Sort by
Items per page

Send to

Choose Destination

Search results

Items: 25


Characterizing Atypical BCL6 Signal Patterns Detected by Digital Fluorescence In Situ Hybridization (FISH) Analysis.

Liew M, Rowe LR, Szankasi P, Paxton CN, Kelley T, Toydemir RM, Salama ME.

Ann Lab Med. 2018 Nov;38(6):619-622. doi: 10.3343/alm.2018.38.6.619. No abstract available.


Genomic Analyses Identify Recurrent Alterations in Immune Evasion Genes in Diffuse Large B-Cell Lymphoma, Leg Type.

Zhou XA, Louissaint A Jr, Wenzel A, Yang J, Martinez-Escala ME, Moy AP, Morgan EA, Paxton CN, Hong B, Andersen EF, Guitart J, Behdad A, Cerroni L, Weinstock DM, Choi J.

J Invest Dermatol. 2018 Nov;138(11):2365-2376. doi: 10.1016/j.jid.2018.04.038. Epub 2018 May 30.


Detection of genome-wide copy number variants in myeloid malignancies using next-generation sequencing.

Shen W, Paxton CN, Szankasi P, Longhurst M, Schumacher JA, Frizzell KA, Sorrells SM, Clayton AL, Jattani RP, Patel JL, Toydemir R, Kelley TW, Xu X.

J Clin Pathol. 2018 Apr;71(4):372-378. doi: 10.1136/jclinpath-2017-204823. Epub 2017 Dec 2.


Genetic evaluation of juvenile xanthogranuloma: genomic abnormalities are uncommon in solitary lesions, advanced cases may show more complexity.

Paxton CN, O'Malley DP, Bellizzi AM, Alkapalan D, Fedoriw Y, Hornick JL, Perkins SL, South ST, Andersen EF.

Mod Pathol. 2017 Sep;30(9):1234-1240. doi: 10.1038/modpathol.2017.50. Epub 2017 Jul 28.


Genomic analysis of follicular dendritic cell sarcoma by molecular inversion probe array reveals tumor suppressor-driven biology.

Andersen EF, Paxton CN, O'Malley DP, Louissaint A Jr, Hornick JL, Griffin GK, Fedoriw Y, Kim YS, Weiss LM, Perkins SL, South ST.

Mod Pathol. 2017 Sep;30(9):1321-1334. doi: 10.1038/modpathol.2017.34. Epub 2017 Jun 16.


Genomic analysis of adult B-ALL identifies potential markers of shorter survival.

Patel S, Mason CC, Glenn MJ, Paxton CN, South ST, Cessna MH, Asch J, Cobain EF, Bixby DL, Smith LB, Reshmi S, Gastier-Foster JM, Schiffman JD, Miles RR.

Leuk Res. 2017 May;56:44-51. doi: 10.1016/j.leukres.2017.01.034. Epub 2017 Feb 3.


C/EBPβ-1 promotes transformation and chemoresistance in Ewing sarcoma cells.

Gardiner JD, Abegglen LM, Huang X, Carter BE, Schackmann EA, Stucki M, Paxton CN, Lor Randall R, Amatruda JF, Putnam AR, Kovar H, Lessnick SL, Schiffman JD.

Oncotarget. 2017 Apr 18;8(16):26013-26026. doi: 10.18632/oncotarget.14847.


Acute Leukemia and Concurrent Mediastinal Germ Cell Tumor: Case Report and Literature Review.

Maese L, Li KD, Xu X, Afify Z, Paxton CN, Putnam A.

Fetal Pediatr Pathol. 2017 Apr;36(2):168-176. doi: 10.1080/15513815.2016.1273983. Epub 2017 Jan 19. Review.


Genomic Copy Number Analysis of HER2-Equivocal Breast Cancers.

Geiersbach KB, Willmore-Payne C, Pasi AV, Paxton CN, Werner TL, Xu X, Wittwer CT, Gulbahce HE, Downs-Kelly E.

Am J Clin Pathol. 2016 Oct;146(4):439-47. doi: 10.1093/ajcp/aqw130. Epub 2016 Sep 10.


Pediatric-type nodal follicular lymphoma: a biologically distinct lymphoma with frequent MAPK pathway mutations.

Louissaint A Jr, Schafernak KT, Geyer JT, Kovach AE, Ghandi M, Gratzinger D, Roth CG, Paxton CN, Kim S, Namgyal C, Morin R, Morgan EA, Neuberg DS, South ST, Harris MH, Hasserjian RP, Hochberg EP, Garraway LA, Harris NL, Weinstock DM.

Blood. 2016 Aug 25;128(8):1093-100. doi: 10.1182/blood-2015-12-682591. Epub 2016 Jun 20.


Two Unrelated Burkitt Lymphomas Seven Years Apart in a Patient With X-Linked Lymphoproliferative Disease Type 1 (XLP1).

Zhou D, Paxton CN, Kelley TW, Afify Z, South ST, Miles RR.

