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Loss of Msx2 Function Down-Regulates the FoxE3 Expression and Results in Anterior Segment Dysgenesis Resembling Peters Anomaly

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/1526-968x(200006)27:2<81::aid-gene50>3.0.co;2-nopenalex-snapshot
ForkheadFoxe3 maps to thedysgenetic lens locus and is critical in lens development and differentiation
inferredcites →https://doi.org/10.1002/dvdy.10367openalex-snapshot
Expression of murine ELL‐associated factor 2 (Eaf2) is developmentally regulated
inferredcites →https://doi.org/10.1002/dvdy.21422openalex-snapshot
Prox1 regulates a transitory state for interneuron neurogenesis in the spinal cord
inferredcites →https://doi.org/10.1002/dvdy.21445openalex-snapshot
Cell autonomous roles for AP‐2α in lens vesicle separation and maintenance of the lens epithelial cell phenotype
inferredcites →https://doi.org/10.1002/dvdy.21924openalex-snapshot
Pitx3 controls multiple aspects of lens development
inferredcites →https://doi.org/10.1002/dvg.20277openalex-snapshot
Abnormal lens morphogenesis and ectopic lens formation in the absence of β‐catenin function
inferredcites →https://doi.org/10.1002/dvg.20380openalex-snapshot
Regulation and function of foxe3 during early zebrafish development
inferredcites →https://doi.org/10.1006/dbio.1998.9114openalex-snapshot
Msx2Gene Dosage Influences the Number of Proliferative Osteogenic Cells in Growth Centers of the Developing Murine Skull: A Possible Mechanism forMSX2-Mediated Craniosynostosis in Humans
inferredcites →https://doi.org/10.1006/dbio.1998.9153openalex-snapshot
BMP7 Acts in Murine Lens Placode Development
inferredcites →https://doi.org/10.1006/dbio.2002.0732openalex-snapshot
The Homeobox Gene Six3 Is a Potential Regulator of Anterior Segment Formation in the Chick Eye
inferredcites →https://doi.org/10.1016/j.bbrc.2009.02.016openalex-snapshot
Analysis of Msx1 and Msx2 transactivation function in the context of the heat shock 70 (Hspa1b) gene promoter
inferredcites →https://doi.org/10.1016/j.devcel.2006.08.009openalex-snapshot
Lens Specification Is the Ground State of All Sensory Placodes, from which FGF Promotes Olfactory Identity
inferredcites →https://doi.org/10.1016/j.devcel.2007.04.020openalex-snapshot
Time of Exposure to BMP Signals Plays a Key Role in the Specification of the Olfactory and Lens Placodes Ex Vivo
inferredcites →https://doi.org/10.1016/j.exer.2008.03.004openalex-snapshot
Anterior segment dysgenesis in the eyes of mice deficient for the high-mobility-group transcription factor Sox11
inferredcites →https://doi.org/10.1016/j.mod.2004.11.012openalex-snapshot
Zebrafish pitx3 is necessary for normal lens and retinal development
inferredcites →https://doi.org/10.1016/j.preteyeres.2007.07.002openalex-snapshot
Genetic and epigenetic mechanisms of gene regulation during lens development
inferredcites →https://doi.org/10.1016/j.semcdb.2006.10.005openalex-snapshot
Lens induction in vertebrates: Variations on a conserved theme of signaling events
inferredcites →https://doi.org/10.1016/j.survophthal.2006.02.006openalex-snapshot
A Review of Anterior Segment Dysgeneses
inferredcites →https://doi.org/10.1016/j.tig.2005.09.001openalex-snapshot
msh/Msx gene family in neural development
inferredcites →https://doi.org/10.1016/j.ydbio.2006.09.021openalex-snapshot
Foxe3 is required for morphogenesis and differentiation of the anterior segment of the eye and is sensitive to Pax6 gene dosage
inferredcites →https://doi.org/10.1016/j.ydbio.2007.05.037openalex-snapshot
