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Search results 1 to 100 out of 150 for Crb1

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Category: Publication
Type Details Score
Publication
First Author: van de Pavert SA
Year: 2007
Journal: Glia
Title: Crb1 is a determinant of retinal apical Müller glia cell features.
Volume: 55
Issue: 14
Pages: 1486-97
Publication  
First Author: Pak JS
Year: 2015
Journal: Mol Vis
Title: The retinal phenotype of Grk1-/- is compromised by a Crb1 rd8 mutation.
Volume: 21
Pages: 1281-94
Publication
First Author: Watanabe T
Year: 2004
Journal: Biochem Biophys Res Commun
Title: Expression of a novel secretory form (Crb1s) of mouse Crumbs homologue Crb1 in skin development.
Volume: 313
Issue: 2
Pages: 263-70
Publication
First Author: Mehalow AK
Year: 2003
Journal: Hum Mol Genet
Title: CRB1 is essential for external limiting membrane integrity and photoreceptor morphogenesis in the mammalian retina.
Volume: 12
Issue: 17
Pages: 2179-89
Publication
First Author: Pellissier LP
Year: 2013
Journal: PLoS Genet
Title: Targeted ablation of CRB1 and CRB2 in retinal progenitor cells mimics Leber congenital amaurosis.
Volume: 9
Issue: 12
Pages: e1003976
Publication
First Author: van Rossum AG
Year: 2006
Journal: Hum Mol Genet
Title: Pals1/Mpp5 is required for correct localization of Crb1 at the subapical region in polarized Muller glia cells.
Volume: 15
Issue: 18
Pages: 2659-72
Publication
First Author: Alves CH
Year: 2013
Journal: Hum Mol Genet
Title: Loss of CRB2 in the mouse retina mimics human retinitis pigmentosa due to mutations in the CRB1 gene.
Volume: 22
Issue: 1
Pages: 35-50
Publication
First Author: van de Pavert SA
Year: 2007
Journal: J Neurosci
Title: A single amino acid substitution (Cys249Trp) in Crb1 causes retinal degeneration and deregulates expression of pituitary tumor transforming gene Pttg1.
Volume: 27
Issue: 3
Pages: 564-73
Publication
First Author: Chen X
Year: 2013
Journal: J Neuropathol Exp Neurol
Title: Rd8 mutation in the Crb1 gene of CD11c-eYFP transgenic reporter mice results in abnormal numbers of CD11c-positive cells in the retina.
Volume: 72
Issue: 8
Pages: 782-90
Publication
First Author: Mattapallil MJ
Year: 2012
Journal: Invest Ophthalmol Vis Sci
Title: The Rd8 mutation of the Crb1 gene is present in vendor lines of C57BL/6N mice and embryonic stem cells, and confounds ocular induced mutant phenotypes.
Volume: 53
Issue: 6
Pages: 2921-7
Publication  
First Author: Roh H
Year: 2023
Journal: Front Cell Neurosci
Title: Electrically-evoked responses for retinal prostheses are differentially altered depending on ganglion cell types in outer retinal neurodegeneration caused by Crb1 gene mutation.
Volume: 17
Pages: 1115703
Publication
First Author: Ray TA
Year: 2020
Journal: Nat Commun
Title: Comprehensive identification of mRNA isoforms reveals the diversity of neural cell-surface molecules with roles in retinal development and disease.
Volume: 11
Issue: 1
Pages: 3328
Publication  
First Author: Concas D
Year: 2017
Journal: F1000Res
Title: A scoring system for the evaluation of the mutated Crb1/rd8-derived retinal lesions in C57BL/6N mice.
Volume: 6
Pages: 404
Publication
First Author: Lajko M
Year: 2017
Journal: PLoS One
Title: Photoreceptor oxidative stress in hyperoxia-induced proliferative retinopathy accelerates rd8 degeneration.
Volume: 12
Issue: 7
Pages: e0180384
Publication  
First Author: Schnabolk G
Year: 2014
Journal: Exp Eye Res
Title: A comparative analysis of C57BL/6J and 6N substrains; chemokine/cytokine expression and susceptibility to laser-induced choroidal neovascularization.
Volume: 129
Pages: 18-23
Publication
First Author: Low BE
Year: 2014
Journal: Invest Ophthalmol Vis Sci
Title: Correction of the Crb1rd8 allele and retinal phenotype in C57BL/6N mice via TALEN-mediated homology-directed repair.
