scholarly article | Q13442814 |
P356 | DOI | 10.1007/S00018-018-2833-9 |
P698 | PubMed publication ID | 29748894 |
P50 | author | Jessica M. Stringer | Q48443999 |
Amy Winship | Q50423867 | ||
Karla J Hutt | Q61096480 | ||
P2093 | author name string | Seng H Liew | |
P2860 | cites work | Different fates of oocytes with DNA double-strand breaks in vitro and in vivo | Q36189081 |
Expression profile of genes coding for DNA repair in human oocytes using pangenomic microarrays, with a special focus on ROS linked decays | Q36268732 | ||
DNA damage induces a meiotic arrest in mouse oocytes mediated by the spindle assembly checkpoint | Q36319891 | ||
The Fanconi Anemia/BRCA pathway: new faces in the crowd | Q36343120 | ||
Direct reversal of DNA alkylation damage | Q36389617 | ||
DNA damage-induced primordial follicle oocyte apoptosis and loss of fertility require TAp63-mediated induction of Puma and Noxa | Q36392786 | ||
The multifaceted mismatch-repair system | Q36448284 | ||
Functions of the MRE11 complex in the development and maintenance of oocytes | Q36526067 | ||
Balancing repair and tolerance of DNA damage caused by alkylating agents | Q36651488 | ||
Requirement of poly(ADP-ribose) polymerase in recovery from DNA damage in mice and in cells | Q36654891 | ||
Chromosomal aberrations in PARP(-/-) mice: genome stabilization in immortalized cells by reintroduction of poly(ADP-ribose) polymerase cDNA. | Q36668248 | ||
Increased susceptibility to ultraviolet-B and carcinogens of mice lacking the DNA excision repair gene XPA | Q36694656 | ||
Activation of a system for the joining of nonhomologous DNA ends during Xenopus egg maturation | Q36813402 | ||
Mre11-Rad50-Nbs1 is a keystone complex connecting DNA repair machinery, double-strand break signaling, and the chromatin template. | Q36916670 | ||
Pregnancy after chemotherapy in male and female survivors of childhood cancer treated between 1970 and 1999: a report from the Childhood Cancer Survivor Study cohort. | Q37004233 | ||
From primordial germ cells to primordial follicles: a review and visual representation of early ovarian development in mice | Q37024648 | ||
Cellular and molecular aspects of ovarian follicle ageing | Q37073306 | ||
Persistence of histone H2AX phosphorylation after meiotic chromosome synapsis and abnormal centromere cohesion in poly (ADP-ribose) polymerase (Parp-1) null oocytes | Q37335451 | ||
Mutator phenotype may be required for multistage carcinogenesis | Q37732904 | ||
Structures and functions of DNA glycosylases | Q37952078 | ||
The mechanism of double-strand DNA break repair by the nonhomologous DNA end-joining pathway | Q22065419 | ||
ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage | Q24306743 | ||
Xeroderma pigmentosum group C protein complex is the initiator of global genome nucleotide excision repair | Q24312736 | ||
The mismatch repair system is required for S-phase checkpoint activation | Q24321503 | ||
Complementation of defective translesion synthesis and UV light sensitivity in xeroderma pigmentosum variant cells by human and mouse DNA polymerase eta | Q24515346 | ||
Second pathway for completion of human DNA base excision-repair: reconstitution with purified proteins and requirement for DNase IV (FEN1). | Q24532243 | ||
Synapsis of DNA ends by DNA-dependent protein kinase | Q24536754 | ||
Distinct DNA-damage-dependent and -independent responses drive the loss of oocytes in recombination-defective mouse mutants | Q24557469 | ||
MutS homolog 4 localization to meiotic chromosomes is required for chromosome pairing during meiosis in male and female mice | Q24606421 | ||
The DNA-damage response in human biology and disease | Q24606586 | ||
Dynamics of DNA damage response proteins at DNA breaks: a focus on protein modifications | Q24608343 | ||
How the fanconi anemia pathway guards the genome | Q24634556 | ||
Retracted: A common mutational pattern in Cockayne syndrome patients from xeroderma pigmentosum group G: implications for a second XPG function | Q24678938 | ||
Deletion of Ku70, Ku80, or both causes early aging without substantially increased cancer | Q24681223 | ||
