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Search results 501 to 600 out of 649 for Fbn1

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Type Details Score
Publication
29769563 | J:262736
First Author: Renard M
Year: 2018
Journal: Sci Rep
Title: Expressed repetitive elements are broadly applicable reference targets for normalization of reverse transcription-qPCR data in mice.
Volume: 8
Issue: 1
Pages: 7642
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Publication
21493863 | J:171337
First Author: Habashi JP
Year: 2011
Journal: Science
Title: Angiotensin II type 2 receptor signaling attenuates aortic aneurysm in mice through ERK antagonism.
Volume: 332
Issue: 6027
Pages: 361-5
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Publication
29520069 | J:260742
First Author: Lino Cardenas CL
Year: 2018
Journal: Nat Commun
Title: An HDAC9-MALAT1-BRG1 complex mediates smooth muscle dysfunction in thoracic aortic aneurysm.
Volume: 9
Issue: 1
Pages: 1009
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Publication
25086405 | J:299130
First Author: Cui JZ
Year: 2014
Journal: J Struct Biol
Title: Quantification of aortic and cutaneous elastin and collagen morphology in Marfan syndrome by multiphoton microscopy.
Volume: 187
Issue: 3
Pages: 242-253
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Publication
33175881 | J:297559
First Author: Hara H
Year: 2020
Journal: PLoS One
Title: Inhibition of transforming growth factor-β signaling in myeloid cells ameliorates aortic aneurysmal formation in Marfan syndrome.
Volume: 15
Issue: 11
Pages: e0239908
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Publication
36812308 | J:333676
First Author: Feng B
Year: 2023
Journal: Sci Adv
Title: Asprosin promotes feeding through SK channel-dependent activation of AgRP neurons.
Volume: 9
Issue: 8
Pages: eabq6718
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Publication
8603845 | J:31798
First Author: Smith RS
Year: 1996
Journal: Invest Ophthalmol Vis Sci
Title: Corn1: a mouse model for corneal surface disease and neovascularization.
Volume: 37
Issue: 2
Pages: 397-404
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Publication
19349279 | J:151111
First Author: Ono RN
Year: 2009
Journal: J Biol Chem
Title: Latent transforming growth factor beta-binding proteins and fibulins compete for fibrillin-1 and exhibit exquisite specificities in binding sites.
Volume: 284
Issue: 25
Pages: 16872-81
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Publication
7902327 | J:14564
First Author: Siracusa LD
Year: 1993
Journal: Genomics
Title: The tight skin (Tsk) mutation in the mouse, a model for human fibrotic diseases, is tightly linked to the beta 2-microglobulin (B2m) gene on chromosome 2.
Volume: 17
Issue: 3
Pages: 748-51
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Publication
8006086 | J:18222
 
First Author: Davis EC
Year: 1994
Journal: J Cell Sci
Title: Immunolocalization of microfibril and microfibril-associated proteins in the subendothelial matrix of the developing mouse aorta.
Volume: 107 ( Pt 3)
Pages: 727-36
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Publication
- | J:30359
       
First Author: Sundberg JP (ed.)
Year: 1994
Title: Handbook of Mouse Mutations with Skin and Hair Abnormalities: Animal Models and Biomedical Tools
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Publication
29093270 | J:282119
 
