|  Help  |  About  |  Contact Us

Search our database by keyword

- or -

Examples

  • Search this entire website. Enter identifiers, names or keywords for genes, diseases, strains, ontology terms, etc. (e.g. Pax6, Parkinson, ataxia)
  • Use OR to search for either of two terms (e.g. OR mus) or quotation marks to search for phrases (e.g. "dna binding").
  • Boolean search syntax is supported: e.g. Balb* for partial matches or mus AND NOT embryo to exclude a term

Search results 1 to 100 out of 101 for Wrn

Category restricted to Publication (x)

<< First    < Previous  |  Next >    Last >>
0.04s

Categories

Category: Publication
« show all
Type Details Score
Publication
10871373 | J:62921
First Author: Huang S
Year: 2000
Journal: Nucleic Acids Res
Title: Characterization of the human and mouse WRN 3'-->5' exonuclease.
Volume: 28
Issue: 12
Pages: 2396-405
•
•
•
•
•
Publication
22301954 | J:205393
First Author: Moser R
Year: 2012
Journal: Mol Cancer Res
Title: MYC-driven tumorigenesis is inhibited by WRN syndrome gene deficiency.
Volume: 10
Issue: 4
Pages: 535-45
•
•
•
•
•
Publication
10757812 | J:61567
First Author: Lombard DB
Year: 2000
Journal: Mol Cell Biol
Title: Mutations in the WRN gene in mice accelerate mortality in a p53-null background.
Volume: 20
Issue: 9
Pages: 3286-91
•
•
•
•
•
Publication
33907225 | J:313779
First Author: Kang SM
Year: 2021
Journal: Sci Rep
Title: Human WRN is an intrinsic inhibitor of progerin, abnormal splicing product of lamin A.
Volume: 11
Issue: 1
Pages: 9122
•
•
•
•
•
Publication
26447695 | J:243692
First Author: Aumailley L
Year: 2015
Journal: PLoS One
Title: Metabolic and Phenotypic Differences between Mice Producing a Werner Syndrome Helicase Mutant Protein and Wrn Null Mice.
Volume: 10
Issue: 10
Pages: e0140292
•
•
•
•
•
Publication
11863428 | J:75032
First Author: Xue Y
Year: 2002
Journal: Biochemistry
Title: A minimal exonuclease domain of WRN forms a hexamer on DNA and possesses both 3'- 5' exonuclease and 5'-protruding strand endonuclease activities.
Volume: 41
Issue: 9
Pages: 2901-12
•
•
•
•
•
Publication
29452565 | J:273808
First Author: Aumailley L
Year: 2018
Journal: FASEB J
Title: Serum vitamin C levels modulate the lifespan and endoplasmic reticulum stress response pathways in mice synthesizing a nonfunctional mutant WRN protein.
Volume: 32
Issue: 7
Pages: 3623-3640
•
•
•
•
•
Publication
16330174 | J:106446
First Author: Massip L
Year: 2006
Journal: Exp Gerontol
Title: Increased insulin, triglycerides, reactive oxygen species, and cardiac fibrosis in mice with a mutation in the helicase domain of the Werner syndrome gene homologue.
Volume: 41
Issue: 2
Pages: 157-68
•
•
•
•
•
Publication
16264192 | J:102524
First Author: Laud PR
Year: 2005
Journal: Genes Dev
Title: Elevated telomere-telomere recombination in WRN-deficient, telomere dysfunctional cells promotes escape from senescence and engagement of the ALT pathway.
Volume: 19
Issue: 21
Pages: 2560-70
•
•
•
•
•
Publication
10782115 | J:61954
First Author: Shen JC
Year: 2000
Journal: Trends Genet
Title: The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases.
Volume: 16
Issue: 5
Pages: 213-20
•
•
•
•
•
Publication
15743673 | J:97864
First Author: Chang S
Year: 2005
Journal: Int J Biochem Cell Biol
Title: A mouse model of Werner Syndrome: what can it tell us about aging and cancer?
Volume: 37
Issue: 5
Pages: 991-9
•
•
•
•
•
Publication
18588880 | J:137828
First Author: Kahyo T
Year: 2008
Journal: FEBS Lett
Title: Sirtuin-mediated deacetylation pathway stabilizes Werner syndrome protein.
Volume: 582
Issue: 17
Pages: 2479-83
•
•
•
•
•
Publication
29494634 | J:258744
First Author: Aumailley L
Year: 2018
Journal: PLoS One
Title: Vitamin C alters the amount of specific endoplasmic reticulum associated proteins involved in lipid metabolism in the liver of mice synthesizing a nonfunctional Werner syndrome (Wrn) mutant protein.
Volume: 13
Issue: 3
Pages: e0193170
•
•
•
•
•
Publication
26521679 | J:325816
 
