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Search results 1 to 100 out of 128 for Fras1

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Category: Publication
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Type Details Score
Publication
32333816 | J:303217
     
First Author: Kalpachidou T
Year: 2020
Journal: Eur J Neurosci
Title: Behavioural effects of extracellular matrix protein Fras1 depletion in the mouse.
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Publication
12766770 | J:83746
First Author: Vrontou S
Year: 2003
Journal: Nat Genet
Title: Fras1 deficiency results in cryptophthalmos, renal agenesis and blebbed phenotype in mice.
Volume: 34
Issue: 2
Pages: 209-14
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Publication
29618029 | J:262964
First Author: Jordan VK
Year: 2018
Journal: Hum Mol Genet
Title: The role of FREM2 and FRAS1 in the development of congenital diaphragmatic hernia.
Volume: 27
Issue: 12
Pages: 2064-2075
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Publication
17240369 | J:119509
First Author: Petrou P
Year: 2007
Journal: Exp Cell Res
Title: Overlapping and divergent localization of Frem1 and Fras1 and its functional implications during mouse embryonic development.
Volume: 313
Issue: 5
Pages: 910-20
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Publication
24101214 | J:206208
First Author: Makrygiannis AK
Year: 2013
Journal: Histochem Cell Biol
Title: Segmental and restricted localization pattern of Fras1 in the developing meningeal basement membrane in mouse.
Volume: 140
Issue: 5
Pages: 595-601
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Publication
16880404 | J:111788
First Author: Kiyozumi D
Year: 2006
Journal: Proc Natl Acad Sci U S A
Title: Breakdown of the reciprocal stabilization of QBRICK/Frem1, Fras1, and Frem2 at the basement membrane provokes Fraser syndrome-like defects.
Volume: 103
Issue: 32
Pages: 11981-6
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Publication
12766769 | J:83745
First Author: McGregor L
Year: 2003
Journal: Nat Genet
Title: Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein.
Volume: 34
Issue: 2
Pages: 203-8
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Publication
23221805 | J:192553
First Author: Beck TF
Year: 2013
Journal: Hum Mol Genet
Title: Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and mice.
Volume: 22
Issue: 5
Pages: 1026-38
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Publication
15345741 | J:92613
First Author: Smyth I
Year: 2004
Journal: Proc Natl Acad Sci U S A
Title: The extracellular matrix gene Frem1 is essential for the normal adhesion of the embryonic epidermis.
Volume: 101
Issue: 37
Pages: 13560-5
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Publication
15838507 | J:98344
First Author: Jadeja S
Year: 2005
Journal: Nat Genet
Title: Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs.
Volume: 37
Issue: 5
Pages: 520-5
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Publication
18787044 | J:142530
First Author: Pitera JE
Year: 2008
Journal: Hum Mol Genet
Title: Fras1, a basement membrane-associated protein mutated in Fraser syndrome, mediates both the initiation of the mammalian kidney and the integrity of renal glomeruli.
Volume: 17
Issue: 24
Pages: 3953-64
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Publication
23536828 | J:200175
First Author: Beck TF
Year: 2013
Journal: PLoS One
Title: Novel frem1-related mouse phenotypes and evidence of genetic interactions with gata4 and slit3.
Volume: 8
Issue: 3
Pages: e58830
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Publication
17462874 | J:124197
First Author: Kiyozumi D
Year: 2007
Journal: Matrix Biol
Title: Frem3, a member of the 12 CSPG repeats-containing extracellular matrix protein family, is a basement membrane protein with tissue distribution patterns distinct from those of Fras1, Frem2, and QBRICK/Frem1.
Volume: 26
Issue: 6
Pages: 456-62
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Publication
17596926 | J:128304
First Author: Petrou P
Year: 2007
Journal: Matrix Biol
Title: Basement membrane localization of Frem3 is independent of the Fras1/Frem1/Frem2 protein complex within the sublamina densa.
Volume: 26
Issue: 8
Pages: 652-8
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Publication
17251066 | J:117883
First Author: Chiotaki R
Year: 2007
Journal: Gene Expr Patterns
Title: Spatiotemporal distribution of Fras1/Frem proteins during mouse embryonic development.
Volume: 7
Issue: 4
Pages: 381-8
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Publication
22613833 | J:185210
First Author: Kiyozumi D
Year: 2012
Journal: J Cell Biol
Title: Basement membrane assembly of the integrin α8β1 ligand nephronectin requires Fraser syndrome-associated proteins.
Volume: 197
Issue: 5
Pages: 677-89
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Publication
14730302 | J:88266
First Author: Takamiya K
Year: 2004
Journal: Nat Genet
Title: A direct functional link between the multi-PDZ domain protein GRIP1 and the Fraser syndrome protein Fras1.
Volume: 36
Issue: 2
Pages: 172-7
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Publication
23064016 | J:317601
First Author: Pitera JE
Year: 2012
Journal: J Am Soc Nephrol
Title: Sprouty1 haploinsufficiency prevents renal agenesis in a model of Fraser syndrome.
Volume: 23
Issue: 11
Pages: 1790-6
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Publication
36495293 | J:335090
First Author: McLaughlin MT
Year: 2023
Journal: Dev Dyn
Title: Frem1 activity is regulated by Sonic hedgehog signaling in the cranial neural crest mesenchyme during midfacial morphogenesis.
Volume: 252
Issue: 4
Pages: 483-494
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Publication
6391574 | J:7673
First Author: Brown KS
Year: 1984
Journal: Birth Defects Orig Artic Ser
Title: Craniofacial consequences of connective tissue disorders in mice.
Volume: 20
Issue: 3
Pages: 113-36
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Publication
22730198 | J:190659
First Author: Pitera JE
Year: 2012
Journal: Genesis
Title: Generation of mice with a conditional null Fraser syndrome 1 (Fras1) allele.
Volume: 50
Issue: 12
Pages: 892-8
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Publication
24232570 | J:208091
First Author: Richardson RJ
Year: 2014
Journal: J Invest Dermatol
Title: AMACO is a component of the basement membrane-associated Fraser complex.
Volume: 134
Issue: 5
Pages: 1313-1322
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Publication
24143185 | J:208682
First Author: Miller KA
Year: 2013
Journal: PLoS One
Title: bfb, a novel ENU-induced blebs mutant resulting from a missense mutation in Fras1.
Volume: 8
Issue: 10
Pages: e76342
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Publication
27002738 | J:231949
 