First Author: Koenig SN
Year: 2017
Journal: JCI Insight
Title: Notch1 haploinsufficiency causes ascending aortic aneurysms in mice.
Volume: 2
Issue: 21
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Publication
24531548 | J:209641
First Author: Cook JR
Year: 2014
Journal: J Clin Invest
Title: Abnormal muscle mechanosignaling triggers cardiomyopathy in mice with Marfan syndrome.
Volume: 124
Issue: 3
Pages: 1329-39
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Publication
35768505 | J:335104
First Author: Sladitschek-Martens HL
Year: 2022
Journal: Nature
Title: YAP/TAZ activity in stromal cells prevents ageing by controlling cGAS-STING.
Volume: 607
Issue: 7920
Pages: 790-798
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Publication
21778429 | J:188834
First Author: Shen D
Year: 2011
Journal: Circ Res
Title: Aortic aneurysm generation in mice with targeted deletion of integrin-linked kinase in vascular smooth muscle cells.
Volume: 109
Issue: 6
Pages: 616-28
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Publication
30429287 | J:268288
First Author: Hu C
Year: 2018
Journal: J Immunol
Title: Complement Inhibitor CRIg/FH Ameliorates Renal Ischemia Reperfusion Injury via Activation of PI3K/AKT Signaling.
Volume: 201
Issue: 12
Pages: 3717-3730
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Publication
21493862 | J:171338
First Author: Holm TM
Year: 2011
Journal: Science
Title: Noncanonical TGFβ signaling contributes to aortic aneurysm progression in Marfan syndrome mice.
Volume: 332
Issue: 6027
Pages: 358-61
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Publication
8111131 | J:16399
First Author: Everett ET
Year: 1994
Journal: Mamm Genome
Title: The tight-skin (Tsk) mutation is closely linked to B2m on mouse chromosome 2.
Volume: 5
Issue: 1
Pages: 55-7
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Publication
7959775 | J:19416
First Author: Douté RC
Year: 1994
Journal: Genomics
Title: Tight-skin (Tsk) maps on mouse chromosome 2 within the region of linkage homology with human chromosome 15.
Volume: 22
Issue: 1
Pages: 223-5
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Publication
17015622 | J:114987
First Author: Ge G
Year: 2006
Journal: J Cell Biol
Title: BMP1 controls TGFbeta1 activation via cleavage of latent TGFbeta-binding protein.
Volume: 175
Issue: 1
Pages: 111-20
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Publication
32948785 | J:296352
First Author: Imhof T
Year: 2020
Journal: Sci Rep
Title: EMILIN proteins are novel extracellular constituents of the dentin-pulp complex.
Volume: 10
Issue: 1
Pages: 15320
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Publication
37252932 | J:336178
First Author: Yao SQ
Year: 2023
Journal: PLoS One
Title: Retinal transcriptome of neonatal mice after optic nerve injury.
Volume: 18
Issue: 5
Pages: e0286344
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Publication
11470817 | J:70592
First Author: Arteaga-Solis E
Year: 2001
Journal: J Cell Biol
Title: Regulation of limb patterning by extracellular microfibrils.
Volume: 154
Issue: 2
Pages: 275-81
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Publication
23055981 | J:190996
 
First Author: d'Amaro R
Year: 2012
Journal: Front Physiol
Title: Putative functions of extracellular matrix glycoproteins in secondary palate morphogenesis.
Volume: 3
Pages: 377
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Publication
31201465 | J:295274
First Author: Oichi T
Year: 2019
Journal: Cell Mol Life Sci
Title: Adamts17 is involved in skeletogenesis through modulation of BMP-Smad1/5/8 pathway.
Volume: 76
Issue: 23
Pages: 4795-4809
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Publication
10848613 | J:62831
First Author: Shipley JM
Year: 2000
Journal: Mol Cell Biol
Title: Developmental expression of latent transforming growth factor beta binding protein 2 and its requirement early in mouse development.
Volume: 20
Issue: 13
Pages: 4879-87
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Publication
36779913 | J:334253
 
First Author: Stavely R
Year: 2023
Journal: Development
Title: A distinct transcriptome characterizes neural crest-derived cells at the migratory wavefront during enteric nervous system development.
Volume: 150
Issue: 5
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Publication
30738849 | J:280264
 
