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Search results 1 to 100 out of 209 for Foxc1

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Category: Publication
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Type Details Score
Publication
19668217 | J:152710
First Author: Aldinger KA
Year: 2009
Journal: Nat Genet
Title: FOXC1 is required for normal cerebellar development and is a major contributor to chromosome 6p25.3 Dandy-Walker malformation.
Volume: 41
Issue: 9
Pages: 1037-42
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Publication
26912704 | J:229528
First Author: Wang L
Year: 2016
Journal: Science
Title: Foxc1 reinforces quiescence in self-renewing hair follicle stem cells.
Volume: 351
Issue: 6273
Pages: 613-7
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Publication
25513817 | J:266747
   
First Author: Haldipur P
Year: 2014
Journal: Elife
Title: Foxc1 dependent mesenchymal signalling drives embryonic cerebellar growth.
Volume: 3
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Publication
22522965 | J:188816
First Author: Sasman A
Year: 2012
Journal: Genesis
Title: Generation of conditional alleles for Foxc1 and Foxc2 in mice.
Volume: 50
Issue: 10
Pages: 766-74
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Publication
28223138 | J:240396
First Author: Motojima M
Year: 2017
Journal: Exp Cell Res
Title: Foxc1 and Foxc2 are necessary to maintain glomerular podocytes.
Volume: 352
Issue: 2
Pages: 265-272
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Publication
23862012 | J:199438
First Author: Siegenthaler JA
Year: 2013
Journal: Biol Open
Title: Foxc1 is required by pericytes during fetal brain angiogenesis.
Volume: 2
Issue: 7
Pages: 647-59
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Publication
25808752 | J:221866
 
First Author: Yoshida M
Year: 2015
Journal: Nat Commun
Title: The transcription factor Foxc1 is necessary for Ihh-Gli2-regulated endochondral ossification.
Volume: 6
Pages: 6653
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Publication
37154714 | J:337938
First Author: Tan C
Year: 2023
Journal: EMBO Rep
Title: Endothelial FOXC1 and FOXC2 promote intestinal regeneration after ischemia-reperfusion injury.
Volume: 24
Issue: 7
Pages: e56030
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Publication
25733312 | J:221192
First Author: Prasitsak T
Year: 2015
Journal: Dev Dyn
Title: Foxc1 is required for early stage telencephalic vascular development.
Volume: 244
Issue: 5
Pages: 703-11
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Publication
31588228 | J:297206
First Author: Lee YH
Year: 2019
Journal: Theranostics
Title: Role of FOXC1 in regulating APSCs self-renewal via STI-1/PrPC signaling.
Volume: 9
Issue: 22
Pages: 6443-6465
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Publication
38580085 | J:352624
First Author: Wei W
Year: 2024
Journal: Genomics
Title: Variants in FOXC1 and FOXC2 identified in patients with conotruncal heart defects.
Volume: 116
Issue: 3
Pages: 110840
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Publication
29070831 | J:255407
First Author: Gao B
Year: 2017
Journal: Sci Rep
Title: Inhibition of lobuloalveolar development by FOXC1 overexpression in the mouse mammary gland.
Volume: 7
Issue: 1
Pages: 14017
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Publication
24590069 | J:210256
First Author: Omatsu Y
Year: 2014
Journal: Nature
Title: Foxc1 is a critical regulator of haematopoietic stem/progenitor cell niche formation.
Volume: 508
Issue: 7497
Pages: 536-40
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Publication
14512019 | J:85739
First Author: Rice R
Year: 2003
Journal: Dev Biol
Title: Progression of calvarial bone development requires Foxc1 regulation of Msx2 and Alx4.
Volume: 262
Issue: 1
Pages: 75-87
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Publication
27592801 | J:238355
First Author: Cui CY
Year: 2017
Journal: J Invest Dermatol
Title: Foxc1 Ablated Mice Are Anhidrotic and Recapitulate Features of Human Miliaria Sweat Retention Disorder.
Volume: 137
Issue: 1
Pages: 38-45
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Publication
32510325 | J:290955
   