First Author: San Agustin JT
Year: 2016
Journal: Nat Commun
Title: Genetic link between renal birth defects and congenital heart disease.
Volume: 7
Pages: 11103
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Publication
15623520 | J:137010
First Author: Petrou P
Year: 2005
Journal: J Biol Chem
Title: Basement membrane distortions impair lung lobation and capillary organization in the mouse model for fraser syndrome.
Volume: 280
Issue: 11
Pages: 10350-6
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Publication
26813283 | J:231083
First Author: Hines EA
Year: 2016
Journal: Dev Dyn
Title: Syndactyly in a novel Fras1(rdf) mutant results from interruption of signals for interdigital apoptosis.
Volume: 245
Issue: 4
Pages: 497-507
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Publication
23669348 | J:199586
First Author: Wang F
Year: 2013
Journal: Hum Mol Genet
Title: Genome-wide loss of 5-hmC is a novel epigenetic feature of Huntington's disease.
Volume: 22
Issue: 18
Pages: 3641-53
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Publication
2166630 | J:30923
First Author: Winter RM
Year: 1990
Journal: Clin Genet
Title: Fraser syndrome and mouse 'bleb' mutants.
Volume: 37
Issue: 6
Pages: 494-5
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Publication
16244325 | J:102757
 
First Author: Smyth I
Year: 2005
Journal: Hum Mol Genet
Title: The genetics of Fraser syndrome and the blebs mouse mutants.
Volume: 14 Spec No. 2
Pages: R269-74
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Publication
25807483 | J:222159
First Author: Li Y
Year: 2015
Journal: Nature
Title: Global genetic analysis in mice unveils central role for cilia in congenital heart disease.
Volume: 521
Issue: 7553
Pages: 520-4
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Publication
- | J:175213
     
