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Items: 1 to 20 of 78

1.

Genome-wide association analysis identifies TXNRD2, ATXN2 and FOXC1 as susceptibility loci for primary open-angle glaucoma.

Bailey JN, Loomis SJ, Kang JH, Allingham RR, Gharahkhani P, Khor CC, Burdon KP, Aschard H, Chasman DI, Igo RP Jr, Hysi PG, Glastonbury CA, Ashley-Koch A, Brilliant M, Brown AA, Budenz DL, Buil A, Cheng CY, Choi H, Christen WG, Curhan G, De Vivo I, Fingert JH, Foster PJ, Fuchs C, Gaasterland D, Gaasterland T, Hewitt AW, Hu F, Hunter DJ, Khawaja AP, Lee RK, Li Z, Lichter PR, Mackey DA, McGuffin P, Mitchell P, Moroi SE, Perera SA, Pepper KW, Qi Q, Realini T, Richards JE, Ridker PM, Rimm E, Ritch R, Ritchie M, Schuman JS, Scott WK, Singh K, Sit AJ, Song YE, Tamimi RM, Topouzis F, Viswanathan AC, Verma SS, Vollrath D, Wang JJ, Weisschuh N, Wissinger B, Wollstein G, Wong TY, Yaspan BL, Zack DJ, Zhang K, Study EN; ANZRAG Consortium, Weinreb RN, Pericak-Vance MA, Small K, Hammond CJ, Aung T, Liu Y, Vithana EN, MacGregor S, Craig JE, Kraft P, Howell G, Hauser MA, Pasquale LR, Haines JL, Wiggs JL.

Nat Genet. 2016 Feb;48(2):189-94. doi: 10.1038/ng.3482. Epub 2016 Jan 11.

2.

Forkhead box transcription factors in embryonic heart development and congenital heart disease.

Zhu H.

Life Sci. 2016 Jan 1;144:194-201. doi: 10.1016/j.lfs.2015.12.001. Epub 2015 Dec 2. Review.

PMID:
26656470
3.

miR-4792 inhibits epithelial-mesenchymal transition and invasion in nasopharyngeal carcinoma by targeting FOXC1.

Li Y, Chen X.

Biochem Biophys Res Commun. 2015 Dec 25;468(4):863-9. doi: 10.1016/j.bbrc.2015.11.045. Epub 2015 Nov 14.

PMID:
26585487
4.

Aberrantly Expressed OTX Homeobox Genes Deregulate B-Cell Differentiation in Hodgkin Lymphoma.

Nagel S, Ehrentraut S, Meyer C, Kaufmann M, Drexler HG, MacLeod RA.

PLoS One. 2015 Sep 25;10(9):e0138416. doi: 10.1371/journal.pone.0138416. eCollection 2015.

5.

A VARIANT CASE OF 6p24 DELETION SYNDROME (OMIM #612582).

Ergin RN, Cigerciogullari E, Alanay Y, Yayla M.

Genet Couns. 2015;26(2):237-41.

PMID:
26349195
6.

Mutation analysis of the genes associated with anterior segment dysgenesis, microcornea and microphthalmia in 257 patients with glaucoma.

Huang X, Xiao X, Jia X, Li S, Li M, Guo X, Liu X, Zhang Q.

Int J Mol Med. 2015 Oct;36(4):1111-7. doi: 10.3892/ijmm.2015.2325. Epub 2015 Aug 24.

PMID:
26310487
7.

FoxC1: Novel Regulator of Inflammation-Induced Metastasis in Hepatocellular Carcinoma.

Aravalli RN, Greten TF.

Gastroenterology. 2015 Oct;149(4):861-3. doi: 10.1053/j.gastro.2015.08.032. Epub 2015 Aug 21. No abstract available.

PMID:
26302490
8.

Interleukin-8 Induces Expression of FOXC1 to Promote Transactivation of CXCR1 and CCL2 in Hepatocellular Carcinoma Cell Lines and Formation of Metastases in Mice.

Huang W, Chen Z, Zhang L, Tian D, Wang D, Fan D, Wu K, Xia L.

Gastroenterology. 2015 Oct;149(4):1053-67.e14. doi: 10.1053/j.gastro.2015.05.058. Epub 2015 Jun 9.

PMID:
26065367
9.

Dual regulation by microRNA-200b-3p and microRNA-200b-5p in the inhibition of epithelial-to-mesenchymal transition in triple-negative breast cancer.

Rhodes LV, Martin EC, Segar HC, Miller DF, Buechlein A, Rusch DB, Nephew KP, Burow ME, Collins-Burow BM.

Oncotarget. 2015 Jun 30;6(18):16638-52.

10.