Involvement of global genome repair, transcription coupled repair, and chromatin remodeling in UV DNA damage response changes during development | Q27347595 | ||
The DNA Damage Response: Making It Safe to Play with Knives | Q27861055 | ||
Eukaryotic DNA mismatch repair | Q27939116 | ||
Functional specificity of MutL homologs in yeast: evidence for three Mlh1-based heterocomplexes with distinct roles during meiosis in recombination and mismatch correction | Q27939611 | ||
How Is the Number of Primordial Follicles in the Ovarian Reserve Established? | Q28084803 | ||
Novel human and mouse homologs of Saccharomyces cerevisiae DNA polymerase eta | Q28116380 | ||
Transcription of eukaryotic protein-coding genes | Q28138540 | ||
Mice with a targeted disruption of the Fanconi anemia homolog Fanca | Q28142089 | ||
Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads to growth retardation, strain-specific microphthalmia, meiotic defects and primordial germ cell hypoplasia | Q28201015 | ||
Interaction of the Fanconi anemia proteins and BRCA1 in a common pathway | Q28203777 | ||
DNA double-strand breaks: signaling, repair and the cancer connection | Q28204231 | ||
Mouse models for human DNA mismatch-repair gene defects | Q28214396 | ||
DNA mismatch repair | Q28256190 | ||
The DNA damage response: ten years after | Q28261230 | ||
Genetic investigation of four meiotic genes in women with premature ovarian failure | Q28263196 | ||
Molecular mechanisms of mammalian DNA repair and the DNA damage checkpoints | Q28266170 | ||
A constant rate of spontaneous mutation in DNA-based microbes | Q28271032 | ||
Inactivation of Fac in mice produces inducible chromosomal instability and reduced fertility reminiscent of Fanconi anaemia | Q28278800 | ||
Involvement of mouse Mlh1 in DNA mismatch repair and meiotic crossing over | Q28282791 | ||
Impairment of BRCA1-related DNA double-strand break repair leads to ovarian aging in mice and humans | Q28285540 | ||
Mammalian MutS homologue 5 is required for chromosome pairing in meiosis | Q28295022 | ||
Mice lacking ADPRT and poly(ADP-ribosyl)ation develop normally but are susceptible to skin disease | Q28298870 | ||
Advances in understanding the complex mechanisms of DNA interstrand cross-link repair | Q28299636 | ||
Defective transcription-coupled repair of oxidative base damage in Cockayne syndrome patients from XP group G | Q28302894 | ||
Reversal of female infertility by Chk2 ablation reveals the oocyte DNA damage checkpoint pathway | Q28306981 | ||
Enhancing survival of mouse oocytes following chemotherapy or aging by targeting Bax and Rad51 | Q28472878 | ||
Disruption of mouse ERCC1 results in a novel repair syndrome with growth failure, nuclear abnormalities and senescence | Q28505334 | ||
Characterization of defective nucleotide excision repair in XPC mutant mice | Q28506912 | ||
Targeted disruption of ATM leads to growth retardation, chromosomal fragmentation during meiosis, immune defects, and thymic lymphoma | Q28509780 | ||
Meiotic pachytene arrest in MLH1-deficient mice | Q28510650 | ||
PARP-2, A novel mammalian DNA damage-dependent poly(ADP-ribose) polymerase | Q28511873 | ||
p63 protects the female germ line during meiotic arrest | Q28586825 | ||
p63 null mutation protects mouse oocytes from radio-induced apoptosis | Q28591572 | ||
The Mre11 complex influences DNA repair, synapsis, and crossing over in murine meiosis | Q28592328 | ||
A mouse model for the basal transcription/DNA repair syndrome trichothiodystrophy | Q28593147 | ||
Meiotic arrest and aneuploidy in MLH3-deficient mice | Q28593875 | ||
Premature aging in mice deficient in DNA repair and transcription | Q28593981 | ||
Transcription-coupled nucleotide excision repair as a determinant of cisplatin sensitivity of human cells | Q28627137 | ||
Proliferating cell nuclear antigen-dependent abasic site repair in Xenopus laevis oocytes: an alternative pathway of base excision DNA repair | Q28645707 | ||
A Surveillance Mechanism Ensures Repair of DNA Lesions during Zygotic Reprogramming | Q28817178 | ||
