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1. Full Text Regulation of sororin by cdk1-mediated phosphorylation
by Dreier, Megan R and Bekier, Michael E and Taylor, William R
Journal of Cell Science, ISSN 0021-9533, 09/2011, Volume 124, Issue 17, pp. 2976 - 2987
Tumor cells are commonly aneuploid, a condition contributing to cancer progression and drug resistance. Understanding how chromatids are linked and separated... 
Cohesion | Sister chromatids | Aneuploid | Spindle assembly checkpoint | Cell cycle | SISTER-CHROMATID COHESION | ANAPHASE | CELLS | LOCALIZATION | COMPLEX | PROTEIN | CHROMOSOME ARMS | KINASE | CELL BIOLOGY | RESPONSES | PROPHASE | CDC2 Protein Kinase - genetics | Phosphorylation | Mutagenesis, Site-Directed | Chromosomal Proteins, Non-Histone - metabolism | Chromatids - genetics | Humans | Cell Cycle Proteins - metabolism | Chromatids - enzymology | CDC2 Protein Kinase - metabolism | Chromatids - metabolism | Transfection | Mitosis - physiology | Sister Chromatid Exchange | HeLa Cells | Adaptor Proteins, Signal Transducing - metabolism | M Phase Cell Cycle Checkpoints - physiology | Index Medicus
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2. Full Text Regulation of DNA repair pathway choice in S and G2 phases by the NHEJ inhibitor CYREN
by Arnoult, Nausica and Correia, Adriana and Ma, Jiao and Merlo, Anna and Garcia-Gomez, Sara and Maric, Marija and Tognetti, Marco and Benner, Christopher W and Boulton, Simon J and Saghatelian, Alan and Karlseder, Jan
Nature, ISSN 0028-0836, 09/2017, Volume 549, Issue 7673, pp. 548 - 552
Classical non-homologous end joining(1) (cNHEJ) and homologous recombination(2) compete for the repair of double-stranded DNA breaks during the cell cycle.... 
STRAND BREAK REPAIR | MECHANISM | RESECTION | MULTIDISCIPLINARY SCIENCES | END-PROTECTION | DAMAGE SIGNAL | ATM | HOMOLOGOUS RECOMBINATION | IDENTIFICATION | TRF2 | TELOMERES | Cell Line | Chromatids - genetics | DNA End-Joining Repair - genetics | Recombinational DNA Repair - genetics | Humans | Ku Autoantigen - chemistry | Ku Autoantigen - metabolism | DNA End-Joining Repair - physiology | DNA Breaks, Double-Stranded | Chromatids - metabolism | G1 Phase | Recombinational DNA Repair - physiology | S Phase | Chromosome Aberrations | G2 Phase | Protein Binding | Telomere - metabolism | Telomere - genetics | Genetic research | Research | Genetic regulation | DNA repair | Medical research | Sister chromatids | DNA damage | Homologous recombination | Homology | Kinases | Proteins | Telomeres | Phases | Inhibitors | Chromatids | Cell cycle | Non-homologous end joining | Aberration | Damage accumulation | Telomerase | Chromosomes | Chromosome aberrations | Deoxyribonucleic acid--DNA | Cancer | G1 phase | Index Medicus
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3. Full Text Investigating the Interplay between Sister Chromatid Cohesion and Homolog Pairing in Drosophila Nuclei
by Senaratne, T. Niroshini and Joyce, Eric F and Nguyen, Son C and Wu, C.-Ting
PLoS Genetics, ISSN 1553-7390, 08/2016, Volume 12, Issue 8, pp. e1006169 - e1006169
Following DNA replication, sister chromatids must stay connected for the remainder of the cell cycle in order to ensure accurate segregation in the subsequent... 