First Author: Lo C
Year: 2011
Journal: MGI Direct Data Submission (B2B/CvDC)
Title: Information submitted by the NHLBI Cardiovascular Development Consortium (CvDC), Bench to Bassinet Program (B2B/CvDC)
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Publication
18757743 | J:139122
First Author: Manabe R
Year: 2008
Journal: Proc Natl Acad Sci U S A
Title: Transcriptome-based systematic identification of extracellular matrix proteins.
Volume: 105
Issue: 35
Pages: 12849-54
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Publication
20843830 | J:166958
First Author: Yates LL
Year: 2010
Journal: Hum Mol Genet
Title: The planar cell polarity gene Vangl2 is required for mammalian kidney-branching morphogenesis and glomerular maturation.
Volume: 19
Issue: 23
Pages: 4663-76
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Publication
- | J:13501
 
First Author: Phillips RJS
Year: 1970
Journal: Mouse News Lett
Title: Blebbed, bl
Volume: 42
Pages: 26
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22159717 | J:265604
First Author: Naba A
Year: 2012
Journal: Mol Cell Proteomics
Title: The matrisome: in silico definition and in vivo characterization by proteomics of normal and tumor extracellular matrices.
Volume: 11
Issue: 4
Pages: M111.014647
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Publication
23469164 | J:199856
First Author: Caruana G
Year: 2013
Journal: PLoS One
Title: Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease.
Volume: 8
Issue: 3
Pages: e55429
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12693553 | J:83413
First Author: Okazaki N
Year: 2003
Journal: DNA Res
Title: Prediction of the coding sequences of mouse homologues of KIAA gene: II. The complete nucleotide sequences of 400 mouse KIAA-homologous cDNAs identified by screening of terminal sequences of cDNA clones randomly sampled from size-fractionated libraries.
Volume: 10
Issue: 1
Pages: 35-48
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Publication
17360634 | J:125902
First Author: Koster MI
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: p63 induces key target genes required for epidermal morphogenesis.
Volume: 104
Issue: 9
Pages: 3255-60
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26921296 | J:244712
First Author: Navarro N
Year: 2016
Journal: G3 (Bethesda)
Title: Does 3D Phenotyping Yield Substantial Insights in the Genetics of the Mouse Mandible Shape?
Volume: 6
Issue: 5
Pages: 1153-63
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Publication
- | J:265051
     
First Author: MGI and IMPC
Year: 2018
Journal: Database Release
Title: MGI Load of Endonuclease-Mediated Alleles (CRISPR) from the International Mouse Phenotyping Consortium (IMPC)
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Publication
24550112 | J:208419
First Author: Basta JM
Year: 2014
Journal: Development
Title: Sall1 balances self-renewal and differentiation of renal progenitor cells.
Volume: 141
Issue: 5
Pages: 1047-58
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Publication
- | J:72247
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2001
Title: Gene Ontology Annotation by the MGI Curatorial Staff
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Publication
- | J:293217
       
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
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Publication
- | J:342604
       
First Author: UniProt-GOA
Year: 2012
Title: Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
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Publication
- | J:60000
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2000
Title: Gene Ontology Annotation by electronic association of SwissProt Keywords with GO terms
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Publication
12466851 | J:80000
First Author: Okazaki Y
Year: 2002
Journal: Nature
Title: Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
Volume: 420
Issue: 6915
Pages: 563-73
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Publication
21267068 | J:153498
First Author: Diez-Roux G
Year: 2011
Journal: PLoS Biol
Title: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Volume: 9
Issue: 1
Pages: e1000582
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Publication
- | J:57747
     
First Author: MGI Genome Annotation Group and UniGene Staff
Year: 2015
Journal: Database Download
Title: MGI-UniGene Interconnection Effort
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Publication
- | J:161428
       