Msx1 and Msx2 regulate survival of secondary heart field precursors and post-migratory proliferation of cardiac neural crest in the outflow tract
inferredcites →https://doi.org/10.1016/s0378-1119(00)00081-0openalex-snapshot
Roles for Msx and Dlx homeoproteins in vertebrate development
inferredcites →https://doi.org/10.1016/s0960-9822(07)00562-3openalex-snapshot
Modification of gene activity in mouse embryos in utero by a tamoxifen-inducible form of Cre recombinase
inferredcites →https://doi.org/10.1021/bi971008xopenalex-snapshot
Structure−Function Analysis of Msx2-Mediated Transcriptional Suppression
inferredcites →https://doi.org/10.1038/5007openalex-snapshot
Generalized lacZ expression with the ROSA26 Cre reporter strain
inferredcites →https://doi.org/10.1038/6844openalex-snapshot
Prox1 function is crucial for mouse lens-fibre elongation
inferredcites →https://doi.org/10.1038/74231openalex-snapshot
Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
inferredcites →https://doi.org/10.1038/ejhg.2010.210openalex-snapshot
A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly
inferredcites →https://doi.org/10.1038/nature04175openalex-snapshot
BMP inhibition-driven regulation of six-3 underlies induction of newt lens regeneration
inferredcites →https://doi.org/10.1038/ng1144openalex-snapshot
Prox1 function controls progenitor cell proliferation and horizontal cell genesis in the mammalian retina
inferredcites →https://doi.org/10.1038/sj.emboj.7601398openalex-snapshot
Six3 activation of Pax6 expression is essential for mammalian lens induction and specification
inferredcites →https://doi.org/10.1038/sj.eye.6702852openalex-snapshot
Molecular and developmental mechanisms of anterior segment dysgenesis
inferredcites →https://doi.org/10.1046/j.1365-2443.2001.00466.xopenalex-snapshot
Regulation of the activity of the transcription factor Runx2 by two homeobox proteins, Msx2 and Dlx5
inferredcites →https://doi.org/10.1073/pnas.0707202104openalex-snapshot
BMP signaling mediates stem/progenitor cell-induced retina regeneration
inferredcites →https://doi.org/10.1073/pnas.92.13.6137openalex-snapshot
Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull.
inferredcites →https://doi.org/10.1074/jbc.m305472200openalex-snapshot
Smad4 and β-Catenin Co-activators Functionally Interact with Lymphoid-enhancing Factor to Regulate Graded Expression of Msx2
inferredcites →https://doi.org/10.1074/jbc.m403621200openalex-snapshot
Reciprocal Roles of Msx2 in Regulation of Osteoblast and Adipocyte Differentiation
inferredcites →https://doi.org/10.1074/jbc.m800851200openalex-snapshot
Msx2 Exerts Bone Anabolism via Canonical Wnt Signaling
inferredcites →https://doi.org/10.1093/hmg/11.1.33openalex-snapshot
Domain disruption and mutation of the bZIP transcription factor, MAF,associated with cataract, ocular anterior segment dysgenesis and coloboma
inferredcites →https://doi.org/10.1093/hmg/11.10.1185openalex-snapshot
Anterior segment dysgenesis and the developmental glaucomas are complex traits
inferredcites →https://doi.org/10.1097/iio.0b013e318169526copenalex-snapshot
Anterior Segment Dysgenesis: Peters Anomaly and Sclerocornea
inferredcites →https://doi.org/10.1101/gad.184000openalex-snapshot
Pax6 activity in the lens primordium is required for lens formation and for correct placement of a single retina in the eye
inferredcites →https://doi.org/10.1128/mcb.25.20.8854-8863.2005openalex-snapshot
Severe Defects in Proliferation and Differentiation of Lens Cells in Foxe3 Null Mice
