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Search results 1 to 77 out of 77 for Ufd1

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Category: Publication
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Type Details Score
Publication
10811609 | J:220517
First Author: Meyer HH
Year: 2000
Journal: EMBO J
Title: A complex of mammalian ufd1 and npl4 links the AAA-ATPase, p97, to ubiquitin and nuclear transport pathways.
Volume: 19
Issue: 10
Pages: 2181-92
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Publication
10024240 | J:65948
First Author: Yamagishi H
Year: 1999
Journal: Science
Title: A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects.
Volume: 283
Issue: 5405
Pages: 1158-61
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Publication
17202270 | J:248232
First Author: Pye VE
Year: 2007
Journal: Proc Natl Acad Sci U S A
Title: Structural insights into the p97-Ufd1-Npl4 complex.
Volume: 104
Issue: 2
Pages: 467-72
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Publication
22773186 | J:188543
First Author: Piccirillo R
Year: 2012
Journal: EMBO J
Title: The p97/VCP ATPase is critical in muscle atrophy and the accelerated degradation of muscle proteins.
Volume: 31
Issue: 15
Pages: 3334-50
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Publication
9063746 | J:38618
First Author: Pizzuti A
Year: 1997
Journal: Hum Mol Genet
Title: UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome.
Volume: 6
Issue: 2
Pages: 259-65
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Publication
11435701 | J:70472
First Author: Ratti A
Year: 2001
Journal: Cytogenet Cell Genet
Title: Cloning and molecular characterization of three ubiquitin fusion degradation 1 (Ufd1) ortholog genes from Xenopus laevis, Gallus gallus and Drosophila melanogaster.
Volume: 92
Issue: 3-4
Pages: 279-82
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Publication
- | J:70100
   
