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Search results 401 to 487 out of 487 for Timeless

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0.036s
Type Details Score
Allele  
Name: timeless interacting protein; gene trap OST431478, Lexicon Genetics
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap XT0299, Wellcome Trust Sanger Institute
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap PST10830, Mammalian Functional Genomics Centre
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap E001G05, German Gene Trap Consortium
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap OST253427, Lexicon Genetics
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap EUCE0044g03, Helmholtz Zentrum Muenchen GmbH
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap PST10996, Mammalian Functional Genomics Centre
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap OST62644, Lexicon Genetics
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap OST225627, Lexicon Genetics
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap IST14472C11, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap EUCE0275g10, Helmholtz Zentrum Muenchen GmbH
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap EUCE00155f04, Helmholtz Zentrum Muenchen GmbH
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap EUCE0023f06, Helmholtz Zentrum Muenchen GmbH
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap E301D09, German Gene Trap Consortium
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap E301E04, German Gene Trap Consortium
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap EUCE00136f07, Helmholtz Zentrum Muenchen GmbH
Allele Type: Gene trapped
Allele
Name: timeless circadian clock 1; targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
Allele Type: Targeted
Attribute String: Null/knockout, Reporter
Allele  
Name: timeless circadian clock 1; gene trap AB0255, Wellcome Trust Sanger Institute
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap Q016E05, German Gene Trap Consortium
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap IST14509B9, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele
Name: timeless circadian clock 1; targeted mutation 1e, Helmholtz Zentrum Muenchen GmbH
Allele Type: Targeted
Attribute String: Null/knockout, Reporter
Allele
Name: timeless circadian clock 1; targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH
Allele Type: Targeted
Attribute String: Conditional ready, Null/knockout, Reporter
Strain
Attribute String: coisogenic, endonuclease-mediated mutation, mutant strain
Allele  
Name: timeless circadian clock 1; gene trap PST20418, Mammalian Functional Genomics Centre
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap PST620, Mammalian Functional Genomics Centre
Allele Type: Gene trapped
Strain
Attribute String: congenic, mutant strain, targeted mutation
Strain
Attribute String: mutant strain, targeted mutation, congenic
Allele  
Name: timeless circadian clock 1; gene trap A050B05, German Gene Trap Consortium
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap IST10977D12, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap EUCE00104c09, Helmholtz Zentrum Muenchen GmbH
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap IST13907A10, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap P065A09, German Gene Trap Consortium
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap IST15026H8, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless circadian clock 1; gene trap IST13203E7, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST13779C2, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap 411H3, Centre for Modeling Human Disease
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap 400H10, Centre for Modeling Human Disease
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST13996B5, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap GC0406, Telethon Institute of Genetics and Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST15070G5, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST14592H7, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap GC0470, Telethon Institute of Genetics and Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST13441H9, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST14841F11, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST14228E1, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST15076D8, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST13636C2, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap GC0741, Telethon Institute of Genetics and Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST14176A6, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST14785C5, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST13957F3, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST14517D6, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST14641C3, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Allele  
Name: timeless interacting protein; gene trap IST13262A12, Texas A&M Institute for Genomic Medicine
Allele Type: Gene trapped
Genotype
Symbol: Timeless/Timeless
Background: involves: 129S4/SvJae
Zygosity: hm
Has Mutant Allele: true
Publication
First Author: Howden R
Year: 2012
Journal: Am J Respir Cell Mol Biol
Title: Cardiac physiologic and genetic predictors of hyperoxia-induced acute lung injury in mice.
Volume: 46
Issue: 4
Pages: 470-8
Strain
Attribute String: coisogenic, mutant strain, targeted mutation
Strain
Attribute String: coisogenic, targeted mutation
Strain
Attribute String: mutant strain, coisogenic, targeted mutation
Genotype
Symbol: Timeless/Timeless
Background: C57BL/6N-Timeless/Wtsi
Zygosity: hm
Has Mutant Allele: true
Genotype
Symbol: Timeless/Timeless<+>
Background: involves: 129S4/SvJae
Zygosity: ht
Has Mutant Allele: true
Genotype
Symbol: Timeless/Timeless<+>
Background: B6.129S6-Timeless
Zygosity: ht
Has Mutant Allele: true
Publication
First Author: Kume K
Year: 1999
Journal: Cell
Title: mCRY1 and mCRY2 are essential components of the negative limb of the circadian clock feedback loop.