inferredcites →https://doi.org/10.1158/0008-5472.749.65.3openalex-snapshot
Homeobox Msx1 Interacts with p53 Tumor Suppressor and Inhibits Tumor Growth by Inducing Apoptosis
inferredcites →https://doi.org/10.1167/iovs.02-0317openalex-snapshot
Microphthalmia Resulting from Msx2 -Induced Apoptosis in the Optic Vesicle
inferredcites →https://doi.org/10.1167/iovs.06-0472openalex-snapshot
Genotype-Phenotype Correlations in Axenfeld-Rieger Malformation and Glaucoma Patients with FOXC1 and PITX2 Mutations
inferredcites →https://doi.org/10.1167/iovs.08-2217openalex-snapshot
Functions of the Type 1 BMP Receptor Acvr1 (Alk2) in Lens Development: Cell Proliferation, Terminal Differentiation, and Survival
inferredcites →https://doi.org/10.1186/1471-213x-8-27openalex-snapshot
Crucial role of zebrafish prox1in hypothalamic catecholaminergic neurons development
inferredcites →https://doi.org/10.1186/1750-1172-2-47openalex-snapshot
Anophthalmia and microphthalmia
inferredcites →https://doi.org/10.1242/dev.000117openalex-snapshot
Foxe view of lens development and disease
inferredcites →https://doi.org/10.1242/dev.001495openalex-snapshot
pygopus 2 has a crucial, Wnt pathway-independent function in lens induction
inferredcites →https://doi.org/10.1242/dev.00201openalex-snapshot
`Cyclic alopecia' inMsx2mutants: defects in hair cycling and hair shaft differentiation
inferredcites →https://doi.org/10.1242/dev.00399openalex-snapshot
Cell-autonomous involvement ofMab21l1is essential for lens placode development
inferredcites →https://doi.org/10.1242/dev.00878openalex-snapshot
Regulation of Msx genes by a Bmp gradient is essential for neural crest specification
inferredcites →https://doi.org/10.1242/dev.009548openalex-snapshot
Convergence of a head-field selector Otx2 and Notch signaling: a mechanism for lens specification
inferredcites →https://doi.org/10.1242/dev.02022openalex-snapshot
Regulation of ocular lens development by Smad-interacting protein 1 involvingFoxe3activation
inferredcites →https://doi.org/10.1242/dev.129.16.3795openalex-snapshot
Bone morphogenetic protein signaling and the initiation of lens fiber cell differentiation
inferredcites →https://doi.org/10.1387/ijdb.041903rlopenalex-snapshot
Pathways regulating lens induction in the mouse
inferredcites →https://doi.org/10.1523/jneurosci.21-04-01292.2001openalex-snapshot
BMP4 Mediates Apoptotic Cell Death in the Developing Chick Eye
inferredcites →https://doi.org/10.1590/s0004-27492010000400014openalex-snapshot
Anomalia de Peters, seus aspectos clínicos e terapêuticos: relato de caso
inferredcites →https://doi.org/10.2144/00291bm09openalex-snapshot
Preparation of PCR-Quality Mouse Genomic DNA with Hot Sodium Hydroxide and Tris (HotSHOT)

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4681866openalex-extracted
ASD Gene Jigsaw: Decrypting the CPAMD8 Puzzle in Chinese Patients with Congenital Ectopia Lentis
inferred← citeshttps://doi.org/10.1002/dvdy.24303openalex-snapshot
Deficiency of the RNA binding protein caprin2 causes lens defects and features of peters anomaly
inferred← citeshttps://doi.org/10.1007/978-4-431-54300-8_1openalex-snapshot
From Zygote to Lens: Emergence of the Lens Epithelium
inferred← citeshttps://doi.org/10.1007/978-981-10-2627-0_1openalex-snapshot
Embryonic Development of the Human Lens
inferred← citeshttps://doi.org/10.1016/b978-0-443-13820-1.00052-9openalex-snapshot
Lens Induction: Specification, Determination, and Placode Morphogenesis
inferred← citeshttps://doi.org/10.1016/j.bbrc.2024.151032openalex-snapshot
