scholarly article | Q13442814 |
P2093 | author name string | Arthur J Lustig | |
P2860 | cites work | How shelterin solves the telomere end-protection problem | Q44220453 |
Oxidative DNA damage in Barrett mucosa: correlation with telomeric dysfunction and p53 mutation | Q44769510 | ||
Saccharomyces telomeres assume a non-nucleosomal chromatin structure | Q44967865 | ||
Analysis of telomeres in peripheral blood cells from patients with bone marrow failure. | Q45986493 | ||
Tumor size-independence of telomere length indicates an aggressive feature of HCC. | Q47400426 | ||
The study on telomere length for age estimation in a Thai population. | Q50692278 | ||
RIF1: a novel regulatory factor for DNA replication and DNA damage response signaling. | Q50693600 | ||
Fission yeast Rap1 homolog is a telomere-specific silencing factor and interacts with Taz1p. | Q52546098 | ||
A quantitative real-time PCR method for absolute telomere length. | Q54533151 | ||
RAP1 and telomere structure regulate telomere position effects in Saccharomyces cerevisiae. | Q54655346 | ||
The Shortest Telomere, Not Average Telomere Length, Is Critical for Cell Viability and Chromosome Stability | Q56508014 | ||
Differential effects of the mismatch repair genes MSH2 and MSH3 on homeologous recombination in Saccharomyces cerevisiae | Q57451646 | ||
Telomere length in vascular tissues from patients with atherosclerotic disease | Q59275515 | ||
Tel1p Preferentially Associates with Short Telomeres to Stimulate Their Elongation | Q61314294 | ||
Action of a RAP1 carboxy-terminal silencing domain reveals an underlying competition between HMR and telomeres in yeast | Q72572914 | ||
Est1 and Cdc13 as comediators of telomerase access | Q73042124 | ||
Telomere maintenance in fission yeast requires an Est1 ortholog | Q73216287 | ||
Functional reconstitution of human telomerase expressed in Saccharomyces cerevisiae | Q73297605 | ||
Ku suppresses formation of telomeric circles and alternative telomere lengthening in Arabidopsis | Q80571138 | ||
Real-time PCR assay for measurement of mouse telomeres | Q82752078 | ||
Functional conservation of the telomerase protein Est1p in humans | Q24299999 | ||
RPA-like mammalian Ctc1-Stn1-Ten1 complex binds to single-stranded DNA and protects telomeres independently of the Pot1 pathway | Q24310294 | ||
TRF2 recruits RTEL1 to telomeres in S phase to promote t-loop unwinding | Q24316035 | ||
Telomere measurement by quantitative PCR | Q24529938 | ||
The Stability of Broken Ends of Chromosomes in Zea Mays. | Q24533277 | ||
Control of human telomere length by TRF1 and TRF2 | Q24554302 | ||
Finding the end: recruitment of telomerase to telomeres | Q24606549 | ||
Characterization of the yeast telomere nucleoprotein core: Rap1 binds independently to each recognition site | Q24612886 | ||
DNA end resection: many nucleases make light work | Q24654725 | ||
Telomere protection by TPP1 is mediated by POT1a and POT1b | Q24654732 | ||
Telomere rapid deletion regulates telomere length in Arabidopsis thaliana | Q24681584 | ||
Analyses of Candida Cdc13 Orthologues Revealed a Novel OB Fold Dimer Arrangement, Dimerization-Assisted DNA Binding, and Substantial Structural Differences between Cdc13 and RPA70 | Q27675212 | ||
Structure of Est3 reveals a bimodal surface with differential roles in telomere replication | Q27680909 | ||
A mutant with a defect in telomere elongation leads to senescence in yeast | Q27930429 | ||
The Saccharomyces telomere-binding protein Cdc13p interacts with both the catalytic subunit of DNA polymerase alpha and the telomerase-associated est1 protein | Q27931011 | ||
Multiple pathways regulate 3' overhang generation at S. cerevisiae telomeres. | Q27931150 | ||
Deletion of Ogg1 DNA glycosylase results in telomere base damage and length alteration in yeast | Q27933719 | ||
Telomerase and Tel1p preferentially associate with short telomeres in S. cerevisiae. | Q27934956 | ||
Rap1 prevents telomere fusions by nonhomologous end joining | Q27936253 | ||
Involvement of the silencer and UAS binding protein RAP1 in regulation of telomere length | Q27938798 | ||
Normal mammalian cells negatively regulate telomere length by telomere trimming | Q28114927 | ||
Break-induced replication and recombinational telomere elongation in yeast | Q28244552 | ||
