Harvard Catalyst Profiles

Contact, publication, and social network information about Harvard faculty and fellows.

Search Result Details

This page shows the details of why an item matched the keywords from your search.
One or more keywords matched the following items that are connected to Fletcher, Jonathan
Item TypeName
Academic Article Cytogenetics and molecular biology of soft tissue tumors.
Academic Article Cytogenetics of soft tissue tumors.
Academic Article Cloning of an Alpha-TFEB fusion in renal tumors harboring the t(6;11)(p21;q13) chromosome translocation.
Academic Article Soft tissue sarcomas of adults: state of the translational science.
Academic Article Translocation (12;22)(q13-14;q12) is a nonrandom aberration in soft-tissue clear-cell sarcoma.
Academic Article Trisomy 5 and trisomy 7 are nonrandom aberrations in pigmented villonodular synovitis: confirmation of trisomy 7 in uncultured cells.
Academic Article Aneurysmal bone cyst variant translocations upregulate USP6 transcription by promoter swapping with the ZNF9, COL1A1, TRAP150, and OMD genes.
Academic Article FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome.
Academic Article Skeletal and extraskeletal myxoid chondrosarcoma: related or distinct tumors?
Academic Article Breakpoints of the t(11;18)(q21;q21) in mucosa-associated lymphoid tissue (MALT) lymphoma lie within or near the previously undescribed gene MALT1 in chromosome 18.
Academic Article Chromosomal abnormalities in nodal and extranodal CD30+ anaplastic large cell lymphomas: infrequent detection of the t(2;5) in extranodal lymphomas.
Academic Article Identification of chromosomal aberrations associated with disease progression and a novel 3q13.31 deletion involving LSAMP gene in osteosarcoma.
Academic Article Frequent fusion of the JAZF1 and JJAZ1 genes in endometrial stromal tumors.
Academic Article BRD4 bromodomain gene rearrangement in aggressive carcinoma with translocation t(15;19).
Academic Article Variant translocations involving 16q22 and 17p13 in solid variant and extraosseous forms of aneurysmal bone cyst.
Academic Article HMGI(Y) activation by chromosome 6p21 rearrangements in multilineage mesenchymal cells from pulmonary hamartoma.
Academic Article Upper respiratory tract carcinoma with chromosomal translocation 15;19: evidence for a distinct disease entity of young patients with a rapidly fatal course.
Academic Article Gains of chromosome 8 are confined to mesenchymal components in pleuropulmonary blastoma.
Academic Article Clonal 6p21 rearrangement is restricted to the mesenchymal component of an endometrial polyp.
Academic Article Congenital mesoblastic nephroma t(12;15) is associated with ETV6-NTRK3 gene fusion: cytogenetic and molecular relationship to congenital (infantile) fibrosarcoma.
Academic Article PDGFRA activating mutations in gastrointestinal stromal tumors.
Academic Article Lineage-restricted clonality in biphasic solid tumors.
Academic Article Solid variants of papillary (chromophil) renal cell carcinoma: clinicopathologic and genetic features.
Academic Article DNA in situ hybridization as an adjunct in tumor diagnosis.
Academic Article Isochromosome 7q in adult Wilms' tumors: diagnostic and pathogenetic implications.
Academic Article Re: O'Sullivan MJ, Kyriakos M, Zhu X, Wick MR, Swanson PE, Dehner LP, Humphrey PA, Pfeifer JD: malignant peripheral nerve sheath tumors with t(X;18). A pathologic and molecular genetic study. Mod pathol 2000;13:1336-46.
Academic Article Molecular genetic characterization of the EWS/CHN and RBP56/CHN fusion genes in extraskeletal myxoid chondrosarcoma.
Academic Article PKC412 inhibits the zinc finger 198-fibroblast growth factor receptor 1 fusion tyrosine kinase and is active in treatment of stem cell myeloproliferative disorder.
Academic Article Papillary renal cell carcinoma: quantitation of chromosomes 7 and 17 by FISH, analysis of chromosome 3p for LOH, and DNA ploidy.
Academic Article Human pancreatic cancer cells (MPanc-96) recognized by autologous tumor-infiltrating lymphocytes after in vitro as well as in vivo tumor expansion.
Academic Article Isolation and characterization of a mammalian homolog of the Drosophila white gene.
Academic Article Frequency and implications of chromosome 8 and 12 gains in Ewing sarcoma.
Academic Article Primary cutaneous Ewing's sarcoma: immunophenotypic and molecular cytogenetic evaluation of five cases.
Academic Article Laboratory investigation and genetics in sarcomas.
Academic Article Peripheral nerve sheath tumors from patients with neurofibromatosis type 1 do not have the chromosomal translocation t(X;18).
Academic Article The chimeric FUS/CREB3l2 gene is specific for low-grade fibromyxoid sarcoma.
