Year |
Citation |
Score |
2013 |
Earnshaw WC, Allshire RC, Black BE, Bloom K, Brinkley BR, Brown W, Cheeseman IM, Choo KH, Copenhaver GP, Deluca JG, Desai A, Diekmann S, Erhardt S, Fitzgerald-Hayes M, Foltz D, et al. Esperanto for histones: CENP-A, not CenH3, is the centromeric histone H3 variant. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 21: 101-6. PMID 23580138 DOI: 10.1007/S10577-013-9347-Y |
0.371 |
|
2007 |
Stoler S, Rogers K, Weitze S, Morey L, Fitzgerald-Hayes M, Baker RE. Scm3, an essential Saccharomyces cerevisiae centromere protein required for G2/M progression and Cse4 localization. Proceedings of the National Academy of Sciences of the United States of America. 104: 10571-6. PMID 17548816 DOI: 10.1073/Pnas.0703178104 |
0.56 |
|
2004 |
Morey L, Barnes K, Chen Y, Fitzgerald-Hayes M, Baker RE. The histone fold domain of Cse4 is sufficient for CEN targeting and propagation of active centromeres in budding yeast Eukaryotic Cell. 3: 1533-1543. PMID 15590827 DOI: 10.1128/Ec.3.6.1533-1543.2004 |
0.62 |
|
2000 |
Keith KC, Fitzgerald-Hayes M. CSE4 genetically interacts with the Saccharomyces cerevisiae centromere DNA elements CDE I and CDE II but not CDE III: Implications for the path of the centromere DNA around a Cse4p variant nucleosome Genetics. 156: 973-981. PMID 11063678 |
0.501 |
|
2000 |
Chen Y, Baker RE, Keith KC, Harris K, Stoler S, Fitzgerald-Hayes M. The N terminus of the centromere H3-like protein Cse4p performs an essential function distinct from that of the histone fold domain Molecular and Cellular Biology. 20: 7037-7048. PMID 10958698 DOI: 10.1128/Mcb.20.18.7037-7048.2000 |
0.603 |
|
1999 |
Keith KC, Baker RE, Chen Y, Harris K, Stoler S, Fitzgerald-Hayes M. Analysis of primary structural determinants that distinguish the centromere-specific function of histone variant Cse4p from histone H3 Molecular and Cellular Biology. 19: 6130-6139. PMID 10454560 DOI: 10.1128/Mcb.19.9.6130 |
0.605 |
|
1999 |
Schroeder AJ, Chen XH, Xiao Z, Fitzgerald-Hayes M. Genetic evidence for interactions between yeast importin α (Srp1p) and its nuclear export receptor, Cse1p Molecular and General Genetics. 261: 788-795. PMID 10394916 |
0.36 |
|
1995 |
Xiao ZX, Fitzgerald-Hayes M. Functional interaction between the CSE2 gene product and centromeres in Saccharomyces cerevisiae Journal of Molecular Biology. 248: 255-263. PMID 7739039 DOI: 10.1016/S0022-2836(95)80048-4 |
0.521 |
|
1995 |
Stoler S, Keith KC, Curnick KE, Fitzgerald-Hayes M. A mutation in CSE4, an essential gene encoding a novel chromatin-associated protein in yeast, causes chromosome nondisjunction and cell cycle arrest at mitosis Genes and Development. 9: 573-586. PMID 7698647 DOI: 10.1101/Gad.9.5.573 |
0.661 |
|
1994 |
Chen XH, Xiao Z, Fitzgerald-Hayes M. SCM2, a tryptophan permease in Saccharomyces cerevisiae, is important for cell growth Mgg Molecular &Amp; General Genetics. 244: 260-268. PMID 8058037 DOI: 10.1007/Bf00285453 |
0.471 |
|
1993 |