Shelterin: the protein complex that shapes and safeguards human telomeres | Q28272546 | ||
The Saccharomyces cerevisiae telomerase subunit Est3 binds telomeres in a cell cycle- and Est1-dependent manner and interacts directly with Est1 in vitro | Q28478064 | ||
The telomere capping complex CST has an unusual stoichiometry, makes multipartite interaction with G-Tails, and unfolds higher-order G-tail structures | Q28484817 | ||
Histone H3 and H4 N-termini interact with SIR3 and SIR4 proteins: a molecular model for the formation of heterochromatin in yeast | Q29614857 | ||
Sgs1 helicase and two nucleases Dna2 and Exo1 resect DNA double-strand break ends | Q29615269 | ||
Reverse transcriptase motifs in the catalytic subunit of telomerase | Q29618392 | ||
Purification of telomerase from Euplotes aediculatus: requirement of a primer 3' overhang | Q30469368 | ||
Three Ever Shorter Telomere (EST) genes are dispensable for in vitro yeast telomerase activity | Q30471100 | ||
Characteristics of age-related changes in cultured human vocal fold fibroblasts | Q30490794 | ||
Estimating telomere length from whole genome sequence data | Q30773501 | ||
Computel: computation of mean telomere length from whole-genome next-generation sequencing data | Q30940378 | ||
Telomeric circles: universal players in telomere maintenance? | Q33696452 | ||
Telomeric protein TRF2 protects Holliday junctions with telomeric arms from displacement by the Werner syndrome helicase. | Q33959427 | ||
An mre11 mutation that promotes telomere recombination and an efficient bypass of senescence | Q34007895 | ||
Intrachromatid excision of telomeric DNA as a mechanism for telomere size control in Saccharomyces cerevisiae | Q34012288 | ||
Reliability and short-term intra-individual variability of telomere length measurement using monochrome multiplexing quantitative PCR. | Q34045020 | ||
Alternative lengthening of telomeres in cancer stem cells in vivo | Q34054060 | ||
Xenopus laevis Ctc1-Stn1-Ten1 (xCST) protein complex is involved in priming DNA synthesis on single-stranded DNA template in Xenopus egg extract | Q34075356 | ||
T-loop assembly in vitro involves binding of TRF2 near the 3' telomeric overhang | Q34082359 | ||
A yeast telomerase complex containing the Est1 recruitment protein is assembled early in the cell cycle | Q34231755 | ||
Regulated assembly and disassembly of the yeast telomerase quaternary complex | Q34271328 | ||
Removal of shelterin reveals the telomere end-protection problem | Q34272638 | ||
Selaginella moellendorffii telomeres: conserved and unique features in an ancient land plant lineage | Q34352194 | ||
Telomeres and telomerase: their mechanisms of action and the effects of altering their functions | Q34389435 | ||
Improving qPCR telomere length assays: Controlling for well position effects increases statistical power | Q34466538 | ||
RAD50 and RAD51 define two pathways that collaborate to maintain telomeres in the absence of telomerase | Q34606774 | ||
High-throughput telomere length quantification by FISH and its application to human population studies | Q34609809 | ||
Differential processing of leading- and lagging-strand ends at Saccharomyces cerevisiae telomeres revealed by the absence of Rad27p nuclease | Q34616720 | ||
A quantitative PCR method for measuring absolute telomere length | Q34618088 | ||
Recombination can cause telomere elongations as well as truncations deep within telomeres in wild-type Kluyveromyces lactis cells | Q34739230 | ||
Leukocyte telomere length variation due to DNA extraction method | Q34897500 | ||
Increased telomere length and proliferative potential in peripheral blood mononuclear cells of adults of different ages stimulated with concanavalin A. | Q34996356 | ||
The Ctf18RFC clamp loader is essential for telomere stability in telomerase-negative and mre11 mutant alleles | Q35095480 | ||
G-quadruplex-mediated regulation of telomere binding protein POT1 gene expression | Q35121313 | ||
Stimulation of yeast telomerase activity by the ever shorter telomere 3 (Est3) subunit is dependent on direct interaction with the catalytic protein Est2. | Q35128162 | ||
Telomere maintenance and DNA replication: how closely are these two connected? | Q35193731 | ||
