|
1
|
Parkin DM, Bray F, Ferlay J and Pisani P:
Global cancer statistics, 2002. CA Cancer J Clin. 55:74–108. 2005.
View Article : Google Scholar : PubMed/NCBI
|
|
2
|
Landis SH, Murray T, Bolden S and Wingo
PA: Cancer statistics, 1999. CA Cancer J Clin. 49:8–31. 1999.
View Article : Google Scholar : PubMed/NCBI
|
|
3
|
Wu A: Epidemiological analysis of
gynecological malignant carcinoma. Bulletin of Chinese Cancer.
6:3–5. 1997.(In Chinese).
|
|
4
|
Weinberg RA: Tumor suppressor genes.
Science. 254:1138–1146. 1991. View Article : Google Scholar : PubMed/NCBI
|
|
5
|
Mears AJ, Jordan T, Mirzayans F, Dubois S,
Kume T, Parlee M, Ritch R, Koop B, Kuo WL, Collins C, et al:
Mutations of the forkhead/winged-helix gene, FKHL7, in patients
with Axenfeld-Rieger anomaly. Am J Hum Genet. 63:1316–1328. 1998.
View Article : Google Scholar : PubMed/NCBI
|
|
6
|
Nishimura DY, Swiderski RE, Alward WL,
Searby CC, Patil SR, Bennet SR, Kanis AB, Gastier JM, Stone EM and
Sheffield VC: The forkhead transcription factor gene FKHL7 is
responsible for glaucoma phenotypes which map to 6p25. Nat Genet.
19:140–147. 1998. View
Article : Google Scholar : PubMed/NCBI
|
|
7
|
Lai E, Clark KL, Burley SK and Darnell JE
Jr: Hepatocyte nuclear factor 3/fork head or ‘winged helix’
proteins. A family of transcription factors of diverse biologic
function. Proc Natl Acad Sci USA. 90:10421–10423. 1993. View Article : Google Scholar : PubMed/NCBI
|
|
8
|
Xuan S, Baptista CA, Balas G, Tao W,
Soares VC and Lai E: Winged helix transcription factor BF-1 is
essential for the development of the cerebral hemispheres. Neuron.
14:1141–1152. 1995. View Article : Google Scholar : PubMed/NCBI
|
|
9
|
Kume T, Jiang H, Topczewska JM and Hogan
BL: The murine winged helix transcription factors, Foxc1 and Foxc2,
are both required for cardiovascular development and somitogenesis.
Genes Dev. 15:2470–2482. 2001. View Article : Google Scholar : PubMed/NCBI
|
|
10
|
Shu W, Yang H, Zhang L, Lu MM and Morrisey
EE: Characterization of a new subfamily of winged-helix/forkhead
(Fox) genes that are expressed in the lung and act as
transcriptional repressors. J Biol Chem. 276:27488–27497. 2001.
View Article : Google Scholar : PubMed/NCBI
|
|
11
|
Hatini V, Huh SO, Herzlinger D, Soares VC
and Lai E: Essential role of stromal mesenchyme in kidney
morphogenesis revealed by targeted disruption of Winged Helix
transcription factor BF-2. Genes Dev. 10:1467–1478. 1996.
View Article : Google Scholar : PubMed/NCBI
|
|
12
|
Lehmann OJ, Sowden JC, Carlsson P, Jordan
T and Bhattacharya SS: Fox's in development and disease. Trends
Genet. 19:339–344. 2003. View Article : Google Scholar : PubMed/NCBI
|
|
13
|
Ang SL and Rossant J: HNF-3 beta is
essential for node and notochord formation in mouse development.
Cell. 78:561–574. 1994. View Article : Google Scholar : PubMed/NCBI
|
|
14
|
Brody SL, Yan XH, Wuerffel MK, Song SK and
Shapiro SD: Ciliogenesis and left-right axis defects in forkhead
factor HFH-4-null mice. Am J Respir Cell Mol Biol. 23:45–51. 2000.
View Article : Google Scholar : PubMed/NCBI
|
|
15
|
Pierrou S, Hellqvist M, Samuelsson L,
Enerbäck S and Carlsson P: Cloning and characterization of seven
human forkhead proteins, binding site specificity and DNA bending.
Embo J. 13:5002–5012. 1994.PubMed/NCBI
|
|
16
|
Gould DB, Mears AJ, Pearce WG and Walter
MA: Autosomal dominant Axenfeld-Rieger anomaly maps to 6p25. Am J
Hum Genet. 61:765–768. 1997. View
Article : Google Scholar : PubMed/NCBI
|
|
17
|
Mirzayans F, Mears AJ, Guo SW, Pearce WG
and Walter MA: Identification of the human chromosomal region
containing the iridogoniodysgenesis anomaly locus by
genomic-mismatch scanning. Am J Hum Genet. 61:111–119. 1997.