Payne WE, Fitzgerald-Hayes M. A mutation in PLC1, a candidate phosphoinositide-specific phospholipase C gene from Saccharomyces cerevisiae, causes aberrant mitotic chromosome segregation Molecular and Cellular Biology. 13: 4351-4364. PMID 8391635 DOI: 10.1128/Mcb.13.7.4351 |
0.529 |
|
1993 |
Xiao Z, Mcgrew JT, Schroeder AJ, Fitzgerald-Hayes M. CSE1 and CSE2, Two New Genes Required for Accurate Mitotic Chromosome Segregation in Saccharomyces cerevisiae Molecular and Cellular Biology. 13: 4691-4702. PMID 8336709 DOI: 10.1128/Mcb.13.8.4691 |
0.51 |
|
1991 |
Densmore L, Payne WE, Fitzgerald-Hayes M. In vivo genomic footprint of a yeast centromere. Molecular and Cellular Biology. 11: 154-65. PMID 1986217 DOI: 10.1128/Mcb.11.1.154 |
0.522 |
|
1991 |
Murphy MR, Fowlkes DM, Fitzgerald-Hayes M. Analysis of centromere function in Saccharomyces cerevisiae using synthetic centromere mutants Chromosoma. 101: 189-197. PMID 1790732 DOI: 10.1007/Bf00355368 |
0.528 |
|
1990 |
Murphy M, Fitzgerald-Hayes M. Cis- and trans-acting factors involved in centromere function in Saccharomyces cerevisiae. Molecular Microbiology. 4: 329-36. PMID 2192227 DOI: 10.1111/J.1365-2958.1990.Tb00600.X |
0.385 |
|
1989 |
McGrew JT, Xiao ZX, Fitzgerald-Hayes M. Saccharomyces cerevisiae mutants defective in chromosome segregation Yeast (Chichester, England). 5: 271-284. PMID 2675488 DOI: 10.1002/Yea.320050407 |
0.528 |
|
1989 |
Gaudet A, Fitzgerald-Hayes M. Mutations in CEN3 cause aberrant chromosome segregation during meiosis in Saccharomyces cerevisiae Genetics. 121: 477-489. PMID 2653962 |
0.427 |
|
1988 |
Saunders M, Fitzgerald-Hayes M, Bloom K. Chromatin structure of altered yeast centromeres Proceedings of the National Academy of Sciences of the United States of America. 85: 175-179. PMID 2829168 DOI: 10.1073/Pnas.85.1.175 |
0.4 |
|
1987 |
Gaudet A, Fitzgerald-Hayes M. Alterations in the adenine-plus-thymine-rich region of CEN3 affect centromere function in Saccharomyces cerevisiae Molecular and Cellular Biology. 7: 68-75. PMID 3550426 |
0.323 |
|
1987 |
Koshland D, Rutledge L, Fitzgerald-Hayes M, Hartwell LH. A genetic analysis of dicentric minichromosomes in Saccharomyces cerevisiae. Cell. 48: 801-12. PMID 3545498 DOI: 10.1016/0092-8674(87)90077-8 |
0.421 |
|
1987 |
Fitzgerald-Hayes M. Yeast centromeres Yeast (Chichester, England). 3: 187-200. PMID 3332973 |
0.457 |
|
1986 |
McGrew J, Diehl B, Fitzgerald-Hayes M. Single base-pair mutations in centromere element III cause aberrant chromosome segregation in Saccharomyces cerevisiae Molecular and Cellular Biology. 6: 530-538. PMID 3537689 |
0.339 |
|
1982 |
Fitzgerald-Hayes M, Clarke L, Carbon J. Nucleotide sequence comparisons and functional analysis of yeast centromere DNAs Cell. 29: 235-244. PMID 7049398 DOI: 10.1016/0092-8674(82)90108-8 |
0.41 |
|
1982 |
Fitzgerald-Hayes M, Buhler JM, Cooper TG, Carbon J. Isolation and subcloning analysis of functional centromere DNA (CEN11) from Saccharomyces cerevisiae chromosome XI Molecular and Cellular Biology. 2: 82-87. PMID 6287222 DOI: 10.1128/mcb.2.1.82-87.1982 |
0.447 |
|
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