First Author: Norden PR
Year: 2020
Journal: Elife
Title: Shear stimulation of FOXC1 and FOXC2 differentially regulates cytoskeletal activity during lymphatic valve maturation.
Volume: 9
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Publication
22022403 | J:178103
First Author: McKeone R
Year: 2011
Journal: PLoS One
Title: Foxf2: a novel locus for anterior segment dysgenesis adjacent to the Foxc1 gene.
Volume: 6
Issue: 10
Pages: e25489
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Publication
10767326 | J:61775
First Author: Smith RS
Year: 2000
Journal: Hum Mol Genet
Title: Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development.
Volume: 9
Issue: 7
Pages: 1021-32
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Publication
15196959 | J:91443
First Author: Wilm B
Year: 2004
Journal: Dev Biol
Title: The forkhead genes, Foxc1 and Foxc2, regulate paraxial versus intermediate mesoderm cell fate.
Volume: 271
Issue: 1
Pages: 176-89
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Publication
29322554 | J:264474
First Author: Mya N
Year: 2018
Journal: Congenit Anom (Kyoto)
Title: Transcription factor Foxc1 is involved in anterior part of cranial base formation.
Volume: 58
Issue: 5
Pages: 158-166
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Publication
15906377 | J:98808
First Author: Rice R
Year: 2005
Journal: Dev Dyn
Title: Foxc1 integrates Fgf and Bmp signalling independently of twist or noggin during calvarial bone development.
Volume: 233
Issue: 3
Pages: 847-52
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Publication
32259372 | J:302064
First Author: Sanchez J
Year: 2020
Journal: Genesis
Title: Conditional inactivation of Foxc1 and Foxc2 in neural crest cells leads to cardiac abnormalities.
Volume: 58
Issue: 7
Pages: e23364
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Publication
18422524 | J:137357
First Author: Vivatbutsiri P
Year: 2008
Journal: J Anat
Title: Impaired meningeal development in association with apical expansion of calvarial bone osteogenesis in the Foxc1 mutant.
Volume: 212
Issue: 5
Pages: 603-11
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Publication
27214551 | J:237068
First Author: Fatima A
Year: 2016
Journal: J Clin Invest
Title: Foxc1 and Foxc2 deletion causes abnormal lymphangiogenesis and correlates with ERK hyperactivation.
Volume: 126
Issue: 7
Pages: 2437-51
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Publication
23677979 | J:202056
First Author: Sizemore GM
Year: 2013
Journal: Biol Reprod
Title: FOXC1 is enriched in the mammary luminal progenitor population, but is not necessary for mouse mammary ductal morphogenesis.
Volume: 89
Issue: 1
Pages: 10
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Publication
11782474 | J:75459
First Author: Berry FB
Year: 2002
Journal: J Biol Chem
Title: FOXC1 transcriptional regulation is mediated by N- and C-terminal activation domains and contains a phosphorylated transcriptional inhibitory domain.
Volume: 277
Issue: 12
Pages: 10292-7
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Publication
28253399 | J:254700
First Author: Seo S
Year: 2017
Journal: Invest Ophthalmol Vis Sci
Title: Foxc1 and Foxc2 in the Neural Crest Are Required for Ocular Anterior Segment Development.
Volume: 58
Issue: 3
Pages: 1368-1377
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Publication
16412416 | J:105944
First Author: Mattiske D
Year: 2006
Journal: Dev Biol
Title: The mouse forkhead gene Foxc1 is required for primordial germ cell migration and antral follicle development.
Volume: 290
Issue: 2
Pages: 447-58
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Publication
34331943 | J:310856
First Author: Almubarak A
Year: 2021
Journal: J Biol Chem
Title: Loss of Foxc1 and Foxc2 function in chondroprogenitor cells disrupts endochondral ossification.
Volume: 297
Issue: 3
Pages: 101020
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Publication
24385915 | J:223126
First Author: Inman KE
Year: 2013
Journal: PLoS Genet
Title: Interaction between Foxc1 and Fgf8 during mammalian jaw patterning and in the pathogenesis of syngnathia.
Volume: 9
Issue: 12
Pages: e1003949
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Publication
22171010 | J:181974
First Author: Seo S
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Forkhead box transcription factor FoxC1 preserves corneal transparency by regulating vascular growth.
Volume: 109
Issue: 6
Pages: 2015-20
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Publication
16839542 | J:119303
First Author: Seo S
Year: 2006
Journal: Dev Biol
Title: Forkhead transcription factors, Foxc1 and Foxc2, are required for the morphogenesis of the cardiac outflow tract.
Volume: 296
Issue: 2
Pages: 421-36
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Publication
39012257 | J:353623
 