Mechanism of eukaryotic homologous recombination | Q29547709 | ||
Repair of endogenous DNA damage | Q35132488 | ||
Transcription-coupled repair of oxidative DNA damage in human cells: mechanisms and consequences | Q35132516 | ||
Xeroderma pigmentosum complementation group G associated with Cockayne syndrome | Q35194613 | ||
DNA replication fidelity | Q35677447 | ||
Mismatch repair and DNA damage signalling | Q35848516 | ||
DNA interstrand crosslinks: natural and drug-induced DNA adducts that induce unique cellular responses | Q36002324 | ||
In vivo evidence for endogenous DNA alkylation damage as a source of spontaneous mutation in eukaryotic cells | Q36155707 | ||
The DNA damage response and cancer therapy | Q37977004 | ||
DNA damage by reactive species: Mechanisms, mutation and repair. | Q38023114 | ||
Genetics of early miscarriage | Q38026354 | ||
Male mice defective in the DNA mismatch repair gene PMS2 exhibit abnormal chromosome synapsis in meiosis | Q38293261 | ||
The magnitude of gonadotoxicity of chemotherapy drugs on ovarian follicles and granulosa cells varies depending upon the category of the drugs and the type of granulosa cells | Q38296008 | ||
Identifying new human oocyte marker genes: a microarray approach. | Q38304751 | ||
Mlh1 is unique among mismatch repair proteins in its ability to promote crossing-over during meiosis | Q38344945 | ||
Gene expression profiles of single human mature oocytes in relation to age. | Q38346535 | ||
Transcriptome analyses of rhesus monkey preimplantation embryos reveal a reduced capacity for DNA double-strand break repair in primate oocytes and early embryos | Q38375832 | ||
Age-related changes in gene expression patterns of immature and aged rat primordial follicles | Q38438495 | ||
Regulators of ovarian preantral follicle development | Q38513465 | ||
Cellular and molecular regulation of the activation of mammalian primordial follicles: somatic cells initiate follicle activation in adulthood | Q38558604 | ||
Causes and consequences of oxidative stress in spermatozoa. | Q38803634 | ||
The Fanconi anaemia pathway: new players and new functions | Q38825562 | ||
Ovarian Folliculogenesis | Q38853367 | ||
PARP is important for genomic stability but dispensable in apoptosis | Q40442742 | ||
Risk for congenital anomalies in offspring of childhood, adolescent and young adult cancer survivors | Q40710343 | ||
Chromosome abnormalities in human beings. | Q40872596 | ||
The base excision repair pathway | Q40930021 | ||
Ku70: a candidate tumor suppressor gene for murine T cell lymphoma | Q41017020 | ||
The Atr and Atm protein kinases associate with different sites along meiotically pairing chromosomes. | Q41164271 | ||
The genetic defect in ataxia-telangiectasia | Q41464274 | ||
Cisplatin-induced primordial follicle oocyte killing and loss of fertility are not prevented by imatinib | Q42400795 | ||
Transcript profiling during mouse oocyte development and the effect of gonadotropin priming and development in vitro | Q42484089 | ||
Detection of DNA damage in oocytes of small ovarian follicles following phosphoramide mustard exposures of cultured rodent ovaries in vitro | Q42744619 | ||
Oxidative status in granulosa cells of infertile women undergoing IVF. | Q43834526 | ||
Effect of chemotherapy on primordial follicular reserve of rat: an animal model of premature ovarian failure and infertility | Q44847798 | ||
Dramatic changes in the ratio of homologous recombination to nonhomologous DNA-end joining in oocytes and early embryos of Xenopus laevis | Q46497248 | ||
The presence of a truncated base excision repair pathway in human spermatozoa that is mediated by OGG1. | Q46549643 | ||
HP1-beta mobilization promotes chromatin changes that initiate the DNA damage response. | Q46625510 | ||
DNA polymerases eta and kappa are responsible for error-free translesion DNA synthesis activity over a cis-syn thymine dimer in Xenopus laevis oocyte extracts | Q46627865 | ||
Reactive oxygen species in follicular fluid may serve as biochemical markers to determine ovarian aging and follicular metabolic age. | Q46867754 | ||