First Author: Hubmacher D
Year: 2019
Journal: Matrix Biol
Title: Limb- and tendon-specific Adamtsl2 deletion identifies a role for ADAMTSL2 in tendon growth in a mouse model for geleophysic dysplasia.
Volume: 82
Pages: 38-53
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Publication
21780244 | J:174611
First Author: Azhar M
Year: 2011
Journal: Dev Dyn
Title: Transforming growth factor Beta2 is required for valve remodeling during heart development.
Volume: 240
Issue: 9
Pages: 2127-41
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Publication
20498044 | J:161299
First Author: Ito Y
Year: 2010
Journal: Proc Natl Acad Sci U S A
Title: The Mohawk homeobox gene is a critical regulator of tendon differentiation.
Volume: 107
Issue: 23
Pages: 10538-42
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Publication
26405179 | J:226844
First Author: Collin GB
Year: 2015
Journal: Hum Mol Genet
Title: Disruption of murine Adamtsl4 results in zonular fiber detachment from the lens and in retinal pigment epithelium dedifferentiation.
Volume: 24
Issue: 24
Pages: 6958-74
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Publication
7633422 | J:24936
First Author: Chiannilkulchai N
Year: 1995
Journal: Hum Mol Genet
Title: A primary expression map of the chromosome 15q15 region containing the recessive form of limb-girdle muscular dystrophy (LGMD2A) gene.
Volume: 4
Issue: 4
Pages: 717-25
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Publication
9415455 | J:44473
First Author: Nakajima Y
Year: 1997
Journal: Anat Rec
Title: Distribution of fibronectin, type I collagen, type IV collagen, and laminin in the cardiac jelly of the mouse embryonic heart with retinoic acid-induced complete transposition of the great arteries.
Volume: 249
Issue: 4
Pages: 478-85
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Publication
25670798 | J:218158
First Author: Turner CJ
Year: 2015
Journal: Development
Title: α5 and αv integrins cooperate to regulate vascular smooth muscle and neural crest functions in vivo.
Volume: 142
Issue: 4
Pages: 797-808
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Publication
15733672 | J:96550
First Author: Williams TM
Year: 2005
Journal: Dev Biol
Title: Candidate downstream regulated genes of HOX group 13 transcription factors with and without monomeric DNA binding capability.
Volume: 279
Issue: 2
Pages: 462-80
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Publication
33722956 | J:306108
 
First Author: Karpinski BA
Year: 2022
Journal: Dis Model Mech
Title: Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome.
Volume: 15
Issue: 2
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Publication
36207400 | J:329931
First Author: Molla MR
Year: 2022
Journal: Commun Biol
Title: Vascular smooth muscle RhoA counteracts abdominal aortic aneurysm formation by modulating MAP4K4 activity.
Volume: 5
Issue: 1
Pages: 1071
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Publication
18651661 | J:139011
First Author: Wilkinson GA
Year: 2008
Journal: Dev Dyn
Title: Role for ephrinB2 in postnatal lung alveolar development and elastic matrix integrity.
Volume: 237
Issue: 8
Pages: 2220-34
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Publication
31550482 | J:278988
     
First Author: Tian C
Year: 2019
Journal: Dev Biol
Title: TBX1 is required for normal stria vascularis and semicircular canal development.
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Publication
29567669 | J:283038
First Author: Gharibeh L
Year: 2018
Journal: Circulation
Title: GATA6 Regulates Aortic Valve Remodeling, and Its Haploinsufficiency Leads to Right-Left Type Bicuspid Aortic Valve.
Volume: 138
Issue: 10
Pages: 1025-1038
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Publication
11518254 | J:72151
First Author: Drake TA
Year: 2001
Journal: J Orthop Res
Title: Genetic loci influencing natural variations in femoral bone morphometry in mice.
Volume: 19
Issue: 4
Pages: 511-7
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Publication
18258849 | J:132011
First Author: Sun J
Year: 2008
Journal: Am J Pathol
Title: Prenatal lung epithelial cell-specific abrogation of Alk3-bone morphogenetic protein signaling causes neonatal respiratory distress by disrupting distal airway formation.
Volume: 172
Issue: 3
Pages: 571-82
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Publication
28302382 | J:251389
 
First Author: Zakariyah AF
Year: 2017
Journal: J Mol Cell Cardiol
Title: Congenital heart defect causing mutation in Nkx2.5 displays in vivo functional deficit.
Volume: 105
Pages: 89-98
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Publication
21979435 | J:179089
First Author: Jaffe M
Year: 2012
Journal: Arterioscler Thromb Vasc Biol
Title: Transforming growth factor-β signaling in myogenic cells regulates vascular morphogenesis, differentiation, and matrix synthesis.
Volume: 32
Issue: 1
Pages: e1-11
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Publication
35894043 | J:334587
First Author: Wang L
Year: 2022
Journal: Circ Res
Title: Endothelial Loss of ETS1 Impairs Coronary Vascular Development and Leads to Ventricular Non-Compaction.
Volume: 131
Issue: 5
Pages: 371-387
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Publication
34189436 | J:311873
First Author: Ye S
Year: 2021
Journal: iScience
Title: Adamts18 modulates the development of the aortic arch and common carotid artery.
Volume: 24
Issue: 6
Pages: 102672
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Publication
27527664 | J:241460
 
