Isolation of novel human and mouse genes of the recA/RAD51 recombination- repair gene family.Cartwright R., Dunn A.M., Simpson P.J., Tambini C.E., Thacker J.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNucleic Acids Res. 26:1653-1659 (1998)Cited in3Mapped to17
Identification, characterization, and genetic mapping of Rad51d, a new mouse and human RAD51/RecA-related gene.Pittman D.L., Weinberg L.R., Schimenti J.C.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenomics 49:103-111 (1998)Cited in2Mapped to12
Multiple alternative transcripts of the human homologue of the mouse TRAD/R51H3/RAD51D gene, a member of the recA/RAD51 gene family.Kawabata M., Saeki K.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA], ALTERNATIVE SPLICING (ISOFORMS 2; 3; 4; 5; 6 AND 7)TissueBrainCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBiochem. Biophys. Res. Commun. 257:156-162 (1999)Cited in1Mapped to13
No title available.NIEHS SNPs programCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA], VARIANTS SER-24; GLN-165; THR-225; GLN-232 AND GLY-233CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)Submission Submitted to EMBL/GenBank/DDBJ databases (MAY-2004)Cited in13
Complete sequencing and characterization of 21,243 full-length human cDNAs.Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H.[...], Sugano S.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 8)TissueThalamusCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Genet. 36:40-45 (2004)Cited in99+99+
DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.Zody M.C., Garber M., Adams D.J., Sharpe T., Harrow J., Lupski J.R., Nicholson C., Searle S.M., Wilming L.[...], Nusbaum C.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 440:1045-1049 (2006)Cited in99+99+
No title available.Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., Lippert R., Walenz B., Shatkay H.[...], Venter J.C.Cited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)Submission Submitted to EMBL/GenBank/DDBJ databases (SEP-2005)Cited in99+
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).The MGC Project TeamView abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1)TissueSkinCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenome Res. 14:2121-2127 (2004)Cited in99+99+
The full-ORF clone resource of the German cDNA consortium.Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U., Wellenreuther R., Mehrle A., Schuster C., Bahr A.[...], Schupp I.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 156-328TissueUterusCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBMC Genomics 8:399-399 (2007)Cited in99+
The RAD51 family member, RAD51L3, is a DNA-stimulated ATPase that forms a complex with XRCC2.Braybrooke J.P., Spink K.G., Thacker J., Hickson I.D.View abstractCited forFUNCTION, INTERACTION WITH XRCC2CategoriesFunction, InteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 275:29100-29106 (2000)Cited in1Mapped to1
Identification and purification of two distinct complexes containing the five RAD51 paralogs.Masson J.Y., Tarsounas M.C., Stasiak A.Z., Stasiak A., Shah R., McIlwraith M.J., Benson F.E., West S.C.View abstractCited forFUNCTION, IDENTIFICATION IN A COMPLEX WITH RAD51C; RAD51D AND XRCC2CategoriesFunction, InteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenes Dev. 15:3296-3307 (2001)Cited in5Mapped to21
Homologous pairing and ring and filament structure formation activities of the human Xrcc2*Rad51D complex.Kurumizaka H., Ikawa S., Nakada M., Enomoto R., Kagawa W., Kinebuchi T., Yamazoe M., Yokoyama S., Shibata T.View abstractCited forFUNCTION, SUBUNITCategoriesFunction, InteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 277:14315-14320 (2002)Cited in2Mapped to2
Involvement of Rad51C in two distinct protein complexes of Rad51 paralogs in human cells.Liu N., Schild D., Thelen M.P., Thompson L.H.View abstractCited forFUNCTION, IDENTIFICATION IN A COMPLEX WITH RAD51C; RAD51D AND XRCC2CategoriesFunction, InteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNucleic Acids Res. 30:1009-1015 (2002)Cited in6