COMPLEX | TOPOISOMERASE-II | MITOTIC CHROMOSOME | YEAST COHESIN | DNA | GENETICS & HEREDITY | CHROMOSOME CONDENSATION | CENTROMERIC-HETEROCHROMATIN | GENE-EXPRESSION | TRANSVECTION | SEGREGATION | Sister Chromatid Exchange - genetics | Chromatids - genetics | In Situ Hybridization, Fluorescence | Multiprotein Complexes - genetics | DNA-Binding Proteins - genetics | Mitosis - genetics | Drosophila melanogaster - genetics | Animals | Cell Nucleus - genetics | Metaphase - genetics | RNA Interference | Chromosomes - genetics | DNA Replication - genetics | Adenosine Triphosphatases - genetics | Chromosome Segregation - genetics | DNA replication | Drosophila | Cell cycle | Genetic research | Genetic aspects | Research | Chromosomes | Proteins | Yeast | Insects | Cell division | Gene expression | Experiments | Deoxyribonucleic acid--DNA | Index Medicus | Deoxyribonucleic acid
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4. Full Text Replication-Dependent Loss of 5-Hydroxymethylcytosine in Mouse Preimplantation Embryos
by Azusa Inoue and Yi Zhang
Science, ISSN 0036-8075, 10/2011, Volume 334, Issue 6053, pp. 194 - 194
Although global erasure of DNA methylation has been observed in zygotes and primordial germ cells, the responsible enzyme(s) have been elusive. The... 
Zygotes | Blastomeres | DNA | Chromatids | Chromosomes | Embryos | BREVIA | Pronucleus | PATERNAL GENOME | MAMMALIAN DNA | 5-METHYLCYTOSINE | CONVERSION | MULTIDISCIPLINARY SCIENCES | ACTIVE DNA DEMETHYLATION | TET PROTEINS | 5-CARBOXYLCYTOSINE | Proto-Oncogene Proteins - metabolism | Cytosine - analogs & derivatives | Mitosis | Blastocyst - metabolism | Zygote - metabolism | DNA Replication | Embryonic Development | Chromatids - metabolism | DNA-Binding Proteins - metabolism | Animals | 5-Methylcytosine - metabolism | Cytosine - metabolism | Sister Chromatid Exchange | Mice | Chromosomes, Mammalian - metabolism | Proteins | DNA methylation | Enzymes | Animal reproduction | Rodents | Index Medicus
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5. Full Text The hybrid incompatibility genes Lhr and Hmr are required for sister chromatid detachment during anaphase but not for centromere function
by Blum, Jacob A and Bonaccorsi, Silvia and Marzullo, Marta and Palumbo, Valeria and Yamashita, Yukiko M and Barbash, Daniel A and Gatti, Maurizio
Genetics, ISSN 0016-6731, 12/2017, Volume 207, Issue 4, pp. 1457 - 1472
Crosses between Drosophila melanogaster females and Drosophila simulans males produce hybrid sons that die at the larval stage. This hybrid lethality is... 
Interspecific hybrids | Drosophila | Lhr | Hmr | Sister chromatid separation | Anaphase | Chromosome aberrations | chromosome aberrations | CELLS | TOPOISOMERASE-II | PROTEIN | DROSOPHILA-MELANOGASTER | anaphase | DNA-DAMAGE | RESOLUTION | SEGREGATION | sister chromatid separation | MITOSIS | interspecific hybrids | CHROMOSOME-ABERRATIONS | HETEROCHROMATIN | GENETICS & HEREDITY | Sister Chromatid Exchange - genetics | Chromatids - genetics | Male | Drosophila melanogaster - genetics | DNA Transposable Elements | Anaphase - genetics | Animals | Heterochromatin - genetics | Larva | Centromere - genetics | Hybridization, Genetic | Genes, Lethal - genetics | Female | Drosophila Proteins - genetics | X Chromosome - genetics | Research | Gene mutations | Analysis | Hybrids | Chromatin | Genes | Centromeres | Lethality | Males | Kinases | Defects | Proteins | Heterochromatin | Metaphase | Euchromatin | Division | Chromosomes | Deoxyribonucleic acid--DNA | Incompatibility | Sister chromatids | Mutants | Bridges | Gene amplification | Detachment | Insects | Chromatids | Breakage | Mutation | Aberration | Females | Index Medicus | Investigations
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6. Full Text Esco1 and Esco2 regulate distinct cohesin functions during cell cycle progression
by Alomer, Reem M and Da Silva, Eulália M. L and Chen, Jingrong and Piekarz, Katarzyna M and McDonald, Katherine and Sansam, Courtney G and Sansam, Christopher L and Rankin, Susannah
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 09/2017, Volume 114, Issue 37, pp. 9906 - 9911
Sister chromatids are tethered together by the cohesin complex from the time they are made until their separation at anaphase. The ability of cohesin to tether... 
