Pages that link to "Q28289730"
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The following pages link to Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia (Q28289730):
Displaying 50 items.
- xeroderma pigmentosum (Q612693) (← links)
- DNA Damage: A Main Determinant of Vascular Aging (Q26746962) (← links)
- Interplay between Fanconi anemia and homologous recombination pathways in genome integrity (Q26753126) (← links)
- Photosensitive human syndromes (Q26800642) (← links)
- Why does the bone marrow fail in Fanconi anemia? (Q26823574) (← links)
- Mechanism and regulation of incisions during DNA interstrand cross-link repair (Q26865523) (← links)
- Fanconi anemia and the cell cycle: new perspectives on aneuploidy (Q27014905) (← links)
- Cell-autonomous progeroid changes in conditional mouse models for repair endonuclease XPG deficiency (Q27312602) (← links)
- The Fanconi Anemia C Protein Binds to and Regulates Stathmin-1 Phosphorylation (Q27312678) (← links)
- The MHF complex senses branched DNA by binding a pair of crossover DNA duplexes (Q27681193) (← links)
- A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination (Q28115483) (← links)
- XPF-ERCC1 acts in Unhooking DNA interstrand crosslinks in cooperation with FANCD2 and FANCP/SLX4 (Q28238027) (← links)
- DNA repair diseases: What do they tell us about cancer and aging? (Q28238854) (← links)
- Advances in understanding the complex mechanisms of DNA interstrand cross-link repair (Q28299636) (← links)
- The Cerebro-oculo-facio-skeletal Syndrome Point Mutation F231L in the ERCC1 DNA Repair Protein Causes Dissociation of the ERCC1-XPF Complex (Q29542538) (← links)
- A never-ending story: the steadily growing family of the FA and FA-like genes (Q30100995) (← links)
- The genomics of inherited bone marrow failure: from mechanism to the clinic. (Q30235895) (← links)
- ERCC6L2 mutations link a distinct bone-marrow-failure syndrome to DNA repair and mitochondrial function (Q32884456) (← links)
- A unified model for the molecular basis of Xeroderma pigmentosum-Cockayne Syndrome. (Q33361700) (← links)
- The histone-fold complex MHF is remodeled by FANCM to recognize branched DNA and protect genome stability (Q33571367) (← links)
- A concomitant loss of dormant origins and FANCC exacerbates genome instability by impairing DNA replication fork progression. (Q33635514) (← links)
- Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology. (Q33698638) (← links)
- Cellular Repair of DNA-DNA Cross-Links Induced by 1,2,3,4-Diepoxybutane (Q33755415) (← links)
- Hypersensitivity of primordial germ cells to compromised replication-associated DNA repair involves ATM-p53-p21 signaling (Q33880788) (← links)
- Tumor suppressor RecQL5 controls recombination induced by DNA crosslinking agents (Q33926029) (← links)
- Understanding nucleotide excision repair and its roles in cancer and ageing. (Q34426055) (← links)
- CSB interacts with SNM1A and promotes DNA interstrand crosslink processing (Q34453793) (← links)
- Endogenous Formaldehyde Is a Hematopoietic Stem Cell Genotoxin and Metabolic Carcinogen. (Q34498633) (← links)
- Restricted diet delays accelerated ageing and genomic stress in DNA-repair-deficient mice (Q34538349) (← links)
- Increased meiotic crossovers and reduced genome stability in absence of Schizosaccharomyces pombe Rad16 (XPF). (Q34636209) (← links)
- Coordinate nuclear targeting of the FANCD2 and FANCI proteins via a FANCD2 nuclear localization signal (Q35054036) (← links)
- The Fanconi anemia group C protein interacts with uncoordinated 5A and delays apoptosis. (Q35133827) (← links)
- The ERCC1 and ERCC4 (XPF) genes and gene products (Q35663361) (← links)
- Characterization of medulloblastoma in Fanconi Anemia: a novel mutation in the BRCA2 gene and SHH molecular subgroup (Q35710253) (← links)
- Comparison of mice with accelerated aging caused by distinct mechanisms (Q35732338) (← links)
- Primary Ovarian Insufficiency Induced by Fanconi Anemia E Mutation in a Mouse Model (Q38634882) (← links)
- Dearth and Delayed Maturation of Testicular Germ Cells in Fanconi Anemia E Mutant Male Mice (Q36093679) (← links)
- Deep phenotyping of 89 xeroderma pigmentosum patients reveals unexpected heterogeneity dependent on the precise molecular defect (Q36658965) (← links)
- Nuclear lamins in cancer (Q37207687) (← links)
- Mutation analysis of the ERCC4/FANCQ gene in hereditary breast cancer (Q37499453) (← links)
- The Fanconi anemia pathway has a dual function in Dickkopf-1 transcriptional repression (Q37587769) (← links)
- High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis. (Q37649522) (← links)
- Xeroderma pigmentosum-Cockayne syndrome complex (Q37736827) (← links)
- Nuclease delivery: versatile functions of SLX4/FANCP in genome maintenance (Q38220992) (← links)
- Stress and DNA repair biology of the Fanconi anemia pathway (Q38252562) (← links)
- Development of effective skin cancer treatment and prevention in xeroderma pigmentosum (Q38266357) (← links)
- Molecular regulation of UV-induced DNA repair (Q38298148) (← links)
- Unscheduled DNA synthesis: the clinical and functional assay for global genomic DNA nucleotide excision repair (Q38371998) (← links)
- XPF knockout via CRISPR/Cas9 reveals that ERCC1 is retained in the cytoplasm without its heterodimer partner XPF. (Q38719028) (← links)
- FANCD2 limits BLM-dependent telomere instability in the alternative lengthening of telomeres pathway (Q38757606) (← links)