Volume: 98
Issue: 2
Pages: 193-205
Protein Domain
Type: Domain
Description: This entry represents the N-terminal domain of the Timeless protein. The timeless gene in Drosophila melanogasteris involved in circadian rhythm control []. Drosophila contains two paralogs, dTIM and dTIM2, acting in clock/photoreception and chromosome integrity/photoreception respectively. The mammalian TIMELESS (TIM) protein, originally identified based on its similarity to Drosophila dTIM, interacts with the clock proteins dCRY and dPER and is essential for circadian rhythm generation and photo-entrainment in the fly []. However, phylogenetic sequence analysis has demonstrated that dTIM2 is likely to be the orthologue of mammalian TIM and other widely conserved TIM-like proteins in eukaryotes []. These proteins include Saccharomyces cerevisiae Tof1, Schizosaccharomyces pombe Swi1, and Caenorhabditis elegans TIM. These proteins are not involved in the core clock mechanism, but instead play important roles in chromosome integrity, efficient cell growth and/or development [, ], with the exception of dTIM-2, that has an additional function in retinal photoreception [].Saccharomyces cerevisiae Tof1 is a subunit of a replication-pausing checkpoint complex (Tof1-Mrc1-Csm3) that acts at the stalled replication fork to promote sister chromatid cohesion after DNA damage, facilitating gap repair of damaged DNA [, ]. Schizosaccharomyces pombe Swi1 and Swi3 form the fork protection complex that coordinates leading- and lagging-strand synthesis and stabilizes stalled replication forks []. In humans timeless forms a stable complex with its partner protein Tipin. The Timeless-Tipin complex has been reported to travel along with the replication fork during unperturbed DNA replication. Moreover, the Timeless-Tipin-Claspin complex contributes to full activation of the ATR-Chk1 signaling pathway through the recruitment of Chk1 to arrested replication forks for sufficient ATR-mediated phosphorylation. It also interacts with PARP-1, and this interaction is required for efficient homologous recombination repair [].
Protein Domain
Type: Domain
Description: This entry represents the C-terminal domain found in the Timeless (TIM) proteins. This domain can be found in TIM homologues mostly from animals. This domain found in hTIM has been shown to bind to the PARP-1 catalytic domain [].The timeless gene in Drosophila melanogasteris involved in circadian rhythm control []. Drosophila contains two paralogs, dTIM and dTIM2, acting in clock/photoreception and chromosome integrity/photoreception respectively. The mammalian TIMELESS (TIM) protein, originally identified based on its similarity to Drosophila dTIM, interacts with the clock proteins dCRY and dPER and is essential for circadian rhythm generation and photo-entrainment in the fly []. However, phylogenetic sequence analysis has demonstrated that dTIM2 is likely to be the orthologue of mammalian TIM and other widely conserved TIM-like proteins in eukaryotes []. These proteins include Saccharomyces cerevisiae Tof1, Schizosaccharomyces pombe Swi1, and Caenorhabditis elegans TIM. These proteins are not involved in the core clock mechanism, but instead play important roles in chromosome integrity, efficient cell growth and/or development [, ], with the exception of dTIM-2, that has an additional function in retinal photoreception [].Saccharomyces cerevisiae Tof1 is a subunit of a replication-pausing checkpoint complex (Tof1-Mrc1-Csm3) that acts at the stalled replication fork to promote sister chromatid cohesion after DNA damage, facilitating gap repair of damaged DNA [, ]. Schizosaccharomyces pombe Swi1 and Swi3 form the fork protection complex that coordinates leading- and lagging-strand synthesis and stabilizes stalled replication forks []. In humans timeless forms a stable complex with its partner protein Tipin. The Timeless-Tipin complex has been reported to travel along with the replication fork during unperturbed DNA replication. Moreover, the Timeless-Tipin-Claspin complex contributes to full activation of the ATR-Chk1 signaling pathway through the recruitment of Chk1 to arrested replication forks for sufficient ATR-mediated phosphorylation. It also interacts with PARP-1, and this interaction is required for efficient homologous recombination repair [].
