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Differentiation of leukemic blasts is not completely blocked in acute myeloid leukemia.

Agarwal A, Bolosky WJ, Wilson DB, Eide CA, Olson SB, Fan G, Druker BJ.

Proc Natl Acad Sci U S A. 2019 Dec 3;116(49):24593-24599. doi: 10.1073/pnas.1904091116. Epub 2019 Nov 21.


ADDENDUM: Section E9 of the American College of Medical Genetics Technical Standards and Guidelines: Fluorescence in situ hybridization.

Mascarello JT, Hirsch B, Kearney HM, Ketterling RP, Olson SB, Quigley DI, Rao KW, Tepperberg JH, Tsuchiya KD, Wiktor AE; A Working Group of the American College of Medical Genetics (ACMG) Laboratory Quality Assurance Committee.

Genet Med. 2019 Oct;21(10):2405. doi: 10.1038/s41436-019-0508-z. No abstract available.


Early Treatment at a Referral Center Improves Outcomes for Patients with Acute Vascular Disease.

Harris DG, Olson SB, Rosen CB, Kalsi R, Taylor BS, Diaz JJ, Flohr TR, Crawford RS.

Ann Vasc Surg. 2018 Jul;50:52-59. doi: 10.1016/j.avsg.2018.01.088. Epub 2018 Mar 5.


Androgen receptor amplification is concordant between circulating tumor cells and biopsies from men undergoing treatment for metastatic castration resistant prostate cancer.

Podolak J, Eilers K, Newby T, Slottke R, Tucker E, Olson SB, Lue HW, Youngren J, Aggarwal R, Small EJ, Graff JN, Alumkal JJ, Beer TM, Thomas GV.

Oncotarget. 2017 Mar 13;8(42):71447-71455. doi: 10.18632/oncotarget.16169. eCollection 2017 Sep 22.


MYC immunohistochemical and cytogenetic analysis are required for identification of clinically relevant aggressive B cell lymphoma subtypes.

Raess PW, Moore SR, Cascio MJ, Dunlap J, Fan G, Gatter K, Olson SB, Braziel RM.

Leuk Lymphoma. 2018 Jun;59(6):1391-1398. doi: 10.1080/10428194.2017.1370547. Epub 2017 Sep 3.


A New Rhesus Macaque Karyotype Based on Human-rhesus Synteny.

Owen NM, Lawce HJ, Olson SB.

J Assoc Genet Technol. 2016;42(4):178-179.


Sponge Sampling with Fluorescent In Situ Hybridization as a Screening Tool for the Early Detection of Esophageal Cancer.

Haisley KR, Dolan JP, Olson SB, Toledo-Valdovinos SA, Hart KD, Bakis G, Enestvedt BK, Hunter JG.

J Gastrointest Surg. 2017 Feb;21(2):215-221. doi: 10.1007/s11605-016-3239-3. Epub 2016 Aug 25.


Cytokine overproduction and crosslinker hypersensitivity are unlinked in Fanconi anemia macrophages.

Garbati MR, Hays LE, Rathbun RK, Jillette N, Chin K, Al-Dhalimy M, Agarwal A, Newell AE, Olson SB, Bagby GC Jr.

J Leukoc Biol. 2016 Mar;99(3):455-65. doi: 10.1189/jlb.3A0515-201R. Epub 2015 Oct 2.


The New Equivocal: Changes to HER2 FISH Results When Applying the 2013 ASCO/CAP Guidelines.

Long TH, Lawce H, Durum C, Moore SR, Olson SB, Gatter K, Troxell ML.

Am J Clin Pathol. 2015 Aug;144(2):253-62. doi: 10.1309/AJCP3Q9WFOQTKUVV.


Bloom syndrome radials are predominantly non-homologous and are suppressed by phosphorylated BLM.

Owen N, Hejna J, Rennie S, Mitchell A, Newell AH, Ziaie N, Moses RE, Olson SB.

Cytogenet Genome Res. 2014;144(4):255-263. doi: 10.1159/000375247. Epub 2015 Feb 28.


Acquisition of Relative Interstrand Crosslinker Resistance and PARP Inhibitor Sensitivity in Fanconi Anemia Head and Neck Cancers.

Lombardi AJ, Hoskins EE, Foglesong GD, Wikenheiser-Brokamp KA, Wiesm├╝ller L, Hanenberg H, Andreassen PR, Jacobs AJ, Olson SB, Keeble WW, Hays LE, Wells SI.

Clin Cancer Res. 2015 Apr 15;21(8):1962-72. doi: 10.1158/1078-0432.CCR-14-2616. Epub 2015 Jan 21.