First Author: Nakamichi R
Year: 2016
Journal: Nat Commun
Title: Mohawk promotes the maintenance and regeneration of the outer annulus fibrosus of intervertebral discs.
Volume: 7
Pages: 12503
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Publication
23658023 | J:213088
First Author: Soteriou D
Year: 2013
Journal: J Biol Chem
Title: Comparative proteomic analysis of supportive and unsupportive extracellular matrix substrates for human embryonic stem cell maintenance.
Volume: 288
Issue: 26
Pages: 18716-31
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Publication
30578393 | J:296772
 
First Author: Yin W
Year: 2019
Journal: Eur Respir J
Title: Fibrillin-2 is a key mediator of smooth muscle extracellular matrix homeostasis during mouse tracheal tubulogenesis.
Volume: 53
Issue: 3
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Publication
35167946 | J:321553
 
First Author: Neupane S
Year: 2022
Journal: Matrix Biol
Title: O-fucosylation of thrombospondin type 1 repeats is essential for ECM remodeling and signaling during bone development.
Volume: 107
Pages: 77-96
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Publication
32882513 | J:306850
First Author: Lu T
Year: 2020
Journal: iScience
Title: ADAMTS18 Deficiency Leads to Pulmonary Hypoplasia and Bronchial Microfibril Accumulation.
Volume: 23
Issue: 9
Pages: 101472
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Publication
34323105 | J:321251
First Author: Yang N
Year: 2022
Journal: J Dent Res
Title: Adamts18 Deficiency Causes Spontaneous SMG Fibrogenesis in Adult Mice.
Volume: 101
Issue: 2
Pages: 226-234
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Publication
30389913 | J:268349
First Author: Kim HT
Year: 2018
Journal: Nat Commun
Title: Myh10 deficiency leads to defective extracellular matrix remodeling and pulmonary disease.
Volume: 9
Issue: 1
Pages: 4600
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Publication
- | J:169366
     
First Author: MouseBookTM
Year: 2005
Journal: Unpublished
Title: Information obtained from MouseBookTM, Medical Research Council Mammalian Genetics Unit, Harwell, UK.
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Publication
28071719 | J:265607
 
First Author: Naba A
Year: 2017
Journal: Sci Rep
Title: Quantitative proteomic profiling of the extracellular matrix of pancreatic islets during the angiogenic switch and insulinoma progression.
Volume: 7
Pages: 40495
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Publication
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
19334288 | J:148410
First Author: Combes AN
Year: 2009
Journal: Dev Dyn
Title: Three-dimensional visualization of testis cord morphogenesis, a novel tubulogenic mechanism in development.
Volume: 238
Issue: 5
Pages: 1033-41
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Publication
24006456 | J:221550
First Author: Abonnenc M
Year: 2013
Journal: Circ Res
Title: Extracellular matrix secretion by cardiac fibroblasts: role of microRNA-29b and microRNA-30c.
Volume: 113
Issue: 10
Pages: 1138-47
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Publication
- | J:238766
     
First Author: Shanghai Model Organisms Center
Year: 2017
Journal: MGI Direct Data Submission
Title: Information obtained from the Shanghai Model Organisms Center (SMOC), Shanghai, China
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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:346132
       
First Author: The Gene Ontology Consortium
Year: 2016
Title: Automatic assignment of GO terms using logical inference, based on on inter-ontology links
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Publication
- | J:80155
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations for FANTOM2 data
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Publication
- | J:326541
       
First Author: Cyagen Biosciences Inc.
Year: 2022
Title: Cyagen Biosciences Website.
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Publication
- | J:171409
     
