DOCSLIB.ORG
Explore
Sign Up
Log In
Upload
Search
Home
» Tags
» DBF4
DBF4
Mcm2 Is a Target of Regulation by Cdc7–Dbf4 During the Initiation of DNA Synthesis
Three Dact Gene Family Members Are Expressed During Embryonic Development
DNA Replication Stress Response Involving PLK1, CDC6, POLQ
Characterization of Budding Yeast Orc6 : a Dimerization Domain Is
"The Genecards Suite: from Gene Data Mining to Disease Genome Sequence Analyses". In: Current Protocols in Bioinformat
Regulation of the Cell Cycle and DNA Damage-Induced Checkpoint Activation
The Role of Dbf4-Dependent Protein Kinase in DNA Polymerase Ζ
A High-Throughput Approach to Uncover Novel Roles of APOBEC2, a Functional Orphan of the AID/APOBEC Family
Anti-DBF4B (Aa 1-50) Polyclonal Antibody (DPABH- 12596) This Product Is for Research Use Only and Is Not Intended for Diagnostic Use
Crystal Structure of Rad53 Bound to Dbf4 and Cdc7 Received: 27 July 2016 Ahmad W
Downregulation of SNRPG Induces Cell Cycle Arrest and Sensitizes Human Glioblastoma Cells to Temozolomide by Targeting Myc Through a P53-Dependent Signaling Pathway
A Graph-Theoretic Approach to Model Genomic Data and Identify Biological Modules Asscociated with Cancer Outcomes
CDC45 Is Required in Conjunction with CDC7/DBF4 to Trigger the Initiation
An N-Terminal Domain of Dbf4p Mediates Interaction with Both Origin Recognition Complex (ORC) and Rad53p and Can Deregulate Late Origin Firing
The Characterization of Dbf4 Interactions and Roles in Genome Replication
Cell Cycle Arrest Through Indirect Transcriptional Repression by P53: I Have a DREAM
The Drosophila Dbf4 Ortholog Chiffon Forms a Complex with Gcn5 That Is Necessary for Histone Acetylation and Viability Eliana F
Antagonistic Control of DDK Binding to Licensed Replication Origins by Mcm2 and Rad53 Syafiq Abd Wahab1,2, Dirk Remus1,2*
Top View
Checkpoint Inhibition of Origin Firing Prevents Inappropriate Replication
Mechanisms Governing DDK Regulation of the Initiation of DNA Replication
Identification of Novel Anti-Tumor Therapeutic Target Via Proteomic
Amplification of a Broad Transcriptional Program by a Common Factor Triggers the Meiotic Cell Cycle in Mice
CDC7 Kinase Antibody
Structural and Mechanistic Insights Into Mcm2-7 Double-Hexamer Assembly
Analysis of the Crystal Structure of an Active MCM Hexamer Justin M Miller†, Buenafe T Arachea†, Leslie B Epling, Eric J Enemark*
Cryo-EM Structure of Mcm2-7 Double Hexamer on DNA Suggests A
Schwann Cell Reprogramming and Lung Cancer Progression: a Meta-Analysis of Transcriptome Data
FARE2015 WINNERS Sorted by Study Section
Incorporation Into the Prereplicative Complex Activates the Mcm2–7 Helicase for Cdc7–Dbf4 Phosphorylation
Distinct Surfaces on Cdc5/PLK Polo-Box Domain Orchestrate Combinatorial Substrate Recognition During Cell Division Ahmad W
The Role of Dbf4-Dependent Kinase in Maintaining Genome Stability
Dbf4 Recruitment by Forkhead Transcription Factors Defines an Upstream Rate-Limiting Step in Determining Origin Firing Timing
In Silico Study for Decoding the Correlated Role of MCM7 Gene in Progression of Breast Cancer and Alzheimer’S Disorder
Macrophage Activation JUNB Is a Key Transcriptional Modulator Of
Characterization of the Association of Dbf4 and Cdc7 with Mcm2-7 And
1 Global Rnaseq of Ocular Cells Reveals Gene Dysregulation in Both
Checkpoint Inhibition of Origin Firing Prevents Inappropriate
Concerted Activities of Mcm4, Sld3, and Dbf4 in Control of Origin Activation and DNA Replication Fork Progression
Interplay Between S-Cyclin-Dependent Kinase and Dbf4-Dependent Kinase in Controlling DNA Replication Through Phosphorylation of Yeast Mcm4 N-Terminal Domain
Temperature-Sensitive Cdc7 Mutations of Saccharomyces