Characterizing the ovotoxicity of cyclophosphamide metabolites on cultured mouse ovaries | Q46871046 | ||
Chromosomal Abnormalities in Offspring of Young Cancer Survivors: A Population-Based Cohort Study in Denmark | Q47566662 | ||
Functions of poly(ADP-ribose) polymerase in controlling telomere length and chromosomal stability | Q48564987 | ||
Fertilization stimulates 8-hydroxy-2'-deoxyguanosine repair and antioxidant activity to prevent mutagenesis in the embryo. | Q48572457 | ||
Oocytes progress beyond prophase in the presence of DNA damage. | Q48649125 | ||
The primordial follicle reserve is not renewed after chemical or γ-irradiation mediated depletion | Q48656079 | ||
Expression profiling of DNA repair genes in human oocytes and blastocysts using microarrays | Q48718101 | ||
Antioxidants and reactive oxygen species in follicular fluid of women undergoing IVF: relationship to outcome | Q48819466 | ||
Base excision repair assay using Xenopus laevis oocyte extracts | Q48911053 | ||
Antioxidants reversibly inhibit the spontaneous resumption of meiosis | Q48921076 | ||
Atm deficiency results in severe meiotic disruption as early as leptonema of prophase I. | Q48932881 | ||
Age-related decline in fertility: a link to degenerative oocytes? | Q48954472 | ||
A novel ovarian xenografting model to characterize the impact of chemotherapy agents on human primordial follicle reserve. | Q50463372 | ||
Maternal gene transcription in mouse oocytes: genes implicated in oocyte maturation and fertilization. | Q50641283 | ||
High incidence of chromosomal abnormalities in oocyte donors. | Q50642887 | ||
Caspase-2 involvement during ionizing radiation-induced oocyte death in the mouse ovary. | Q50643031 | ||
Gene expression profiling of early follicular development in primordial, primary, and secondary follicles. | Q50653701 | ||
Developmental regulation and in vitro culture effects on expression of DNA repair and cell cycle checkpoint control genes in rhesus monkey oocytes and embryos. | Q50666210 | ||
Transcript profiling during preimplantation mouse development. | Q50672706 | ||
Eicosatetraynoic and eicosatriynoic acids, lipoxygenase inhibitors, block meiosis via antioxidant action. | Q50719773 | ||
DNA polymerases alpha and beta are required for DNA repair in an efficient nuclear extract from Xenopus oocytes. | Q50761981 | ||
Collaborative work on evaluation of ovarian toxicity. 6) Two- or four-week repeated-dose studies and fertility study of cisplatin in female rats. | Q51642754 | ||
Age as a determinant of reproductive success among captive female rhesus macaques (Macaca mulatta). | Q51753138 | ||
The response of Parp knockout mice against DNA damaging agents. | Q52538829 | ||
Oocyte DNA damage quality control requires consecutive interplay of CHK2 and CK1 to activate p63. | Q52684301 | ||
Both ATM and ATR promote the efficient and accurate processing of programmed meiotic double-strand breaks. | Q53481054 | ||
Deficiency in the response to DNA double-strand breaks in mouse early preimplantation embryos. | Q53553547 | ||
Inactivation of the poly(ADP-ribose) polymerase gene affects oxygen radical and nitric oxide toxicity in islet cells. | Q54172665 | ||
Base selection, proofreading, and mismatch repair during DNA replication in Escherichia coli. | Q54648245 | ||
Human gene expression first occurs between the four- and eight-cell stages of preimplantation development | Q59084361 | ||
Two Pathways for Base Excision Repair in Mammalian Cells | Q60702220 | ||
Detrimental effect of visible light on meiosis of mammalian eggs in vitro | Q67016863 | ||
Ultraviolet light-induced unscheduled DNA synthesis in mouse oocytes during meiotic maturation | Q67427857 | ||
Chromosomal analysis in mouse eggs fertilized in vitro with sperma exposed to ultraviolet light (UV) and methyl and ethyl methanesulfonate (MMS and EMS) | Q68297301 | ||
Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH | Q83343914 | ||
Base-excision repair of oxidative DNA damage | Q29615373 | ||
Transcriptional control of human p53-regulated genes | Q29617650 | ||