First Author: Strausberg R
Year: 2001
Journal: GenBank Submission
Title: Mus musculus, clone MGC: 11477, mRNA, complete cds
Pages: BC006630
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Publication
10517636 | J:57757
First Author: Lindsay EA
Year: 1999
Journal: Nature
Title: Congenital heart disease in mice deficient for the DiGeorge syndrome region.
Volume: 401
Issue: 6751
Pages: 379-83
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Publication
11416137 | J:70008
First Author: Yoshida K
Year: 2001
Journal: Mol Cell Biol
Title: Requirement of CDC45 for postimplantation mouse development.
Volume: 21
Issue: 14
Pages: 4598-603
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Publication
11578863 | J:71907
First Author: Kunte A
Year: 2001
Journal: Mech Dev
Title: A common cis-acting sequence in the DiGeorge critical region regulates bi-directional transcription of UFD1L and CDC45L.
Volume: 108
Issue: 1-2
Pages: 81-92
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Publication
9284932 | J:42506
First Author: Botta A
Year: 1997
Journal: Cytogenet Cell Genet
Title: Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 gene.
Volume: 77
Issue: 3-4
Pages: 264-5
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Publication
17000876 | J:221559
First Author: Wang Q
Year: 2006
Journal: J Cell Biol
Title: Regulation of retrotranslocation by p97-associated deubiquitinating enzyme ataxin-3.
Volume: 174
Issue: 7
Pages: 963-71
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Publication
11242049 | J:67409
First Author: Lindsay EA
Year: 2001
Journal: Nature
Title: Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice.
Volume: 410
Issue: 6824
Pages: 97-101
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Publication
12847084 | J:220515
First Author: Ye Y
Year: 2003
Journal: J Cell Biol
Title: Function of the p97-Ufd1-Npl4 complex in retrotranslocation from the ER to the cytosol: dual recognition of nonubiquitinated polypeptide segments and polyubiquitin chains.
Volume: 162
Issue: 1
Pages: 71-84
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Publication
22232657 | J:245245
First Author: Bebeacua C
Year: 2012
Journal: Proc Natl Acad Sci U S A
Title: Distinct conformations of the protein complex p97-Ufd1-Npl4 revealed by electron cryomicroscopy.
Volume: 109
Issue: 4
Pages: 1098-103
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Publication
11804793 | J:74505
First Author: Maynard TM
Year: 2002
Journal: Mech Dev
Title: RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction.
Volume: 111
Issue: 1-2
Pages: 177-80
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Publication
18775783 | J:142422
First Author: Maynard TM
Year: 2008
Journal: Mol Cell Neurosci
Title: Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes.
Volume: 39
Issue: 3
Pages: 439-51
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Publication
27184122 | J:240212
First Author: Devaraju P
Year: 2017
Journal: Mol Psychiatry
Title: Haploinsufficiency of the 22q11.2 microdeletion gene Mrpl40 disrupts short-term synaptic plasticity and working memory through dysregulation of mitochondrial calcium.
Volume: 22
Issue: 9
Pages: 1313-1326
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Publication
9383280 | J:44451
First Author: Botta A
Year: 1997
Journal: Mamm Genome
Title: Comparative mapping of the DiGeorge syndrome region in mouse shows inconsistent gene order and differential degree of gene conservation.
Volume: 8
Issue: 12
Pages: 890-5
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Publication
17097888 | J:116629
First Author: Meechan DW
Year: 2006
Journal: Mol Cell Neurosci
Title: Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome.
Volume: 33
Issue: 4
Pages: 412-28
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Publication
10625532 | J:59338
First Author: Clouthier DE
Year: 2000
Journal: Dev Biol
Title: Signaling pathways crucial for craniofacial development revealed by endothelin-A receptor-deficient mice.
Volume: 217
Issue: 1
Pages: 10-24
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Publication
9740669 | J:49844
First Author: Sutherland HF
Year: 1998
Journal: Genomics
Title: Cloning and comparative mapping of the DiGeorge syndrome critical region in the mouse.
Volume: 52
Issue: 1
Pages: 37-43
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19805316 | J:153232
First Author: Meechan DW
Year: 2009
Journal: Proc Natl Acad Sci U S A
Title: Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome.
Volume: 106
Issue: 38
Pages: 16434-45
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Publication
11389549 | J:69146
First Author: Hwang SY
Year: 2001
Journal: Mol Reprod Dev
Title: Expression of genes involved in mammalian meiosis during the transition from egg to embryo.
Volume: 59
Issue: 2
Pages: 144-58
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Publication
23077214 | J:191130
First Author: Maynard TM
Year: 2013
Journal: Hum Mol Genet
Title: 22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development.
Volume: 22
Issue: 2
Pages: 300-12
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Publication
10963672 | J:64380
First Author: Puech A
Year: 2000
Journal: Proc Natl Acad Sci U S A
Title: Normal cardiovascular development in mice deficient for 16 genes in 550 kb of the velocardiofacial/DiGeorge syndrome region.
Volume: 97
Issue: 18
Pages: 10090-5
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Publication
15778864 | J:98850
First Author: Prescott K
Year: 2005
Journal: Hum Genet
Title: Microarray analysis of the Df1 mouse model of the 22q11 deletion syndrome.
Volume: 116
Issue: 6
Pages: 486-96
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Publication
10704284 | J:60871
First Author: Lund J
Year: 2000
Journal: Genomics
Title: Comparative sequence analysis of 634 kb of the mouse chromosome 16 region of conserved synteny with the human velocardiofacial syndrome region on chromosome 22q11.2.
Volume: 63
Issue: 3
Pages: 374-83
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Publication
9405660 | J:45079
First Author: Puech A
Year: 1997
Journal: Proc Natl Acad Sci U S A
Title: Comparative mapping of the human 22q11 chromosomal region and the orthologous region in mice reveals complex changes in gene organization.
Volume: 94
Issue: 26
Pages: 14608-13
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Publication
10337614 | J:54501
First Author: Lund J
Year: 1999
Journal: Mamm Genome
Title: Sequence-ready physical map of the mouse chromosome 16 region with conserved synteny to the human velocardiofacial syndrome region on 22q11.2.
Volume: 10
Issue: 5
Pages: 438-43
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Publication
25452572 | J:235630
First Author: Paronett EM
Year: 2015
Journal: Cereb Cortex
Title: Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.
Volume: 25
Issue: 10
Pages: 3977-93
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Publication
14614146 | J:86704
First Author: Maynard TM
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: A comprehensive analysis of 22q11 gene expression in the developing and adult brain.
Volume: 100
Issue: 24
Pages: 14433-8
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Publication
24357327 | J:213451
First Author: Karpinski BA
Year: 2014
Journal: Dis Model Mech
Title: Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome.
Volume: 7
Issue: 2
Pages: 245-57
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Publication
- | J:342601
       