Differential expression of keratin and keratin associated proteins are linked with hair loss condition in spontaneously mutated inbred mice
inferred← citeshttps://doi.org/10.1016/j.exer.2013.09.010openalex-snapshot
Regulation of mouse lens maturation and gene expression by Krüppel-like factor 4
inferred← citeshttps://doi.org/10.1016/j.exer.2016.03.010openalex-snapshot
Systems biology of lens development: A paradigm for disease gene discovery in the eye
inferred← citeshttps://doi.org/10.1016/j.ydbio.2026.04.006openalex-snapshot
Meis1 and Meis2 are jointly required for advanced stages of mouse lens morphogenesis
inferred← citeshttps://doi.org/10.1038/s41374-018-0180-yopenalex-snapshot
Lens-specific conditional knockout of Msx2 in mice leads to ocular anterior segment dysgenesis via activation of a calcium signaling pathway
inferred← citeshttps://doi.org/10.1038/s41419-026-08487-6openalex-snapshot
Unveiling ZNF124 as a novel determinant in neurodegeneration: orchestration of photoreceptor homeostasis through MSX2 transcriptional regulation
inferred← citeshttps://doi.org/10.1111/1365-2656.12503openalex-snapshot
Evidence of the phenotypic expression of a lethal recessive allele under inbreeding in a wild population of conservation concern
inferred← citeshttps://doi.org/10.1111/dgd.12128openalex-snapshot
The lens equator: A platform for molecular machinery that regulates the switch from cell proliferation to differentiation in the vertebrate lens
inferred← citeshttps://doi.org/10.1155/2013/103947openalex-snapshot
Ocular Surface Development and Gene Expression
inferred← citeshttps://doi.org/10.1177/0300060518774687openalex-snapshot
Lens-specific deletion of the Msx2 gene increased apoptosis by enhancing the caspase-3/caspase-8 signaling pathway
inferred← citeshttps://doi.org/10.1242/dev.107953openalex-snapshot
The cellular and molecular mechanisms of vertebrate lens development
inferred← citeshttps://doi.org/10.1242/dev.137760openalex-snapshot
Control of lens development by Lhx2-regulated neuroretinal FGFs
inferred← citeshttps://doi.org/10.1371/journal.pone.0115442openalex-snapshot
Differential Binding of Lef1 and Msx1/2 Transcription Factors to Dkk1 CNEs Correlates with Reporter Gene Expression In Vivo
inferred← citeshttps://doi.org/10.1371/journal.pone.0159639openalex-snapshot
Requirement of Smad4 from Ocular Surface Ectoderm for Retinal Development
inferred← citeshttps://doi.org/10.1371/journal.pone.0172302openalex-snapshot
Lens apoptosis in the Astyanax blind cavefish is not triggered by its small size or defects in morphogenesis
inferred← citeshttps://doi.org/10.1387/ijdb.130193jgopenalex-snapshot
Pitx3 directly regulates Foxe3 during early lens development
inferred← citeshttps://doi.org/10.18240/ijo.2016.07.02openalex-snapshot
Anterior segment dysgenesis correlation with epithelial-mesenchymal transition in Smad4 knockout mice
inferred← citeshttps://doi.org/10.3109/13816810.2014.886270openalex-snapshot
MSX2Gene Duplication in a Patient with Eye Development Defects
inferred← citeshttps://doi.org/10.3390/genes13071138openalex-snapshot
QTL Mapping for Age-Related Eye Pigmentation in the Pink-Eyed Dilution Castaneus Mutant Mouse
inferred← citeshttps://doi.org/10.3980/j.issn.2222-3959.2013.03.04openalex-snapshot
Msx2 plays a critical role in lens epithelium cell cycle control.
inferred← citeshttps://doi.org/10.64898/2026.02.15.706040openalex-snapshot
Studies of mice with a large deletion of the ARPKD-associated Pkhd1 locus likely explain its GWAS association with glaucoma in humans
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