RAD51C interacts with RAD51B and is central to a larger protein complex in vivo exclusive of RAD51.Miller K.A., Yoshikawa D.M., McConnell I.R., Clark R., Schild D., Albala J.S.View abstractCited forSUBUNITCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 277:8406-8411 (2002)Cited in5Mapped to4
Interactions involving the Rad51 paralogs Rad51C and XRCC3 in human cells.Wiese C., Collins D.W., Albala J.S., Thompson L.H., Kronenberg A., Schild D.View abstractCited forIDENTIFICATION IN A COMPLEX WITH RAD51C; RAD51D AND XRCC2CategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNucleic Acids Res. 30:1001-1008 (2002)Cited in4
Functional interaction between the Bloom's syndrome helicase and the RAD51 paralog, RAD51L3 (RAD51D).Braybrooke J.P., Li J.L., Wu L., Caple F., Benson F.E., Hickson I.D.View abstractCited forFUNCTION OF THE BCDX2 COMPLEX, INTERACTION WITH BLM AND XRCC2CategoriesFunction, InteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 278:48357-48366 (2003)Cited in1Mapped to8
Telomere maintenance requires the RAD51D recombination/repair protein.Tarsounas M., Munoz P., Claas A., Smiraldo P.G., Pittman D.L., Blasco M.A., West S.C.View abstractCited forFUNCTION, SUBCELLULAR LOCATIONCategoriesFunction, Subcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCCell 117:337-347 (2004)Cited in2Mapped to23
An unappreciated role for RNA surveillance.Hillman R.T., Green R.E., Brenner S.E.View abstractCited forSPLICE ISOFORM(S) THAT ARE POTENTIAL NMD TARGET(S)CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenome Biol. 5:R8.1-R8.16 (2004)Cited in96
Sws1 is a conserved regulator of homologous recombination in eukaryotic cells.Martin V., Chahwan C., Gao H., Blais V., Wohlschlegel J., Yates J.R. III, McGowan C.H., Russell P.View abstractCited forINTERACTION WITH ZSWIM7 AND XRCC2CategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCEMBO J. 25:2564-2574 (2006)Cited in6Mapped to4
Homologous recombination proteins are associated with centrosomes and are required for mitotic stability.Cappelli E., Townsend S., Griffin C., Thacker J.View abstractCited forSUBCELLULAR LOCATIONCategoriesSubcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCExp. Cell Res. 317:1203-1213 (2011)Cited in4Mapped to10
hSWS1.SWSAP1 is an evolutionarily conserved complex required for efficient homologous recombination repair.Liu T., Wan L., Wu Y., Chen J., Huang J.View abstractCited forINTERACTION WITH SWSAP1 AND ZSWIM7CategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 286:41758-41766 (2011)Cited in7Mapped to2
Germline mutations in RAD51D confer susceptibility to ovarian cancer.Loveday C., Turnbull C., Ramsay E., Hughes D., Ruark E., Frankum J.R., Bowden G., Kalmyrzaev B., Warren-Perry M.[...], Rahman N.View abstractCited forINVOLVEMENT IN BROVCA4CategoriesDisease & VariantsSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Genet. 43:879-882 (2011)Cited in1
Rad51 paralog complexes BCDX2 and CX3 act at different stages in the BRCA1-BRCA2-dependent homologous recombination pathway.Chun J., Buechelmaier E.S., Powell S.N.View abstractCited forFUNCTION OF THE BCDX2 COMPLEXCategoriesFunction, InteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCMol. Cell. Biol. 33:387-395 (2013)Cited in5Mapped to99+
Structural and functional characterization of the N-terminal domain of human Rad51D.Kim Y.M., Choi B.S.View abstractCited forSTRUCTURE BY NMR OF 1-83, DNA-BINDINGCategoriesFunction, StructureSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCInt. J. Biochem. Cell Biol. 43:416-422 (2011)Cited in1
MAGI2 mutations cause congenital nephrotic syndrome.NephroS, UK study of Nephrotic SyndromeBierzynska A., Soderquest K., Dean P., Colby E., Rollason R., Jones C., Inward C.D., McCarthy H.J., Simpson M.A.[...], Saleem M.A.View abstractCited forVARIANT SER-9CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Am. Soc. Nephrol. 28:1614-1621 (2017)Cited in7Mapped to4