Pages that link to "Q28508100"
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The following pages link to BRCA1 is required for common-fragile-site stability via its G2/M checkpoint function (Q28508100):
Displaying 50 items.
- Breast cancer 1, early onset (Q14862232) (← links)
- Fragile histidine triad gene (Q21979944) (← links)
- BRCA1 is an essential regulator of heart function and survival following myocardial infarction (Q24300290) (← links)
- Inhibition of topoisomerase I prevents chromosome breakage at common fragile sites (Q24622097) (← links)
- Comparative genomics and molecular dynamics of DNA repeats in eukaryotes (Q24650948) (← links)
- Common fragile sites: genomic hotspots of DNA damage and carcinogenesis (Q26825040) (← links)
- PALB2: the hub of a network of tumor suppressors involved in DNA damage responses (Q28243398) (← links)
- Expanded roles of the Fanconi anemia pathway in preserving genomic stability (Q28749668) (← links)
- DNA secondary structure at chromosomal fragile sites in human disease (Q30300009) (← links)
- 45S rDNA regions are chromosome fragile sites expressed as gaps in vitro on metaphase chromosomes of root-tip meristematic cells in Lolium spp. (Q33334417) (← links)
- Stably transfected common fragile site sequences exhibit instability at ectopic sites (Q33350550) (← links)
- Over half of breakpoints in gene pairs involved in cancer-specific recurrent translocations are mapped to human chromosomal fragile sites (Q33404454) (← links)
- DNA structure and the Werner protein modulate human DNA polymerase delta-dependent replication dynamics within the common fragile site FRA16D. (Q33700188) (← links)
- ATR preferentially interacts with common fragile site FRA3B and the binding requires its kinase activity in response to aphidicolin treatment (Q33712256) (← links)
- Secondary structure formation and DNA instability at fragile site FRA16B (Q33871196) (← links)
- Transcriptional regulation of the base excision repair pathway by BRCA1 (Q33911232) (← links)
- Potential biomarkers of DNA replication stress in cancer (Q33913808) (← links)
- DNA instability at chromosomal fragile sites in cancer (Q34152853) (← links)
- Premature condensation induces breaks at the interface of early and late replicating chromosome bands bearing common fragile sites (Q34212683) (← links)
- Human TopBP1 ensures genome integrity during normal S phase (Q34230830) (← links)
- Plant 45S rDNA clusters are fragile sites and their instability is associated with epigenetic alterations (Q34235590) (← links)
- Cycles of chromosome instability are associated with a fragile site and are increased by defects in DNA replication and checkpoint controls in yeast (Q34324101) (← links)
- Are common fragile sites merely structural domains or highly organized "functional" units susceptible to oncogenic stress? (Q34515728) (← links)
- The SNM1B/APOLLO DNA nuclease functions in resolution of replication stress and maintenance of common fragile site stability. (Q34829867) (← links)
- Common fragile sites are conserved features of human and mouse chromosomes and relate to large active genes (Q35056705) (← links)
- A deletion at the mouse Xist gene exposes trans-effects that alter the heterochromatin of the inactive X chromosome and the replication time and DNA stability of both X chromosomes (Q35175983) (← links)
- Increased common fragile site expression, cell proliferation defects, and apoptosis following conditional inactivation of mouse Hus1 in primary cultured cells (Q35650781) (← links)
- Chromatin changes in the development and pathology of the Fragile X-associated disorders and Friedreich ataxia (Q36016607) (← links)
- The role of fragile sites in sporadic papillary thyroid carcinoma (Q36063579) (← links)
- Regulation of the Fanconi anemia pathway by a CUE ubiquitin-binding domain in the FANCD2 protein (Q36220736) (← links)
- Chromosomal radiosensitivity of human immunodeficiency virus positive/negative cervical cancer patients in South Africa (Q36390334) (← links)
- Replication stress induces tumor-like microdeletions in FHIT/FRA3B (Q36423451) (← links)
- Increased level of chromosomal damage after irradiation of lymphocytes from BRCA1 mutation carriers (Q36613591) (← links)
- Replication stress induces specific enrichment of RECQ1 at common fragile sites FRA3B and FRA16D (Q36874183) (← links)
- FANCJ at the FORK. (Q36952290) (← links)
- Haploinsufficiency of DNA Damage Response Genes and their Potential Influence in Human Genomic Disorders (Q37185705) (← links)
- The biological effects of simple tandem repeats: lessons from the repeat expansion diseases (Q37204533) (← links)
- Telomeric allelic imbalance indicates defective DNA repair and sensitivity to DNA-damaging agents (Q37251187) (← links)
- The role of DNA damage response pathways in chromosome fragility in Fragile X syndrome (Q37273647) (← links)
- Somatic copy number changes in DPYD are associated with lower risk of recurrence in triple-negative breast cancers (Q37279312) (← links)
- Mammalian telomeres resemble fragile sites and require TRF1 for efficient replication (Q37297007) (← links)
- Regulation of the activation of the Fanconi anemia pathway by the p21 cyclin-dependent kinase inhibitor (Q37682205) (← links)
- Interplay between genetic and epigenetic factors governs common fragile site instability in cancer (Q38258279) (← links)
- Fragile sites in cancer: more than meets the eye. (Q39455549) (← links)
- Homologous recombination and nonhomologous end-joining repair pathways regulate fragile site stability (Q39705486) (← links)
- Relationship between FRA11F and 11q13 gene amplification in oral cancer (Q40209226) (← links)
- Genome rearrangements caused by depletion of essential DNA replication proteins in Saccharomyces cerevisiae (Q42321840) (← links)
- The mINO80 chromatin remodeling complex is required for efficient telomere replication and maintenance of genome stability (Q42853694) (← links)
- Werner syndrome helicase activity is essential in maintaining fragile site stability (Q42972865) (← links)
- FRA18C: a new aphidicolin-inducible fragile site on chromosome 18q22, possibly associated with in vivo chromosome breakage (Q43232398) (← links)