Year |
Citation |
Score |
2023 |
Le H, Jin E, Jewell A, Jackson-Cook C, Haskell GT, Couser N. Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features. American Journal of Medical Genetics. Part A. PMID 36941760 DOI: 10.1002/ajmg.a.63186 |
0.363 |
|
2022 |
Gillam J, Catic A, Paulraj P, Dalton J, Lai G, Jackson-Cook C, Turner S, Ferreira-Gonzalez A, Barrie E. Acute megakaryoblastic leukemia with trisomy 3 and CBFA2T3::GLIS2: A case report. Genes, Chromosomes & Cancer. PMID 35294081 DOI: 10.1002/gcc.23039 |
0.339 |
|
2021 |
Rafferty K, Archer KJ, Turner K, Brown R, Jackson-Cook C. Trisomy 21-associated increases in chromosomal instability are unmasked by comparing isogenic trisomic/disomic leukocytes from people with mosaic Down syndrome. Plos One. 16: e0254806. PMID 34283872 DOI: 10.1371/journal.pone.0254806 |
0.413 |
|
2020 |
Gheghiani L, Wang L, Zhang Y, Moore XTR, Zhang J, Smith SC, Tian Y, Wang L, Turner K, Jackson-Cook CK, Mukhopadhyay ND, Fu Z. PLK1 induces chromosomal instability and overrides cell cycle checkpoints to drive tumorigenesis. Cancer Research. PMID 33376114 DOI: 10.1158/0008-5472.CAN-20-1377 |
0.341 |
|
2019 |
Jackson-Cook C. A hypothesis: Could telomere length and/or epigenetic alterations contribute to infertility in females with Turner syndrome? American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 181: 108-116. PMID 30741474 DOI: 10.1002/ajmg.c.31684 |
0.414 |
|
2016 |
Rafferty K, Charalsawadi C, Jackson-Cook C. An Isogenic Trisomic–Disomic Model System Using Cells from People with Mosaic Down Syndrome Unmasks Trisomy 21 Associated Increases in Age-Related Chromosomal Instability, Senescence Associated Distension of Satellites, and Telomere Shortening Cancer Genetics and Cytogenetics. 209: 238. DOI: 10.1016/J.Cancergen.2016.05.029 |
0.76 |
|
2015 |
Aboalela N, Lyon D, Elswick RK, Kelly DL, Brumelle J, Bear HD, Jackson-Cook C. Perceived Stress Levels, Chemotherapy, Radiation Treatment and Tumor Characteristics Are Associated with a Persistent Increased Frequency of Somatic Chromosomal Instability in Women Diagnosed with Breast Cancer: A One Year Longitudinal Study. Plos One. 10: e0133380. PMID 26177092 DOI: 10.1371/Journal.Pone.0133380 |
0.308 |
|
2015 |
Papavassiliou P, Charalsawadi C, Rafferty K, Jackson-Cook C. Mosaicism for trisomy 21: a review. American Journal of Medical Genetics. Part A. 167: 26-39. PMID 25412855 DOI: 10.1002/Ajmg.A.36861 |
0.683 |
|
2013 |
York TP, Brumelle J, Juusola J, Kendler KS, Eaves LJ, Amstadter AB, Aggen SH, Jones KH, Ferreira-Gonzalez A, Jackson-Cook C. Increased frequency of micronuclei in adults with a history of childhood sexual abuse: a discordant monozygotic twin study. Plos One. 8: e55337. PMID 23383158 DOI: 10.1371/journal.pone.0055337 |
0.375 |
|
2013 |
Dragoescu E, Jackson-Cook C, Domson G, Massey D, Foster WC. Small cell osteosarcoma with Ewing sarcoma breakpoint region 1 gene rearrangement detected by interphase fluorescence in situ hybridization. Annals of Diagnostic Pathology. 17: 377-82. PMID 22971270 DOI: 10.1016/J.Anndiagpath.2012.08.004 |
0.351 |
|
2012 |
Jones KH, York TP, Jackson-Cook C. Mechanisms leading to the formation of micronuclei containing sex chromosomes differ with age. Mutation Research. 747: 207-17. PMID 22613870 DOI: 10.1016/j.mrgentox.2012.05.004 |
0.419 |
|
2012 |
Jackson-Cook C. Constitutional and acquired autosomal aneuploidy. Clinics in Laboratory Medicine. 31: 481-511, vii. PMID 22118733 DOI: 10.1016/j.cll.2011.08.002 |
0.405 |
|
2009 |
Papavassiliou P, York TP, Gursoy N, Hill G, Nicely LV, Sundaram U, McClain A, Aggen SH, Eaves L, Riley B, Jackson-Cook C. The phenotype of persons having mosaicism for trisomy 21/Down syndrome reflects the percentage of trisomic cells present in different tissues. American Journal of Medical Genetics. Part A. 149: 573-83. PMID 19291777 DOI: 10.1002/Ajmg.A.32729 |
