| Item Type | Name |
|
Academic Article
|
i(5p) and del(6q) are nonrandom abnormalities in carcinoma cervix uteri. Cytogenetics of two newly developed cell lines.
|
|
Academic Article
|
Consistent chromosomal losses in head and neck squamous cell carcinoma cell lines.
|
|
Academic Article
|
The t(9;14)(p13;q32) chromosomal translocation associated with lymphoplasmacytoid lymphoma involves the PAX-5 gene.
|
|
Academic Article
|
BCL8, a novel gene involved in translocations affecting band 15q11-13 in diffuse large-cell lymphoma.
|
|
Academic Article
|
The t(2;3)(q21;q27) translocation in non-Hodgkin's lymphoma displays BCL6 mutations in the 5' regulatory region and chromosomal breakpoints distant from the gene.
|
|
Academic Article
|
Chromosomal and gene amplification in diffuse large B-cell lymphoma.
|
|
Academic Article
|
Spectral karyotyping identifies new rearrangements, translocations, and clinical associations in diffuse large B-cell lymphoma.
|
|
Academic Article
|
Analysis of a 69-kb contiguous genomic sequence at a putative tumor suppressor gene locus on human chromosome 6q27.
|
|
Academic Article
|
The utility of spectral karyotyping in the cytogenetic analysis of newly diagnosed pediatric acute lymphoblastic leukemia.
|
|
Academic Article
|
Deletions involving two distinct regions of 6q in B-cell non-Hodgkin lymphoma.
|
|
Academic Article
|
IRTA1 and IRTA2, novel immunoglobulin superfamily receptors expressed in B cells and involved in chromosome 1q21 abnormalities in B cell malignancy.
|
|
Academic Article
|
Frequent amplification and rearrangement of chromosomal bands 6p12-p21 and 17p11.2 in osteosarcoma.
|
|
Academic Article
|
Overexpression of E2F-1 in lung and liver metastases of human colon cancer is associated with gene amplification.
|
|
Academic Article
|
Amplification of MGC2177, PLAG1, PSMC6P, and LYN in a malignant mixed tumor of salivary gland detected by cDNA microarray with tyramide signal amplification.
|
|
Academic Article
|
The p73 locus is commonly deleted in non-Hodgkin's lymphomas.
|
|
Academic Article
|
Amplification of the 3q26.3 locus is associated with progression to invasive cancer and is a negative prognostic factor in head and neck squamous cell carcinomas.
|
|
Academic Article
|
Genetic analysis identifies putative tumor suppressor sites at 2q35-q36.1 and 2q36.3-q37.1 involved in cervical cancer progression.
|
|
Academic Article
|
Alternative translocation breakpoint cluster region 5' to BCL-6 in B-cell non-Hodgkin's lymphoma.
|
|
Academic Article
|
Genomic and expression analysis of the 12p11-p12 amplicon using EST arrays identifies two novel amplified and overexpressed genes.
|
|
Academic Article
|
Medulloblastomas overexpress the p53-inactivating oncogene WIP1/PPM1D.
|
|
Academic Article
|
Juvenile juxtacortical chondromyxoid fibroma of bone: a case report.
|
|
Academic Article
|
Chromosomal amplifications, 3q gain and deletions of 2q33-q37 are the frequent genetic changes in cervical carcinoma.
|
|
Academic Article
|
Genome-wide array comparative genomic hybridization analysis reveals distinct amplifications in osteosarcoma.
|
|
Academic Article
|
Novel chromosomal rearrangements and break points at the t(6;9) in salivary adenoid cystic carcinoma: association with MYB-NFIB chimeric fusion, MYB expression, and clinical outcome.
|
|
Academic Article
|
Transformation of human kidney proximal tubule cells by a src-containing retrovirus.
|
|
Academic Article
|
Medulloblastoma outcome is adversely associated with overexpression of EEF1D, RPL30, and RPS20 on the long arm of chromosome 8.
|
|
Academic Article
|
Squamous cell carcinoma related oncogene/DCUN1D1 is highly conserved and activated by amplification in squamous cell carcinomas.
|
|
Academic Article
|
Molecular cytogenetic analysis of follicular lymphoma (FL) provides detailed characterization of chromosomal instability associated with the t(14;18)(q32;q21) positive and negative subsets and histologic progression.
|
|
Academic Article
|
Cell cycle regulator gene CDC5L, a potential target for 6p12-p21 amplicon in osteosarcoma.
|
|
Academic Article
|
Deletion of 1p32-p36 is the most frequent genetic change and poor prognostic marker in adenoid cystic carcinoma of the salivary glands.
|
|
Academic Article
|
Molecular characterization of permanent cell lines from primary, metastatic and recurrent malignant peripheral nerve sheath tumors (MPNST) with underlying neurofibromatosis-1.
|
|
Academic Article
|
Translocation t(6;14) as the sole chromosomal abnormality in adenoid cystic carcinoma of the base of tongue.
|
|
Academic Article
|
11p13-15 is a specific region of chromosomal rearrangement in gastric and esophageal adenocarcinomas.
|
|
Academic Article
|
De novo B lymphoblastic leukemia/lymphoma in an adult with t(14;18)(q32;q21) and c-MYC gene rearrangement involving 10p13.
