11914272
[TBL] [Abstract][Full Text] [Related]
27. Shmt1 and de novo thymidylate biosynthesis underlie folate-responsive neural tube defects in mice.
Beaudin AE; Abarinov EV; Noden DM; Perry CA; Chu S; Stabler SP; Allen RH; Stover PJ
Am J Clin Nutr; 2011 Apr; 93(4):789-98. PubMed ID: 21346092
[TBL] [Abstract][Full Text] [Related]
28. Pax3 lineage-specific deletion of Gpr161 is associated with spinal neural tube and craniofacial malformations during embryonic development.
Kim SE; Chothani PJ; Shaik R; Pollard W; Finnell RH
Dis Model Mech; 2023 Nov; 16(11):. PubMed ID: 37885410
[TBL] [Abstract][Full Text] [Related]
29. Functional interactions between the LRP6 WNT co-receptor and folate supplementation.
Gray JD; Nakouzi G; Slowinska-Castaldo B; Dazard JE; Rao JS; Nadeau JH; Ross ME
Hum Mol Genet; 2010 Dec; 19(23):4560-72. PubMed ID: 20843827
[TBL] [Abstract][Full Text] [Related]
30. 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]
31. Mouse mutants with neural tube closure defects and their role in understanding human neural tube defects.
Harris MJ; Juriloff DM
Birth Defects Res A Clin Mol Teratol; 2007 Mar; 79(3):187-210. PubMed ID: 17177317
[TBL] [Abstract][Full Text] [Related]
32. Modifier locus for exencephaly in Cecr2 mutant mice is syntenic to the 10q25.3 region associated with neural tube defects in humans.
Davidson CE; Li Q; Churchill GA; Osborne LR; McDermid HE
Physiol Genomics; 2007 Oct; 31(2):244-51. PubMed ID: 17623803
[TBL] [Abstract][Full Text] [Related]
33. Migration of cardiac neural crest cells in Splotch embryos.
Epstein JA; Li J; Lang D; Chen F; Brown CB; Jin F; Lu MM; Thomas M; Liu E; Wessels A; Lo CW
Development; 2000 May; 127(9):1869-78. PubMed ID: 10751175
[TBL] [Abstract][Full Text] [Related]
34. A transgenic neuroanatomical marker identifies cranial neural crest deficiencies associated with the Pax3 mutant Splotch.
Tremblay P; Kessel M; Gruss P
Dev Biol; 1995 Oct; 171(2):317-29. PubMed ID: 7556916
[TBL] [Abstract][Full Text] [Related]
35. PAX3 Promotes Proliferation of Human Glioma Cells by WNT/β-Catenin Signaling Pathways.
Liang X; Dong Z; Bin W; Dekang N; Xuhang Z; Shuyuan Z; Liwen L; Kai J; Caixing S
J Mol Neurosci; 2019 May; 68(1):66-77. PubMed ID: 30826985
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Genetic interactions between planar cell polarity genes cause diverse neural tube defects in mice.
Murdoch JN; Damrau C; Paudyal A; Bogani D; Wells S; Greene ND; Stanier P; Copp AJ
Dis Model Mech; 2014 Oct; 7(10):1153-63. PubMed ID: 25128525
[TBL] [Abstract][Full Text] [Related]
38. Fate Specification of Neural Plate Border by Canonical Wnt Signaling and Grhl3 is Crucial for Neural Tube Closure.
Kimura-Yoshida C; Mochida K; Ellwanger K; Niehrs C; Matsuo I
EBioMedicine; 2015 Jun; 2(6):513-27. PubMed ID: 26288816
[TBL] [Abstract][Full Text] [Related]
39. Canonical Wnt/β-catenin signaling is required for maintenance but not activation of Pitx2 expression in neural crest during eye development.
Zacharias AL; Gage PJ
Dev Dyn; 2010 Dec; 239(12):3215-25. PubMed ID: 20960542
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