First Author: Aumailley L
Year: 2015
Journal: Exp Gerontol
Title: Impact of vitamin C on the cardiometabolic and inflammatory profiles of mice lacking a functional Werner syndrome protein helicase.
Volume: 72
Pages: 192-203
•
•
•
•
•
Publication
15235603 | J:91715
First Author: Chang S
Year: 2004
Journal: Nat Genet
Title: Essential role of limiting telomeres in the pathogenesis of Werner syndrome.
Volume: 36
Issue: 8
Pages: 877-82
•
•
•
•
•
Publication
9681877 | J:48529
First Author: Wu J
Year: 1998
Journal: Mech Ageing Dev
Title: Effect of age and apoptosis on the mouse homologue of the huWRN gene.
Volume: 103
Issue: 1
Pages: 27-44
•
•
•
•
•
Publication
11301316 | J:69903
First Author: Kawabe Yi
Year: 2001
Journal: J Biol Chem
Title: A novel protein interacts with the Werner's syndrome gene product physically and functionally.
Volume: 276
Issue: 23
Pages: 20364-9
•
•
•
•
•
Publication
10806190 | J:118820
First Author: Kawabe Y
Year: 2000
Journal: J Biol Chem
Title: Covalent modification of the Werner's syndrome gene product with the ubiquitin-related protein, SUMO-1.
Volume: 275
Issue: 28
Pages: 20963-6
•
•
•
•
•
Publication
22753033 | J:199686
First Author: Kanagaraj R
Year: 2012
Journal: Nucleic Acids Res
Title: Involvement of Werner syndrome protein in MUTYH-mediated repair of oxidative DNA damage.
Volume: 40
Issue: 17
Pages: 8449-59
•
•
•
•
•
Publication
12803543 | J:85650
First Author: Bachrati CZ
Year: 2003
Journal: Biochem J
Title: RecQ helicases: suppressors of tumorigenesis and premature aging.
Volume: 374
Issue: Pt 3
Pages: 577-606
•
•
•
•
•
Publication
15367665 | J:93016
First Author: Du X
Year: 2004
Journal: Mol Cell Biol
Title: Telomere shortening exposes functions for the mouse Werner and Bloom syndrome genes.
Volume: 24
Issue: 19
Pages: 8437-46
•
•
•
•
•
Publication
9789047 | J:48424
First Author: Lebel M
Year: 1998
Journal: Proc Natl Acad Sci U S A
Title: A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity.
Volume: 95
Issue: 22
Pages: 13097-102
•
•
•
•
•
Publication
18028256 | J:214652
First Author: Pignolo RJ
Year: 2008
Journal: Aging Cell
Title: Defects in telomere maintenance molecules impair osteoblast differentiation and promote osteoporosis.
Volume: 7
Issue: 1
Pages: 23-31
•
•
•
•
•
Publication
16195394 | J:103920
First Author: Deschênes F
Year: 2005
Journal: Hum Mol Genet
Title: In vivo misregulation of genes involved in apoptosis, development and oxidative stress in mice lacking both functional Werner syndrome protein and poly(ADP-ribose) polymerase-1.
Volume: 14
Issue: 21
Pages: 3293-308
•
•
•
•
•
Publication
12707040 | J:83068
First Author: Lebel M
Year: 2003
Journal: Am J Pathol
Title: Genetic cooperation between the Werner syndrome protein and poly(ADP-ribose) polymerase-1 in preventing chromatid breaks, complex chromosomal rearrangements, and cancer in mice.
Volume: 162
Issue: 5
Pages: 1559-69
•
•
•
•
•
Publication
12242664 | J:79056
First Author: Leder A
Year: 2002
Journal: Oncogene
Title: Genetic interaction between the unstable v-Ha-RAS transgene (Tg.AC) and the murine Werner syndrome gene: transgene instability and tumorigenesis.
Volume: 21
Issue: 43
Pages: 6657-68
•
•
•
•
•
Publication
11420665 | J:69659
First Author: Suzuki T
Year: 2001
Journal: Oncogene
Title: Diverged nuclear localization of Werner helicase in human and mouse cells.
Volume: 20
Issue: 20
Pages: 2551-8
•
•
•
•
•
Publication
12944467 | J:85464
First Author: Cheng WH
Year: 2003
Journal: Mol Cell Biol
Title: Werner syndrome protein phosphorylation by abl tyrosine kinase regulates its activity and distribution.
Volume: 23
Issue: 18
Pages: 6385-95
•
•
•
•
•
Publication
11756244 | J:73919
First Author: Lebel M
Year: 2002
Journal: Carcinogenesis
Title: Increased frequency of DNA deletions in pink-eyed unstable mice carrying a mutation in the Werner syndrome gene homologue.
Volume: 23
Issue: 1
Pages: 213-6
•
•
•
•
•
Publication
11280729 | J:68488
First Author: Lebel M
Year: 2001
Journal: Cancer Res
Title: Tumorigenic effect of nonfunctional p53 or p21 in mice mutant in the Werner syndrome helicase.
Volume: 61
Issue: 5
Pages: 1816-9
•
•
•
•
•
Publication
9143515 | J:39875
First Author: Imamura O
Year: 1997
Journal: Genomics
Title: Cloning of a mouse homologue of the human Werner syndrome gene and assignment to 8A4 by fluorescence in situ hybridization.
Volume: 41
Issue: 2
Pages: 298-300
•
•
•
•
•
Publication
28119126 | J:249400
 