Sister chromatid cohesion | Chromosome biology | Esco enzymes | Cell cycle | SISTER-CHROMATID COHESION | COMPLEX | SORORIN | cell cycle | ACETYLATION | MULTIDISCIPLINARY SCIENCES | CTCF | ESTABLISHMENT | CCCTC-BINDING FACTOR | HUMAN GENOME | sister chromatid cohesion | chromosome biology | ARCHITECTURE | S-PHASE | Cohesion | Deactivation | Sister chromatids | Transcription | Cell division | Inactivation | DNA repair | Studies | Proteins | Vertebrates | Cell growth | Chromatids | Cohesin | Acetylation | Chromosomes | Anaphase | Deoxyribonucleic acid--DNA | Index Medicus | Biological Sciences
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7. Full Text Tracking Chromatid Segregation to Identify Human Cardiac Stem Cells That Regenerate Extensively the Infarcted Myocardium
by Kajstura, Jan and Bai, Yingnan and Cappetta, Donato and Kim, Junghyun and Arranto, Christian and Sanada, Fumihiro and DʼAmario, Domenico and Matsuda, Alex and Bardelli, Silvana and Ferreira-Martins, João and Hosoda, Toru and Leri, Annarosa and Rota, Marcello and Loscalzo, Joseph and Anversa, Piero
Circulation Research, ISSN 0009-7330, 09/2012, Volume 111, Issue 7, pp. 894 - 906
RATIONALE:According to the immortal DNA strand hypothesis, dividing stem cells selectively segregate chromosomes carrying the old template DNA, opposing... 
immortal DNA strand hypothesis | proliferation | asymmetrical chromatid segregation | cell cycle | myocardial infarction | symmetrical chromatid segregation | myocardial regeneration | adult stem cells | asymmetrical stem cell division | PROGENITOR CELLS | ACTIVATION | CARDIOMYOGENESIS | CARDIAC & CARDIOVASCULAR SYSTEMS | MOUSE | TO-PRO-3 | TEMPLATE DNA STRANDS | DIVISION | HEART | IMMORTAL STRAND HYPOTHESIS | BROMODEOXYURIDINE | PERIPHERAL VASCULAR DISEASE | HEMATOLOGY | Chromatids - physiology | Cell Proliferation | Telomere - ultrastructure | Heart - physiology | Humans | Middle Aged | Rats, Inbred F344 | Child, Preschool | Bromodeoxyuridine | Infant | Male | Stem Cells - cytology | Stem Cell Transplantation | Young Adult | Myocardial Infarction - therapy | DNA - physiology | Myocardial Infarction - pathology | Aged, 80 and over | Chromosome Segregation - physiology | Adult | Chromatids - ultrastructure | Female | Models, Animal | Myocardial Infarction - physiopathology | Child | Cells, Cultured | Rats | Regeneration - physiology | Myocardium - cytology | Animals | Adolescent | Stem Cells - physiology | Aged | In Vitro Techniques | Index Medicus | asymmetric stem cell division | symmetric chromatid segregation | asymmetric chromatid segregation | Immortal DNA strand hypothesis
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8. Full Text Rtt101‐Mms1‐Mms22 coordinates replication‐coupled sister chromatid cohesion and nucleosome assembly
by Zhang, Jingjing and Shi, Di and Li, Xiaoli and Ding, Lin and Tang, Jun and Liu, Cong and Shirahige, Katsuhiko and Cao, Qinhong and Lou, Huiqiang
EMBO reports, ISSN 1469-221X, 08/2017, Volume 18, Issue 8, pp. 1294 - 1305
Two sister chromatids must be held together by a cohesion process from their synthesis during S phase to segregation in anaphase. Despite its pivotal role in... 