First Author: Almubarak A
Year: 2024
Journal: Development
Title: FOXC1 and FOXC2 regulate growth plate chondrocyte maturation towards hypertrophy in the embryonic mouse limb skeleton.
Volume: 151
Issue: 16
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Publication
24472616 | J:212049
First Author: Silla ZT
Year: 2014
Journal: Exp Cell Res
Title: Signals from the lens and Foxc1 regulate the expression of key genes during the onset of corneal endothelial development.
Volume: 322
Issue: 2
Pages: 381-8
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Publication
23344708 | J:194058
First Author: Sun J
Year: 2013
Journal: Development
Title: Foxc1 controls the growth of the murine frontal bone rudiment by direct regulation of a Bmp response threshold of Msx2.
Volume: 140
Issue: 5
Pages: 1034-44
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Publication
27671872 | J:237944
First Author: Mishra S
Year: 2016
Journal: Dev Biol
Title: Cerebrovascular defects in Foxc1 mutants correlate with aberrant WNT and VEGF-A pathways downstream of retinoic acid from the meninges.
Volume: 420
Issue: 1
Pages: 148-165
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Publication
11562355 | J:71693
First Author: Kume T
Year: 2001
Journal: Genes Dev
Title: The murine winged helix transcription factors, Foxc1 and Foxc2, are both required for cardiovascular development and somitogenesis.
Volume: 15
Issue: 18
Pages: 2470-82
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Publication
16678147 | J:119144
First Author: Seo S
Year: 2006
Journal: Dev Biol
Title: The forkhead transcription factors, Foxc1 and Foxc2, are required for arterial specification and lymphatic sprouting during vascular development.
Volume: 294
Issue: 2
Pages: 458-70
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Publication
10704385 | J:60834
First Author: Kume T
Year: 2000
Journal: Development
Title: Murine forkhead/winged helix genes Foxc1 (Mf1) and Foxc2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract.
Volume: 127
Issue: 7
Pages: 1387-95
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17715063 | J:136459
First Author: Zarbalis K
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: Cortical dysplasia and skull defects in mice with a Foxc1 allele reveal the role of meningeal differentiation in regulating cortical development.
Volume: 104
Issue: 35
Pages: 14002-7
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Publication
28092268 | J:253288
   
First Author: Haldipur P
Year: 2017
Journal: Elife
Title: Phenotypic outcomes in Mouse and Human Foxc1 dependent Dandy-Walker cerebellar malformation suggest shared mechanisms.
Volume: 6
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Publication
11165495 | J:67310
First Author: Topczewska JM
Year: 2001
Journal: Mech Dev
Title: Sequence and expression of zebrafish foxc1a and foxc1b, encoding conserved forkhead/winged helix transcription factors.
Volume: 100
Issue: 2
Pages: 343-7
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Publication
11179011 | J:67859
First Author: Saleem RA
Year: 2001
Journal: Am J Hum Genet
Title: Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1.
Volume: 68
Issue: 3
Pages: 627-41
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Publication
18187037 | J:131323
First Author: Hayashi H
Year: 2008
Journal: Biochem Biophys Res Commun
Title: Forkhead transcription factors regulate expression of the chemokine receptor CXCR4 in endothelial cells and CXCL12-induced cell migration.
Volume: 367
Issue: 3
Pages: 584-9
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Publication
12624268 | J:82280
First Author: Libby RT
Year: 2003
Journal: Science
Title: Modification of ocular defects in mouse developmental glaucoma models by tyrosinase.
Volume: 299
Issue: 5612
Pages: 1578-81
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Publication
16470615 | J:107208
First Author: Mattiske D
Year: 2006
Journal: Dev Dyn
Title: The role of the forkhead transcription factor, Foxc1, in the development of the mouse lacrimal gland.
Volume: 235
Issue: 4
Pages: 1074-80
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Publication
29959321 | J:266245
First Author: Hirukawa A
Year: 2018
Journal: Nat Commun
Title: Targeting EZH2 reactivates a breast cancer subtype-specific anti-metastatic transcriptional program.
Volume: 9
Issue: 1
Pages: 2547
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Publication
30943405 | J:291738
First Author: Adane B
Year: 2019
Journal: Cell Rep
Title: The Hematopoietic Oxidase NOX2 Regulates Self-Renewal of Leukemic Stem Cells.
Volume: 27
Issue: 1
Pages: 238-254.e6
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Publication
23145080 | J:195028
First Author: Mirzayans F
Year: 2012
Journal: PLoS One
Title: Initiation of early osteoblast differentiation events through the direct transcriptional regulation of Msx2 by FOXC1.
Volume: 7
Issue: 11
Pages: e49095
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Publication
15465483 | J:93150
First Author: Dagenais SL
Year: 2004
Journal: Gene Expr Patterns
Title: Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome.
Volume: 4
Issue: 6
Pages: 611-9
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Publication
19879845 | J:157301
First Author: Siegenthaler JA
Year: 2009
Journal: Cell
Title: Retinoic acid from the meninges regulates cortical neuron generation.
Volume: 139
Issue: 3
Pages: 597-609
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Publication
16207763 | J:102847
First Author: Matt N
Year: 2005
Journal: Development
Title: Retinoic acid-dependent eye morphogenesis is orchestrated by neural crest cells.
Volume: 132
Issue: 21
Pages: 4789-800
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Publication
12015277 | J:76673
First Author: Lines MA
Year: 2002
Journal: Hum Mol Genet
Title: Molecular genetics of Axenfeld-Rieger malformations.
Volume: 11
Issue: 10
Pages: 1177-84
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Publication
18545664 | J:137147
First Author: Hayashi H
Year: 2008
Journal: PLoS One
Title: Foxc transcription factors directly regulate Dll4 and Hey2 expression by interacting with the VEGF-Notch signaling pathways in endothelial cells.
Volume: 3
Issue: 6
Pages: e2401
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Publication
16759280 | J:356614
First Author: Sommer P
Year: 2006
Journal: Dev Growth Differ
Title: Identification of Tgf beta1i4 as a downstream target of Foxc1.
Volume: 48
Issue: 5
Pages: 297-308
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Publication
31845891 | J:291752
   