First Author: Rekik K
Year: 2017
Journal: Behav Brain Res
Title: Cognitive deficit in hippocampal-dependent tasks in Werner syndrome mouse model.
Volume: 323
Pages: 68-77
•
•
•
•
•
Publication
24626990 | J:213181
First Author: Brennan TA
Year: 2014
Journal: Dis Model Mech
Title: Mouse models of telomere dysfunction phenocopy skeletal changes found in human age-related osteoporosis.
Volume: 7
Issue: 5
Pages: 583-92
•
•
•
•
•
Publication
10757074 | J:61970
First Author: Oshima J
Year: 2000
Journal: In Vivo
Title: Comparative aspects of the Werner syndrome gene.
Volume: 14
Issue: 1
Pages: 165-72
•
•
•
•
•
Publication
8602509 | J:46871
First Author: Yu CE
Year: 1996
Journal: Science
Title: Positional cloning of the Werner's syndrome gene.
Volume: 272
Issue: 5259
Pages: 258-62
•
•
•
•
•
Publication
23974989 | J:345735
First Author: Wang H
Year: 2013
Journal: J Mol Med (Berl)
Title: R-Spondin 1 promotes vibration-induced bone formation in mouse models of osteoporosis.
Volume: 91
Issue: 12
Pages: 1421-9
•
•
•
•
•
Publication
24608430 | J:218627
First Author: Chung L
Year: 2015
Journal: Oncogene
Title: The FEN1 E359K germline mutation disrupts the FEN1-WRN interaction and FEN1 GEN activity, causing aneuploidy-associated cancers.
Volume: 34
Issue: 7
Pages: 902-11
•
•
•
•
•
Publication
22621437 | J:214714
First Author: Wang H
Year: 2012
Journal: Aging Cell
Title: Impairment of osteoblast differentiation due to proliferation-independent telomere dysfunction in mouse models of accelerated aging.
Volume: 11
Issue: 4
Pages: 704-13
•
•
•
•
•
Publication
26195664 | J:227293
First Author: Drosopoulos WC
Year: 2015
Journal: J Cell Biol
Title: BLM helicase facilitates telomere replication during leading strand synthesis of telomeres.
Volume: 210
Issue: 2
Pages: 191-208
•
•
•
•
•
Publication
25921537 | J:228364
First Author: Yu Q
Year: 2015
Journal: Cell Rep
Title: DNA-damage-induced type I interferon promotes senescence and inhibits stem cell function.
Volume: 11
Issue: 5
Pages: 785-797
•
•
•
•
•
Publication
11087671 | J:66161
First Author: Dron M
Year: 2000
Journal: Genomics
Title: Mouse scrapie responsive gene 1 (Scrg1): genomic organization, physical linkage to sap30, genetic mapping on chromosome 8, and expression in neuronal primary cell cultures.
Volume: 70
Issue: 1
Pages: 140-9
•
•
•
•
•
Publication
16785251 | J:112037
First Author: Sebastiani G
Year: 2006
Journal: Hum Mol Genet
Title: Mapping genetic modulators of amyloid plaque deposition in TgCRND8 transgenic mice.
Volume: 15
Issue: 15
Pages: 2313-23
•
•
•
•
•
Publication
14595844 | J:86589
First Author: McClive PJ
Year: 2003
Journal: Genesis
Title: Subtractive hybridisation screen identifies sexually dimorphic gene expression in the embryonic mouse gonad.
Volume: 37
Issue: 2
Pages: 84-90
•
•
•
•
•
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
•
•
•
•
•
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)
•
•
•
•
•
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
•
•
•
•
•
Publication
- | J:342608
       
