Item Type | Name |
Concept
|
Chromosomes, Human, Pair 18
|
Concept
|
Chromosomes, Human, Pair 12
|
Concept
|
Chromosomes, Human, Pair 15
|
Concept
|
Chromosomes, Human, X
|
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 7
|
Concept
|
Chromosomes, Human, Pair 6
|
Concept
|
Chromosomes, Human, Pair 2
|
Concept
|
Chromosomes, Human, Pair 13
|
Concept
|
Chromosomes, Human, Pair 9
|
Concept
|
Chromosomes, Human, Pair 22
|
Academic Article
|
TET2 mutations, myelodysplastic features, and a distinct immunoprofile characterize blastic plasmacytoid dendritic cell neoplasm in the bone marrow.
|
Academic Article
|
Chronic lymphocytic leukemia with t(14;18)(q32;q21).
|
Academic Article
|
B acute lymphoblastic leukemia with t(14;19)(q32;p13.1) involving IGH/EPOR: a clinically aggressive subset of disease.
|
Academic Article
|
Cytogenetic risk stratification of 417 patients with chronic myelomonocytic leukemia from a single institution.
|
Academic Article
|
Homozygous inv(11)(q21q23) and MLL gene rearrangement in two patients with myeloid neoplasms.
|
Academic Article
|
MLL gene amplification in acute myeloid leukemia and myelodysplastic syndromes is associated with characteristic clinicopathological findings and TP53 gene mutation.
|
Academic Article
|
Association of bcl-1 rearrangements with lymphocytic lymphoma of intermediate differentiation.
|
Academic Article
|
Numerical cytogenetic abnormalities of chromosomes 3, 7, and 12 in marginal zone B-cell lymphomas.
|
Academic Article
|
5'-->3' exonuclease-based real-time PCR assays for detecting the t(14;18)(q32;21): a survey of 162 malignant lymphomas and reactive specimens.
|
Academic Article
|
Anaplastic large cell lymphoma arising in bone: report of a case of the monomorphic variant with the t(2;5)(p23;q35) translocation.
|
Academic Article
|
Cyclin D1 and E2F-1 immunoreactivity in bone marrow biopsy specimens of multiple myeloma: relationship to proliferative activity, cytogenetic abnormalities and DNA ploidy.
|
Academic Article
|
Mature B-cell leukemias with more than 55% prolymphocytes. A heterogeneous group that includes an unusual variant of mantle cell lymphoma.
|
Academic Article
|
Differential expression of BCL-2 family proteins in ALK-positive and ALK-negative anaplastic large cell lymphoma of T/null-cell lineage.
|
Academic Article
|
Quantitative real-time polymerase chain reaction for monitoring minimal residual disease in patients with advanced indolent lymphomas treated with rituximab, fludarabine, mitoxantrone, and dexamethasone.
|
Academic Article
|
Lymphoid neoplasms associated with concurrent t(14;18) and 8q24/c-MYC translocation generally have a poor prognosis.
|
Academic Article
|
Acute myeloid leukemia associated with variant t(8;21) detected by conventional cytogenetic and molecular studies: a report of four cases and review of the literature.
|
Academic Article
|
Translocation (3;8)(q26;q24): a recurrent chromosomal abnormality in myelodysplastic syndrome and acute myeloid leukemia.
|
Academic Article
|
Acute myeloid leukemia harboring t(8;21)(q22;q22): a heterogeneous disease with poor outcome in a subset of patients unrelated to secondary cytogenetic aberrations.
|
Academic Article
|
Therapy-related acute myeloid leukemia with t(8;21) (q22;q22) shares many features with de novo acute myeloid leukemia with t(8;21)(q22;q22) but does not have a favorable outcome.
|
Academic Article
|
Chronic lymphocytic leukemia With t(2;14)(p16;q32) involves the BCL11A and IgH genes and is associated with atypical morphologic features and unmutated IgVH genes.
|
Academic Article
|
Trisomy 11 in myelodysplastic syndromes defines a unique group of disease with aggressive clinicopathologic features.
|
Academic Article
|
JAK2 V617F mutation is uncommon in patients with the 3q21q26 syndrome.
|
Academic Article
|
Myelodysplastic syndromes with deletions of chromosome 11q lack cryptic MLL rearrangement and exhibit characteristic clinicopathologic features.
|
Academic Article
|
The B cell antigen receptor in atypical chronic lymphocytic leukemia with t(14;19)(q32;q13) demonstrates remarkable stereotypy.
|
Academic Article
|
Chromosome 20q deletion: a recurrent cytogenetic abnormality in patients with chronic myelogenous leukemia in remission.
|
Academic Article
|
Activation of the p53 pathway by the MDM2 inhibitor nutlin-3a overcomes BCL2 overexpression in a preclinical model of diffuse large B-cell lymphoma associated with t(14;18)(q32;q21).