Publication
First Author: Shearman LP
Year: 2000
Journal: Science
Title: Interacting molecular loops in the mammalian circadian clock.
Volume: 288
Issue: 5468
Pages: 1013-9
Publication
First Author: Mayer ML
Year: 2004
Journal: Mol Biol Cell
Title: Identification of protein complexes required for efficient sister chromatid cohesion.
Volume: 15
Issue: 4
Pages: 1736-45
Publication
First Author: Nedelcheva MN
Year: 2005
Journal: J Mol Biol
Title: Uncoupling of unwinding from DNA synthesis implies regulation of MCM helicase by Tof1/Mrc1/Csm3 checkpoint complex.
Volume: 347
Issue: 3
Pages: 509-21
Protein Domain
Type: Family
Description: Proteins in this family contain a domain found in yeast chromosome segregation in meiosis protein 3. Proteins include:Chromosome segregation in meiosis protein 3, which is required for required for chromosome segregation during meiosis and DNA damage repair, forming a fork protection complex with TOF1 [, ].TIMELESS-interacting protein (also known as TIPIN), which is a nuclear protein that associates with the replicative helicase, and is required for efficient cell cycle arrest in response to DNA damage. It forms a checkpoint complex with TIMELESS []. Protein TIPIN homolog, which is the orthologue of TIPIN from Caenorhabditis elegans and Drosophila melanogaster.Swi1-interacting protein swi3, from Schizosaccharomyces pombe, which forms a fork protection complex with swi1 [].
Protein
Organism: Mus musculus/domesticus
Length: 278  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 111  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 93  
Fragment?: true
Protein
Organism: Mus musculus/domesticus
Length: 93  
Fragment?: true
Publication
First Author: Dorval V
Year: 2014
Journal: PLoS One
Title: Gene and MicroRNA transcriptome analysis of Parkinson's related LRRK2 mouse models.
Volume: 9
Issue: 1
Pages: e85510
Publication
First Author: Kumada T
Year: 2010
Journal: Dev Dyn
Title: Ttyh1, a Ca(2+)-binding protein localized to the endoplasmic reticulum, is required for early embryonic development.
Volume: 239
Issue: 8
Pages: 2233-45
Publication
First Author: Hennig S
Year: 2009
Journal: PLoS Biol
Title: Structural and functional analyses of PAS domain interactions of the clock proteins Drosophila PERIOD and mouse PERIOD2.
Volume: 7
Issue: 4
Pages: e94
Publication
First Author: Cobellis G
Year: 2005
Journal: Nucleic Acids Res
Title: Tagging genes with cassette-exchange sites.
Volume: 33
Issue: 4
Pages: e44
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: FANTOM2 Data Curation in Mouse Genome Informatics
Publication      
First Author: GUDMAP Consortium
Year: 2004
Journal: www.gudmap.org
Title: GUDMAP: the GenitoUrinary Development Molecular Anatomy Project
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2001
Title: Gene Ontology Annotation by the MGI Curatorial Staff
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Chromosome assignment of mouse genes using the Mouse Genome Sequencing Consortium (MGSC) assembly and the ENSEMBL Database
Publication
First Author: Gerhard DS
Year: 2004
Journal: Genome Res
Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).
Volume: 14
Issue: 10B
Pages: 2121-7
Publication
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
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
Publication
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
First Author: Huttlin EL
Year: 2010
Journal: Cell
Title: A tissue-specific atlas of mouse protein phosphorylation and expression.
Volume: 143
Issue: 7
Pages: 1174-89
Publication
First Author: Church DM
Year: 2009
Journal: PLoS Biol
Title: Lineage-specific biology revealed by a finished genome assembly of the mouse.
Volume: 7
Issue: 5
Pages: e1000112