These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
248 related articles for article (PubMed ID: 11641221)
1. Severe nasal clefting and abnormal embryonic apoptosis in Alx3/Alx4 double mutant mice. Beverdam A; Brouwer A; Reijnen M; Korving J; Meijlink F Development; 2001 Oct; 128(20):3975-86. PubMed ID: 11641221 [TBL] [Abstract][Full Text] [Related]
2. Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene. Twigg SR; Versnel SL; Nürnberg G; Lees MM; Bhat M; Hammond P; Hennekam RC; Hoogeboom AJ; Hurst JA; Johnson D; Robinson AA; Scambler PJ; Gerrelli D; Nürnberg P; Mathijssen IM; Wilkie AO Am J Hum Genet; 2009 May; 84(5):698-705. PubMed ID: 19409524 [TBL] [Abstract][Full Text] [Related]
3. Goosecoid acts cell autonomously in mesenchyme-derived tissues during craniofacial development. Rivera-Pérez JA; Wakamiya M; Behringer RR Development; 1999 Sep; 126(17):3811-21. PubMed ID: 10433910 [TBL] [Abstract][Full Text] [Related]
4. The OAR/aristaless domain of the homeodomain protein Cart1 has an attenuating role in vivo. Brouwer A; ten Berge D; Wiegerinck R; Meijlink F Mech Dev; 2003 Feb; 120(2):241-52. PubMed ID: 12559496 [TBL] [Abstract][Full Text] [Related]
5. Crucial and Overlapping Roles of Six1 and Six2 in Craniofacial Development. Liu Z; Li C; Xu J; Lan Y; Liu H; Li X; Maire P; Wang X; Jiang R J Dent Res; 2019 May; 98(5):572-579. PubMed ID: 30905259 [TBL] [Abstract][Full Text] [Related]
6. Physical and genetic interactions between Alx4 and Cart1. Qu S; Tucker SC; Zhao Q; deCrombrugghe B; Wisdom R Development; 1999 Jan; 126(2):359-69. PubMed ID: 9847249 [TBL] [Abstract][Full Text] [Related]
7. Potocki-Shaffer deletion encompassing ALX4 in a patient with frontonasal dysplasia phenotype. Ferrarini A; Gaillard M; Guerry F; Ramelli G; Heidi F; Keddache CV; Wieland I; Beckmann JS; Jaquemont S; Martinet D Am J Med Genet A; 2014 Feb; 164A(2):346-52. PubMed ID: 24376213 [TBL] [Abstract][Full Text] [Related]
9. Cranial anomaly of homozygous rSey rat is associated with a defect in the migration pathway of midbrain crest cells. Osumi-Yamashita N; Kuratani S; Ninomiya Y; Aoki K; Iseki S; Chareonvit S; Doi H; Fujiwara M; Watanabe T; Eto K Dev Growth Differ; 1997 Feb; 39(1):53-67. PubMed ID: 9079035 [TBL] [Abstract][Full Text] [Related]
10. Defective neural crest migration revealed by a Zebrafish model of Alx1-related frontonasal dysplasia. Dee CT; Szymoniuk CR; Mills PE; Takahashi T Hum Mol Genet; 2013 Jan; 22(2):239-51. PubMed ID: 23059813 [TBL] [Abstract][Full Text] [Related]
11. Alx4 and Msx2 play phenotypically similar and additive roles in skull vault differentiation. Antonopoulou I; Mavrogiannis LA; Wilkie AO; Morriss-Kay GM J Anat; 2004 Jun; 204(6):487-99. PubMed ID: 15198690 [TBL] [Abstract][Full Text] [Related]
12. Lineage-specific requirements of Alx4 function in craniofacial and hair development. Lan Y; Wu Z; Liu H; Jiang R Dev Dyn; 2024 Oct; 253(10):940-948. PubMed ID: 38481039 [TBL] [Abstract][Full Text] [Related]
13. The aristaless-like homeobox protein Alx3 as an etiopathogenic factor for diabetes mellitus. Vallejo M Islets; 2011; 3(2):66-8. PubMed ID: 21350340 [TBL] [Abstract][Full Text] [Related]
14. Embryonic defence mechanisms against glucose-dependent oxidative stress require enhanced expression of Alx3 to prevent malformations during diabetic pregnancy. García-Sanz P; Mirasierra M; Moratalla R; Vallejo M Sci Rep; 2017 Mar; 7(1):389. PubMed ID: 28341857 [TBL] [Abstract][Full Text] [Related]
15. Mouse Alx3: an aristaless-like homeobox gene expressed during embryogenesis in ectomesenchyme and lateral plate mesoderm. ten Berge D; Brouwer A; el Bahi S; Guénet JL; Robert B; Meijlink F Dev Biol; 1998 Jul; 199(1):11-25. PubMed ID: 9676189 [TBL] [Abstract][Full Text] [Related]
16. Hoxb2 and hoxb4 act together to specify ventral body wall formation. Manley NR; Barrow JR; Zhang T; Capecchi MR Dev Biol; 2001 Sep; 237(1):130-44. PubMed ID: 11518511 [TBL] [Abstract][Full Text] [Related]
17. Vertical transmission of a frontonasal phenotype caused by a novel ALX4 mutation. Bertola DR; Rodrigues MG; Quaio CR; Kim CA; Passos-Bueno MR Am J Med Genet A; 2013 Mar; 161A(3):600-4. PubMed ID: 23401352 [TBL] [Abstract][Full Text] [Related]
18. Developmental origin of the mammalian premaxilla. Iyyanar PPR; Qin C; Adhikari N; Liu H; Hu YC; Jiang R; Lan Y Dev Biol; 2023 Nov; 503():1-9. PubMed ID: 37524195 [TBL] [Abstract][Full Text] [Related]
19. Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5. Acampora D; Merlo GR; Paleari L; Zerega B; Postiglione MP; Mantero S; Bober E; Barbieri O; Simeone A; Levi G Development; 1999 Sep; 126(17):3795-809. PubMed ID: 10433909 [TBL] [Abstract][Full Text] [Related]
20. DeltaEF1, a zinc finger and homeodomain transcription factor, is required for skeleton patterning in multiple lineages. Takagi T; Moribe H; Kondoh H; Higashi Y Development; 1998 Jan; 125(1):21-31. PubMed ID: 9389660 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]