Paxton CN - Search Results

1

Identification of differentially expressed genes in early inner ear development.

Paxton CN, Bleyl SB, Chapman SC, Schoenwolf GC. Paxton CN, et al. Gene Expr Patterns. 2010 Jan;10(1):31-43. doi: 10.1016/j.gep.2009.11.002. Epub 2009 Nov 11. Gene Expr Patterns. 2010. PMID: 19913109 Free PMC article.

2

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. Urness LD, et al. Among authors: paxton cn. Dev Biol. 2010 Apr 15;340(2):595-604. doi: 10.1016/j.ydbio.2010.02.016. Epub 2010 Feb 18. Dev Biol. 2010. PMID: 20171206 Free PMC article.

3

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

Paxton CN, Brothman AR, Geiersbach KB. Paxton CN, et al. Prenat Diagn. 2013 Jan;33(1):25-31. doi: 10.1002/pd.4003. Epub 2012 Nov 8. Prenat Diagn. 2013. PMID: 23138848

4

Differentiation of genetic abnormalities in early pregnancy loss.

Romero ST, Geiersbach KB, Paxton CN, Rose NC, Schisterman EF, Branch DW, Silver RM. Romero ST, et al. Among authors: paxton cn. Ultrasound Obstet Gynecol. 2015 Jan;45(1):89-94. doi: 10.1002/uog.14713. Ultrasound Obstet Gynecol. 2015. PMID: 25358469 Free PMC article.

5

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. Liew M, et al. Among authors: paxton cn. Ann Lab Med. 2018 Nov;38(6):619-622. doi: 10.3343/alm.2018.38.6.619. Ann Lab Med. 2018. PMID: 30027711 Free PMC article. No abstract available.

6

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

Paxton CN, Rowe LR, South ST. Paxton CN, et al. Mol Cytogenet. 2015 Aug 7;8:60. doi: 10.1186/s13039-015-0156-1. eCollection 2015. Mol Cytogenet. 2015. PMID: 26257825 Free PMC article.

7

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. Furtado LV, et al. Among authors: paxton cn. Arch Pathol Lab Med. 2013 Jan;137(1):55-63. doi: 10.5858/arpa.2012-0047-OA. Arch Pathol Lab Med. 2013. PMID: 23276175 Free article.

8

Zhou D, Paxton CN, Kelley TW, Afify Z, South ST, Miles RR. Zhou D, et al. Among authors: paxton cn. Am J Clin Pathol. 2016 Aug;146(2):248-53. doi: 10.1093/ajcp/aqw036. Epub 2016 Jun 10. Am J Clin Pathol. 2016. PMID: 27287777

9

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. Lloyd IE, et al. Among authors: paxton cn. Pediatr Dev Pathol. 2014 Sep-Oct;17(5):360-5. doi: 10.2350/14-04-1474-CR.1. Epub 2014 Jun 19. Pediatr Dev Pathol. 2014. PMID: 24945981

10

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. Geiersbach KB, et al. Among authors: paxton cn. Cancer Genet. 2011 Nov;204(11):596-602. doi: 10.1016/j.cancergen.2011.10.002. Cancer Genet. 2011. PMID: 22200085

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