Volume: 55
Issue: 1
Pages: 387-95
Publication
First Author: Quinn PM
Year: 2019
Journal: Hum Mol Genet
Title: Loss of CRB2 in Müller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype.
Volume: 28
Issue: 1
Pages: 105-123
Publication  
First Author: Richard M
Year: 2006
Journal: Hum Mol Genet
Title: Towards understanding CRUMBS function in retinal dystrophies.
Volume: 15 Spec No 2
Pages: R235-43
Publication
First Author: den Hollander AI
Year: 2002
Journal: Mech Dev
Title: Isolation of Crb1, a mouse homologue of Drosophila crumbs, and analysis of its expression pattern in eye and brain.
Volume: 110
Issue: 1-2
Pages: 203-7
Publication
First Author: Dolón JF
Year: 2018
Journal: Sci Rep
Title: Expression and localization of the polarity protein CRB2 in adult mouse brain: a comparison with the CRB1rd8 mutant mouse model.
Volume: 8
Issue: 1
Pages: 11652
Publication
First Author: Pellissier LP
Year: 2014
Journal: Hum Mol Genet
Title: CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in mice.
Volume: 23
Issue: 14
Pages: 3759-71
Publication
First Author: Quinn PM
Year: 2018
Journal: Hum Mol Genet
Title: CRB2 in immature photoreceptors determines the superior-inferior symmetry of the developing retina to maintain retinal structure and function.
Volume: 27
Issue: 18
Pages: 3137-3153
Publication  
First Author: Alves CH
Year: 2019
Journal: Int J Mol Sci
Title: CRB2 Loss in Rod Photoreceptors Is Associated with Progressive Loss of Retinal Contrast Sensitivity.
Volume: 20
Issue: 17
Publication
First Author: Alves CH
Year: 2013
Journal: PLoS One
Title: Microarray and morphological analysis of early postnatal CRB2 mutant retinas on a pure C57BL/6J genetic background.
Volume: 8
Issue: 12
Pages: e82532
Publication
First Author: Son S
Year: 2020
Journal: Biochem Biophys Res Commun
Title: Crumbs proteins regulate layered retinal vascular development required for vision.
Volume: 521
Issue: 4
Pages: 939-946
Publication
First Author: Luhmann UF
Year: 2015
Journal: Hum Mol Genet
Title: The severity of retinal pathology in homozygous Crb1rd8/rd8 mice is dependent on additional genetic factors.
Volume: 24
Issue: 1
Pages: 128-41
Publication  
First Author: Aredo B
Year: 2015
Journal: J Neuroinflammation
Title: Differences in the distribution, phenotype and gene expression of subretinal microglia/macrophages in C57BL/6N (Crb1 rd8/rd8) versus C57BL6/J (Crb1 wt/wt) mice.
Volume: 12
Pages: 6
Publication
First Author: Aleman TS
Year: 2011
Journal: Invest Ophthalmol Vis Sci
Title: Human CRB1-associated retinal degeneration: comparison with the rd8 Crb1-mutant mouse model.
Volume: 52
Issue: 9
Pages: 6898-910
Publication
First Author: Greferath U
Year: 2014
Journal: PLoS One
Title: The role of histamine in the retina: studies on the Hdc knockout mouse.
Volume: 9
Issue: 12
Pages: e116025
Publication
First Author: Fischer MD
Year: 2009
Journal: PLoS One
Title: Noninvasive, in vivo assessment of mouse retinal structure using optical coherence tomography.
Volume: 4
Issue: 10
Pages: e7507
Publication
First Author: Kwon YS
Year: 2020
Journal: Dev Biol
Title: Cytoglobin deficiency potentiates Crb1-mediated retinal degeneration in rd8 mice.
Volume: 458
Issue: 2
Pages: 141-152
Publication
First Author: van de Pavert SA
Year: 2004
Journal: J Cell Sci
Title: Crumbs homologue 1 is required for maintenance of photoreceptor cell polarization and adhesion during light exposure.
Volume: 117
Issue: Pt 18
Pages: 4169-77
Publication
First Author: Cho SH
Year: 2019
Journal: Dev Biol
Title: Targeted deletion of Crb1/Crb2 in the optic vesicle models key features of leber congenital amaurosis 8.
Volume: 453
Issue: 2
Pages: 141-154
Publication  
First Author: Luhmann UF
Year: 2013
Journal: Exp Eye Res
Title: Ccl2, Cx3cr1 and Ccl2/Cx3cr1 chemokine deficiencies are not sufficient to cause age-related retinal degeneration.