First Author: Marc Feuermann, Huaiyu Mi, Pascale Gaudet, Dustin Ebert, Anushya Muruganujan, Paul Thomas
Year: 2010
Title: Annotation inferences using phylogenetic trees
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Publication
- | J:262123
     
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
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Publication
- | J:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
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Publication
- | J:75000
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations
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Publication
- | J:144087
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
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Publication
- | J:63103
     
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
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Publication
- | J:85324
     
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
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Publication
- | J:53168
     
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
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Publication
- | J:91388
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
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Publication
- | J:155721
     
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
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- | J:90438
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
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Publication
- | J:144086
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
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Publication
34321999 | J:313619
 
First Author: Bedogni F
Year: 2021
Journal: Front Mol Neurosci
Title: Cell-Type-Specific Gene Expression in Developing Mouse Neocortex: Intermediate Progenitors Implicated in Axon Development.
Volume: 14
Pages: 686034
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Publication
- | J:157972
     
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome U74 Array Platform (A, B, C v2).
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Publication
21507892 | J:200884
First Author: Slavotinek AM
Year: 2011
Journal: J Med Genet
Title: Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1.
Volume: 48
Issue: 6
Pages: 375-82
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Publication
- | J:136583
     
First Author: Curtain MM
Year: 2008
Journal: MGI Direct Data Submission
Title: A Spontaneous Mouse Strain with Cryptophthalmos
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Publication
- | J:14847
 
First Author: Little CC
Year: 1923
Journal: Am J Roentgenol
Title: The occurrence of two heritable types of abnormality among descendants of X-rayed mice.
Volume: 10
Pages: 975-989
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Publication
- | J:13050
First Author: Carter TC
Year: 1959
Journal: J Genet
Title: Embryology of the Little and Bagg X-rayed mouse stock.
Volume: 56
Issue: 3
Pages: 401-434
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Publication
- | J:221
First Author: Carter TC
Year: 1956
Journal: J Genet
Title: Genetics of the little and Bagg X-rayed mouse stock.
Volume: 54
Issue: 2
Pages: 311-26
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8055142 | J:20762
First Author: Darling S
Year: 1994
Journal: Clin Dysmorphol
Title: A mouse model for Fraser syndrome?
Volume: 3
Issue: 2
Pages: 91-5
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405279 | J:5810
First Author: Center EM
Year: 1977
Journal: Genet Res
Title: Genetical and embryological comparison of two mutations which cause foetal blebs in mice.
Volume: 29
Issue: 2
Pages: 147-57
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Publication
- | J:185265
     
First Author: Karst SY
Year: 2012
Journal: MGI Direct Data Submission
Title: No eyelid is a spontaneous missense mutation in Frem2
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Publication
17246673 | J:155930
First Author: Little CC
Year: 1932
Journal: Genetics
Title: Further Studies on the Genetics of Abnormalities Appearing in the Descendants of X-Rayed Mice.
Volume: 17
Issue: 6
Pages: 674-88
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1515706 | J:1440
First Author: Center EM
Year: 1992
Journal: Histol Histopathol
Title: Etiology of the developing eye in myelencephalic blebs (my) mice.
Volume: 7
Issue: 2
Pages: 231-6
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Publication
6793660 | J:6609
First Author: Varnum DS
Year: 1981
Journal: J Hered
Title: Head blebs: a new mutation on chromosome 4 of the mouse.
Volume: 72
Issue: 4
Pages: 293
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Publication
- | J:64448
 