First Author: Portal C
Year: 2019
Journal: Elife
Title: Primary cilia deficiency in neural crest cells models anterior segment dysgenesis in mouse.
Volume: 8
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39217245 | J:353558
First Author: Havrylov S
Year: 2024
Journal: Sci Rep
Title: Pleiotropy in FOXC1-attributable phenotypes involves altered ciliation and cilia-dependent signaling.
Volume: 14
Issue: 1
Pages: 20278
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Publication
24417671 | J:213450
First Author: Machida A
Year: 2014
Journal: Congenit Anom (Kyoto)
Title: Difference in apical and basal growth of the frontal bone primordium in Foxc1ch/ch mice.
Volume: 54
Issue: 3
Pages: 172-7
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26718006 | J:229010
First Author: Wang J
Year: 2016
Journal: Development
Title: Yap and Taz play a crucial role in neural crest-derived craniofacial development.
Volume: 143
Issue: 3
Pages: 504-15
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Publication
22248045 | J:181175
 
First Author: Zarbalis K
Year: 2012
Journal: Neural Dev
Title: Meningeal defects alter the tangential migration of cortical interneurons in Foxc1hith/hith mice.
Volume: 7
Pages: 2
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16459152 | J:109569
First Author: Mitchell EK
Year: 2006
Journal: Gene Expr Patterns
Title: Differential gene expression in the developing mouse ureter.
Volume: 6
Issue: 5
Pages: 519-38
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20976766 | J:250521
First Author: Hecht JH
Year: 2010
Journal: Ann Neurol
Title: Primary cellular meningeal defects cause neocortical dysplasia and dyslamination.
Volume: 68
Issue: 4
Pages: 454-64
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Publication
26839363 | J:240081
First Author: Mayeuf-Louchart A
Year: 2016
Journal: Development
Title: Endothelial cell specification in the somite is compromised in Pax3-positive progenitors of Foxc1/2 conditional mutants, with loss of forelimb myogenesis.
Volume: 143
Issue: 5
Pages: 872-9
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Publication
33898467 | J:306327
 