Comparison of chromosome breakage in non-mosaic and mosaic patients with Fanconi anemia, relatives, and patients with other inherited bone marrow failure syndromes.

Fargo JH, Rochowski A, Giri N, Savage SA, Olson SB, Alter BP.

Cytogenet Genome Res. 2014;144(1):15-27. doi: 10.1159/000366251. Epub 2014 Sep 11.


Aberrations of MYC are a common event in B-cell prolymphocytic leukemia.

Flatley E, Chen AI, Zhao X, Jaffe ES, Dunlap JB, Pittaluga S, Abdullah S, Olson SB, Spurgeon SE, Fan G.

Am J Clin Pathol. 2014 Sep;142(3):347-54. doi: 10.1309/AJCPUBHM8U7ZFLOB.


Mosaic variegated aneuploidy in mouse BubR1 deficient embryos and pregnancy loss in human.

Schmid M, Steinlein C, Tian Q, Hanlon Newell AE, Gessler M, Olson SB, Rosenwald A, Kneitz B, Fedorov LM.

Chromosome Res. 2014 Sep;22(3):375-92. doi: 10.1007/s10577-014-9432-x. Epub 2014 Jul 1. Erratum in: Chromosome Res. 2014 Dec;22(4):645-6.


MDM2 Amplification and PI3KCA Mutation in a Case of Sclerosing Rhabdomyosarcoma.

Kikuchi K, Wettach GR, Ryan CW, Hung A, Hooper JE, Beadling C, Warrick A, Corless CL, Olson SB, Keller C, Mansoor A.

Sarcoma. 2013;2013:520858. doi: 10.1155/2013/520858. Epub 2013 May 20.


In vivo selection of transplanted hepatocytes by pharmacological inhibition of fumarylacetoacetate hydrolase in wild-type mice.

Paulk NK, Wursthorn K, Haft A, Pelz C, Clarke G, Newell AH, Olson SB, Harding CO, Finegold MJ, Bateman RL, Witte JF, McClard R, Grompe M.

Mol Ther. 2012 Oct;20(10):1981-7. doi: 10.1038/mt.2012.154. Epub 2012 Aug 7.


Aneuploidy as a mechanism for stress-induced liver adaptation.

Duncan AW, Hanlon Newell AE, Bi W, Finegold MJ, Olson SB, Beaudet AL, Grompe M.

J Clin Invest. 2012 Sep;122(9):3307-15. doi: 10.1172/JCI64026. Epub 2012 Aug 6.


FANCL ubiquitinates ╬▓-catenin and enhances its nuclear function.

Dao KH, Rotelli MD, Petersen CL, Kaech S, Nelson WD, Yates JE, Hanlon Newell AE, Olson SB, Druker BJ, Bagby GC.

Blood. 2012 Jul 12;120(2):323-34. doi: 10.1182/blood-2011-11-388355. Epub 2012 May 31.


Patients with Fanconi anemia and AML have different cytogenetic clones than de novo cases of AML.

Rochowski A, Olson SB, Alonzo TA, Gerbing RB, Lange BJ, Alter BP.

Pediatr Blood Cancer. 2012 Nov;59(5):922-4. doi: 10.1002/pbc.24168. Epub 2012 Apr 19. Review.


Formaldehyde-induced genome instability is suppressed by an XPF-dependent pathway.

Kumari A, Lim YX, Newell AH, Olson SB, McCullough AK.

DNA Repair (Amst). 2012 Mar 1;11(3):236-46. doi: 10.1016/j.dnarep.2011.11.001. Epub 2011 Dec 18.


Frequent aneuploidy among normal human hepatocytes.

Duncan AW, Hanlon Newell AE, Smith L, Wilson EM, Olson SB, Thayer MJ, Strom SC, Grompe M.

Gastroenterology. 2012 Jan;142(1):25-8. doi: 10.1053/j.gastro.2011.10.029. Epub 2011 Nov 2.


Section E9 of the American College of Medical Genetics technical standards and guidelines: fluorescence in situ hybridization.

Mascarello JT, Hirsch B, Kearney HM, Ketterling RP, Olson SB, Quigley DI, Rao KW, Tepperberg JH, Tsuchiya KD, Wiktor AE; Working Group of the American College of Medical Genetics Laboratory Quality Assurance Committee.

Genet Med. 2011 Jul;13(7):667-75. doi: 10.1097/GIM.0b013e3182227295.


Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene.

Click ES, Cox B, Olson SB, Grompe M, Akkari Y, Moreau LA, Shimamura A, Sternen DL, Liu YJ, Leppig KA, Matthews DC, Parisi MA.

Am J Med Genet A. 2011 Jul;155A(7):1673-9. doi: 10.1002/ajmg.a.34024. Epub 2011 May 27.