First Author: UniProt-GOA
Year: 2012
Title: Gene Ontology annotation based on UniPathway vocabulary mapping
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Publication
- | J:157064
     
First Author: University of California, Davis
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by the University of California, Davis
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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
12520002 | J:91812
First Author: Stryke D
Year: 2003
Journal: Nucleic Acids Res
Title: BayGenomics: a resource of insertional mutations in mouse embryonic stem cells.
Volume: 31
Issue: 1
Pages: 278-81
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Publication
- | J:57656
     
First Author: Lennon G
Year: 1999
Journal: Database Download
Title: WashU-HHMI Mouse EST Project
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Publication
- | J:148605
     
First Author: Wellcome Trust Sanger Institute
Year: 2009
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by the Wellcome Trust Sanger Institute
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Publication
18799693 | J:142754
First Author: Hansen GM
Year: 2008
Journal: Genome Res
Title: Large-scale gene trapping in C57BL/6N mouse embryonic stem cells.
Volume: 18
Issue: 10
Pages: 1670-9
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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: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: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
11217851 | J:65060
First Author: Kawai J
Year: 2001
Journal: Nature
Title: Functional annotation of a full-length mouse cDNA collection.
Volume: 409
Issue: 6821
Pages: 685-90
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14610273 | J:86696
First Author: Zambrowicz BP
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.
Volume: 100
Issue: 24
Pages: 14109-14
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Publication
- | J:23000
       
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
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Publication
- | J:141210
     
First Author: Mouse Genome Informatics (MGI) and National Center for Biotechnology Information (NCBI)
Year: 2008
Journal: Database Download
Title: Mouse Gene Trap Data Load from dbGSS
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21677750 | J:173534
First Author: Skarnes WC
Year: 2011
Journal: Nature
Title: A conditional knockout resource for the genome-wide study of mouse gene function.
Volume: 474
Issue: 7351
Pages: 337-42
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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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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: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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- | 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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- | 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:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
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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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- | 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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- | 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
16004872 | -
First Author: Park S
Year: 2005
Journal: Structure
Title: Ufd1 exhibits the AAA-ATPase fold with two distinct ubiquitin interaction sites.
Volume: 13
Issue: 7
Pages: 995-1005
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Publication
20206597 | -
First Author: Barbin L
Year: 2010
Journal: Biochem Biophys Res Commun
Title: The Cdc48-Ufd1-Npl4 complex is central in ubiquitin-proteasome triggered catabolite degradation of fructose-1,6-bisphosphatase.
Volume: 394
Issue: 2
Pages: 335-41
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Publication
28355556 | -
First Author: Maric M
Year: 2017
Journal: Cell Rep
Title: Ufd1-Npl4 Recruit Cdc48 for Disassembly of Ubiquitylated CMG Helicase at the End of Chromosome Replication.
Volume: 18
Issue: 13
Pages: 3033-3042
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26471729 | J:227762
First Author: Hao Q
Year: 2015
Journal: EMBO J
Title: A non-canonical role of the p97 complex in RIG-I antiviral signaling.
Volume: 34
Issue: 23
Pages: 2903-20
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17880284 | -
First Author: Galvão RM
Year: 2008
Journal: Biochem J
Title: Characterization of a new family of protein kinases from Arabidopsis containing phosphoinositide 3/4-kinase and ubiquitin-like domains.
Volume: 409
Issue: 1
Pages: 117-27
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28254780 | -
First Author: Song S
Year: 2017
Journal: Plant Cell
Title: OsFTIP1-Mediated Regulation of Florigen Transport in Rice Is Negatively Regulated by the Ubiquitin-Like Domain Kinase OsUbDKγ4.
Volume: 29
Issue: 3
Pages: 491-507
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20691684 | J:201304
First Author: Kaneko Y
Year: 2010
Journal: FEBS Lett
Title: Isolation of a point-mutated p47 lacking binding affinity to p97ATPase.
Volume: 584
Issue: 18
Pages: 3873-7
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11740563 | J:73327
First Author: Ye Y
Year: 2001
Journal: Nature
Title: The AAA ATPase Cdc48/p97 and its partners transport proteins from the ER into the cytosol.
Volume: 414
Issue: 6864
Pages: 652-6
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