Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1SALEEM, Ramsey A; BANERJEE-BASU, Sharmila; BERRY, Fred B et al.Human molecular genetics (Print). 2003, Vol 12, Num 22, pp 2993-3005, issn 0964-6906, 13 p.Article

Axenfeld—Rieger Anomaly and Axenfeld—Rieger Syndrome: Clinical, Molecular-Cytogenetic, and DNA Array Analyses of Three Patients With Chromosomal Defects at 6p25TONOKI, Hidefumi; HARADA, Naoki; SHIMOKAWA, Osamu et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 12, pp 2925-2932, issn 1552-4825, 8 p.Article

Clinical report. Absence of PITX2, BARX1, and FOXC1 mutations in De Hauwere syndrome (Axenfeld-Rieger anomaly, hydrocephaly, hearing loss): A 25-year follow upLOWRY, R. Brian; GOULD, Douglas B; WALTER, Michael A et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 11, pp 1227-1230, issn 1552-4825, 4 p.Article

Molecular and developmental mechanisms of anterior segment dysgenesisSOWDEN, J. C.Eye (London. 1987). 2007, Vol 21, Num 10, pp 1310-1318, issn 0950-222X, 9 p.Conference Paper

Iris development in vertebrates; genetic and molecular considerationsDAUIS-SILBERMAN, Noa; ASHERY-PADAN, Ruth.Brain research. 2008, Vol 1192, pp 17-28, issn 0006-8993, 12 p.Article

Dysregulation of microRNA-204 mediates migration and invasion of endometrial cancer by regulating FOXC1CHUNG, T. K. H; LAU, T. S; BARROILHET, L. M et al.International journal of cancer (Print). 2012, Vol 130, Num 5, pp 1036-1045, issn 0020-7136, 10 p.Article

PITX2 and FOXC1 spectrum of mutations in ocular syndromesREIS, Linda M; TYLER, Rebecca C; SEMINA, Elena V et al.European journal of human genetics. 2012, Vol 20, Num 12, pp 1224-1233, issn 1018-4813, 10 p.Article

A Complex 6p25 Rearrangement in a Child With Multiple Epiphyseal DysplasiaBEDOYAN, Jirair K; LESPERANCE, Marci M; ACKLEY, Todd et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 1, pp 154-163, issn 1552-4825, 10 p.Article

FOXC1 Is Enriched in the Mammary Luminal Progenitor Population, but Is Not Necessary for Mouse Mammary Ductal MorphogenesisSIZEMORE, Gina M; SIZEMORE, Steven T; PAL, Bhupinder et al.Biology of reproduction. 2013, Vol 89, Num 1, issn 0006-3363, 10.1-10.10Article

Pre- and Postnatal Phenotype of 6p25 Deletions Involving the FOXC1 GeneDELAHAYE, Andrée; KHUNG-SAVATOVSKY, Suonavy; HUEL, Chan et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 10, pp 2430-2438, issn 1552-4825, 9 p.Article

A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomalyWEISSCHUH, N; WOLF, C; WISSINGER, B et al.Clinical genetics. 2008, Vol 74, Num 5, pp 476-480, issn 0009-9163, 5 p.Article

A 12 Mb deletion of 6p24.1 → pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneysCHEN, Chih-Ping; TZEN, Chin-Yuan; CHERN, Schu-Rern et al.European journal of medical genetics. 2009, Vol 52, Num 1, pp 59-61, issn 1769-7212, 3 p.Article

Exclusion of a PAX6, FOXC1, PITX2, and MYCN Mutation in Another Patient With Apple Peel Intestinal Atresia, Ocular Anomalies and Microcephaly and Review of the LiteratureVAN BEVER, Yolande; VAN HEST, Liselotte; WOLFS, Roger et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 4, pp 500-504, issn 1552-4825, 5 p.Article

Subtelomeric deletions of chromosome 6p : Molecular and cytogenetic characterization of three new cases with phenotypic overlap with ritscher-schinzel (3C) syndromeDESCIPIO, Cheryl; SCHNEIDER, Lori; MENON, Ammini et al.American journal of medical genetics. 2005, Vol 134A, Num 1, pp 3-11, issn 0148-7299, 9 p.Article

FOXC1, a target of polycomb, inhibits metastasis of breast cancer cellsJUAN DU; LIN LI; JUN LU et al.Breast cancer research and treatment. 2012, Vol 131, Num 1, pp 65-73, issn 0167-6806, 9 p.Article

Subtelomeric 6p deletion : Clinical, FISH, and array CGH characterization of two casesLE CAIGNEC, Cédric; DE MAS, Philippe; VINCENT, Marie-Claire et al.American journal of medical genetics. 2005, Vol 132A, Num 2, pp 175-180, issn 0148-7299, 6 p.Article

Identification of FOXC1 as a TGF-β1 responsive gene and its involvement in negative regulation of cell growthYONG ZHOU; KATO, Hidenori; ASANOMA, Kazuo et al.Genomics (San Diego, Calif.). 2002, Vol 80, Num 5, pp 465-472, issn 0888-7543, 8 p.Article

Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1SALEEM, Ramsey A; BANERJEE-BASU, Sharmila; BERRY, Fred B et al.American journal of human genetics. 2001, Vol 68, Num 3, pp 627-641, issn 0002-9297Article

Chromosomal duplication involving the forkhead transcription factor gene FOXC1 causes iris hypoplasia and glaucomaLEHMANN, Ordan J; EBENEZER, Neil D; KHAW, Peng T et al.American journal of human genetics. 2000, Vol 67, Num 5, pp 1129-1135, issn 0002-9297Article

Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletionsLEHMANN, Ordan J; EBENEZER, Neil D; POVEY, Sue et al.Investigative ophthalmology & visual science. 2002, Vol 43, Num 6, pp 1843-1849, issn 0146-0404Article

Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairmentANDERLID, Britt-Marie; SCHOUMANS, Jacqueline; HALLQVIST, Asa et al.European journal of human genetics. 2003, Vol 11, Num 1, pp 89-92, issn 1018-4813, 4 p.Article

Molecular genetics of Axenfeld-Rieger malformationsLINES, Matthew A; KOZLOWSKI, Kathy; WALTER, Michael A et al.Human molecular genetics (Print). 2002, Vol 11, Num 10, pp 1177-1184, issn 0964-6906Article

Array-CGH and Clinical Characterization in a Patient With Subtelomeric 6p Deletion Without Ocular DysgenesisPICCIONE, Maria; ANTONA, R; SALZANO, E et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 1, pp 150-154, issn 1552-4825, 5 p.Article

Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular developmentSMITH, R. S; ZABALETA, A; KUME, T et al.Human molecular genetics (Print). 2000, Vol 9, Num 7, pp 1021-1032, issn 0964-6906Article