Complex cytogenetic analysis of early lethality mouse embryos.

Tian Q, Hanlon Newell AE, Wang Y, Olson SB, Fedorov LM.

Chromosome Res. 2011 May;19(4):567-74. doi: 10.1007/s10577-011-9209-4. Epub 2011 Apr 20.


The ploidy conveyor of mature hepatocytes as a source of genetic variation.

Duncan AW, Taylor MH, Hickey RD, Hanlon Newell AE, Lenzi ML, Olson SB, Finegold MJ, Grompe M.

Nature. 2010 Oct 7;467(7316):707-10. doi: 10.1038/nature09414. Epub 2010 Sep 22.


Human FANCC is hypomorphic in murine Fancc-deficient cells.

Hays LE, Keeble WW, Yates JE, Rathbun RK, Koretsky T, Olson SB, Sun Z, Clapp DW, Bagby GC Jr.

Blood. 2010 Sep 23;116(12):2057-60. doi: 10.1182/blood-2010-02-266411. Epub 2010 Jun 16.


Embryonic lethality after combined inactivation of Fancd2 and Mlh1 in mice.

van de Vrugt HJ, Eaton L, Hanlon Newell A, Al-Dhalimy M, Liskay RM, Olson SB, Grompe M.

Cancer Res. 2009 Dec 15;69(24):9431-8. doi: 10.1158/0008-5472.CAN-09-2452.


Wilms tumor, AML, and medulloblastoma in a child with cancer prone syndrome of total premature chromatid separation and Fanconi anemia.

Alter BP, Olson SB.

Pediatr Blood Cancer. 2010 Mar;54(3):488; author reply 489. doi: 10.1002/pbc.22333. No abstract available.


Characterizing the HER2/neu status and metastatic potential of breast cancer stem/progenitor cells.

Pommier SJ, Quan GG, Christante D, Muller P, Newell AE, Olson SB, Diggs B, Muldoon L, Neuwelt E, Pommier RF.

Ann Surg Oncol. 2010 Feb;17(2):613-23. doi: 10.1245/s10434-009-0730-z. Epub 2009 Oct 17.


Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agents.

Hemphill AW, Akkari Y, Newell AH, Schultz RA, Grompe M, North PS, Hickson ID, Jakobs PM, Rennie S, Pauw D, Hejna J, Olson SB, Moses RE.

Cytogenet Genome Res. 2009;125(3):165-75. doi: 10.1159/000230001. Epub 2009 Sep 4.


DNA interstrand crosslink repair in mammalian cells.

McCabe KM, Olson SB, Moses RE.

J Cell Physiol. 2009 Sep;220(3):569-73. doi: 10.1002/jcp.21811. Review.


Validation of Fanconi anemia complementation Group A assignment using molecular analysis.

Moghrabi NN, Johnson MA, Yoshitomi MJ, Zhu X, Al-Dhalimy MJ, Olson SB, Grompe M, Richards CS.

Genet Med. 2009 Mar;11(3):183-92. doi: 10.1097/GIM.0b013e318193ba67.


Ploidy reductions in murine fusion-derived hepatocytes.

Duncan AW, Hickey RD, Paulk NK, Culberson AJ, Olson SB, Finegold MJ, Grompe M.

PLoS Genet. 2009 Feb;5(2):e1000385. doi: 10.1371/journal.pgen.1000385. Epub 2009 Feb 20.


Loss of homologous recombination or non-homologous end-joining leads to radial formation following DNA interstrand crosslink damage.

Hanlon Newell AE, Hemphill A, Akkari YM, Hejna J, Moses RE, Olson SB.

Cytogenet Genome Res. 2008;121(3-4):174-80. doi: 10.1159/000138882. Epub 2008 Aug 28.


ERCC1 is required for FANCD2 focus formation.

McCabe KM, Hemphill A, Akkari Y, Jakobs PM, Pauw D, Olson SB, Moses RE, Grompe M.

Mol Genet Metab. 2008 Sep-Oct;95(1-2):66-73. doi: 10.1016/j.ymgme.2008.06.009. Epub 2008 Jul 30.


Cigarette smoke induces genetic instability in airway epithelial cells by suppressing FANCD2 expression.

Hays LE, Zodrow DM, Yates JE, Deffebach ME, Jacoby DB, Olson SB, Pankow JF, Bagby GC.

Br J Cancer. 2008 May 20;98(10):1653-61. doi: 10.1038/sj.bjc.6604362. Epub 2008 May 13.


Role for DNA polymerase kappa in the processing of N2-N2-guanine interstrand cross-links.

Minko IG, Harbut MB, Kozekov ID, Kozekova A, Jakobs PM, Olson SB, Moses RE, Harris TM, Rizzo CJ, Lloyd RS.