Volume: 107
Pages: 80-7
Publication  
First Author: Badia A
Year: 2021
Journal: Exp Eye Res
Title: Transcriptomics analysis of Ccl2/Cx3cr1/Crb1rd8 deficient mice provides new insights into the pathophysiology of progressive retinal degeneration.
Volume: 203
Pages: 108424
Publication
First Author: Weatherly SM
Year: 2022
Journal: PLoS Genet
Title: Identification of Arhgef12 and Prkci as genetic modifiers of retinal dysplasia in the Crb1rd8 mouse model.
Volume: 18
Issue: 6
Pages: e1009798
Publication  
First Author: Markand S
Year: 2016
Journal: Exp Eye Res
Title: Mthfr as a modifier of the retinal phenotype of Crb1(rd8/rd8) mice.
Volume: 145
Pages: 164-172
Publication
First Author: Chang B
Year: 2018
Journal: Invest Ophthalmol Vis Sci
Title: Spontaneous Posterior Segment Vascular Disease Phenotype of a Mouse Model, rnv3, Is Dependent on the Crb1rd8 Allele.
Volume: 59
Issue: 12
Pages: 5127-5139
Publication
First Author: Tonelli Gombalová Z
Year: 2020
Journal: J Comp Neurol
Title: Majority of cerebrospinal fluid-contacting neurons in the spinal cord of C57Bl/6N mice is present in ectopic position unlike in other studied experimental mice strains and mammalian species.
Volume: 528
Issue: 15
Pages: 2523-2550
Publication  
First Author: Sahu B
Year: 2015
Journal: Mol Vis
Title: Presence of rd8 mutation does not alter the ocular phenotype of late-onset retinal degeneration mouse model.
Volume: 21
Pages: 273-84
Publication
First Author: Cho SH
Year: 2012
Journal: Hum Mol Genet
Title: Genetic ablation of Pals1 in retinal progenitor cells models the retinal pathology of Leber congenital amaurosis.
Volume: 21
Issue: 12
Pages: 2663-76
Publication
First Author: Gosens I
Year: 2008
Journal: Exp Eye Res
Title: Composition and function of the Crumbs protein complex in the mammalian retina.
Volume: 86
Issue: 5
Pages: 713-26
Publication
First Author: Nagai N
Year: 2015
Journal: Am J Pathol
Title: Novel CCR3 Antagonists Are Effective Mono- and Combination Inhibitors of Choroidal Neovascular Growth and Vascular Permeability.
Volume: 185
Issue: 9
Pages: 2534-49
Publication
First Author: Nagai N
Year: 2014
Journal: Invest Ophthalmol Vis Sci
Title: Spontaneous CNV in a novel mutant mouse is associated with early VEGF-A-driven angiogenesis and late-stage focal edema, neural cell loss, and dysfunction.
Volume: 55
Issue: 6
Pages: 3709-19
Publication
First Author: Saul AB
Year: 2017
Journal: Doc Ophthalmol
Title: Detailed electroretinographic findings in rd8 mice.
Volume: 134
Issue: 3
Pages: 195-203
Publication  
First Author: Perkins GA
Year: 2012
Journal: Mol Vis
Title: Bcl-xL-mediated remodeling of rod and cone synaptic mitochondria after postnatal lead exposure: electron microscopy, tomography and oxygen consumption.
Volume: 18
Pages: 3029-48
Publication
First Author: Moore BA
Year: 2018
Journal: Invest Ophthalmol Vis Sci
Title: A Population Study of Common Ocular Abnormalities in C57BL/6N rd8 Mice.
Volume: 59
Issue: 6
Pages: 2252-2261
Publication
First Author: Stojic A
Year: 2017
Journal: Invest Ophthalmol Vis Sci
Title: Murine Autoimmune Optic Neuritis Is Not Phenotypically Altered by the Retinal Degeneration 8 Mutation.
Volume: 58
Issue: 1
Pages: 318-328
Publication
First Author: Dando SJ
Year: 2016
Journal: Glia
Title: A case of mistaken identity: CD11c-eYFP(+) cells in the normal mouse brain parenchyma and neural retina display the phenotype of microglia, not dendritic cells.
Volume: 64
Issue: 8
Pages: 1331-49
Publication
First Author: Aartsen WM
Year: 2010
Journal: PLoS One
Title: GFAP-driven GFP expression in activated mouse Müller glial cells aligning retinal blood vessels following intravitreal injection of AAV2/6 vectors.