Academic Article Midline carcinoma of children and young adults with NUT rearrangement.
Academic Article A t(2;19)(p13;p13.2) in a giant invasive cardiac lipoma from a patient with multiple lipomatosis.
Academic Article Trisomy 18 is a consistent cytogenetic feature in pilomatricoma.
Academic Article Identification of genetically aberrant cell lineages in Wilms' tumors.
Academic Article Cardiac synovial sarcoma with translocation (X;18) associated with asbestos exposure.
Academic Article Fluorescent in situ hybridization assessment of chromosome 7 copy number in uncultured lung and kidney cells.
Academic Article Subtracted, unique-sequence, in situ hybridization: experimental and diagnostic applications.
Academic Article Molecular and clinical analysis of locally advanced dermatofibrosarcoma protuberans treated with imatinib: Imatinib Target Exploration Consortium Study B2225.
Academic Article Cytogenetic aberrations in perineurioma: variation with subtype.
Academic Article Acute lymphocytic leukemia with eosinophilia and unusual karyotype.
Academic Article Prognostic implications of cytogenetic studies in an intensively treated group of children with acute lymphoblastic leukemia.
Academic Article 14-3-3 fusion oncogenes in high-grade endometrial stromal sarcoma.
Academic Article Chromosome aberrations in desmoid tumors. Trisomy 8 may be a predictor of recurrence.
Academic Article Limitations of chromosome classification by multicolor karyotyping.
Academic Article Diagnostic relevance of clonal cytogenetic aberrations in malignant soft-tissue tumors.
Academic Article Ovarian granulosa-stromal cell tumors are characterized by trisomy 12.
Academic Article Reporting of diagnostic cytogenetic results.
Academic Article Codeletion of p15 and p16 in primary malignant mesothelioma.
Academic Article Cytogenetic findings in pediatric adipose tumors: consistent rearrangement of chromosome 8 in lipoblastoma.
Academic Article Sustained complete remission of metastatic dermatofibrosarcoma protuberans with imatinib mesylate.
Academic Article Translocation (9;22) is associated with extremely poor prognosis in intensively treated children with acute lymphoblastic leukemia.
Academic Article Cytogenetic abnormalities in uterine leiomyomata.
Academic Article Ring chromosomes in dermatofibrosarcoma protuberans are composed of interspersed sequences from chromosomes 17 and 22.
Academic Article A polymerase chain reaction assay for non-random X chromosome inactivation identifies monoclonal endometrial cancers and precancers.
Academic Article Chromosome aberrations in uterine smooth muscle tumors: potential diagnostic relevance of cytogenetic instability.
Academic Article Cytogenetic aberrations in osteosarcomas. Nonrandom deletions, rings, and double-minute chromosomes.
Academic Article Cytogenetics and fluorescence in situ hybridization as adjuncts to cytology in the diagnosis of malignant mesothelioma.
Academic Article Fluorescence in situ hybridization evaluation of chromosome deletion patterns in prostate cancer.
Academic Article Trisomy 3 in renal cell carcinoma.
Academic Article Extremely poor prognosis of pediatric acute lymphoblastic leukemia with translocation (9;22): updated experience.
Academic Article Primary renal neoplasms with the ASPL-TFE3 gene fusion of alveolar soft part sarcoma: a distinctive tumor entity previously included among renal cell carcinomas of children and adolescents.
Academic Article Activation of the GLI oncogene through fusion with the beta-actin gene (ACTB) in a group of distinctive pericytic neoplasms: pericytoma with t(7;12).
Academic Article The pericentromeric inversion, inv (6)(p25q13), is a novel diagnostic marker in chondromyxoid fibroma.
Academic Article Trisomy 12 in pediatric granulosa-stromal cell tumors. Demonstration by a modified method of fluorescence in situ hybridization on paraffin-embedded material.
Academic Article Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma.
Academic Article Clonal rearrangement of chromosome band 6p21 in the mesenchymal component of pulmonary chondroid hamartoma.
Academic Article Consistent cytogenetic aberrations in hepatoblastoma: a common pathway of genetic alterations in embryonal liver and skeletal muscle malignancies?
Academic Article PLAG1 alterations in lipoblastoma: involvement in varied mesenchymal cell types and evidence for alternative oncogenic mechanisms.
Academic Article Chromogenic in situ hybridization and FISH in pathology.
Academic Article Detection of chromosome 18 rearrangement in synovial sarcoma by fluorescence in situ hybridization.
Academic Article Novel fluorescence in situ hybridization approaches in solid tumors. Characterization of frozen specimens, touch preparations, and cytological preparations.
Academic Article Cystic neuroblastoma: emphasis on gene expression, morphology, and pathogenesis.