J Biol Chem. 2008 Jun 20;283(25):17075-82. doi: 10.1074/jbc.M801238200. Epub 2008 Apr 22.


Tip60 is required for DNA interstrand cross-link repair in the Fanconi anemia pathway.

Hejna J, Holtorf M, Hines J, Mathewson L, Hemphill A, Al-Dhalimy M, Olson SB, Moses RE.

J Biol Chem. 2008 Apr 11;283(15):9844-51. doi: 10.1074/jbc.M709076200. Epub 2008 Feb 8.


Mammalian SNM1 is required for genome stability.

Hemphill AW, Bruun D, Thrun L, Akkari Y, Torimaru Y, Hejna K, Jakobs PM, Hejna J, Jones S, Olson SB, Moses RE.

Mol Genet Metab. 2008 May;94(1):38-45. doi: 10.1016/j.ymgme.2007.11.012. Epub 2008 Jan 3.


Evaluation of Her-2/neu status in carcinomas with amplified chromosome 17 centromere locus.

Troxell ML, Bangs CD, Lawce HJ, Galperin IB, Baiyee D, West RB, Olson SB, Cherry AM.

Am J Clin Pathol. 2006 Nov;126(5):709-16.


Cytogenetic instability in ovarian epithelial cells from women at risk of ovarian cancer.

Pejovic T, Yates JE, Liu HY, Hays LE, Akkari Y, Torimaru Y, Keeble W, Rathbun RK, Rodgers WH, Bale AE, Ameziane N, Zwaan CM, Errami A, Thuillier P, Cappuccini F, Olson SB, Cain JM, Bagby GC Jr.

Cancer Res. 2006 Sep 15;66(18):9017-25.


CRELD2: gene mapping, alternate splicing, and comparative genomic identification of the promoter region.

Maslen CL, Babcock D, Redig JK, Kapeli K, Akkari YM, Olson SB.

Gene. 2006 Nov 1;382:111-20. Epub 2006 Jul 7.


The role for preimplantation genetic diagnosis in balanced translocation carriers.

Sampson JE, Ouhibi N, Lawce H, Patton PE, Battaglia DE, Burry KA, Olson SB.

Am J Obstet Gynecol. 2004 Jun;190(6):1707-11; discussion 1711-3.


Interstrand crosslink-induced radials form between non-homologous chromosomes, but are absent in sex chromosomes.

Newell AE, Akkari YM, Torimaru Y, Rosenthal A, Reifsteck CA, Cox B, Grompe M, Olson SB.

DNA Repair (Amst). 2004 May 4;3(5):535-42.


Transplanted adult hematopoietic stems cells differentiate into functional endothelial cells.

Bailey AS, Jiang S, Afentoulis M, Baumann CI, Schroeder DA, Olson SB, Wong MH, Fleming WH.

Blood. 2004 Jan 1;103(1):13-9. Epub 2003 Sep 4.


Cisplatin and the sensitive cell.

Bagby GC, Olson SB.

Nat Med. 2003 May;9(5):513-4. No abstract available.


Demonstration of Philadelphia chromosome negative abnormal clones in patients with chronic myelogenous leukemia during major cytogenetic responses induced by imatinib mesylate.

O'Dwyer ME, Gatter KM, Loriaux M, Druker BJ, Olson SB, Magenis RE, Lawce H, Mauro MJ, Maziarz RT, Braziel RM.

Leukemia. 2003 Mar;17(3):481-7.


Acquired FANCA dysfunction and cytogenetic instability in adult acute myelogenous leukemia.

Lensch MW, Tischkowitz M, Christianson TA, Reifsteck CA, Speckhart SA, Jakobs PM, O'Dwyer ME, Olson SB, Le Beau MM, Hodgson SV, Mathew CG, Larson RA, Bagby GC Jr.

Blood. 2003 Jul 1;102(1):7-16. Epub 2003 Mar 13.


Identification, genomic organization and mRNA expression of CRELD1, the founding member of a unique family of matricellular proteins.

Rupp PA, Fouad GT, Egelston CA, Reifsteck CA, Olson SB, Knosp WM, Glanville RW, Thornburg KL, Robinson SW, Maslen CL.

Gene. 2002 Jun 26;293(1-2):47-57.


Hematopathologic and cytogenetic findings in imatinib mesylate-treated chronic myelogenous leukemia patients: 14 months' experience.

Braziel RM, Launder TM, Druker BJ, Olson SB, Magenis RE, Mauro MJ, Sawyers CL, Paquette RL, O'Dwyer ME.

Blood. 2002 Jul 15;100(2):435-41.


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