PubMed for id: 1677473082

Year	Number of Results
1992	3
1993	1
1999	2
2001	1
2006	1
2022	1
2023	1
2024	2

1

Comparative study on the expression of Pax3, Rad51 and VEGF-C in esophageal gastric junction adenocarcinoma and distal gastric adenocarcinoma.

Pan Q, Liu X, Xu C, Yu C. Pan Q, et al. Cell Mol Biol (Noisy-le-grand). 2024 Jan 31;70(1):40-45. doi: 10.14715/cmb/2024.70.1.6. Cell Mol Biol (Noisy-le-grand). 2024. PMID: 38372116

2

PAX3 mutation suppress otic progenitors proliferation and induce apoptosis by inhibiting WNT1/β-catenin signaling pathway in WS1 patient iPSC-derived inner ear organoids.

Li S, He C, Mei L, Wu X, Feng Y, Song J. Li S, et al. Biochem Biophys Res Commun. 2024 Feb 26;698:149510. doi: 10.1016/j.bbrc.2024.149510. Epub 2024 Jan 13. Biochem Biophys Res Commun. 2024. PMID: 38278051

3

PAX3-FOXO1 dictates myogenic reprogramming and rhabdomyosarcoma identity in endothelial progenitors.

Searcy MB, Larsen RK 4th, Stevens BT, Zhang Y, Jin H, Drummond CJ, Langdon CG, Gadek KE, Vuong K, Reed KB, Garcia MR, Xu B, Kimbrough DW, Adkins GE, Djekidel N, Porter SN, Schreiner PA, Pruett-Miller SM, Abraham BJ, Rehg JE, Hatley ME. Searcy MB, et al. Nat Commun. 2023 Nov 15;14(1):7291. doi: 10.1038/s41467-023-43044-1. Nat Commun. 2023. PMID: 37968277 Free PMC article.

4

Waardenburg Syndrome Type I.

Milunsky JM. Milunsky JM. 2001 Jul 30 [updated 2022 Oct 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2001 Jul 30 [updated 2022 Oct 20]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301703 Free Books & Documents. Review.

5

Functional analysis of alternative isoforms of the transcription factor PAX3 in melanocytes in vitro.

Wang Q, Kumar S, Slevin M, Kumar P. Wang Q, et al. Cancer Res. 2006 Sep 1;66(17):8574-80. doi: 10.1158/0008-5472.CAN-06-0947. Cancer Res. 2006. PMID: 16951170

6

PAX3 gene structure, alternative splicing and evolution.

Barber TD, Barber MC, Cloutier TE, Friedman TB. Barber TD, et al. Gene. 1999 Sep 17;237(2):311-9. doi: 10.1016/s0378-1119(99)00339-x. Gene. 1999. PMID: 10521655

7

Functional characterization of the human PAX3 gene regulatory region.

Okladnova O, Syagailo YV, Tranitz M, Riederer P, Stöber G, Mössner R, Lesch KP. Okladnova O, et al. Genomics. 1999 Apr 1;57(1):110-9. doi: 10.1006/geno.1998.5711. Genomics. 1999. PMID: 10191090

8

Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene.

Tassabehji M, Read AP, Newton VE, Harris R, Balling R, Gruss P, Strachan T. Tassabehji M, et al. Nature. 1992 Feb 13;355(6361):635-6. doi: 10.1038/355635a0. Nature. 1992. PMID: 1347148

9

Waardenburg syndrome associated with meningomyelocele.

Carezani-Gavin M, Clarren SK, Steege T. Carezani-Gavin M, et al. Am J Med Genet. 1992 Jan 1;42(1):135-6. doi: 10.1002/ajmg.1320420127. Am J Med Genet. 1992. PMID: 1308353 No abstract available.

10

A frameshift mutation in the HuP2 paired domain of the probable human homolog of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indonesian family.

Morell R, Friedman TB, Moeljopawiro S, Hartono, Soewito, Asher JH Jr. Morell R, et al. Hum Mol Genet. 1992 Jul;1(4):243-7. doi: 10.1093/hmg/1.4.243. Hum Mol Genet. 1992. PMID: 1303193

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