chromosome replication | nucleosome assembly | cohesin acetyltransferase | sister chromatid cohesion | PROMOTES REPLICATION | DNA-POLYMERASE-EPSILON | UBIQUITIN LIGASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | MMS22L-NFKBIL2 COMPLEX | SACCHAROMYCES-CEREVISIAE | S-PHASE CHECKPOINT | CELL BIOLOGY | ESTABLISHMENT FACTOR | CHROMOSOME BIOLOGY | HOMOLOGOUS RECOMBINATION | ACETYLATION CYCLE | Acetyltransferases - metabolism | Chromatids - physiology | Chromatids - genetics | Saccharomyces cerevisiae - genetics | Acetyltransferases - genetics | Cell Cycle Proteins - genetics | Cullin Proteins - metabolism | Acetylation | Nuclear Proteins - genetics | Saccharomyces cerevisiae - physiology | Chromosomal Proteins, Non-Histone - metabolism | Cell Cycle Proteins - metabolism | Ubiquitin-Protein Ligases - metabolism | Chromatin Assembly and Disassembly | DNA Replication | Nuclear Proteins - metabolism | Nucleosomes - genetics | Nucleosomes - physiology | Saccharomyces cerevisiae Proteins - genetics | Chromosomal Proteins, Non-Histone - genetics | Cullin Proteins - genetics | Point Mutation | Saccharomyces cerevisiae Proteins - metabolism | DNA Replication Timing | Ubiquitin-Protein Ligases - genetics | Ubiquitin | Temperature requirements | Cohesion | Chromatin | Yeast | Stability | Sister chromatids | Crosstalk | Genomes | Dosage | Suppressors | Mutants | Defects | Temperature effects | S phase | Chromatids | Proliferating cell nuclear antigen | Replication | Cohesin | Mutation | Chromosomes | Anaphase | Assembly | Index Medicus | Chromatin, Epigenetics, Genomics & Functional Genomics | DNA Replication, Repair & Recombination
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9. Full Text The mre11 A470 alleles influence the hereditability and the segregation of telosomes in Saccharomyces cerevisiae
by Baek, In-Joon and Moss, Daniel S and Lustig, Arthur J
PLoS ONE, ISSN 1932-6203, 09/2017, Volume 12, Issue 9, pp. e0183549 - e0183549
Telomeres, the nucleoprotein complexes at the termini of linear chromosomes, are essential for the processes of end replication, end protection, and chromatin... 
YEAST | MAINTENANCE | DNA-BINDING | REPLICATION | MECHANISM | RAP1 | ELONGATION | MULTIDISCIPLINARY SCIENCES | HETEROCHROMATIN | GENE-EXPRESSION | TELOMERE LENGTH | Chromatids - metabolism | Saccharomyces cerevisiae - metabolism | Chromatin Immunoprecipitation | Chromatids - genetics | Saccharomyces cerevisiae - genetics | Alleles | Saccharomyces cerevisiae Proteins - metabolism | Telomere - metabolism | Saccharomyces cerevisiae Proteins - genetics | Mutation - genetics | Telomere - genetics | DNA structure | Chromatin | Phosphorylation | Yeast | Immunoprecipitation | Homeostasis | Biochemistry | Genomes | Saccharomyces | DNA repair | Proteins | MRE11 protein | Chromosomes | Telomerase | Deoxyribonucleic acid--DNA | Crystal structure | Integration | Sister chromatids | Nucleotide sequence | Base pairs | Digestion | Gene expression | Simple sequence repeats | Telomeres | Chromatids | Replication | Heritability | Molecular biology | Saccharomyces cerevisiae | Cellular structure | Index Medicus | Quantitative Biology - Subcellular Processes | Deoxyribonucleic acid | DNA
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10. Full Text H4K20me0 recognition by BRCA1-BARD1 directs homologous recombination to sister chromatids
by Nakamura, Kyosuke and Saredi, Giulia and Becker, Jordan R and Foster, Benjamin M and Nguyen, Nhuong V and Beyer, Tracey E and Cesa, Laura C and Faull, Peter A and Lukauskas, Saulius and Frimurer, Thomas and Chapman, J Ross and Bartke, Till and Groth, Anja
Nature cell biology, ISSN 1465-7392, 03/2019, Volume 21, Issue 3, pp. 311 - 318
Genotoxic DNA double-strand breaks (DSBs) can be repaired by error-free homologous recombination (HR) or mutagenic non-homologous end-joining . HR supresses... 
