Sort by

Send to

Choose Destination

Search results

Items: 16


Single-base LOH can be used as Specific Marker to Classify BRCAx Familial Breast Cancer into More Homogenous Subtypes.

Downs B, Xiao F, Kim YC, Chen PX, Huang D, Fleissner EA, Cowan K, Wang SM.

Breast J. 2017 Jan 24. doi: 10.1111/tbj.12777. [Epub ahead of print] No abstract available.


Tumoral TP53 and/or CDKN2A alterations are not reliable prognostic biomarkers in patients with localized Ewing sarcoma: a report from the Children's Oncology Group.

Lerman DM, Monument MJ, McIlvaine E, Liu XQ, Huang D, Monovich L, Beeler N, Gorlick RG, Marina NM, Womer RB, Bridge JA, Krailo MD, Randall RL, Lessnick SL; Children's Oncology Group Ewing Sarcoma Biology Committee..

Pediatr Blood Cancer. 2015 May;62(5):759-65. doi: 10.1002/pbc.25340.


Osseous myxochondroid sarcoma: a detailed study of 5 cases of extraskeletal myxoid chondrosarcoma of the bone.

Demicco EG, Wang WL, Madewell JE, Huang D, Bui MM, Bridge JA, Meis JM.

Am J Surg Pathol. 2013 May;37(5):752-62. doi: 10.1097/PAS.0b013e3182796e46.


Genomic imbalances in benign metastasizing leiomyoma: characterization by conventional karyotypic, fluorescence in situ hybridization, and whole genome SNP array analysis.

Bowen JM, Cates JM, Kash S, Itani D, Gonzalez A, Huang D, Oliveira A, Bridge JA.

Cancer Genet. 2012 May;205(5):249-54. doi: 10.1016/j.cancergen.2012.04.005.


Pericytoma with t(7;12) and ACTB-GLI1 fusion arising in bone.

Bridge JA, Sanders K, Huang D, Nelson M, Neff JR, Muirhead D, Walker C, Seemayer TA, Sumegi J.

Hum Pathol. 2012 Sep;43(9):1524-9. doi: 10.1016/j.humpath.2012.01.019.


Translocation t(12;17)(q24.1;q21) as the sole anomaly in a nasal chondromesenchymal hamartoma arising in a patient with pleuropulmonary blastoma.

Behery RE, Bedrnicek J, Lazenby A, Nelson M, Grove J, Huang D, Smith R, Bridge JA.

Pediatr Dev Pathol. 2012 May-Jun;15(3):249-53. doi: 10.2350/11-11-1121-CR.1.


Extraskeletal Ewing's sarcoma of the thoracic epidural space: case report and review of the literature.

Yasuda T, Suzuki K, Kanamori M, Hori T, Huang D, Bridge JA, Kimura T.

Oncol Rep. 2011 Sep;26(3):711-5. doi: 10.3892/or.2011.1326. Review.


Renal cell carcinoma with novel VCL-ALK fusion: new representative of ALK-associated tumor spectrum.

Debelenko LV, Raimondi SC, Daw N, Shivakumar BR, Huang D, Nelson M, Bridge JA.

Mod Pathol. 2011 Mar;24(3):430-42. doi: 10.1038/modpathol.2010.213.


C11orf95-MKL2 is the resulting fusion oncogene of t(11;16)(q13;p13) in chondroid lipoma.

Huang D, Sumegi J, Dal Cin P, Reith JD, Yasuda T, Nelson M, Muirhead D, Bridge JA.

Genes Chromosomes Cancer. 2010 Sep;49(9):810-8. doi: 10.1002/gcc.20788.


Tissue-based quantification of 8-hydroxy-2'-deoxyguanosine in human prostate biopsies using quantitative fluorescence imaging analysis.

Richardson T, McCanse W, Casale GP, Huang D, Tian J, Elkahwaji JE, Lele S, Hemstreet GP.

Urology. 2009 Nov;74(5):1174-9. doi: 10.1016/j.urology.2009.01.052.


Udp-glucose dehydrogenase as a novel field-specific candidate biomarker of prostate cancer.

Huang D, Casale GP, Tian J, Lele SM, Pisarev VM, Simpson MA, Hemstreet GP 3rd.

Int J Cancer. 2010 Jan 15;126(2):315-27. doi: 10.1002/ijc.24820.


Quantitative fluorescence imaging analysis for cancer biomarker discovery: application to beta-catenin in archived prostate specimens.

Huang D, Casale GP, Tian J, Wehbi NK, Abrahams NA, Kaleem Z, Smith LM, Johansson SL, Elkahwaji JE, Hemstreet GP 3rd.

Cancer Epidemiol Biomarkers Prev. 2007 Jul;16(7):1371-81.


Identification and characterization of a novel gene disrupted by a pericentric inversion inv(4)(p13.1q21.1) in a family with cleft lip.

Beiraghi S, Zhou M, Talmadge CB, Went-Sumegi N, Davis JR, Huang D, Saal H, Seemayer TA, Sumegi J.

Gene. 2003 Apr 24;309(1):11-21.


Identification of the mouse and rat orthologs of the gene mutated in Usher syndrome type IIA and the cellular source of USH2A mRNA in retina, a target tissue of the disease.

Huang D, Eudy JD, Uzvolgyi E, Davis JR, Talmadge CB, Pretto D, Weston MD, Lehman JE, Zhou M, Seemayer TA, Ahmad I, Kimberling WJ, Sumegi J.

Genomics. 2002 Aug;80(2):195-203.


A spectrum of mutations in SH2D1A that causes X-linked lymphoproliferative disease and other Epstein-Barr virus-associated illnesses.

Sumegi J, Seemayer TA, Huang D, Davis JR, Morra M, Gross TG, Yin L, Romco G, Klein E, Terhorst C, Lanyi A.

Leuk Lymphoma. 2002 Jun;43(6):1189-201. Review.


Usher syndrome type III: revised genomic structure of the USH3 gene and identification of novel mutations.

Fields RR, Zhou G, Huang D, Davis JR, Möller C, Jacobson SG, Kimberling WJ, Sumegi J.

Am J Hum Genet. 2002 Sep;71(3):607-17.

Items per page

Supplemental Content

Loading ...
Support Center