Clinical correlations of chromosome change in human solid tumors: the tip of the iceberg?

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Methods in molecular medicine·2012

Chromosome Microdissection for Detection of Subchromosomal Alterations by FISH.

Methods in molecular medicine·2011

Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.

Oncogene·2007

The value of molecular haplotypes in a family-based linkage study.

American journal of human genetics·2006

A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.

Journal of medical genetics·2005

Time trends of human papillomavirus-attributable head and neck cancers: the BROADEN study.

Journal of the National Cancer Institute·2026

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Colonoscopy screening outcomes in Lynch syndrome and differential colorectal cancer paths among MLH1/MSH2 carriers.

Journal of the National Cancer Institute·2026

Identification of prediagnostic proteomic biomarkers for colon and rectal cancer in 3 prospective cohorts.

Journal of the National Cancer Institute·2026

Claims-based frailty, dual eligibility, and potential unmet home-health needs in older breast cancer survivors.

Journal of the National Cancer Institute·2026

Lifestyle and genetic risk factors for postmenopausal breast cancer in the multiethnic cohort.

Journal of the National Cancer Institute·2026

A Novel cccDNA-Binding Protein HSPA1B Promotes HBV Transcription and HBx-Mediated HCC Metastasis via Downregulating SOX4.

Journal of medical virology·2026

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Angewandte Chemie (International ed. in English)·2026

Syntaxin11 deficiency inhibits CRAC channel priming to suppress cytotoxicity and gene expression in T lymphocytes independent of membrane trafficking.

eLife·2026

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Stroke·2026

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Clinical correlations of chromosome change in human solid tumors: the tip of the iceberg?

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A recurrent germline BAP1 mutation and extension of the BAP1 tumor predisposition spectrum to include basal cell carcinoma.

Isolation of tumor suppressor genes in melanoma by cDNA microarray.

Chromosome Microdissection for Detection of Subchromosomal Alterations by FISH.

Frequent activating FGFR2 mutations in endometrial carcinomas parallel germline mutations associated with craniosynostosis and skeletal dysplasia syndromes.

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A common nonsense mutation in EphB2 is associated with prostate cancer risk in African American men with a positive family history.

Time trends of human papillomavirus-attributable head and neck cancers: the BROADEN study.

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A Novel cccDNA-Binding Protein HSPA1B Promotes HBV Transcription and HBx-Mediated HCC Metastasis via Downregulating SOX4.

Downsizing Electrophilic MAX-Derived Helical Zipper Peptides to Covalently Bind and Degrade Oncogenic MYC.

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Clinical correlations of chromosome change in human solid tumors: the tip of the iceberg?

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