First Author: Xu J
Year: 2021
Journal: Front Cell Dev Biol
Title: Cis-Repression of Foxq1 Expression Affects Foxf2-Mediated Gene Expression in Palate Development.
Volume: 9
Pages: 665109
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Publication
19369394 | J:148019
First Author: Huang J
Year: 2009
Journal: Development
Title: FGF-regulated BMP signaling is required for eyelid closure and to specify conjunctival epithelial cell fate.
Volume: 136
Issue: 10
Pages: 1741-50
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24055172 | J:203791
First Author: Kuracha MR
Year: 2013
Journal: Dev Biol
Title: Spry1 and Spry2 are necessary for eyelid closure.
Volume: 383
Issue: 2
Pages: 227-38
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9767123 | J:50469
First Author: Hiemisch H
Year: 1998
Journal: Gene
Title: The mouse Fkh1/Mf1 gene: cDNA sequence, chromosomal localization and expression in adult tissues.
Volume: 220
Issue: 1-2
Pages: 77-82
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Publication
- | J:75733
First Author: Gruneberg H
Year: 1943
Journal: J Genet
Title: Congenital hydrocephalus in the mouse, a case of spurious pleiotropism.
Volume: 45
Issue: 1
Pages: 1-21
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4269479 | J:5368
First Author: Breen M
Year: 1973
Journal: Biochim Biophys Acta
Title: Acidic glycosaminoglycans in developing sterno-costal cartilage of the hydrocephalic (ch+-ch+) mouse.
Volume: 304
Issue: 3
Pages: 828-36
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Publication
- | J:14980
First Author: Gruneberg H
Year: 1953
Journal: J Genet
Title: Genetical studies on the skeleton of the mouse. VII. Congenital hydrocephalus.
Volume: 51
Issue: 2
Pages: 327-58
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9792859 | J:51159
First Author: Mears AJ
Year: 1998
Journal: Am J Hum Genet
Title: Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.
Volume: 63
Issue: 5
Pages: 1316-28
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Publication
10474162 | J:57295
First Author: Swiderski RE
Year: 1999
Journal: Dev Dyn
Title: Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defects.
Volume: 216
Issue: 1
Pages: 16-27
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Publication
- | J:209
First Author: Phillips RJS
Year: 1956
Journal: J Hered
Title: The linkages of congenital hydrocephalus in the house mouse.
Volume: 47
Issue: 6
Pages: 302-4
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9635428 | J:48079
First Author: Kume T
Year: 1998
Journal: Cell
Title: The forkhead/winged helix gene Mf1 is disrupted in the pleiotropic mouse mutation congenital hydrocephalus.
Volume: 93
Issue: 6
Pages: 985-96
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Publication
11237714 | J:67853
First Author: Agarwala KL
Year: 2001
Journal: Biochem Biophys Res Commun
Title: DSCAM, a highly conserved gene in mammals, expressed in differentiating mouse brain.
Volume: 281
Issue: 3
Pages: 697-705
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Publication
4784576 | J:5426
First Author: Raimondi AJ
Year: 1973
Journal: Surg Neurol
Title: The pathophysiology and morphology of murine hydrocephalus in Hy-3 and Ch mutants.
Volume: 1
Issue: 1
Pages: 50-5
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4819561 | J:5431
First Author: Grüneberg H
Year: 1974
Journal: J Embryol Exp Morphol
Title: A re-examination of two skeletal mutants of the mouse, vestigial-tail (vt) and congenital hydrocephalus (ch).
Volume: 31
Issue: 1
Pages: 207-22
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Publication
9545561 | J:47627
First Author: Hiemisch H
Year: 1998
Journal: Mech Dev
Title: Expression of the mouse Fkh1/Mf1 and Mfh1 genes in late gestation embryos is restricted to mesoderm derivatives.
Volume: 73
Issue: 1
Pages: 129-32
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Publication
- | J:24606
 