Academic Article Lineage-restricted chromosome translocation in a benign fibrous tumor of the breast.
Academic Article Distinctive cytogenetic profile in benign metastasizing leiomyoma: pathogenetic implications.
Academic Article Genetics of soft tissue tumors.
Academic Article USP6 (Tre2) fusion oncogenes in aneurysmal bone cyst.
Academic Article Overexpression, amplification, and androgen regulation of TPD52 in prostate cancer.
Academic Article Cytogenetic evidence of clonality in a case of pigmented villonodular synovitis.
Academic Article Identification of a YAC spanning the translocation breakpoint t(8;22) associated with acute monocytic leukemia.
Academic Article BRD4-NUT fusion oncogene: a novel mechanism in aggressive carcinoma.
Academic Article Reporting of diagnostic cytogenetic results.
Academic Article Cytogenetic and histologic findings in 17 pulmonary chondroid hamartomas: evidence for a pathogenetic relationship with lipomas and leiomyomas.
Academic Article Complex cytogenetic aberrations in a well-differentiated chondrosarcoma.
Academic Article Chromosome aberrations in choroid plexus papillomas.
Academic Article Translocation t(8;13)(p11;q11-12) in stem cell leukemia/lymphoma of T-cell and myeloid lineages.
Academic Article Cytogenetics.
Academic Article Fibrosarcoma in infants and children. Application of new techniques.
Academic Article Isochromosome 7q in adult Wilms' tumor.
Academic Article Reporting of diagnostic cytogenetic results.
Academic Article PLAG1 fusion oncogenes in lipoblastoma.
Academic Article Biology and genetic aspects of gastrointestinal stromal tumors: KIT activation and cytogenetic alterations.
Academic Article Identification of a YAC spanning the translocation breakpoints in uterine leiomyomata, pulmonary chondroid hamartoma, and lipoma: physical mapping of the 12q14-q15 breakpoint region in uterine leiomyomata.
Academic Article Association of trisomy 8 and squamous differentiation in an endometrial adenocarcinoma.
Academic Article Disruption of the architectural factor HMGI-C: DNA-binding AT hook motifs fused in lipomas to distinct transcriptional regulatory domains.
Academic Article Investigation of chromosomal aberrations in hepatocellular carcinoma by fluorescence in situ hybridization.
Academic Article Molecular characterization of a 17q11.2 translocation in a malignant schwannoma cell line.
Academic Article Hemangiopericytoma of the tongue in a 12-year-old child: ultrastructural and cytogenetic observations.
Academic Article Chromosome aberrations in mesoblastic nephroma.
Concept Chromosome Breakpoints
Concept Chromosomes, Human, Pair 7
Concept Chromosome Walking
Concept Chromosome Aberrations
Concept Chromosome Deletion
Concept Chromosomes, Human, Pair 10
Concept Chromosome Inversion
Concept Chromosomes, Human, Pair 3
Concept Chromosomes, Human, Pair 20
Concept Chromosomes, Human, Pair 14
Concept Chromosomes, Human, Pair 11
Concept Chromosomes, Human, Pair 1
Concept Chromosomes, Human, Pair 19
Concept Chromosomes, Human, Pair 4
Concept Chromosomes, Human, Pair 5
Concept Chromosome Banding
Concept Chromosome Breakage
Concept Chromosomes, Human, Pair 21
Concept Chromosomes, Human, Pair 8
Concept Chromosome Painting
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 2
Concept X Chromosome
Concept Chromosomes, Human, Pair 13
Concept Chromosomes, Human, Pair 9
Concept Chromosomes, Human, Pair 6
Concept Chromosomes, Human, Pair 18
Concept Chromosomes, Human, Pair 12
Concept Chromosomes, Human, Pair 15
Concept Sex Chromosome Aberrations
Concept Chromosomes, Human, Pair 16
Concept Chromosome Disorders
Concept Chromosomes, Human, Pair 22
Concept Chromosomes, Human, Pair 17
Concept Philadelphia Chromosome
Academic Article High-resolution genome-wide copy-number analyses identify localized copy-number alterations in Ewing sarcoma.
Academic Article Characterization of the chromosomal translocation t(10;17)(q22;p13) in clear cell sarcoma of kidney.
Academic Article Ewing sarcoma mimicking atypical carcinoid tumor: detection of unexpected genomic alterations demonstrates the use of next generation sequencing as a diagnostic tool.
Academic Article Reporting of Diagnostic Cytogenetic Results.
Academic Article MAX inactivation is an early event in GIST development that regulates p16 and cell proliferation.
Academic Article What is New in Gastrointestinal Stromal Tumor?
Academic Article Mutational inactivation of mTORC1 repressor gene DEPDC5 in human gastrointestinal stromal tumors.
Search Criteria
  • Chromosomes Human Pair 9
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.