Latest papers

Oncogenic FAM131B-BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma.

Genomic analysis reveals the molecular heterogeneity of ovarian clear cell carcinomas.

Molecular karyotypes of Hodgkin and Reed-Sternberg cells at disease onset reveal distinct copy number alterations in chemosensitive versus refractory Hodgkin lymphoma.

High resolution array comparative genomic hybridization identifies copy number alterations in diffuse large B-cell lymphoma that predict response to immuno-chemotherapy.

Analysis of miRNA-gene expression-genomic profiles reveals complex mechanisms of microRNA deregulation in osteosarcoma.

A pathobiological role of the insulin receptor in chronic lymphocytic leukemia.

Syntenic relationships between genomic profiles of fiber-induced murine and human malignant mesothelioma.

[Recent advances in molecular pathology of phyllodes tumor of breast]. FAU - Niu, Yun AU - Niu Y LA - chi PT - Journal Article PT - Review PL - China TA - Zhonghua Bing Li Xue Za Zhi JT - Zhonghua bing li xue za zhi Chinese journal of pathology JID - 0005331 SB - IM MHDA- 2011/10/18 06:00 PST - ppublish SO - Zhonghua Bing Li Xue Za Zhi. 2011 Feb;40(2):135-7.

Association of IFN-gamma signal transduction defects with impaired HLA class I antigen processing in melanoma cell lines.

A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome.

A novel mutation in the RPS6KA3 gene in a patient with Coffin-Lowry syndrome.

A Multi-Sample Based Method for Identifying Common CNVs in Normal Human Genomic Structure Using High-Resolution aCGH Data.

Prenatal diagnosis and molecular characterization of an interstitial 1q24.3-31.3 deletion: case report and review.

The genome and its implications.

New cases and refinement of the critical region in the 1q41q42 microdeletion syndrome

De novo supernumerary marker chromosome originating from chromosome 17 resulting in a normal pregnancy outcome.

Correlation between DNA ploidy, metaphase high-resolution comparative genomic hybridization results and clinical outcome of synovial sarcoma.

Deletions of 16q in Wilms tumors localize to blastemal-anaplastic cells and are associated with reduced expression of the IRXB renal tubulogenesis gene cluster.

The TLX1 oncogene drives aneuploidy in T cell transformation.

Prognostic implication of MET overexpression in myxofibrosarcomas: an integrative array comparative genomic hybridization, real-time quantitative PCR, immunoblotting, and immunohistochemical analysis.