First Author: Wallace ME
Year: 1958
Journal: Heredity
Title: New linkage and independence data for Ruby and Jerker in the mouse
Volume: 12
Pages: 453-62
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Publication
5500588 | J:5191
First Author: Green MC
Year: 1970
Journal: Dev Biol
Title: The developmental effects of congenital hydrocephalus (ch) in the mouse.
Volume: 23
Issue: 4
Pages: 585-608
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Publication
12015278 | J:76672
First Author: Gould DB
Year: 2002
Journal: Hum Mol Genet
Title: Anterior segment dysgenesis and the developmental glaucomas are complex traits.
Volume: 11
Issue: 10
Pages: 1185-93
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Publication
10479458 | J:57677
First Author: Winnier GE
Year: 1999
Journal: Dev Biol
Title: Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles.
Volume: 213
Issue: 2
Pages: 418-31
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Publication
8798505 | J:34243
First Author: Sutton J
Year: 1996
Journal: J Biol Chem
Title: Genesis, a winged helix transcriptional repressor with expression restricted to embryonic stem cells.
Volume: 271
Issue: 38
Pages: 23126-33
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Publication
11688556 | J:71240
First Author: Feiner L
Year: 2001
Journal: Development
Title: Targeted disruption of semaphorin 3C leads to persistent truncus arteriosus and aortic arch interruption.
Volume: 128
Issue: 16
Pages: 3061-70
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Publication
10072431 | J:54407
First Author: Hong HK
Year: 1999
Journal: Hum Mol Genet
Title: Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene.
Volume: 8
Issue: 4
Pages: 625-37
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Publication
18579532 | J:140365
First Author: Hayashi H
Year: 2008
Journal: J Biol Chem
Title: The Foxc2 transcription factor regulates angiogenesis via induction of integrin beta3 expression.
Volume: 283
Issue: 35
Pages: 23791-800
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Publication
9096120 | J:39311
First Author: MacTaggart TE
Year: 1997
Journal: Mamm Genome
Title: Mouse angiotensin receptor genes Agtr1a and Agtr1b map to chromosomes 13 and 3.
Volume: 8
Issue: 4
Pages: 294-5
•
•
•
•
•
Publication
32034090 | J:286545
First Author: Okubo T
Year: 2020
Journal: J Biol Chem
Title: Generation and validation of a PITX2-EGFP reporter line of human induced pluripotent stem cells enables isolation of periocular mesenchymal cells.
Volume: 295
Issue: 11
Pages: 3456-3465
•
•
•
•
•
Publication
8375339 | J:11921
First Author: Sasaki H
Year: 1993
Journal: Development
Title: Differential expression of multiple fork head related genes during gastrulation and axial pattern formation in the mouse embryo.
Volume: 118
Issue: 1
Pages: 47-59
•
•
•
•
•
Publication
10395790 | J:56425
First Author: Kidson SH
Year: 1999
Journal: Dev Biol
Title: The forkhead/winged-helix gene, Mf1, is necessary for the normal development of the cornea and formation of the anterior chamber in the mouse eye.
Volume: 211
Issue: 2
Pages: 306-22
•
•
•
•
•
Publication
8325367 | J:33942
First Author: Miura N
Year: 1993
Journal: FEBS Lett
Title: MFH-1, a new member of the fork head domain family, is expressed in developing mesenchyme.
Volume: 326
Issue: 1-3
Pages: 171-6
•
•
•
•
•
Publication
10364424 | J:55575
First Author: Furumoto TA
Year: 1999
Journal: Dev Biol
Title: Notochord-dependent expression of MFH1 and PAX1 cooperates to maintain the proliferation of sclerotome cells during the vertebral column development.
Volume: 210
Issue: 1
Pages: 15-29
•
•
•
•
•
Publication
12533514 | J:81296
First Author: Yamagishi H
Year: 2003
Journal: Genes Dev
Title: Tbx1 is regulated by tissue-specific forkhead proteins through a common Sonic hedgehog-responsive enhancer.
Volume: 17
Issue: 2
Pages: 269-81
•
•
•
•
•
Publication
23472160 | J:200199
First Author: Harrison-Uy SJ
Year: 2013
Journal: PLoS One
Title: CoupTFI interacts with retinoic acid signaling during cortical development.
Volume: 8
Issue: 3
Pages: e58219
•
•
•
•
•
Publication
33667029 | J:308975
First Author: Takenoshita M
Year: 2021
Journal: Dev Dyn
Title: Cell lineage- and expression-based inference of the roles of forkhead box transcription factor Foxc2 in craniofacial development.
Volume: 250
Issue: 8
Pages: 1125-1139
•
•
•
•
•
Publication
10660670 | J:60307
First Author: Pressman CL
Year: 2000
Journal: Genesis
Title: LMX1B, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye.
Volume: 26
Issue: 1
Pages: 15-25
•
•
•
•
•
Publication
11641716 | J:71411
First Author: Arkell RM
Year: 2001
Journal: Mamm Genome
Title: Genetic, physical, and phenotypic characterization of the Del(13)Svea36H mouse.
Volume: 12
Issue: 9
Pages: 687-94
•
•
•
•
•
Publication
15314648 | J:136795
First Author: Zarbalis K
Year: 2004
Journal: PLoS Biol
Title: A focused and efficient genetic screening strategy in the mouse: identification of mutations that disrupt cortical development.
Volume: 2
Issue: 8
Pages: E219
•
•
•
•
•
Publication
7957066 | J:50747
First Author: Pierrou S
Year: 1994
Journal: EMBO J
Title: Cloning and characterization of seven human forkhead proteins: binding site specificity and DNA bending.
Volume: 13
Issue: 20
Pages: 5002-12
•
•
•
•
•
Publication
9321480 | J:39061
First Author: Zhang ZX
Year: 1997
Journal: Mamm Genome
Title: The methionine synthase (Mtr) gene maps to proximal mouse chromosome 13.
Volume: 8
Issue: 10
Pages: 787-8
•
•
•
•
•




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