Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
about
Severe defects in proliferation and differentiation of lens cells in Foxe3 null miceA mutation in the FOXE3 gene causes congenital primary aphakia in an autosomal recessive consanguineous Pakistani familyHomozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc colobomaIdentification of dominant FOXE3 and PAX6 mutations in patients with congenital cataract and aniridiaFOXE3 plays a significant role in autosomal recessive microphthalmiaA novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomalyHomozygous nonsense mutation in the FOXE3 gene as a cause of congenital primary aphakia in humansPitx3 controls multiple aspects of lens developmentlaminin alpha 1 gene is essential for normal lens development in zebrafish.Molecular mechanisms of pituitary organogenesis: In search of novel regulatory genes.Postnatal manipulation of Pax6 dosage reverses congenital tissue malformation defects.Genetic heterogeneity for recessively inherited congenital cataract microcornea with corneal opacityNiche regulation of corneal epithelial stem cells at the limbus.Whole exome sequence analysis of Peters anomaly.Anterior eye development and ocular mesenchyme: new insights from mouse models and human diseasesAnalysis of FOXD3 sequence variation in human ocular disease.In control of biology: of mice, men and FoxesGenetics of anterior segment dysgenesis disorders.The orphan G protein-coupled receptor, Gpr161, encodes the vacuolated lens locus and controls neurulation and lens development.Impaired ADAMTS9 secretion: A potential mechanism for eye defects in Peters Plus Syndrome.Signaling "cross-talk" is integrated by transcription factors in the development of the anterior segment in the eye.Conserved genetic pathways associated with microphthalmia, anophthalmia, and coloboma.Inherited Congenital Cataract: A Guide to Suspect the Genetic Etiology in the Cataract Genesis.Ocular surface development and gene expression.Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalitiesMutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects.
P2860
Q24337406-C72229E6-8FF9-42A3-A8E6-415A870D3C75Q24610243-66FCE05B-3822-4D71-A387-CB1895FFC0B3Q24615242-56D7778D-404A-4A81-83A3-026A87DBFFE8Q24628643-EBE9085A-542B-4CB0-9D99-53C01555D8F3Q24630469-AA1C25BF-8DF3-4FB6-85FF-1C331DE7DC68Q24633479-48117221-7D09-446F-A44C-37F2B89EC8CEQ24669843-9878C80A-9D1E-4E21-8AD1-AC61BBBC4F47Q28508017-BD3DB848-B185-4A37-8CA1-2057DC7BB1D3Q33235707-4DB729E6-EEB4-4769-9D92-D6C322029C5FQ34017922-D1835BC3-68AD-4612-B302-EE64A70153E4Q34039397-71FE0EC2-42BE-40F6-9D36-96CCC772D5B2Q35221064-D9F8C6E4-9B55-459F-9905-E22D69808467Q35302474-DA39C940-684F-49B4-A12D-A6AAF54B8918Q35395210-5B37D906-1DC6-4CE7-B85E-8041D825FA55Q35731050-AB57E1EE-8C1E-4412-A1EF-B55B16E155D0Q36099721-3B9B8EF5-B4AC-4B98-8C7A-9FEB15DBAFC9Q36515335-50FC8133-83D6-4E33-BD6A-024BAF98A9D8Q36571645-18CDF9ED-3CCF-4BA3-8448-C8106B0BC1DBQ36883085-5DC3E237-D216-4346-8196-A116EE42780EQ37298462-2297FDF9-F0CD-493B-B695-734122E1A95EQ37558392-63C2C060-6543-4DF4-B194-F2EEF9DB8438Q38517281-EE4B64DB-3B32-45B6-AC0C-C037FFF801ABQ39370800-957DCFC3-E7EB-4479-A35D-5D8399A87F5FQ41204566-DC89ADD2-DFED-46BA-B14B-159D8A7EC109Q41979823-97BB8B0D-E7A9-4750-B1B6-210C8226736DQ48286993-1CDED192-A388-48AA-99EF-D0AE723B090A
P2860
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
description
2002 nî lūn-bûn
@nan
2002 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2002 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2002年の論文
@ja
2002年論文
@yue
2002年論文
@zh-hant
2002年論文
@zh-hk
2002年論文
@zh-mo
2002年論文
@zh-tw
2002年论文
@wuu
name
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@ast
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@en
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@en-gb
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@nl
type
label
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@ast
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@en
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@en-gb
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@nl
prefLabel
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@ast
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@en
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@en-gb
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@nl
P2093
P921
P3181
P1476
Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
@en
P2093
Amanda Churchill
Mattias Ormestad
Peter Carlsson
Sven Enerbäck
P304
P3181
P407
P577
2002-05-01T00:00:00Z