|
|
Academic Article
|
Interphase cytogenetics of gastric and esophageal adenocarcinomas.
|
|
Academic Article
|
Cloning of bcl-6, the locus involved in chromosome translocations affecting band 3q27 in B-cell lymphoma.
|
|
Academic Article
|
REL proto-oncogene is frequently amplified in extranodal diffuse large cell lymphoma.
|
|
Academic Article
|
Deregulation of MUM1/IRF4 by chromosomal translocation in multiple myeloma.
|
|
Academic Article
|
Novel chromosomal abnormalities identified by comparative genomic hybridization in parathyroid adenomas.
|
|
Academic Article
|
Multicolor spectral karyotyping identifies new recurring breakpoints and translocations in multiple myeloma.
|
|
Academic Article
|
Chromosomal rearrangement of the PAX-5 locus in lymphoplasmacytic lymphoma with t(9;14)(p13;q32).
|
|
Academic Article
|
Molecular cytogenetic characterization of head and neck squamous cell carcinoma and refinement of 3q amplification.
|
|
Concept
|
Chromosomes, Human, Pair 18
|
|
Concept
|
Chromosomes, Human, Pair 12
|
|
Concept
|
Chromosomes, Human, Pair 15
|
|
Concept
|
Chromosomes, Human, Pair 16
|
|
Concept
|
Chromosomes, Human, Pair 17
|
|
Concept
|
Chromosomes, Human
|
|
Concept
|
Chromosomes, Human, Pair 14
|
|
Concept
|
Chromosomes, Human, Pair 11
|
|
Concept
|
Chromosomes, Human, Pair 1
|
|
Concept
|
Chromosomes, Human, Pair 19
|
|
Concept
|
Chromosomes, Human, Pair 3
|
|
Concept
|
Chromosomes, Human, Pair 20
|
|
Concept
|
Chromosomes, Human, Pair 4
|
|
Concept
|
Chromosomes, Human, Pair 5
|
|
Concept
|
Chromosomes, Human, Pair 21
|
|
Concept
|
Chromosomes, Human, Pair 8
|
|
Concept
|
Chromosomes, Human, Pair 10
|
|
Concept
|
Chromosomes, Human, Pair 7
|
|
Concept
|
Chromosomes, Human, Pair 6
|
|
Concept
|
Chromosomes, Human, Pair 2
|
|
Concept
|
Chromosomes, Human, Pair 9
|
|
Concept
|
Chromosomes, Human, Pair 22
|
|
Academic Article
|
Integrated multimodal genetic testing of Ewing sarcoma--a single-institution experience.
|
|
Academic Article
|
t(3;8) as the sole chromosomal abnormality in a myoepithelial carcinoma ex pleomorphic adenoma: a putative progression event.
|
|
Academic Article
|
Comparative genomic hybridization for analysis of changes in DNA copy number in multiple myeloma.
|
|
Academic Article
|
Trisomy 1q, 2, and 20 in a case of hepatoblastoma: possible significance of 2q35-q37 and 1q12-q21 rearrangements.
|
|
Academic Article
|
An apparent interlocus gene conversion-like event at a putative tumor suppressor gene locus on human chromosome 6q27 in a Burkitt's lymphoma cell line.
|
|
Academic Article
|
Translocation (4;15)(p16;q24): a novel reciprocal translocation in a patient with BCR/ABL negative myeloproliferative syndrome progressing to blastic phase.
|
|
Academic Article
|
Chromosome 18 breakpoint in t(11;18)(q21;q21) translocation associated with MALT lymphoma is proximal to BCL2 and distal to DCC.
|
|
Academic Article
|
Deregulation of BCL6 in non-Hodgkin lymphoma by insertion of IGH sequences in complex translocations involving band 3q27.
|
|
Academic Article
|
Chromosomal amplification is associated with cisplatin resistance of human male germ cell tumors.
|
|
Academic Article
|
Nonsyntenic amplification of MYC with CDK4 and MDM2 in a malignant mixed tumor of salivary gland.
|
|
Academic Article
|
Type I transforming growth factor beta receptor maps to 9q22 and exhibits a polymorphism and a rare variant within a polyalanine tract.
|
|
Academic Article
|
Cloning and mapping of human chromosome 6q26-q27 deleted in B-cell non-Hodgkin lymphoma and multiple tumor types.
|
|
Academic Article
|
Assignment of the human B-cell-derived (BCD1) proto-oncogene to 10p14-p15.
|
|
Academic Article
|
Molecular cytogenetic characterization of mammary neuroendocrine carcinoma.
|
|
Academic Article
|
Translocation t(7;12) as the sole chromosomal abnormality resulting in ACTB-GLI1 fusion in pediatric gastric pericytoma.
|
|
Academic Article
|
Novel t(1;3)(q21,p21) translocation in a basal cell adenocarcinoma of the parotid gland: potential association with tumorigenesis.
|
|
Academic Article
|
Novel MYBL1 Gene Rearrangements with Recurrent MYBL1-NFIB Fusions in Salivary Adenoid Cystic Carcinomas Lacking t(6;9) Translocations.
|