All gene-sized DNA molecules in four species of hypotrichs have the same terminal sequence and an unusual 3' terminus | Q35362394 | ||
Impartial comparative analysis of measurement of leukocyte telomere length/DNA content by Southern blots and qPCR. | Q35468277 | ||
Clues to catastrophic telomere loss in mammals from yeast telomere rapid deletion | Q35591723 | ||
Adding to the ends: what makes telomerase processive and how important is it? | Q35880054 | ||
Increased association of telomerase with short telomeres in yeast. | Q35893631 | ||
Gender and telomere length: systematic review and meta-analysis | Q35911189 | ||
The carboxy termini of Sir4 and Rap1 affect Sir3 localization: evidence for a multicomponent complex required for yeast telomeric silencing | Q36235711 | ||
Telomere dynamics in genome stability | Q36365852 | ||
Telomere loops and homologous recombination-dependent telomeric circles in a Kluyveromyces lactis telomere mutant strain. | Q36421126 | ||
Alternative lengthening of telomeres in normal mammalian somatic cells | Q36557062 | ||
Detection of alternative lengthening of telomeres by telomere quantitative PCR. | Q36559242 | ||
Multiple pathways inhibit NHEJ at telomeres. | Q36585488 | ||
Human telomere biology: pitfalls of moving from the laboratory to epidemiology | Q36602356 | ||
Developmentally controlled telomere addition in wild-type and mutant paramecia | Q36780421 | ||
Robust measurement of telomere length in single cells. | Q36884117 | ||
The length of the shortest telomere as the major determinant of the onset of replicative senescence | Q37063130 | ||
Telomere length measurement by a novel monochrome multiplex quantitative PCR method | Q37108473 | ||
A proposed OB-fold with a protein-interaction surface in Candida albicans telomerase protein Est3 | Q37131017 | ||
Rif1 and rif2 inhibit localization of tel1 to DNA ends. | Q37143974 | ||
TRF2 promotes, remodels and protects telomeric Holliday junctions | Q37151495 | ||
The Est3 protein associates with yeast telomerase through an OB-fold domain | Q37159901 | ||
Control of telomere length by a trimming mechanism that involves generation of t-circles | Q37163052 | ||
Telomere length varies by DNA extraction method: implications for epidemiologic research | Q37308297 | ||
The conserved Est1 protein stimulates telomerase DNA extension activity | Q37394791 | ||
Multiple genetic pathways regulate replicative senescence in telomerase-deficient yeast | Q37600457 | ||
The role of telomere trimming in normal telomere length dynamics | Q37993983 | ||
Molecular steps of G-overhang generation at human telomeres and its function in chromosome end protection | Q39678675 | ||
Unusual telomeric DNAs in human telomerase-negative immortalized cells | Q39915528 | ||
The Ku Heterodimer Performs Separable Activities at Double-Strand Breaks and Chromosome Termini | Q40172226 | ||
Mutual dependence of Candida albicans Est1p and Est3p in telomerase assembly and activation | Q40207099 | ||
Comparison of different protocols for telomere length estimation by combination of quantitative fluorescence in situ hybridization (Q-FISH) and flow cytometry in human cancer cell lines. | Q40427433 | ||
Telomere dynamics and fusion of critically shortened telomeres in plants lacking DNA ligase IV | Q40696254 | ||
Telomere maintenance by recombination in human cells. | Q40839283 | ||
Fission yeast MAP kinase Sty1 is recruited to stress-induced genes | Q41234667 | ||
Rap1p and telomere length regulation in yeast. | Q41730851 | ||
Measurement of telomere length: a new assay using QuantiGene chemistry on a Luminex platform | Q41875208 | ||
Reproducibility of telomere length assessment: an international collaborative study | Q41935897 | ||
Telomere capping in non-dividing yeast cells requires Yku and Rap1. | Q42031994 | ||
Blunt-ended telomeres: an alternative ending to the replication and end protection stories. | Q42275166 | ||
Telomere position effect in human cells | Q43642023 | ||
P433 | issue | 1 | |
P304 | page(s) | 28-37 | |
P577 | publication date | 2015-08-12 | |
P1433 | published in | Journal of cancer epidemiology & treatment | Q27726809 |
P1476 | title | Potential Risks in the Paradigm of Basic to Translational Research: A Critical Evaluation of qPCR Telomere Size Techniques | |
P478 | volume | 1 |