First Author: Varnum DS
Year: 1976
Journal: Mouse News Lett
Title: heb - head bleb
Volume: 55
Pages: 16
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Publication
9302549 | J:43359
First Author: Center EM
Year: 1997
Journal: Histol Histopathol
Title: Acidic glycosaminoglycans and laminin-1 in renal corpuscles of mutant blebs (my) and control mice.
Volume: 12
Issue: 4
Pages: 901-7
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Publication
31554749 | J:291067
First Author: Kiyozumi D
Year: 2020
Journal: Exp Anim
Title: Genetic mutation of Frem3 does not causeFraser syndrome in mice.
Volume: 69
Issue: 1
Pages: 104-109
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Publication
16087869 | J:101189
First Author: Timmer JR
Year: 2005
Journal: Proc Natl Acad Sci U S A
Title: Tissue morphogenesis and vascular stability require the Frem2 protein, product of the mouse myelencephalic blebs gene.
Volume: 102
Issue: 33
Pages: 11746-50
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Publication
24046351 | J:205063
First Author: Wiradjaja F
Year: 2013
Journal: Dis Model Mech
Title: Regulation of PDGFC signalling and extracellular matrix composition by FREM1 in mice.
Volume: 6
Issue: 6
Pages: 1426-33
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Publication
19732862 | J:154319
First Author: Alazami AM
Year: 2009
Journal: Am J Hum Genet
Title: FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndrome.
Volume: 85
Issue: 3
Pages: 414-8
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Publication
21931569 | J:177282
First Author: Vissers LE
Year: 2011
Journal: PLoS Genet
Title: Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice.
Volume: 7
Issue: 9
Pages: e1002278
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Publication
- | J:30758
       
First Author: Gruneberg H
Year: 1952
Title: The Genetics of the Mouse, second edition
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Publication
30802441 | J:279933
 
First Author: Zhang X
Year: 2019
Journal: Exp Eye Res
Title: Loss-of-function mutations in FREM2 disrupt eye morphogenesis.
Volume: 181
Pages: 302-312
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Publication
33490088 | J:304359
 
First Author: Zhang X
Year: 2020
Journal: Front Cell Dev Biol
Title: The Metabolic Reprogramming of Frem2 Mutant Mice Embryos in Cryptophthalmos Development.
Volume: 8
Pages: 625492
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Publication
21693562 | J:247458
First Author: Marean A
Year: 2011
Journal: Hum Mol Genet
Title: Folic acid supplementation can adversely affect murine neural tube closure and embryonic survival.
Volume: 20
Issue: 18
Pages: 3678-83
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Publication
5088022 | J:140462
First Author: Grüneberg H
Year: 1971
Journal: J Embryol Exp Morphol
Title: Exocrine glands and the Chievitz organ of some mouse mutants.
Volume: 25
Issue: 2
Pages: 247-61
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Publication
820740 | J:5671
First Author: Davisson MT
Year: 1976
Journal: J Hered
Title: Genes on chromosome 3 of the mouse.
Volume: 67
Issue: 3
Pages: 155-6
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Publication
6160178 | J:6433
First Author: Eicher EM
Year: 1980
Journal: J Hered
Title: Assignment of LH XVI to chromosome 3 in the mouse.
Volume: 71
Issue: 5
Pages: 315-8
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Publication
- | J:13728
 
First Author: Fox S
Year: 1977
Journal: Mouse News Lett
Title: Er - Gpd-1 linkage.
Volume: 57
Pages: 21
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Publication
16466971 | J:109155
First Author: Hentges KE
Year: 2006
Journal: Gene Expr Patterns
Title: Novel lethal mouse mutants produced in balancer chromosome screens.
Volume: 6
Issue: 6
Pages: 653-65
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Publication
- | J:89098
     
First Author: The Mouse Genome Project at The Baylor College of Medicine
Year: 2004
Journal: MGI Direct Data Submission
Title: Heritable mouse mutants from the Mouse Mutagenesis for Developmental Defects Program
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Publication
15878328 | J:99700
First Author: Kiyozumi D
Year: 2005
Journal: Exp Cell Res
Title: Identification of a novel cell-adhesive protein spatiotemporally expressed in the basement membrane of mouse developing hair follicle.
Volume: 306
Issue: 1
Pages: 9-23
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Publication
26234751 | J:223062
First Author: Palmer K
Year: 2016
Journal: Dev Biol
Title: Discovery and characterization of spontaneous mouse models of craniofacial dysmorphology.
Volume: 415
Issue: 2
Pages: 216-227
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Publication
33875569 | J:313559
     
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