Am J Clin Pathol. 2016 Aug;146(2):248-53. doi: 10.1093/ajcp/aqw036. Epub 2016 Jun 10.


Low miR-187 expression promotes resistance to chemoradiation therapy in vitro and correlates with treatment failure in patients with esophageal adenocarcinoma.

Lynam-Lennon N, Bibby BA, Mongan AM, Marignol L, Paxton CN, Geiersbach K, Bronner MP, O'Sullivan J, Reynolds J, Maher SG.

Mol Med. 2016 May 23;22. doi: 10.2119/molmed.2016.00020.


Pediatric B-Cell Lymphoma With Lymphoblastic Morphology, TdT Expression, MYC Rearrangement, and Features Overlapping With Burkitt Lymphoma.

Meznarich J, Miles R, Paxton CN, Afify Z.

Pediatr Blood Cancer. 2016 May;63(5):938-40. doi: 10.1002/pbc.25907. Epub 2016 Jan 19.


Observations of the genomic landscape beyond 1p19q deletions and EGFR amplification in glioma.

Paxton CN, Rowe LR, South ST.

Mol Cytogenet. 2015 Aug 7;8:60. doi: 10.1186/s13039-015-0156-1. eCollection 2015.


Streamlining the OncoScan® Array Procedure for Use in a Clinical Laboratory.

Paxton CN, Rowe LR, South ST.

J Assoc Genet Technol. 2015;41(2):61-5.


Copy number assessment by competitive PCR with limiting deoxynucleotide triphosphates and high-resolution melting.

Zhou L, Palais RA, Paxton CN, Geiersbach KB, Wittwer CT.

Clin Chem. 2015 May;61(5):724-33. doi: 10.1373/clinchem.2014.236208. Epub 2015 Mar 10.


Differentiation of genetic abnormalities in early pregnancy loss.

Romero ST, Geiersbach KB, Paxton CN, Rose NC, Schisterman EF, Branch DW, Silver RM.

Ultrasound Obstet Gynecol. 2015 Jan;45(1):89-94. doi: 10.1002/uog.14713.


Neural tube defects and atypical deletion on 22q11.2.

Leoni C, Stevenson DA, Geiersbach KB, Paxton CN, Krock BL, Mao R, Rope AF.

Am J Med Genet A. 2014 Nov;164A(11):2701-6. doi: 10.1002/ajmg.a.36701. Epub 2014 Aug 13.


Two cases of Scimitar syndrome associated with multiple congenital skeletal anomalies and lacking abnormalities by genomic microarray analysis.

Lloyd IE, Rowe LR, Erickson LK, Paxton CN, South ST, Alashari M.

Pediatr Dev Pathol. 2014 Sep-Oct;17(5):360-5. doi: 10.2350/14-04-1474-CR.1. Epub 2014 Jun 19.


Diagnostic utility of microsatellite genotyping for molar pregnancy testing.

Furtado LV, Paxton CN, Jama MA, Tripp SR, Wilson AR, Lyon E, Jarboe EA, Thaker HM, Geiersbach KB.

Arch Pathol Lab Med. 2013 Jan;137(1):55-63. doi: 10.5858/arpa.2012-0047-OA.


Rapid aneusomy detection in products of conception using the KaryoLite™ BACs-on-Beads™ assay.

Paxton CN, Brothman AR, Geiersbach KB.

Prenat Diagn. 2013 Jan;33(1):25-31. doi: 10.1002/pd.4003. Epub 2012 Nov 8.


Aneuploidy detection in paraffin embedded tissue from products of conception by mini-STR genotyping.

Furtado LV, Jama MA, Paxton CN, Wilson AA, Gardiner AE, Lyon E, Geiersbach KB.

Fetal Pediatr Pathol. 2013 Apr;32(2):133-50. doi: 10.3109/15513815.2012.681428. Epub 2012 May 18.


FOXL2 mutation and large-scale genomic imbalances in adult granulosa cell tumors of the ovary.

Geiersbach KB, Jarboe EA, Jahromi MS, Baker CL, Paxton CN, Tripp SR, Schiffman JD.

Cancer Genet. 2011 Nov;204(11):596-602. doi: 10.1016/j.cancergen.2011.10.002.


FGF signaling regulates otic placode induction and refinement by controlling both ectodermal target genes and hindbrain Wnt8a.

Urness LD, Paxton CN, Wang X, Schoenwolf GC, Mansour SL.

Dev Biol. 2010 Apr 15;340(2):595-604. doi: 10.1016/j.ydbio.2010.02.016. Epub 2010 Feb 18.


Identification of differentially expressed genes in early inner ear development.

Paxton CN, Bleyl SB, Chapman SC, Schoenwolf GC.

Gene Expr Patterns. 2010 Jan;10(1):31-43. doi: 10.1016/j.gep.2009.11.002. Epub 2009 Nov 11.

Supplemental Content

Loading ...
Support Center