View Article : Google Scholar : PubMed/NCBI
|
|
18
|
Kume T, Deng KY, Winfrey V, Gould DB,
Walter MA and Hogan BL: The forkhead/winged helix gene Mf1 is
disrupted in the pleiotropic mouse mutation congenital
hydrocephalus. Cell. 93:985–996. 1998. View Article : Google Scholar : PubMed/NCBI
|
|
19
|
Winnier GE, Kume T, Deng K, Rogers R,
Bundy J, Raines C, Walter MA, Hogan BL and Conway SJ: Roles for the
winged helix transcription factors MF1 and MFH1 in cardiovascular
development revealed by nonallelic noncomplementation of null
alleles. Dev Biol. 213:418–431. 1999. View Article : Google Scholar : PubMed/NCBI
|
|
20
|
Carlsson P and Mahlapuu M: Forkhead
transcription factors: Key players in development and metabolism.
Dev Biol. 250:1–23. 2002. View Article : Google Scholar : PubMed/NCBI
|
|
21
|
Swiderski RE, Reiter RS, Nishimura DY,
Alward WL, Kalenak JW, Searby CS, Stone EM, Sheffield VC and Lin
JJ: Expression of the Mf1 gene in developing mouse hearts,
Implication in the development of human congenital heart defects.
Dev Dyn. 216:16–27. 1999. View Article : Google Scholar : PubMed/NCBI
|
|
22
|
Lehmann OJ, Ebenezer ND, Jordan T, Fox M,
Ocaka L, Payne A, Leroy BP, Clark BJ, Hitchings RA, Povey S, et al:
Chromosomal duplication involving the forkhead transcription factor
gene FOXC1 causes iris hypoplasia and glaucoma. Am J Hum Genet.
67:1129–1135. 2000. View Article : Google Scholar : PubMed/NCBI
|
|
23
|
van der Heul-Nieuwenhuijsen L, Dits NF and
Jenster G: Gene expression of forkhead transcription factors in the
normal and diseased human prostate. Bju Int. 103:1574–1580. 2009.
View Article : Google Scholar : PubMed/NCBI
|
|
24
|
Zhou Y, Kato H, Asanoma K, Kondo H, Arima
T, Kato K, Matsuda T and Wake N: Identification of FOXC1 as a
TGF-beta1 responsive gene and its involvement in negative
regulation of cell growth. Genomics. 80:465–472. 2002. View Article : Google Scholar : PubMed/NCBI
|
|
25
|
Kaku T, Ogawa S, Kawano Y, Ohishi Y,
Kobayashi H, Hirakawa T and Nakano H: Histological classification
of ovarian cancer. Med Electron Microsc. 36:9–17. 2003. View Article : Google Scholar : PubMed/NCBI
|
|
26
|
Benedet JL, Bender H, Jones H III, Ngan HY
and Pecorelli S: FIGO staging classifications and clinical practice
guidelines in the management of gynecologic cancers. FIGO Committee
on Gynecologic Oncology. Int J Gynaecol Obstet. 70:209–262. 2000.
View Article : Google Scholar : PubMed/NCBI
|
|
27
|
Saleem RA, Banerjee-Basu S, Berry FB,
Baxevanis AD and Walter MA: Analyses of the effects that
disease-causing missense mutations have on the structure and
function of the winged-helix protein FOXC1. Am J Hum Genet.
68:627–641. 2001. View
Article : Google Scholar : PubMed/NCBI
|
|
28
|
Saleem RA, Banerjee-Basu S, Murphy TC,
Baxevanis A and Walter MA: Essential structural and functional
determinants within the forkhead domain of FOXC1. Nucleic Acids
Res. 32:4182–4193. 2004. View Article : Google Scholar : PubMed/NCBI
|
|
29
|
Saleem RA, Banerjee-Basu S, Berry FB,
Baxevanis AD and Walter MA: Structural and functional analyses of
disease-causing missense mutations in the forkhead domain of FOXC1.
Hum Mol Genet. 12:2993–3005. 2003. View Article : Google Scholar : PubMed/NCBI
|
|
30
|
Berry FB, Saleem RA and Walter MA: FOXC1
transcriptional regulation is mediated by N- and C-terminal
activation domains and contains a phosphorylated transcriptional
inhibitory domain. J Biol Chem. 277:10292–10297. 2002. View Article : Google Scholar : PubMed/NCBI
|
|
31
|
Brunet A, Bonni A, Zigmond MJ, Lin MZ, Juo
P, Hu LS, Anderson MJ, Arden KC, Blenis J and Greenberg ME: Akt
promotes cell survival by phosphorylating and inhibiting a Forkhead
transcription factor. Cell. 96:857–868. 1999. View Article : Google Scholar : PubMed/NCBI
|