Poly(ADP-ribose): novel functions for an old molecule | Q29617735 | ||
Cell cycle checkpoint signaling through the ATM and ATR kinases | Q29617837 | ||
Eukaryotic translesion synthesis DNA polymerases: specificity of structure and function | Q29617871 | ||
Atm-deficient mice: a paradigm of ataxia telangiectasia | Q29619532 | ||
Changes in the expression of DNA double strand break repair genes in primordial follicles from immature and aged rats | Q30273988 | ||
Selective degradation of transcripts during meiotic maturation of mouse oocytes | Q30479226 | ||
The association of ATR protein with mouse meiotic chromosome cores | Q30724277 | ||
DNA damage response during mouse oocyte maturation | Q30820071 | ||
The involvement of ataxia-telangiectasia mutated protein activation in nucleotide excision repair-facilitated cell survival with cisplatin treatment | Q33250629 | ||
Fertility of female survivors of childhood cancer: a report from the childhood cancer survivor study | Q33429790 | ||
Mutations in MSH5 in primary ovarian insufficiency | Q33569127 | ||
Light and dark in chromatin repair: repair of UV-induced DNA lesions by photolyase and nucleotide excision repair | Q33784364 | ||
DNA mismatch repair in Xenopus egg extracts: repair efficiency and DNA repair synthesis for all single base-pair mismatches | Q33836666 | ||
Sensing and responding to DNA damage. | Q33840475 | ||
Physical map of 1p36, placement of breakpoints in monosomy 1p36, and clinical characterization of the syndrome | Q33904701 | ||
Molecular mechanisms for constitutional chromosomal rearrangements in humans | Q33926237 | ||
The transition from maternal to embryonic control in the 2-cell mouse embryo. | Q33928353 | ||
Ku-dependent nonhomologous DNA end joining in Xenopus egg extracts | Q33957659 | ||
Requirement for the kinase activity of human DNA-dependent protein kinase catalytic subunit in DNA strand break rejoining | Q33958394 | ||
UV-induced DNA damage and repair: a review | Q34186547 | ||
Proteome of mouse oocytes at different developmental stages | Q34200160 | ||
A genome-wide study of gene activity reveals developmental signaling pathways in the preimplantation mouse embryo. | Q34289900 | ||
Repair and genetic consequences of endogenous DNA base damage in mammalian cells | Q34371854 | ||
DNA double strand breaks but not interstrand crosslinks prevent progress through meiosis in fully grown mouse oocytes. | Q34396087 | ||
XPA: A key scaffold for human nucleotide excision repair | Q34529078 | ||
How nucleotide excision repair protects against cancer | Q34568150 | ||
MGMT: key node in the battle against genotoxicity, carcinogenicity and apoptosis induced by alkylating agents | Q34626127 | ||
Specialized DNA polymerases, cellular survival, and the genesis of mutations | Q34662609 | ||
Changes in DNA repair during aging. | Q34697935 | ||
Base excision repair and lesion-dependent subpathways for repair of oxidative DNA damage | Q34987124 | ||
Catalytic subunit of DNA-dependent protein kinase: impact on lymphocyte development and tumorigenesis | Q34992049 | ||
Functional interaction between PARP-1 and PARP-2 in chromosome stability and embryonic development in mouse | Q35018839 | ||
Poly(ADP-ribose) polymerase-2 contributes to the fidelity of male meiosis I and spermiogenesis | Q35075511 | ||
P433 | issue | 15 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | folliculogenesis | Q2142940 |
P304 | page(s) | 2777-2792 | |
P577 | publication date | 2018-05-10 | |
P1433 | published in | Cellular and Molecular Life Sciences | Q5058352 |
P1476 | title | The capacity of oocytes for DNA repair | |
P478 | volume | 75 |
Q92702430 | Crosstalk between PTEN/PI3K/Akt Signalling and DNA Damage in the Oocyte: Implications for Primordial Follicle Activation, Oocyte Quality and Ageing |
Q60939479 | DNA Damage and Repair in Human Reproductive Cells |
Q61818073 | Genetic Instability and Chromatin Remodeling in Spermatids |
Q90339595 | Kinase-independent inhibition of cyclophosphamide-induced pathways protects the ovarian reserve and prolongs fertility |
Search more.