|
Academic Article
|
Trisomy 11 as an isolated abnormality in acute myeloid leukemia is associated with unfavorable prognosis but not with an NPM1 or KIT mutation.
|
Academic Article
|
Genotypic analysis of diffuse, mixed cell lymphomas. Comparison with morphologic and immunophenotypic findings.
|
Academic Article
|
Follicular center cell lymphoma with the t(14;18) translocation in which the rearranged BCL-2 gene is silent.
|
Academic Article
|
bcl-2 expression in Hodgkin's disease. Correlation with the t(14;18) translocation and Epstein-Barr virus.
|
Academic Article
|
Isochromosome 7q: the primary cytogenetic abnormality in hepatosplenic gammadelta T cell lymphoma.
|
Academic Article
|
Trisomy 14 in myelodysplastic syndromes: report of two cases and review of the literature.
|
Academic Article
|
Hepatosplenic gamma/delta T-cell lymphoma in bone marrow. A sinusoidal neoplasm with blastic cytologic features.
|
Academic Article
|
Cytogenetic findings in lymphoplasmacytic lymphoma/Waldenstr?m macroglobulinemia. Chromosomal abnormalities are associated with the polymorphous subtype and an aggressive clinical course.
|
Academic Article
|
Marginal-zone B-cell lymphoma of extranodal mucosa-associated lymphoid tissue type: molecular genetics provides new insights into pathogenesis.
|
Academic Article
|
Real-Time t(14;18)(q32;q21) PCR assay combined with high-resolution capillary electrophoresis: a novel and rapid approach that allows accurate quantitation and size determination of bcl-2/JH fusion sequences.
|
Academic Article
|
Mantle cell lymphoma with 8q24 chromosomal abnormalities: a report of 5 cases with blastoid features.
|
Academic Article
|
t(8;21)(q22;q22) in blast phase of chronic myelogenous leukemia.
|
Academic Article
|
Expression of bcl-3 in chronic lymphocytic leukemia correlates with trisomy 12 and abnormalities of chromosome 19.
|
Academic Article
|
Chronic myeloproliferative diseases with the t(5;12)(q33;p13): clonal evolution is associated with blast crisis.
|
Academic Article
|
NPM-ALK oncogenic kinase promotes cell-cycle progression through activation of JNK/cJun signaling in anaplastic large-cell lymphoma.
|
Academic Article
|
t(8;13)-positive bilineal lymphomas: report of 6 cases.
|
Academic Article
|
Splenic marginal zone lymphomas are characterized by loss of interstitial regions of chromosome 7q, 7q31.32 and 7q36.2 that include the protection of telomere 1 (POT1) and sonic hedgehog (SHH) genes.
|
Academic Article
|
Translocation (18;22)(q21;q11) in B-cell lymphomas: a report of 4 cases and review of the literature.
|
Academic Article
|
del(15q) is a recurrent minor-route cytogenetic abnormality in the clonal evolution of chronic myelogenous leukemia.
|
Academic Article
|
B-cell lymphomas with MYC/8q24 rearrangements and IGH@BCL2/t(14;18)(q32;q21): an aggressive disease with heterogeneous histology, germinal center B-cell immunophenotype and poor outcome.
|
Academic Article
|
Array comparative genomic hybridization analysis identifies recurrent gain of chromosome 2p25.3 involving the ACP1 and MYCN genes in chronic lymphocytic leukemia.
|
Academic Article
|
Myelodysplastic syndrome/acute myeloid leukemia with t(3;21)(q26.2;q22) is commonly a therapy-related disease associated with poor outcome.
|
Academic Article
|
Therapy-related myeloid neoplasms with isolated del(20q): comparison with cases of de novo myelodysplastic syndrome with del(20q).
|
Academic Article
|
Chromosomal translocation t(14;19) as indicated by bcl-3 rearrangement is a rare phenomenon in non-Hodgkin's lymphoma and chronic lymphocytic leukemia: a molecular genetic analysis of 176 cases.
|
Academic Article
|
Presence of t(8;21)(q22;q22) in myeloperoxidase-positive, myeloid surface antigen-negative acute myeloid leukemia.
|
Academic Article
|
Real-time 5'-->3' exonuclease-based PCR assay for detection of the t(11;14)(q13;q32).
|
Academic Article
|
Detection of chromosome 11q13 breakpoints by interphase fluorescence in situ hybridization. A useful ancillary method for the diagnosis of mantle cell lymphoma.
|
Academic Article
|
Cyclin D1 expression in dysplastic nevi: an immunohistochemical study.
|
Academic Article
|
Leukemic mantle cell lymphoma: clinical and pathologic spectrum of twenty-three cases.
