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Items: 1 to 20 of 36

1.

PAX1 Methylation as a Potential Biomarker to Predict the Progression of Cervical Intraepithelial Neoplasia: A Meta-analysis of Related Studies.

Luan T, Hua Q, Liu X, Xu P, Gu Y, Qian H, Yan L, Xu X, Geng R, Zeng X, Li P.

Int J Gynecol Cancer. 2017 Sep;27(7):1480-1488. doi: 10.1097/IGC.0000000000001011.

PMID:
28472814
2.

Paired boxed gene 1 expression: A single potential biomarker for differentiating endometrial lesions associated with favorable outcomes in patients with endometrial carcinoma.

Liu LC, Lai HC, Chou YC, Huang RL, Yu MH, Lin CP, Tsai WC, Chiang KJ, Wang YC, Chao TK.

J Obstet Gynaecol Res. 2016 Sep;42(9):1159-67. doi: 10.1111/jog.13040. Epub 2016 May 26.

PMID:
27226215
3.
4.

PAX1 methylation as an auxiliary biomarker for cervical cancer screening: a meta-analysis.

Nikolaidis C, Nena E, Panagopoulou M, Balgkouranidou I, Karaglani M, Chatzaki E, Agorastos T, Constantinidis TC.

Cancer Epidemiol. 2015 Oct;39(5):682-6. doi: 10.1016/j.canep.2015.07.008. Epub 2015 Jul 30.

PMID:
26234429
5.

PAX1 methylation as a potential biomarker for cervical cancer screening.

Kan YY, Liou YL, Wang HJ, Chen CY, Sung LC, Chang CF, Liao CI.

Int J Gynecol Cancer. 2014 Jun;24(5):928-34. doi: 10.1097/IGC.0000000000000155.

PMID:
24844223
6.
7.

DNA methylation of PAX1 as a biomarker for oral squamous cell carcinoma.

Huang YK, Peng BY, Wu CY, Su CT, Wang HC, Lai HC.

Clin Oral Investig. 2014 Apr;18(3):801-8. doi: 10.1007/s00784-013-1048-6. Epub 2013 Aug 2.

PMID:
23907469
8.

A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome.

Pohl E, Aykut A, Beleggia F, Karaca E, Durmaz B, Keupp K, Arslan E, Palamar M, Yigit G, Özkinay F, Wollnik B.

Hum Genet. 2013 Nov;132(11):1311-20. doi: 10.1007/s00439-013-1337-9. Epub 2013 Jul 13. Erratum in: Hum Genet. 2013 Nov;132(11):1321. Onay, Melis Palamar [corrected to Palamar, Melis].

PMID:
23851939
9.

Quantitative analysis of methylation status of the PAX1 gene for detection of cervical cancer.

Huang TH, Lai HC, Liu HW, Lin CJ, Wang KH, Ding DC, Chu TY.

Int J Gynecol Cancer. 2010 May;20(4):513-9. doi: 10.1111/IGC.0b013e3181c7fe6e.

PMID:
20442585
10.

[Association of PAX1 gene polymorphisms with susceptibility to congenital scoliosis in Chinese Han population].

Fei Q, Wu ZH, Yuan SM, Wang H, Zhou X, Liu Z, Song HF, Yin RF, Wang YP, Qiu GX.

Zhonghua Yi Xue Za Zhi. 2008 Oct 14;88(37):2597-602. Chinese.

PMID:
19080705
11.

An analysis of PAX1 in the development of vertebral malformations.

Giampietro PF, Raggio CL, Reynolds CE, Shukla SK, McPherson E, Ghebranious N, Jacobsen FS, Kumar V, Faciszewski T, Pauli RM, Rasmussen K, Burmester JK, Zaleski C, Merchant S, David D, Weber JL, Glurich I, Blank RD.

Clin Genet. 2005 Nov;68(5):448-53.

PMID:
16207213
12.

Mutations in PAX1 may be associated with Klippel-Feil syndrome.

McGaughran JM, Oates A, Donnai D, Read AP, Tassabehji M.

Eur J Hum Genet. 2003 Jun;11(6):468-74.

13.

Human PAX gene expression and development of the vertebral column.

Smith CA, Tuan RS.

Clin Orthop Relat Res. 1994 May;(302):241-50.

PMID:
7909508
14.
15.

DNA Methylation Status of PAX1 and ZNF582 in Esophageal Squamous Cell Carcinoma.

Huang J, Wang G, Tang J, Zhuang W, Wang LP, Liou YL, Liu YZ, Zhou HH, Zhu YS.

Int J Environ Res Public Health. 2017 Feb 22;14(2). pii: E216. doi: 10.3390/ijerph14020216.

16.

Hypermethylated ZNF582 and PAX1 are effective biomarkers for detection of oral dysplasia and oral cancer.

Cheng SJ, Chang CF, Lee JJ, Chen HM, Wang HJ, Liou YL, Yen C, Chiang CP.

Oral Oncol. 2016 Nov;62:34-43. doi: 10.1016/j.oraloncology.2016.09.007. Epub 2016 Oct 6.

PMID:
27865370
17.

PAX1/SOX1 DNA methylation and cervical neoplasia detection: a Taiwanese Gynecologic Oncology Group (TGOG) study.

Lai HC, Ou YC, Chen TC, Huang HJ, Cheng YM, Chen CH, Chu TY, Hsu ST, Liu CB, Hung YC, Wen KC, Yu MH, Wang KL.

Cancer Med. 2014 Aug;3(4):1062-74. doi: 10.1002/cam4.253. Epub 2014 May 3.

18.

Susceptibility variants for male-pattern baldness on chromosome 20p11.

Hillmer AM, Brockschmidt FF, Hanneken S, Eigelshoven S, Steffens M, Flaquer A, Herms S, Becker T, Kortüm AK, Nyholt DR, Zhao ZZ, Montgomery GW, Martin NG, Mühleisen TW, Alblas MA, Moebus S, Jöckel KH, Bröcker-Preuss M, Erbel R, Reinartz R, Betz RC, Cichon S, Propping P, Baur MP, Wienker TF, Kruse R, Nöthen MM.

Nat Genet. 2008 Nov;40(11):1279-81. doi: 10.1038/ng.228. Epub 2008 Oct 12.

PMID:
18849994
19.

Diaphanospondylodysostosis: six new cases and exclusion of the candidate genes, PAX1 and MEOX1.

Vatanavicharn N, Graham JM Jr, Curry CJ, Pepkowitz S, Lachman RS, Rimoin DL, Wilcox WR.

Am J Med Genet A. 2007 Oct 1;143A(19):2292-302.

PMID:
17764081
20.

Aberrant Pax1 and Pax9 expression in Jarcho-Levin syndrome: report of two Caucasian siblings and literature review.

Bannykh SI, Emery SC, Gerber JK, Jones KL, Benirschke K, Masliah E.

Am J Med Genet A. 2003 Jul 15;120A(2):241-6. Review.

PMID:
12833407

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