Pages that link to "Q35199532"
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The following pages link to Induction of sister chromatid exchanges at common fragile sites (Q35199532):
Displaying 50 items.
- Concerted evolution of the tandemly repeated genes encoding human U2 snRNA (the RNU2 locus) involves rapid intrachromosomal homogenization and rare interchromosomal gene conversion (Q24532100) (← links)
- Chromosomal instability at common fragile sites in Seckel syndrome (Q24533727) (← links)
- Common fragile sites: genomic hotspots of DNA damage and carcinogenesis (Q26825040) (← links)
- BRCA1 is required for common-fragile-site stability via its G2/M checkpoint function (Q28508100) (← links)
- Nuclear function of Alus (Q28658599) (← links)
- A novel approach to simultaneously scan genes at fragile sites (Q33253255) (← links)
- Induction of distamycin A-inducible rare fragile sites and increased sister chromatid exchanges at the fragile site (Q33353680) (← links)
- Clinical and molecular characterization of patients with distal 11q deletions. (Q33490677) (← links)
- DNA structure and the Werner protein modulate human DNA polymerase delta-dependent replication dynamics within the common fragile site FRA16D. (Q33700188) (← links)
- ATR suppresses telomere fragility and recombination but is dispensable for elongation of short telomeres by telomerase (Q33717036) (← links)
- DNA breaks at fragile sites generate oncogenic RET/PTC rearrangements in human thyroid cells (Q33792630) (← links)
- Secondary structure formation and DNA instability at fragile site FRA16B (Q33871196) (← links)
- Replication delay along FRA7H, a common fragile site on human chromosome 7, leads to chromosomal instability (Q33963998) (← 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)
- Topoisomerase II- and condensin-dependent breakage of MEC1ATR-sensitive fragile sites occurs independently of spindle tension, anaphase, or cytokinesis. (Q34469022) (← links)
- Are common fragile sites merely structural domains or highly organized "functional" units susceptible to oncogenic stress? (Q34515728) (← links)
- Common fragile site tumor suppressor genes and corresponding mouse models of cancer (Q34557827) (← links)
- An AT-rich sequence in human common fragile site FRA16D causes fork stalling and chromosome breakage in S. cerevisiae (Q34659849) (← links)
- Fragile site instability in Saccharomyces cerevisiae causes loss of heterozygosity by mitotic crossovers and break-induced replication. (Q34998370) (← links)
- Increased genetic instability of the common fragile site at 3p14 after integration of exogenous DNA. (Q35195363) (← links)
- Chromosome breakage and recombination at fragile sites (Q35246834) (← links)
- Phosphorylation of the Bloom's syndrome helicase and its role in recovery from S-phase arrest (Q35544616) (← links)
- A genome-wide analysis of common fragile sites: what features determine chromosomal instability in the human genome? (Q36021725) (← links)
- The role of fragile sites in sporadic papillary thyroid carcinoma (Q36063579) (← links)
- Genomic instability in the PARK2 locus is associated with Parkinson's disease (Q36199151) (← links)
- Replication stress induces tumor-like microdeletions in FHIT/FRA3B (Q36423451) (← links)
- A TRF1-controlled common fragile site containing interstitial telomeric sequences (Q36664216) (← links)
- The role of BRCA1 in homologous recombination repair in response to replication stress: significance in tumorigenesis and cancer therapy (Q36689932) (← links)
- TERRA, hnRNP A1, and DNA-PKcs Interactions at Human Telomeres (Q36772057) (← links)
- ZNF365 promotes stability of fragile sites and telomeres. (Q37009684) (← links)
- High chromosomal instability in workers occupationally exposed to solvents and paint removers. (Q37019722) (← links)
- Evidence for a novel mechanism for gene amplification in multiple myeloma: 1q12 pericentromeric heterochromatin mediates breakage-fusion-bridge cycles of a 1q12 approximately 23 amplicon (Q37082758) (← links)
- Mammalian telomeres resemble fragile sites and require TRF1 for efficient replication (Q37297007) (← links)
- SMARCAL1 Resolves Replication Stress at ALT Telomeres. (Q37312254) (← links)
- Sources and structures of mitotic crossovers that arise when BLM helicase is absent in Drosophila (Q37412731) (← links)
- X chromosome inactivation and autoimmunity (Q37571619) (← links)
- Dose-response function for Painter's SCE-model (Q38517146) (← links)
- Repeat expansion in the budding yeast ribosomal DNA can occur independently of the canonical homologous recombination machinery (Q38855771) (← links)
- Infection with retroviral vectors leads to perturbed DNA replication increasing vector integrations into fragile sites (Q39126132) (← links)
- Werner syndrome protein suppresses the formation of large deletions during the replication of human telomeric sequences (Q39300997) (← links)
- Fragile sites in cancer: more than meets the eye. (Q39455549) (← links)
- Failure of Origin Activation in Response to Fork Stalling Leads to Chromosomal Instability at Fragile Sites (Q39512958) (← links)
- Adenovirus Type 12-Induced Fragility of the Human RNU2 Locus Requires p53 Function (Q39578554) (← links)
- Direct cloning and analysis of DNA sequences from a region of the Chinese hamster genome associated with aphidicolin-sensitive fragility (Q41040273) (← links)
- Sister chromatid exchanges are preferentially induced at expressed and nonexpressed common fragile sites (Q41157378) (← links)
- BLM helicase suppresses recombination at G-quadruplex motifs in transcribed genes (Q49195352) (← links)
- Human DNA Helicase B as a Candidate for Unwinding Secondary CGG Repeat Structures at the Fragile X Mental Retardation Gene. (Q55234993) (← links)
- Common Chromosomal Fragile Sites-Conserved Failure Stories (Q60935156) (← links)
- Population cytogenetics of folate-sensitive fragile sites. I. Common fragile sites (Q67980047) (← links)