|
Academic Article
|
Precursor T-cell acute lymphoblastic leukemia in adults: age-related immunophenotypic, cytogenetic, and molecular subsets.
|
Academic Article
|
Characterization of 4 mantle cell lymphoma cell lines.
|
Academic Article
|
CD79b expression in chronic lymphocytic leukemia. Association with trisomy 12 and atypical immunophenotype.
|
Academic Article
|
Quantitative PCR detection of t(14;18) bcl-2/JH fusion sequences in follicular lymphoma patients: comparison of peripheral blood and bone marrow aspirate samples.
|
Academic Article
|
inv(16)(p13q22) in chronic myelogenous leukemia in blast phase: a clinicopathologic, cytogenetic, and molecular study of five cases.
|
Academic Article
|
Immunohistochemical analysis of CBFbeta-SMMHC protein reveals a unique nuclear localization in acute myeloid leukemia with inv(16)(p13q22).
|
Academic Article
|
Therapy may unmask hypoplastic myelodysplastic syndrome that mimics aplastic anemia.
|
Academic Article
|
High-grade B-cell lymphoma/leukemia associated with t(14;18) and 8q24/MYC rearrangement: a neoplasm of germinal center immunophenotype with poor prognosis.
|
Academic Article
|
Deletion 15q as the sole abnormality in acute myeloid leukemia: report of three cases and review of the literature.
|
Academic Article
|
8p11 myeloproliferative syndrome: a review.
|
Academic Article
|
Myelodysplastic syndrome with inv(3)(q21q26.2) or t(3;3)(q21;q26.2) has a high risk for progression to acute myeloid leukemia.
|
Academic Article
|
Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53.
|
Academic Article
|
Splenic B-cell lymphomas with more than 55% prolymphocytes in blood: evidence for prolymphocytoid transformation.
|
Academic Article
|
Patients with diffuse large B-cell lymphoma of germinal center origin with BCL2 translocations have poor outcome, irrespective of MYC status: a report from an International DLBCL rituximab-CHOP Consortium Program Study.
|
Academic Article
|
Fluorescent in situ hybridization in routinely processed bone marrow aspirate clot and core biopsy sections.
|
Academic Article
|
Frequent deletions at 12q14.3 chromosomal locus in adult acute lymphoblastic leukemia.
|
Academic Article
|
Expression of B cell-specific activator protein/PAX5 in acute myeloid leukemia with t(8;21)(q22;q22).
|
Academic Article
|
Comparative analysis of genes regulated in acute myelomonocytic leukemia with and without inv(16)(p13q22) using microarray techniques, real-time PCR, immunohistochemistry, and flow cytometry immunophenotyping.
|
Academic Article
|
Aberrant EVI1 expression in acute myeloid leukemias associated with the t(3;8)(q26;q24).
|
Academic Article
|
De novo acute myeloid leukemia with inv(3)(q21q26.2) or t(3;3)(q21;q26.2): a clinicopathologic and cytogenetic study of an entity recently added to the WHO classification.
|
Academic Article
|
Chronic lymphocytic leukemia with t(14;19)(q32;q13) is characterized by atypical morphologic and immunophenotypic features and distinctive genetic features.
|
Academic Article
|
Molecular and clinicopathologic characterization of AML with isolated trisomy 4.
|
Academic Article
|
Determination of lineage and clonality in diffuse lymphomas using the polymerase chain reaction technique.
|
Academic Article
|
Primary cutaneous diffuse large B-cell lymphoma: a clinicopathologic study of 15 cases.
|
Academic Article
|
Quantitative real-time polymerase chain reaction for detection of circulating cells with t(14;18) in volunteer blood donors and patients with follicular lymphoma.
|
Academic Article
|
Mature B-cell leukemias with more than 55% prolymphocytes: report of 2 cases with Burkitt lymphoma-type chromosomal translocations involving c-myc.
|
Academic Article
|
Dysplasia and high proliferation rate are common in acute myeloid leukemia with inv(16)(p13q22).
|
Academic Article
|
Myeloid sarcoma of the urinary bladder and epididymis as a primary manifestation of acute myeloid leukemia with inv(16).
|
Academic Article
|
The t(14;19)(q32;q13)-positive small B-cell leukaemia: a clinicopathologic and cytogenetic study of seven cases.
|
Academic Article
|
Identification of clinically important chromosomal aberrations in acute myeloid leukemia by array-based comparative genomic hybridization.
|
Academic Article
|
Isolated +15 in bone marrow: disease-associated or a benign finding?
|
Academic Article
|
Identification of a novel fusion gene, IRF2BP2-RARA, in acute promyelocytic leukemia.
|
Academic Article
|
Chromosomal rearrangement involving 11q23 locus in chronic myelogenous leukemia: a rare phenomenon frequently associated with disease progression and poor prognosis.