0.69 |
|
2008 |
Winters J, Markello T, Nance W, Jackson-Cook C. Mosaic "tetrasomy" 8p: case report and review of the literature. Clinical Genetics. 48: 195-198. PMID 8591671 DOI: 10.1111/J.1399-0004.1995.Tb04088.X |
0.483 |
|
2006 |
Compton SA, Elmore LW, Haydu K, Jackson-Cook CK, Holt SE. Induction of nitric oxide synthase-dependent telomere shortening after functional inhibition of Hsp90 in human tumor cells. Molecular and Cellular Biology. 26: 1452-62. PMID 16449656 DOI: 10.1128/Mcb.26.4.1452-1462.2006 |
0.36 |
|
2006 |
Ben-Ezra JM, Jackson-Cook C. Reed-Sternberg Cells Have Shortened Telomere Length. Blood. 108: 4594-4594. DOI: 10.1182/BLOOD.V108.11.4594.4594 |
0.375 |
|
2004 |
Leach NT, Jackson-Cook C. Micronuclei with multiple copies of the X chromosome: Do chromosomes replicate in micronuclei? Mutation Research - Fundamental and Molecular Mechanisms of Mutagenesis. 554: 89-94. PMID 15450407 DOI: 10.1016/J.Mrfmmm.2004.03.004 |
0.758 |
|
2004 |
Leach NT, Rehder C, Jensen K, Holt S, Jackson-Cook C. Human chromosomes with shorter telomeres and large heterochromatin regions have a higher frequency of acquired somatic cell aneuploidy Mechanisms of Ageing and Development. 125: 563-573. PMID 15336914 DOI: 10.1016/J.Mad.2004.06.006 |
0.768 |
|
2004 |
McChesney PA, Turner KC, Jackson-Cook C, Elmore LW, Holt SE. Telomerase resets the homeostatic telomere length and prevents telomere dysfunction in immortalized human cells. Dna and Cell Biology. 23: 293-300. PMID 15199944 DOI: 10.1089/104454904323090921 |
0.439 |
|
2003 |
Liu X, Wu Y, Zehner ZE, Jackson-Cook C, Ware JL. Proteomic analysis of the tumorigenic human prostate cell line M12 after microcell-mediated transfer of chromosome 19 demonstrates reduction of vimentin. Electrophoresis. 24: 3445-53. PMID 14595690 DOI: 10.1002/Elps.200305574 |
0.369 |
|
2003 |
Jackson-Cook C, Zou Y, Turner K, Astbury C, Ware J. A novel tumorigenic human prostate epithelial cell line (M2205): molecular cytogenetic characterization demonstrates C-MYC amplification and jumping translocations. Cancer Genetics and Cytogenetics. 141: 56-64. PMID 12581899 DOI: 10.1016/S0165-4608(02)00665-9 |
0.714 |
|
2002 |
Elmore LW, Turner KC, Gollahon LS, Landon MR, Jackson-Cook CK, Holt SE. Telomerase protects cancer-prone human cells from chromosomal instability and spontaneous immortalization. Cancer Biology & Therapy. 1: 391-7. PMID 12432253 DOI: 10.4161/Cbt.1.4.13 |
0.522 |
|
2002 |
Yu Y, Inamdar KV, Turner K, Jackson-Cook CK, Povirk LF. Base substitutions, targeted single-base deletions, and chromosomal translocations induced by bleomycin in plateau-phase mammary epithelial cells. Radiation Research. 158: 327-38. PMID 12175310 DOI: 10.1667/0033-7587(2002)158[0327:Bstsbd]2.0.Co;2 |
0.307 |
|
2002 |
Elmore LW, Rehder CW, Di X, McChesney PA, Jackson-Cook CK, Gewirtz DA, Holt SE. Adriamycin-induced senescence in breast tumor cells involves functional p53 and telomere dysfunction. The Journal of Biological Chemistry. 277: 35509-15. PMID 12101184 DOI: 10.1074/Jbc.M205477200 |
0.371 |
|
2002 |
Riley RS, Massey D, Jackson-Cook C, Idowu M, Romagnoli G. Immunophenotypic analysis of acute lymphocytic leukemia. Hematology-Oncology Clinics of North America. 16: 245-299. PMID 12094473 DOI: 10.1016/S0889-8588(02)00004-7 |
0.32 |
|
2002 |
Wang P, Lee JW, Yu Y, Turner K, Zou Y, Jackson-Cook CK, Povirk LF. Gene rearrangements induced by the DNA double-strand cleaving agent neocarzinostatin: conservative non-homologous reciprocal exchanges in an otherwise stable genome. Nucleic Acids Research. 30: 2639-46. PMID 12060680 DOI: 10.1093/Nar/Gkf369 |
0.425 |
|
2002 |
Tekin M, Jackson-Cook C, Pandya A. De novo inverted tandem duplication of the short arm of chromosome 12 in a patient with microblepharon. American Journal of Medical Genetics. 104: 42-6. PMID 11746026 DOI: 10.1002/AJMG.10025 |
