Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (15) GO Terms (3) Nucleotides (93) Proteins (48) Interactants (97) Wiki
XB-GENEPAGE-5995329

Papers associated with diaph1



???displayGene.coCitedPapers???

???pagination.result.count???

???pagination.result.page??? 1

Sort Newest To Oldest Sort Oldest To Newest

Xenopus Drf1, a regulator of Cdc7, displays checkpoint-dependent accumulation on chromatin during an S-phase arrest., Yanow SK, Gold DA, Yoo HY, Dunphy WG., J Biol Chem. October 17, 2003; 278 (42): 41083-92.


Identification and characterization of the human FMN1 gene in silico., Katoh M, Katoh M., Int J Mol Med. July 1, 2004; 14 (1): 121-6.


Cdc7-Drf1 is a developmentally regulated protein kinase required for the initiation of vertebrate DNA replication., Takahashi TS, Walter JC., Genes Dev. October 1, 2005; 19 (19): 2295-300.


Xenopus CDC7/DRF1 complex is required for the initiation of DNA replication., Silva T, Bradley RH, Gao Y, Coue M., J Biol Chem. April 28, 2006; 281 (17): 11569-76.


Cdc7-Drf1 kinase links chromosome cohesion to the initiation of DNA replication in Xenopus egg extracts., Takahashi TS, Basu A, Bermudez V, Hurwitz J, Walter JC., Genes Dev. July 15, 2008; 22 (14): 1894-905.            


The role of Dbf4/Drf1-dependent kinase Cdc7 in DNA-damage checkpoint control., Tsuji T, Lau E, Chiang GG, Jiang W., Mol Cell. December 26, 2008; 32 (6): 862-9.


Drf1-dependent kinase interacts with Claspin through a conserved protein motif., Gold DA, Dunphy WG., J Biol Chem. April 23, 2010; 285 (17): 12638-46.


Identification of two novel missense WFS1 mutations, H696Y and R703H, in patients with non-syndromic low-frequency sensorineural hearing loss., Sun Y, Cheng J, Lu Y, Li J, Lu Y, Jin Z, Dai P, Wang R, Yuan H., J Genet Genomics. February 1, 2011; 38 (2): 71-6.


Titration of four replication factors is essential for the Xenopus laevis midblastula transition., Collart C, Allen GE, Bradshaw CR, Smith JC, Zegerman P., Science. August 23, 2013; 341 (6148): 893-6.


Quantitative proteomics of Xenopus laevis embryos: expression kinetics of nearly 4000 proteins during early development., Sun L, Bertke MM, Champion MM, Zhu G, Huber PW, Dovichi NJ., Sci Rep. February 26, 2014; 4 4365.                              


RAD18 Is a Maternal Limiting Factor Silencing the UV-Dependent DNA Damage Checkpoint in Xenopus Embryos., Kermi C, Prieto S, van der Laan S, Tsanov N, Recolin B, Uro-Coste E, Delisle MB, Maiorano D., Dev Cell. August 10, 2015; 34 (3): 364-72.        


Formin Is Associated with Left-Right Asymmetry in the Pond Snail and the Frog., Davison A, McDowell GS, Holden JM, Johnson HF, Koutsovoulos GD, Liu MM, Hulpiau P, Van Roy F, Wade CM, Banerjee R, Yang F, Chiba S, Davey JW, Jackson DJ, Levin M, Blaxter ML., Curr Biol. March 7, 2016; 26 (5): 654-60.            


Helical rotation of the diaphanous-related formin mDia1 generates actin filaments resistant to cofilin., Mizuno H, Tanaka K, Yamashiro S, Narita A, Watanabe N., Proc Natl Acad Sci U S A. May 29, 2018; 115 (22): E5000-E5007.          


Comprehensive analysis of formin localization in Xenopus epithelial cells., Higashi T, Stephenson RE, Miller AL, Miller AL., Mol Biol Cell. January 1, 2019; 30 (1): 82-95.                                


Late-onset hearing loss case associated with a heterozygous truncating variant of DIAPH1., Kim BJ, Miyoshi T, Chaudhry T, Friedman TB, Choi BY, Ueyama T., Clin Genet. April 1, 2022; 101 (4): 466-471.

???pagination.result.page??? 1