Amino Acid Sequence | G2 Phase - genetics | Tumor Suppressor Proteins - metabolism | Chromatids - genetics | HCT116 Cells | Humans | Ubiquitin-Protein Ligases - metabolism | Homologous Recombination | DNA Breaks, Double-Stranded | S Phase - genetics | Chromatids - metabolism | Sequence Homology, Amino Acid | BRCA1 Protein - genetics | BRCA1 Protein - metabolism | DNA Repair | Tumor Suppressor Proteins - genetics | Cell Line, Tumor | Lysine - metabolism | HeLa Cells | Histones - metabolism | Methylation | Ubiquitin-Protein Ligases - genetics | Chromatin | Genetic research | Research | Genetic recombination | Tumor proteins | DNA repair | Health aspects | Yeast | p53 Protein | DNA damage | Homologous recombination | Genotoxicity | Homology | Genomes | ADP | Proteins | Ribose | Cell cycle | Histones | Deoxyribonucleic acid--DNA | Sister chromatids | BRCA1 protein | Routing | Breast cancer | Polymerase | Histone H4 | Lysine | Chromatids | Ankyrin | Mutation | Recognition | Cancer | Index Medicus
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11. Full Text BLM Ortholog, Sgs1, Prevents Aberrant Crossing-over by Suppressing Formation of Multichromatid Joint Molecules
by Oh, Steve D and Lao, Jessica P and Hwang, Patty Yi-Hwa and Taylor, Andrew F and Smith, Gerald R and Hunter, Neil
Cell, ISSN 0092-8674, 2007, Volume 130, Issue 2, pp. 259 - 272
Bloom's helicase (BLM) is thought to prevent crossing-over during DNA double-strand-break repair (DSBR) by disassembling double-Holliday junctions (dHJs) or by... 
PROTEINS | DNA | DNA MISMATCH REPAIR | SISTER CHROMATIDS | SYNDROME GENE-PRODUCT | RECQ HELICASES | BIOCHEMISTRY & MOLECULAR BIOLOGY | RECIPROCAL RECOMBINATION | HOMOLOGOUS RECOMBINATION | SACCHAROMYCES-CEREVISIAE | HOLLIDAY JUNCTIONS | DOUBLE-STRAND-BREAK | MEIOTIC RECOMBINATION | CELL BIOLOGY | DNA Helicases - chemistry | Molecular Weight | RecQ Helicases - metabolism | Saccharomyces cerevisiae - genetics | DNA, Cruciform - metabolism | Meiosis | Mutation - genetics | DNA Breaks, Double-Stranded | Crossing Over, Genetic - genetics | Chromatids - metabolism | DNA-Binding Proteins - metabolism | Saccharomyces cerevisiae - cytology | Sequence Homology, Amino Acid | Transcription Factors - metabolism | Saccharomyces cerevisiae Proteins - metabolism | Sister Chromatid Exchange | Adenosine Triphosphatases - chemistry | Chromatids - ultrastructure | Models, Genetic | Index Medicus
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12. Full Text Meiosis I chromosome segregation is established through regulation of microtubule-kinetochore interactions
by Miller, Matthew P and Ünal, Elçin and Brar, Gloria A and Amon, Angelika
eLife, ISSN 2050-084X, 12/2012, Volume 2012, Issue 1, pp. e00117 - e00117
During meiosis, a single round of DNA replication is followed by two consecutive rounds of nuclear divisions called meiosis I and meiosis II. In meiosis I,... 
SISTER-CHROMATID COHESION | REC8 PHOSPHORYLATION | FISSION YEAST | CENTROMERIC COHESION | ELECTROPHORETIC TRANSFER | HOMOLOGOUS CHROMOSOMES | BIOLOGY | CELL-CYCLE | POLYACRYLAMIDE GELS | PROTEIN PHOSPHATASE 2A | SACCHAROMYCES-CEREVISIAE | Gene Expression Regulation, Fungal | Chromosomes, Fungal | Chromosome Segregation | Kinetochores - metabolism | Signal Transduction | Mitosis | Saccharomyces cerevisiae - genetics | DNA Replication | Meiosis | Saccharomyces cerevisiae - ultrastructure | Saccharomyces cerevisiae Proteins - genetics | Chromatids - metabolism | Saccharomyces cerevisiae - metabolism | Kinetochores - ultrastructure | Microtubules - metabolism | Microtubules - ultrastructure | Saccharomyces cerevisiae Proteins - metabolism | Chromatids - ultrastructure | Cluster analysis | Phosphorylation | Chromatin | Sister chromatids | Laboratories | Kinetochores | Prophase | Cell division | DNA biosynthesis | Proteins | S phase | Microtubules | Chromatids | Cohesin | Chromosomes | Deoxyribonucleic acid--DNA | Index Medicus
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