Frequent p53 Mutations in Head and Neck Cancer

KD Somers, MA Merrick, ME Lopez, LS Incognito… - Cancer Research, 1992 - AACR
Squamous cell carcinomas of the head and neck (SCCHN) are associated strongly with the
use of tobacco and alcohol, but little is known about the molecular pathogenesis of these …

Diagnostic relevance of clonal cytogenetic aberrations in malignant soft-tissue tumors

JA Fletcher, HP Kozakewich, FA Hoffer… - … England Journal of …, 1991 - Mass Medical Soc
Background. Malignant soft-tissue tumors often present substantial diagnostic challenges.
Chromosome aberrations that might be diagnostic have been identified in some types of soft …

Deletion 7q22 in uterine leiomyoma: a cytogenetic review

YY Ozisik, AM Meloni, U Surti, AA Sandberg - Cancer genetics and …, 1993 - Elsevier
The cytogenetic patterns of uterine leiomyomas have been extensively investigated, and
cases characterized by specific clonal changes have been documented in detail. In these …

Synovial chondromatosis: clonal chromosome changes provide further evidence for a neoplastic disorder

R Sciot, P Dal Cin, J Bellemans, I Samson… - Virchows Archiv, 1998 - Springer
Synovial chondromatosis is a rare lesion, which is still believed by most authors to be
reactive rather than neoplastic. We report on a case of synovial chondromatosis with clonal …

DNA-damaging agents greatly increase the transduction of nondividing cells by adeno-associated virus vectors

IE Alexander, DW Russell, AD Miller - Journal of virology, 1994 - Am Soc Microbiol
None of the vector systems currently available for gene therapy applications have been
shown to be capable of both efficient gene transfer into nondividing cells and long-term …

Meningioma: a cytogenetic model of a complex benign human tumor, including data on 394 karyotyped cases

KD Zang - Cytogenetics and cell genetics, 2001 - karger.com
Meningioma is the most frequent tumor of neuroectodermal origin in humans. It is usually
benign. Only a minority of cases shows progression to an anaplastic tumor (WHO grade II …

Complex composition and co‐amplification of SAS and MDM2 in ring and giant rod marker chromosomes in well‐differentiated liposarcoma

F Pedeutour, RF Suijkerbuijk, A Forus… - Genes …, 1994 - Wiley Online Library
Extra abnormal chromosomes (rings and giant rods) containing chromosome 12 sequences
are characteristic of well‐differentiated liposarcoma (WDLPS). By whole chromosome …

Receptor protein-tyrosine phosphatase gamma is a candidate tumor suppressor gene at human chromosome region 3p21.

S LaForgia, B Morse, J Levy… - Proceedings of the …, 1991 - National Acad Sciences
PTPG, the gene for protein-tyrosine phosphatase gamma (PTP gamma), maps to a region of
human chromosome 3, 3p21, that is frequently deleted in renal cell carcinoma and lung …

Involvement of chromosome X in primary cytogenetic change in human neoplasia: nonrandom translocation in synovial sarcoma.

C Turc-Carel, P Dal Cin, J Limon… - Proceedings of the …, 1987 - National Acad Sciences
A translocation that involves chromosome X (band p11. 2) and chromosome 18 (band q11.
2) was observed in short-term in vitro cultures of cells from five synovial sarcomas and one …

Cytogenetic studies of adipose tissue tumors. II. Recurrent reciprocal translocation t (12; 16)(q13; p11) in myxoid liposarcomas

C Turc-Carel, J Limon, P Dal Cin, U Rao… - Cancer genetics and …, 1986 - Elsevier
Detailed chromosome studies, briefly reported previously, from short-term cultures of tumor
cells from myxoid liposarcomas are reported. A common reciprocal translocation, t (12; …