Volume: 5
Issue: 8
Pages: e12387
Publication
First Author: Parr GR
Year: 1976
Journal: Biochemistry
Title: A kinetic study of the subunit dissociation and reassembly of rabbit muscle phosphofructokinase.
Volume: 15
Issue: 4
Pages: 857-62
Publication
First Author: Kozycki CT
Year: 2022
Journal: Ann Rheum Dis
Title: Gain-of-function mutations in ALPK1 cause an NF-κB-mediated autoinflammatory disease: functional assessment, clinical phenotyping and disease course of patients with ROSAH syndrome.
Volume: 81
Issue: 10
Pages: 1453-1464
Publication
First Author: Lakowski J
Year: 2010
Journal: Hum Mol Genet
Title: Cone and rod photoreceptor transplantation in models of the childhood retinopathy Leber congenital amaurosis using flow-sorted Crx-positive donor cells.
Volume: 19
Issue: 23
Pages: 4545-59
Publication  
First Author: Liegel RP
Year: 2014
Journal: Mol Genet Metab Rep
Title: Alkylglycerone phosphate synthase (AGPS) deficient mice: models for rhizomelic chondrodysplasia punctate type 3 (RCDP3) malformation syndrome.
Volume: 1
Pages: 299-311
Publication
First Author: Herrmann P
Year: 2015
Journal: Neurobiol Aging
Title: Cd59a deficiency in mice leads to preferential innate immune activation in the retinal pigment epithelium-choroid with age.
Volume: 36
Issue: 9
Pages: 2637-48
Publication
First Author: Mirza M
Year: 2013
Journal: PLoS One
Title: Progressive retinal degeneration and glial activation in the CLN6 (nclf) mouse model of neuronal ceroid lipofuscinosis: a beneficial effect of DHA and curcumin supplementation.
Volume: 8
Issue: 10
Pages: e75963
Publication
First Author: Wang X
Year: 2016
Journal: J Neurosci
Title: Requirement for Microglia for the Maintenance of Synaptic Function and Integrity in the Mature Retina.
Volume: 36
Issue: 9
Pages: 2827-42
Publication
First Author: Feng L
Year: 2017
Journal: Am J Pathol
Title: A Proinflammatory Function of Toll-Like Receptor 2 in the Retinal Pigment Epithelium as a Novel Target for Reducing Choroidal Neovascularization in Age-Related Macular Degeneration.
Volume: 187
Issue: 10
Pages: 2208-2221
Publication
First Author: Colton CA
Year: 2014
Journal: J Neuropathol Exp Neurol
Title: mNos2 deletion and human NOS2 replacement in Alzheimer disease models.
Volume: 73
Issue: 8
Pages: 752-69
Publication
First Author: Enríquez JA
Year: 2019
Journal: Nat Metab
Title: Mind your mouse strain.
Volume: 1
Issue: 1
Pages: 5-7
Publication
First Author: Datta P
Year: 2015
Journal: Proc Natl Acad Sci U S A
Title: Accumulation of non-outer segment proteins in the outer segment underlies photoreceptor degeneration in Bardet-Biedl syndrome.
Volume: 112
Issue: 32
Pages: E4400-9
Publication
First Author: Chang B
Year: 2013
Journal: Invest Ophthalmol Vis Sci
Title: Survey of common eye diseases in laboratory mouse strains.
Volume: 54
Issue: 7
Pages: 4974-81
Publication
First Author: Fontaine V
Year: 2016
Journal: PLoS One
Title: Norbixin Protects Retinal Pigmented Epithelium Cells and Photoreceptors against A2E-Mediated Phototoxicity In Vitro and In Vivo.
Volume: 11
Issue: 12
Pages: e0167793
Publication
First Author: Borrás T
Year: 2015
Journal: Invest Ophthalmol Vis Sci
Title: A Novel Mgp-Cre Knock-In Mouse Reveals an Anticalcification/Antistiffness Candidate Gene in the Trabecular Meshwork and Peripapillary Scleral Region.
Volume: 56
Issue: 4
Pages: 2203-14
Publication
First Author: Vessey KA
Year: 2015
Journal: Invest Ophthalmol Vis Sci
Title: Assessment of retinal function and morphology in aging Ccl2 knockout mice.