First Author: GO Central curators, GOA curators, Rhea curators
Year: 2020
Title: Automatic Gene Ontology annotation based on Rhea mapping
•
•
•
•
•
Publication
- | J:73065
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2001
Title: Gene Ontology Annotation by the MGI Curatorial Staff
•
•
•
•
•
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)
•
•
•
•
•
Publication
- | J:326541
       
First Author: Cyagen Biosciences Inc.
Year: 2022
Title: Cyagen Biosciences Website.
•
•
•
•
•
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
•
•
•
•
•
Publication
- | J:342605
       
First Author: GOA curators
Year: 2016
Title: Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
•
•
•
•
•
Publication
- | J:155856
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Title: Rat to Mouse ISO GO annotation transfer
•
•
•
•
•
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
•
•
•
•
•
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
•
•
•
•
•
Publication
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
•
•
•
•
•
Publication
- | J:293217
       
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
•
•
•
•
•
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
•
•
•
•
•
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
•
•
•
•
•
Publication
- | J:68900
     
First Author: The Jackson Laboratory Mouse Radiation Hybrid Database
Year: 2004
Journal: Database Release
Title: Mouse T31 Radiation Hybrid Data Load
•
•
•
•
•
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
•
•
•
•
•
Publication
- | J:164563
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Title: Human to Mouse ISO GO annotation transfer
•
•
•
•
•
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
•
•
•
•
•
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).
•
•
•
•
•
Publication
- | J:57747
     
First Author: MGI Genome Annotation Group and UniGene Staff
Year: 2015
Journal: Database Download
Title: MGI-UniGene Interconnection Effort
•
•
•
•
•
Publication
- | J:75000
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations
•
•
•
•
•
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
•
•
•
•
•
Publication
- | J:53168
     
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
•
•
•
•
•
Publication
- | J:91388
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
•
•
•
•
•
Publication
- | J:90438
       
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
•
•
•
•
•
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
•
•
•
•
•
Publication
- | J:155221
     
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
•
•
•
•
•
Publication
- | J:63103
     
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
•
•
•
•
•
Publication
- | J:262123
     
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
•
•
•
•
•
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
•
•
•
•
•
Publication
- | J:85324
     
