Species
|
Resource
|
RRC ID
|
Title
|
Journal
|
Published
|
Link
|
Human and Animal Cells
|
HEV0012(HEV0012)
,
277-LCL(RCB2283)
|
78802
|
Evaluating homologous recombination activity in tissues to predict the risk of hereditary breast and ovarian cancer and olaparib sensitivity.
|
Sci Rep |
2024-4-8 |
Pubmed
Full text
|
Human and Animal Cells
|
HUDEP-2(RCB4557)
|
77291
|
Generation of scalable cancer models by combining AAV-intron-trap, CRISPR/Cas9, and inducible Cre-recombinase.
|
Commun Biol |
2021-10-13 |
Pubmed
Full text
|
C.elegans
|
tm2134
,
tm2026
|
75984
|
Helicase Q promotes homology-driven DNA double-strand break repair and prevents tandem duplications.
|
Nat Commun |
2021-12-8 |
Pubmed
Full text
|
Mice
|
RBRC10583
|
72867
|
BRCA2-DSS1 interaction is dispensable for RAD51 recruitment at replication-induced and meiotic DNA double strand breaks
|
Nature Communications |
2022-12-1 |
Pubmed
Full text
|
Human and Animal Cells
|
LK-2(RCB1970)
,
RERF-LC-AI(RCB0444)
,
EBC-1(RCB1965)
,
LC-1/sq-SF(RCB0438)
|
66847
|
Recruitment of KMT2C/MLL3 to DNA Damage Sites Mediates DNA Damage Responses and Regulates PARP Inhibitor Sensitivity in Cancer.
|
Cancer Res |
2021-6-15 |
Pubmed
Full text
|
Human and Animal Cells
|
KGN(RCB1154)
|
62815
|
FOXL2 directs DNA double-strand break repair pathways by differentially interacting with Ku.
|
Nat Commun |
2020-4-24 |
Pubmed
Full text
|
Drosophila
|
CAS-0004
|
60949
|
The Classic Lobe Eye Phenotype of Drosophila Is Caused by Transposon Insertion-Induced Misexpression of a Zinc-Finger Transcription Factor.
|
Genetics |
2020-9-1 |
Pubmed
Full text
|
Yeast
|
FY32724
,
FY32725
|
60886
|
Rad50 zinc hook functions as a constitutive dimerization module interchangeable with SMC hinge.
|
Nat Commun |
2020-1-17 |
Pubmed
Full text
|
Prokaryotes B. subtilis
|
MBS729
,
MBS730
,
MBS731
,
MBS732
,
MBS733
,
MBS734
,
MBS735
,
MBS736
,
MBS737
,
MBS738
,
...
|
59820
|
Transposition of insertion sequence IS256Bsu1 in Bacillus subtilis 168 is strictly dependent on recA.
|
Genes Genet Syst |
2017-10-18 |
Pubmed
Full text
|
C.elegans
|
tm1524
,
tm2026
,
tm2027
,
tm1842
,
tm1086
,
tm2134
|
59378
|
Meiotic Double-Strand Break Proteins Influence Repair Pathway Utilization.
|
Genetics |
2018-11-1 |
Pubmed
Full text
|
Cellular slime molds
|
G90483
|
57728
|
Recent Advances in CRISPR/Cas9-Mediated Genome Editing in Dictyostelium.
|
Cells |
2019-1-12 |
Pubmed
Full text
|
Prokaryotes E. coli
|
Cloning Vector pJB658
|
56349
|
Markerless gene knockout and integration to express heterologous biosynthetic gene clusters in Pseudomonas putida.
|
Metab Eng |
2018-5-1 |
Pubmed
Full text
|
Prokaryotes E. coli
|
W3110
|
55826
|
Markerless gene knockout and integration to express heterologous biosynthetic gene clusters in Pseudomonas putida.
|
Metab Eng |
2018-5-1 |
Pubmed
Full text
|
C.elegans
|
tm1086
,
tm1145
,
tm1298
,
tm1354
,
tm1670
,
tm1842
,
tm1937
,
tm1981
,
tm2073
,
tm2181
,
...
|
51490
|
Systematic analysis of DNA crosslink repair pathways during development and aging in Caenorhabditis elegans.
|
Nucleic Acids Res |
2017-9-19 |
Pubmed
Full text
|
C.elegans
|
tm1145
,
tm2026
,
tm2842
,
tm2940
|
51419
|
A Role for the Nonsense-Mediated mRNA Decay Pathway in Maintaining Genome Stability in Caenorhabditis elegans.
|
Genetics |
2017-8-1 |
Pubmed
Full text
|
Yeast
|
|
49591
|
The histone variant H2A.Z promotes initiation of meiotic recombination in fission yeast.
|
Nucleic Acids Res |
2018-1-25 |
Pubmed
Full text
|
Algae
|
NIES-1332
|
47412
|
Transformation of the Cyanidioschyzon merolae chloroplast genome: prospects for understanding chloroplast function in extreme environments.
|
Plant Mol Biol |
2017-1-1 |
Pubmed
Full text
|
C.elegans
|
tm1624
,
tm1489
|
46543
|
Rapid de novo centromere formation occurs independently of heterochromatin protein 1 in C. elegans embryos.
|
Curr Biol |
2011-11-8 |
Pubmed
Full text
|
C.elegans
|
tm1791
|
46218
|
Heritable custom genomic modifications in Caenorhabditis elegans via a CRISPR-Cas9 system.
|
Genetics |
2013-11-1 |
Pubmed
Full text
|
Human and Animal Cells
|
HeLa
|
44959
|
Mutations in the FHA-domain of ectopically expressed NBS1 lead to radiosensitization and to no increase in somatic mutation rates via a partial suppression of homologous recombination.
|
J Radiat Res |
2014-7-1 |
Pubmed
Full text
|