| 1 | PHOX2A, PHOX2B
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| Ongoing roles of Phox2 homeodomain transcription factors during neuronal differentiation.
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| Coppola E, d'Autréaux F, Rijli FM, Brunet JF.
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| Development 137(24):4211-20. Epub 2010 Nov 10.
2010
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| 2 | PHOX2A, CHRNA3
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| Transcription factor PHOX2A regulates the human alpha3 nicotinic receptor subunit gene promoter.
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| Benfante R, Flora A, Di Lascio S, Cargnin F, Longhi R, Colombo S, Clementi F, Fornasari D.
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| J Biol Chem 282(18):13290-302. Epub 2007 Mar 7. 2007
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| 3 | TLX2, PHOX2A, PHOX2B
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| Transcriptional regulation of TLX2 and impaired intestinal innervation: possible role of the PHOX2A and PHOX2B genes.
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| Borghini S, Di Duca M, Santamaria G, Vargiolu M, Bachetti T, Cargnin F, Pini Prato A, De Giorgio R, Lerone M, Stanghellini V, Jasonni V, Fornasari D, Ravazzolo R, Ceccherini I.
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| Eur J Hum Genet 15(8):848-55. Epub 2007 May 16. 2007
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| 4 | PHOX2A, FEOM2
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| Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations in PHOX2A.
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| Bosley TM, Oystreck DT, Robertson RL, al Awad A, Abu-Amero K, Engle EC.
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| Brain 129(Pt 9):2363-74. Epub 2006 Jun 30. 2006
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| 5 | PHOX2A, FEOM2
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| ARIX gene polymorphisms in patients with congenital superior oblique muscle palsy.
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| Jiang Y, Matsuo T, Fujiwara H, Hasebe S, Ohtsuki H, Yasuda T.
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| Br J Ophthalmol 88(2):263-7. 2004
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| 6 | PHOX2A, FEOM2
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| A novel PHOX2A/ARIX mutation in an Iranian family with congenital fibrosis of extraocular muscles type 2 (CFEOM2).
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| Yazdani A, Chung DC, Abbaszadegan MR, Al-Khayer K, Chan WM, Yazdani M, Ghodsi K, Engle EC, Traboulsi EI.
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| Am J Ophthalmol 136(5):861-5. 2003
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| 7 | PHOX2A, DBH
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| The paired-like homeodomain protein, Arix, mediates protein kinase A-stimulated dopamine beta-hydroxylase gene transcription through its phosphorylation status.
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| Adachi M, Lewis EJ.
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| J Biol Chem 277(25):22915-24. 2002
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| 8 | PHOX2A, PHOX2B
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| Sp proteins and Phox2b regulate the expression of the human Phox2a gene.
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| Flora A, Lucchetti H, Benfante R, Goridis C, Clementi F, Fornasari D.
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| J Neurosci 21(18):7037-45. 2001
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| 9 | FEOM2, PHOX2A
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| Homozygous mutations in ARIX(PHOX2A) result in congenital fibrosis of the extraocular muscles type 2.
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| Nakano M, Yamada K, Fain J, Sener EC, Selleck CJ, Awad AH, Zwaan J, Mullaney PB, Bosley TM, Engle EC.
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| Nat Genet 29(3):315-20. 2001
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| 10 | PHOX2A
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| Mutations in mouse Aristaless-like4 cause Strong's luxoid polydactyly.
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| Qu S, et al.
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| Development 125(14):2711-21. 1998
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| 11 | ART2P, KRTAP5-9, OMP, TYR, PHOX2A
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| A 5.5-Mb high-resolution integrated map of distal 11q13.
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| Merscher S, et al.
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| Genomics 39 : 340-347. 1997
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| 12 | PHOX2A
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| Polydactyly and ectopic ZPA formation in Alx-4 mutant mice.
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| Qu S, et al.
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| Development 124(20):3999-4008. 1997
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| 13 | PHOX2A
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| Mapping of the ARIX homeodomain gene to mouse chromosome 7 and human chromosome 11q13.
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| Johnson KR, et al.
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| Genomics 33 : 527-531. 1996
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| 14 | CUX1, PHOX2A
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| The mouse homeodomain protein Phox2 regulates Ncam promoter activity in concert with Cux/CDP and is a putative determinant of neurotransmitter phenotype.
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| ValarchŽ I, et al.
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| Development 119 : 881-896. 1993
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