Volume: 56
Issue: 2
Pages: 1238-52
Publication
First Author: Hasegawa E
Year: 2014
Journal: PLoS One
Title: Characterization of a spontaneous retinal neovascular mouse model.
Volume: 9
Issue: 9
Pages: e106507
Publication
First Author: Richert E
Year: 2020
Journal: Adv Med Sci
Title: CRB1rd8 mutation influences the age-related macular degeneration phenotype of NRF2 knockout mice and favors choroidal neovascularization.
Volume: 65
Issue: 1
Pages: 71-77
Publication
First Author: Chen M
Year: 2014
Journal: PLoS One
Title: RAGE regulates immune cell infiltration and angiogenesis in choroidal neovascularization.
Volume: 9
Issue: 2
Pages: e89548
Publication  
First Author: Boatright JH
Year: 2015
Journal: Mol Vis
Title: Methodologies for analysis of patterning in the mouse RPE sheet.
Volume: 21
Pages: 40-60
Publication
First Author: Vessey KA
Year: 2012
Journal: Invest Ophthalmol Vis Sci
Title: Ccl2/Cx3cr1 knockout mice have inner retinal dysfunction but are not an accelerated model of AMD.
Volume: 53
Issue: 12
Pages: 7833-46
Publication
First Author: Ardeljan D
Year: 2014
Journal: PLoS One
Title: Interleukin-17 retinotoxicity is prevented by gene transfer of a soluble interleukin-17 receptor acting as a cytokine blocker: implications for age-related macular degeneration.
Volume: 9
Issue: 4
Pages: e95900
Publication
First Author: Ramkumar HL
Year: 2013
Journal: J Nutr
Title: Nutrient supplementation with n3 polyunsaturated fatty acids, lutein, and zeaxanthin decrease A2E accumulation and VEGF expression in the retinas of Ccl2/Cx3cr1-deficient mice on Crb1rd8 background.
Volume: 143
Issue: 7
Pages: 1129-35
Publication  
First Author: Palko SI
Year: 2022
Journal: Proc Natl Acad Sci U S A
Title: Compartmentalized citrullination in Muller glial endfeet during retinal degeneration.
Volume: 119
Issue: 9
Publication
First Author: Wang Y
Year: 2014
Journal: Lab Invest
Title: Platelet-derived growth factor (PDGF)-C inhibits neuroretinal apoptosis in a murine model of focal retinal degeneration.
Volume: 94
Issue: 6
Pages: 674-82
Publication
First Author: Chen Q
Year: 2017
Journal: Diabetes
Title: Pathogenic Role of microRNA-21 in Diabetic Retinopathy Through Downregulation of PPARα.
Volume: 66
Issue: 6
Pages: 1671-1682
Publication
First Author: Ji X
Year: 2016
Journal: Invest Ophthalmol Vis Sci
Title: Retinal Pigment Epithelium Atrophy 1 (rpea1): A New Mouse Model With Retinal Detachment Caused by a Disruption of Protein Kinase C, θ.
Volume: 57
Issue: 3
Pages: 877-88
Publication  
First Author: Liu YH
Year: 2018
Journal: Exp Eye Res
Title: Partial retinal photoreceptor loss in a transgenic mouse model associated with reduced levels of interphotoreceptor retinol binding protein (IRBP, RBP3).
Volume: 172
Pages: 54-65
Publication
First Author: Hippert C
Year: 2015
Journal: PLoS One
Title: Müller glia activation in response to inherited retinal degeneration is highly varied and disease-specific.
Volume: 10
Issue: 3
Pages: e0120415
Publication
First Author: Flynn E
Year: 2014
Journal: Invest Ophthalmol Vis Sci
Title: Fundus autofluorescence and photoreceptor cell rosettes in mouse models.
Volume: 55
Issue: 9
Pages: 5643-52
Publication
First Author: Campbell CI
Year: 2016
Journal: J Cell Sci
Title: The RNF146 and tankyrase pathway maintains the junctional Crumbs complex through regulation of angiomotin.
Volume: 129
Issue: 18
Pages: 3396-411
Publication
First Author: Chen Y
Year: 2013
Journal: J Biol Chem
Title: Autophagy protects the retina from light-induced degeneration.
Volume: 288
Issue: 11
Pages: 7506-18
Publication
First Author: Liao C
Year: 2020
Journal: J Biol Chem
Title: Activation of JNK signaling promotes all-trans-retinal-induced photoreceptor apoptosis in mice.