The critical and specific transcriptional regulator of the microenvironmental niche for hematopoietic stem and progenitor cells.

Omatsu Y, Nagasawa T.

Curr Opin Hematol. 2015 Jul;22(4):330-6. doi: 10.1097/MOH.0000000000000153. Review.

PMID:
26049754
11.

Diagnosis of Basal-Like Breast Cancer Using a FOXC1-Based Assay.

Jensen TW, Ray T, Wang J, Li X, Naritoku WY, Han B, Bellafiore F, Bagaria SP, Qu A, Cui X, Taylor CR, Ray PS.

J Natl Cancer Inst. 2015 Jun 3;107(8). pii: djv148. doi: 10.1093/jnci/djv148. Print 2015 Aug.

PMID:
26041837
12.

Alternatively spliced isoforms of WT1 control podocyte-specific gene expression.

Lefebvre J, Clarkson M, Massa F, Bradford ST, Charlet A, Buske F, Lacas-Gervais S, Schulz H, Gimpel C, Hata Y, Schaefer F, Schedl A.

Kidney Int. 2015 Aug;88(2):321-31. doi: 10.1038/ki.2015.140. Epub 2015 May 20.

PMID:
25993318
13.

Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma.

Pasutto F, Mauri L, Popp B, Sticht H, Ekici A, Piozzi E, Bonfante A, Penco S, Schlötzer-Schrehardt U, Reis A.

Gene. 2015 Aug 15;568(1):76-80. doi: 10.1016/j.gene.2015.05.015. Epub 2015 May 9.

PMID:
25967385
14.

MicroRNA-138-5p regulates pancreatic cancer cell growth through targeting FOXC1.

Yu C, Wang M, Li Z, Xiao J, Peng F, Guo X, Deng Y, Jiang J, Sun C.

Cell Oncol (Dordr). 2015 Jun;38(3):173-81. doi: 10.1007/s13402-014-0200-x. Epub 2015 Feb 10.

15.

Subtelomeric 6p25 deletion/duplication: Report of a patient with new clinical findings and genotype-phenotype correlations.

Linhares ND, Svartman M, Rodrigues TC, Rosenberg C, Valadares ER.

Eur J Med Genet. 2015 May;58(5):310-8. doi: 10.1016/j.ejmg.2015.02.011. Epub 2015 Mar 24.

PMID:
25817395
16.

The Role of hsa-miR-548l Dysregulation as a Putative Modifier Factor for Glaucoma-Associated FOXC1 Mutations.

Medina-Trillo C, Aroca-Aguilar JD, Ferre-Fernández JJ, Méndez-Hernández CD, Morales L, García-Feijoo J, Escribano J.

Microrna. 2015;4(1):50-6.

PMID:
25809640
17.

The transcription factor Foxc1 is necessary for Ihh-Gli2-regulated endochondral ossification.

Yoshida M, Hata K, Takashima R, Ono K, Nakamura E, Takahata Y, Murakami T, Iseki S, Takano-Yamamoto T, Nishimura R, Yoneda T.

Nat Commun. 2015 Mar 26;6:6653. doi: 10.1038/ncomms7653.

PMID:
25808752
18.

Hypo- and hypermorphic FOXC1 mutations in dominant glaucoma: transactivation and phenotypic variability.

Medina-Trillo C, Sánchez-Sánchez F, Aroca-Aguilar JD, Ferre-Fernández JJ, Morales L, Méndez-Hernández CD, Blanco-Kelly F, Ayuso C, García-Feijoo J, Escribano J.

PLoS One. 2015 Mar 18;10(3):e0119272. doi: 10.1371/journal.pone.0119272. eCollection 2015.

19.

Renal complications in 6p duplication syndrome: microarray-based investigation of the candidate gene(s) for the development of congenital anomalies of the kidney and urinary tract (CAKUT) and focal segmental glomerular sclerosis (FSGS).

Yoshimura-Furuhata M, Nishimura-Tadaki A, Amano Y, Ehara T, Hamasaki Y, Muramatsu M, Shishido S, Aikawa A, Hamada R, Ishikura K, Hataya H, Hidaka Y, Noda S, Koike K, Wakui K, Fukushima Y, Matsumoto N, Awazu M, Miyake N, Kosho T.

Am J Med Genet A. 2015 Mar;167A(3):592-601. doi: 10.1002/ajmg.a.36942. Review.

PMID:
25691411
20.

Anirdia-like phenotype caused by 6p25 dosage aberrations.

Sadagopan KA, Liu GT, Capasso JE, Wuthisiri W, Keep RB, Levin AV.

Am J Med Genet A. 2015 Mar;167A(3):524-8. doi: 10.1002/ajmg.a.36890.

PMID:
25691405
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