First Author: GUDMAP Consortium
Year: 2004
Journal: www.gudmap.org
Title: GUDMAP: the GenitoUrinary Development Molecular Anatomy Project
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Publication
- | J:211773
     
First Author: Mouse Genome Informatics and the International Mouse Phenotyping Consortium (IMPC)
Year: 2014
Journal: Database Release
Title: Obtaining and Loading Phenotype Annotations from the International Mouse Phenotyping Consortium (IMPC) Database
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Publication
- | J:342605
       
First Author: GOA curators
Year: 2016
Title: Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
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Publication
- | J:155856
       
First Author: The Gene Ontology Consortium
Year: 2014
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-rat orthologs
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Publication
16602821 | J:162220
First Author: Magdaleno S
Year: 2006
Journal: PLoS Biol
Title: BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system.
Volume: 4
Issue: 4
Pages: e86
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Publication
16141072 | J:99680
First Author: Carninci P
Year: 2005
Journal: Science
Title: The transcriptional landscape of the mammalian genome.
Volume: 309
Issue: 5740
Pages: 1559-63
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Publication
38355793 | J:345621
First Author: Adams DJ
Year: 2024
Journal: Nature
Title: Genetic determinants of micronucleus formation in vivo.
Volume: 627
Issue: 8002
Pages: 130-136
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Publication
- | J:293217
       
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
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Publication
- | J:60000
       
First Author: UniProt-GOA
Year: 2012
Title: Gene Ontology annotation based on UniProtKB/Swiss-Prot keyword mapping
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Publication
- | J:342587
       
First Author: AgBase, BHF-UCL, Parkinson's UK-UCL, dictyBase, HGNC, Roslin Institute, FlyBase and UniProtKB curators
Year: 2011
Title: Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
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Publication
- | J:68900
     
First Author: The Jackson Laboratory Mouse Radiation Hybrid Database
Year: 2004
Journal: Database Release
Title: Mouse T31 Radiation Hybrid Data Load
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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
- | J:164563
       
First Author: The Gene Ontology Consortium
Year: 2010
Title: Automated transfer of experimentally-verified manual GO annotation data to mouse-human orthologs
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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: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
- | 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: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: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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Publication
- | J:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
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Publication
- | 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
- | 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:262123
     
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
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HT Experiment
GSE202780 | RNAseq of mitral valves from Fbn1 C1039G/+ mice with or without CCR2 deficiency
 
Experiment Type: RNA-Seq
Study Type: WT vs. Mutant
Source: GEO
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GXD Expression
GXD Expression
Probe: MGI:6874592
Assay Type: Immunohistochemistry
Annotation Date: 2022-02-21
Strength: Present
Sex: Not Specified
Emaps: EMAPS:3567624
Pattern: Not Specified
Stage: TS24
Assay Id: MGI:6874604
Age: embryonic day 16.5
Image: 4G/I
Note: Expression of Thsd4 co-localized with Fbn1 in the perichondrium.
Specimen Label: 4G/I
Detected: true
Specimen Num: 1
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DO Term
DOID:0111150 | autosomal dominant isolated ectopia lentis 1
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•
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Allele
Fbn1<em4Smoc> | MGI:7289622
Name: fibrillin 1; endonuclease-mediated mutation 4, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Not Specified
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•
•
•
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DO Term
DOID:0111726 | geleophysic dysplasia 2
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•
•
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Allele
Fbn1<em3Smoc> | MGI:7289621
Name: fibrillin 1; endonuclease-mediated mutation3, Shanghai Model Organisms Center
Allele Type: Endonuclease-mediated
Attribute String: Null/knockout
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•
•
•
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Strain
MGI:6475254 | C57BL/6-Fbn1<em4Smoc>/Smoc
Attribute String: coisogenic, endonuclease-mediated mutation, mutant strain
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•
•
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DO Term
DOID:0111561 | stiff skin syndrome
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•
•
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•
Allele
Fbn1<Tsk> | MGI:1857348
 
Name: fibrillin 1; tight skin
Allele Type: Spontaneous
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•
•
•
•
DO Term
DOID:0111243 | acromicric dysplasia
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•
•
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