Volume: 295
Issue: 20
Pages: 6958-6971
Publication
First Author: Zhang N
Year: 2013
Journal: J Clin Invest
Title: Autosomal recessive retinitis pigmentosa E150K opsin mice exhibit photoreceptor disorganization.
Volume: 123
Issue: 1
Pages: 121-37
Publication
First Author: Barber AC
Year: 2013
Journal: Proc Natl Acad Sci U S A
Title: Repair of the degenerate retina by photoreceptor transplantation.
Volume: 110
Issue: 1
Pages: 354-9
Publication
First Author: Samardzija M
Year: 2014
Journal: Invest Ophthalmol Vis Sci
Title: A mouse model for studying cone photoreceptor pathologies.
Volume: 55
Issue: 8
Pages: 5304-13
Publication
First Author: Beryozkin A
Year: 2021
Journal: Sci Rep
Title: A new mouse model for retinal degeneration due to Fam161a deficiency.
Volume: 11
Issue: 1
Pages: 2030
Publication
First Author: Kohno H
Year: 2014
Journal: J Immunol
Title: CCL3 production by microglial cells modulates disease severity in murine models of retinal degeneration.
Volume: 192
Issue: 8
Pages: 3816-27
Publication
First Author: Gosens I
Year: 2007
Journal: Exp Cell Res
Title: FERM protein EPB41L5 is a novel member of the mammalian CRB-MPP5 polarity complex.
Volume: 313
Issue: 19
Pages: 3959-70
Publication  
First Author: Jiang X
Year: 2018
Journal: Gene Expr Patterns
Title: Asymmetric distribution of CRUMBS polarity complex proteins from compacted 8-cell to blastocyst stage during mouse preimplantation development.
Volume: 27
Pages: 93-98
Publication
First Author: Chang B
Year: 2002
Journal: Vision Res
Title: Retinal degeneration mutants in the mouse.
Volume: 42
Issue: 4
Pages: 517-25
Publication
First Author: Kim JY
Year: 2015
Journal: Gene Expr Patterns
Title: Common and distinctive localization patterns of Crumbs polarity complex proteins in the mammalian eye.
Volume: 17
Issue: 1
Pages: 31-7
Publication
First Author: Ramkumar N
Year: 2015
Journal: PLoS Genet
Title: Protein O-Glucosyltransferase 1 (POGLUT1) Promotes Mouse Gastrulation through Modification of the Apical Polarity Protein CRUMBS2.
Volume: 11
Issue: 10
Pages: e1005551
Publication
First Author: Alldredge A
Year: 2016
Journal: Invest Ophthalmol Vis Sci
Title: Loss of Axin2 Causes Ocular Defects During Mouse Eye Development.
Volume: 57
Issue: 13
Pages: 5253-5262
Publication
First Author: Lee JD
Year: 2007
Journal: Development
Title: The FERM protein Epb4.1l5 is required for organization of the neural plate and for the epithelial-mesenchymal transition at the primitive streak of the mouse embryo.
Volume: 134
Issue: 11
Pages: 2007-16
Publication
First Author: Ramkumar N
Year: 2016
Journal: Nat Cell Biol
Title: Crumbs2 promotes cell ingression during the epithelial-to-mesenchymal transition at gastrulation.
Volume: 18
Issue: 12
Pages: 1281-1291
Publication  
First Author: Dudok JJ
Year: 2016
Journal: Neurosci Res
Title: Crumbs 2 prevents cortical abnormalities in mouse dorsal telencephalon.
Volume: 108
Pages: 12-23
Publication      
First Author: JAX Neuroscience Mutagenesis Facility
Year: 2003
Journal: MGI Direct Data Submission
Title: Heritable mouse mutants from JAX NMF ENU Mutagenesis Program
Publication
First Author: Grego-Bessa J
Year: 2015
Journal: Development
Title: Morphogenesis of the mouse neural plate depends on distinct roles of cofilin 1 in apical and basal epithelial domains.
Volume: 142
Issue: 7
Pages: 1305-14
Publication
First Author: Whiteman EL
Year: 2014
Journal: Mol Cell Biol
Title: Crumbs3 is essential for proper epithelial development and viability.
Volume: 34
Issue: 1
Pages: 43-56
Publication
First Author: Sterling N
Year: 2020
Journal: Hum Mol Genet
Title: De novo variants in MPP5 cause global developmental delay and behavioral changes.
Volume: 29
Issue: 20
Pages: 3388-3401