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
•
•
•
•
•
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
•
•
•
•
•
Publication
10628995 | J:95127
First Author: Wang L
Year: 2000
Journal: Genetics
Title: Cellular Werner phenotypes in mice expressing a putative dominant-negative human WRN gene.
Volume: 154
Issue: 1
Pages: 357-62
•
•
•
•
•
Publication
29483835 | J:319607
First Author: Si X
Year: 2018
Journal: Int J Biol Sci
Title: Loss of p21 promoted tumorigenesis in the background of telomere dysfunctions induced by TRF2 and Wrn deficiency.
Volume: 14
Issue: 2
Pages: 165-177
•
•
•
•
•
Publication
12034829 | -
First Author: Liu H
Year: 2002
Journal: Nucleic Acids Res
Title: Distinct proteins encoded by alternative transcripts of the PURG gene, located contrapodal to WRN on chromosome 8, determined by differential termination/polyadenylation.
Volume: 30
Issue: 11
Pages: 2417-26
•
•
•
•
•
Publication
18639560 | J:139038
First Author: Yamamoto ML
Year: 2008
Journal: Mutat Res
Title: Effects of human Werner helicase on intrachromosomal homologous recombination mediated DNA deletions in mice.
Volume: 644
Issue: 1-2
Pages: 11-6
•
•
•
•
•
Publication
9288107 | -
First Author: Gray MD
Year: 1997
Journal: Nat Genet
Title: The Werner syndrome protein is a DNA helicase.
Volume: 17
Issue: 1
Pages: 100-3
•
•
•
•
•
Publication
9697700 | -
First Author: Yan H
Year: 1998
Journal: Nat Genet
Title: Replication focus-forming activity 1 and the Werner syndrome gene product.
Volume: 19
Issue: 4
Pages: 375-8
•
•
•
•
•
Publication
9224595 | -
First Author: Suzuki N
Year: 1997
Journal: Nucleic Acids Res
Title: DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system.
Volume: 25
Issue: 15
Pages: 2973-8
•
•
•
•
•
Publication
33926956 | -
First Author: Pezo V
Year: 2021
Journal: Science
Title: Noncanonical DNA polymerization by aminoadenine-based siphoviruses.
Volume: 372
Issue: 6541
Pages: 520-524
•
•
•
•
•
Publication
15377656 | -
First Author: Andraos N
Year: 2004
Journal: J Biol Chem
Title: The highly processive DNA polymerase of bacteriophage T5. Role of the unique N and C termini.
Volume: 279
Issue: 48
Pages: 50609-18
•
•
•
•
•
Publication
11979727 | J:85891
First Author: Ichikawa K
Year: 2002
Journal: Nihon Yakurigaku Zasshi
Title: [Preparation of the gene targeted knockout mice for human premature aging diseases, Werner syndrome, and Rothmund-Thomson syndrome caused by the mutation of DNA helicases].
Volume: 119
Issue: 4
Pages: 219-26
•
•
•
•
•
Publication
17587522 | J:126579
First Author: Cheng WH
Year: 2007
Journal: Exp Gerontol
Title: Werner syndrome protein: functions in the response to DNA damage and replication stress in S-phase.
Volume: 42
Issue: 9
Pages: 871-8
•
•
•
•
•
Publication
31754102 | J:283828
First Author: Fang EF
Year: 2019
Journal: Nat Commun
Title: NAD+ augmentation restores mitophagy and limits accelerated aging in Werner syndrome.
Volume: 10
Issue: 1
Pages: 5284
•
•
•
•
•
Publication
10647186 | -
First Author: Liu Z
Year: 1999
Journal: Structure
Title: The three-dimensional structure of the HRDC domain and implications for the Werner and Bloom syndrome proteins.
Volume: 7
Issue: 12
Pages: 1557-66
•
•
•
•
•
Publication
15591044 | -
First Author: Armache KJ
Year: 2005
Journal: J Biol Chem
Title: Structures of complete RNA polymerase II and its subcomplex, Rpb4/7.
Volume: 280
Issue: 8
Pages: 7131-4
•
•
•
•
•
Publication
9397680 | -
First Author: Morozov V
Year: 1997
Journal: Trends Biochem Sci
Title: A putative nucleic acid-binding domain in Bloom's and Werner's syndrome helicases.
Volume: 22
Issue: 11
Pages: 417-8
•
•
•
•
•
Publication
11167012 | J:67348
First Author: Ohhata T
Year: 2000
Journal: Gene
Title: Cloning, genomic structure and chromosomal localization of the gene encoding mouse DNA helicase RecQ helicase protein-like 4.
Volume: 261
Issue: 2
Pages: 251-8
•
•
•
•
•
Publication
17961633 | J:141467
First Author: Pereira M
Year: 2007
Journal: Mech Ageing Dev
Title: Interaction of human SUV3 RNA/DNA helicase with BLM helicase; loss of the SUV3 gene results in mouse embryonic lethality.
Volume: 128
Issue: 11-12
Pages: 609-17
•
•
•
•
•
Publication
19145458 | J:144991
First Author: Paul E
Year: 2009
Journal: Mamm Genome
Title: Disruption of Supv3L1 damages the skin and causes sarcopenia, loss of fat, and death.
Volume: 20
Issue: 2
Pages: 92-108
•
•
•
•
•
Publication
23519127 | J:274834
 
First Author: Bopp A
Year: 2013
Journal: Cell Death Dis
Title: Rac1 modulates acute and subacute genotoxin-induced hepatic stress responses, fibrosis and liver aging.
Volume: 4
Pages: e558
•
•
•
•
•
Publication
31757807 | J:284953
First Author: Morales C
Year: 2020
Journal: J Biol Chem
Title: PDS5 proteins are required for proper cohesin dynamics and participate in replication fork protection.
Volume: 295
Issue: 1
Pages: 146-157
•
•
•
•
•
Publication
31523200 | J:282261
First Author: Zhao J
Year: 2019
Journal: Int J Biol Sci
Title: p53 Mutant p53N236S Induces Neural Tube Defects in Female Embryos.
Volume: 15
Issue: 9
Pages: 2006-2015
•
•
•
•
•
Publication
22296597 | J:214934
First Author: Croteau DL
Year: 2012
Journal: Aging Cell
Title: RECQL4 localizes to mitochondria and preserves mitochondrial DNA integrity.
Volume: 11
Issue: 3
Pages: 456-66
•
•
•
•
•
Publication
25901030 | -
First Author: Newman JA
Year: 2015
Journal: Nucleic Acids Res
Title: Crystal structure of the Bloom's syndrome helicase indicates a role for the HRDC domain in conformational changes.
Volume: 43
Issue: 10
Pages: 5221-35
•
•
•
•
•




MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

Copyright © 2017 by The Jackson Laboratory. All Rights Reserved

© 2002 - 2017 Department of Genetics, University of Cambridge, Downing Street,
Cambridge CB2 3EH, United Kingdom