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10. 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]
11. Loss of GRHL3 leads to TARC/CCL17-mediated keratinocyte proliferation in the epidermis. Goldie SJ; Cottle DL; Tan FH; Roslan S; Srivastava S; Brady R; Partridge DD; Auden A; Smyth IM; Jane SM; Dworkin S; Darido C Cell Death Dis; 2018 Oct; 9(11):1072. PubMed ID: 30341279 [TBL] [Abstract][Full Text] [Related]
12. The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulation. Kousa YA; Zhu H; Fakhouri WD; Lei Y; Kinoshita A; Roushangar RR; Patel NK; Agopian AJ; Yang W; Leslie EJ; Busch TD; Mansour TA; Li X; Smith AL; Li EB; Sharma DB; Williams TJ; Chai Y; Amendt BA; Liao EC; Mitchell LE; Bassuk AG; Gregory S; Ashley-Koch A; Shaw GM; Finnell RH; Schutte BC Hum Mol Genet; 2019 May; 28(10):1726-1737. PubMed ID: 30689861 [TBL] [Abstract][Full Text] [Related]
13. A GRHL3-regulated repair pathway suppresses immune-mediated epidermal hyperplasia. Gordon WM; Zeller MD; Klein RH; Swindell WR; Ho H; Espetia F; Gudjonsson JE; Baldi PF; Andersen B J Clin Invest; 2014 Dec; 124(12):5205-18. PubMed ID: 25347468 [TBL] [Abstract][Full Text] [Related]
14. The Grainyhead-like epithelial transactivator Get-1/Grhl3 regulates epidermal terminal differentiation and interacts functionally with LMO4. Yu Z; Lin KK; Bhandari A; Spencer JA; Xu X; Wang N; Lu Z; Gill GN; Roop DR; Wertz P; Andersen B Dev Biol; 2006 Nov; 299(1):122-36. PubMed ID: 16949565 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. The epidermis of grhl3-null mice displays altered lipid processing and cellular hyperproliferation. Ting SB; Caddy J; Wilanowski T; Auden A; Cunningham JM; Elias PM; Holleran WM; Jane SM Organogenesis; 2005 Apr; 2(2):33-5. PubMed ID: 19521564 [TBL] [Abstract][Full Text] [Related]
17. Inositol- and folate-resistant neural tube defects in mice lacking the epithelial-specific factor Grhl-3. Ting SB; Wilanowski T; Auden A; Hall M; Voss AK; Thomas T; Parekh V; Cunningham JM; Jane SM Nat Med; 2003 Dec; 9(12):1513-9. PubMed ID: 14608380 [TBL] [Abstract][Full Text] [Related]
18. Loss of Grhl3 is correlated with altered cellular protrusions in the non-neural ectoderm during neural tube closure. Jaffe E; Niswander L Dev Dyn; 2021 May; 250(5):732-744. PubMed ID: 33378081 [TBL] [Abstract][Full Text] [Related]
19. Mice lacking the conserved transcription factor Grainyhead-like 3 (Grhl3) display increased apposition of the frontal and parietal bones during embryonic development. Goldie SJ; Arhatari BD; Anderson P; Auden A; Partridge DD; Jane SM; Dworkin S BMC Dev Biol; 2016 Oct; 16(1):37. PubMed ID: 27756203 [TBL] [Abstract][Full Text] [Related]
20. Spatial and temporal expression of the Grainyhead-like transcription factor family during murine development. Auden A; Caddy J; Wilanowski T; Ting SB; Cunningham JM; Jane SM Gene Expr Patterns; 2006 Oct; 6(8):964-70. PubMed ID: 16831572 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]