0.449 |
|
2001 |
Williams MS, Josephson KD, Gursoy N, Jackson-Cook C. Suspected gonadal mosaicism for isochromosomes 18p and 18q unsubstantiated by fluorescence in situ hybridization analysis of sperm Genetics in Medicine. 3: 318-320. PMID 11478534 DOI: 10.1097/00125817-200107000-00010 |
0.722 |
|
2001 |
Leach NT, Jackson-Cook C. The application of spectral karyotyping (SKY) and fluorescent in situ hybridization (FISH) technology to determine the chromosomal content(s) of micronuclei Mutation Research - Genetic Toxicology and Environmental Mutagenesis. 495: 11-19. PMID 11448638 DOI: 10.1016/S1383-5718(01)00194-2 |
0.753 |
|
2001 |
Astbury C, Jackson-Cook CK, Culp SH, Paisley TE, Ware JL. Suppression of tumorigenicity in the human prostate cancer cell line M12 via microcell-mediated restoration of chromosome 19. Genes, Chromosomes & Cancer. 31: 143-55. PMID 11319802 DOI: 10.1002/Gcc.1128 |
0.702 |
|
2001 |
Tekin M, Jackson-Cook C, Buller A, Ferreira-Gonzalez A, Pandya A, Garrett CT, Bodurtha J. Fluorescence in situ hybridization detectable mosaicism for Angelman syndrome with biparental methylation. American Journal of Medical Genetics. 95: 145-9. PMID 11078565 DOI: 10.1002/1096-8628(20001113)95:2<145::Aid-Ajmg10>3.0.Co;2-R |
0.411 |
|
1998 |
Bae VL, Jackson-Cook CK, Maygarden SJ, Plymate SR, Chen J, Ware JL. Metastatic sublines of an SV40 large T antigen immortalized human prostate epithelial cell line Prostate. 34: 275-282. PMID 9496902 DOI: 10.1002/(Sici)1097-0045(19980301)34:4<275::Aid-Pros5>3.0.Co;2-G |
0.425 |
|
1997 |
Wang P, Zhou RH, Zou Y, Jackson-Cook CK, Povirk LF. Highly conservative reciprocal translocations formed by apparent joining of exchanged DNA double-strand break ends Proceedings of the National Academy of Sciences of the United States of America. 94: 12018-12023. PMID 9342355 DOI: 10.1073/Pnas.94.22.12018 |
0.322 |
|
1997 |
Boon C, Markello T, Jackson-Cook C, Pandya A. Partial trisomy 10 mosaicism with cutaneous manifestations: report of a case and review of the literature. Clinical Genetics. 50: 417-21. PMID 9007335 DOI: 10.1111/j.1399-0004.1996.tb02399.x |
0.349 |
|
1996 |
Jackson-Cook C, Bae V, Edelman W, Brothman A, Ware J. Cytogenetic characterization of the human prostate cancer cell line P69SV40T and its novel tumorigenic sublines M2182 and M15 Cancer Genetics and Cytogenetics. 87: 14-23. PMID 8646734 DOI: 10.1016/0165-4608(95)00232-4 |
0.417 |
|
1995 |
Huang B, Meyer JM, Jackson-Cook CK. Heritability and heteromorphic distributions of AluI chromosome banding variants in twins American Journal of Medical Genetics. 57: 429-436. PMID 7677146 DOI: 10.1002/ajmg.1320570313 |
0.452 |
|
1993 |
Shaffer LG, McCaskill C, Haller V, Brown JA, Jackson-Cook CK. Further characterization of 19 cases of rea(21q21q) and delineation as isochromosomes or Robertsonian translocations in Down syndrome American Journal of Medical Genetics. 47: 1218-1222. PMID 7904793 DOI: 10.1002/ajmg.1320470818 |
0.416 |
|
1992 |
Salbert BA, Solomon M, Spence JE, Jackson-Cook C, Brown J, Bodurtha J. Partial trisomy 19p: case report and natural history. Clinical Genetics. 41: 143-6. PMID 1563088 DOI: 10.1111/J.1399-0004.1992.TB03651.X |
0.393 |
|
1992 |
Shaffer LG, Jackson-Cook CK, Stasiowski BA, Spence JE, Brown JA. Parental origin determination in thirty de novo Robertsonian translocations American Journal of Medical Genetics. 43: 957-963. PMID 1357969 DOI: 10.1002/ajmg.1320430611 |
0.461 |
|
1991 |
Shaffer LG, Jackson-Cook CK, Meyer JM, Brown JA, Spence JE. A molecular genetic approach to the identification of isochromosomes of chromosome 21 Human Genetics. 86: 375-382. PMID 1671850 DOI: 10.1007/Bf00201838 |
0.539 |
|
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