|
Academic Article
|
Impact of trisomy 8 on treatment response and survival of patients with chronic myelogenous leukemia in the era of tyrosine kinase inhibitors.
|
Academic Article
|
Del(20q) in patients with chronic lymphocytic leukemia: a therapy-related abnormality involving lymphoid or myeloid cells.
|
Academic Article
|
Clinical significance of newly emerged isolated del(20q) in patients following cytotoxic therapies.
|
Academic Article
|
Isolated del(5q) in Patients Following Therapies for Various Malignancies May Not All Be Clinically Significant.
|
Academic Article
|
Prognostic impact of acquisition of cytogenetic abnormalities during the course of chronic myelomonocytic leukemia.
|
Academic Article
|
De Novo MYC and BCL2 Double-hit B-Cell Precursor Acute Lymphoblastic Leukemia (BCP-ALL) in Pediatric and Young Adult Patients Associated With Poor Prognosis.
|
Academic Article
|
Cytogenetic landscape and impact in blast phase of chronic myeloid leukemia in the era of tyrosine kinase inhibitor therapy.
|
Academic Article
|
Clinical significance of isolated del(7p) in myeloid neoplasms.
|
Academic Article
|
Constitutional pericentric inversion of chromosome 9 has no impact on survival in chronic myelogenous leukemia.
|
Academic Article
|
Myeloid neoplasms with isolated isochromosome 17q demonstrate a high frequency of mutations in SETBP1, SRSF2, ASXL1 and NRAS.
|
Academic Article
|
Prognostic Factors of Hepatosplenic T-cell Lymphoma: Clinicopathologic Study of 28 Cases.
|
Academic Article
|
Clinical significance of acquired loss of the X chromosome in bone marrow.
|
Academic Article
|
Newly emerged isolated Del(7q) in patients with prior cytotoxic therapies may not always be associated with therapy-related myeloid neoplasms.
|
Academic Article
|
Whole-arm translocation of der(5;17)(p10;q10) with concurrent TP53 mutations in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): A unique molecular-cytogenetic subgroup.
|
Academic Article
|
Acute leukaemia and myelodysplastic syndromes with chromosomal rearrangement involving 11q23 locus, but not MLL gene.
|
Academic Article
|
Clinical significance of trisomy 8 that emerges during therapy in chronic myeloid leukemia.
|
Academic Article
|
Genome-wide copy number aberrations and HER2 and FGFR1 alterations in primary breast cancer by molecular inversion probe microarray.
|
Academic Article
|
Myeloproliferative neoplasms with t(8;22)(p11.2;q11.2)/BCR-FGFR1: a meta-analysis of 20 cases shows cytogenetic progression with B-lymphoid blast phase.
|
Academic Article
|
Characteristics and clinical significance of cytogenetic abnormalities in polycythemia vera.
|
Academic Article
|
Additional-structural-chromosomal aberrations are associated with inferior clinical outcome in patients with hyperdiploid multiple myeloma: a single-institution experience.
|
Academic Article
|
3q26.2/EVI1 rearrangement is associated with poor prognosis in classical Philadelphia chromosome-negative myeloproliferative neoplasms.
|
Academic Article
|
8q24/MYC rearrangement is a recurrent cytogenetic abnormality in blastic plasmacytoid dendritic cell neoplasms.
|
Academic Article
|
3q26/EVI1 rearrangement in myelodysplastic/myeloproliferative neoplasms: An early event associated with a poor prognosis.
|
Academic Article
|
Genomic aberrations involving 12p/ETV6 are highly prevalent in blastic plasmacytoid dendritic cell neoplasms and might represent early clonal events.
|
Academic Article
|
Acute myeloid leukemia with t(8;16)(p11.2;p13.3)/KAT6A-CREBBP in adults.
|
Academic Article
|
Acute myeloid leukemia with t(8;21)(q22;q22.1)/RUNX1-RUNX1T1 and KIT Exon 8 mutation is associated with characteristic mastocytosis and dismal outcomes.
|
Academic Article
|
Homogeneously staining region (hsr) on chromosome 11 is highly specific for KMT2A amplification in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS).
|
Academic Article
|
t(11;16)(q23;p13)/KMT2A-CREBBP in hematologic malignancies: presumptive evidence of myelodysplasia or therapy-related neoplasm?
|
Academic Article
|
iAMP21 in acute myeloid leukemia is associated with complex karyotype, TP53 mutation and dismal outcome.
|
Academic Article
|
T(6;14)(q25;q32) involves BCL11B and is highly associated with mixed-phenotype acute leukemia, T/myeloid.
|
Academic Article
|
Myeloid neoplasms associated with t(3;12)(q26.2;p13) are clinically aggressive, show myelodysplasia, and frequently harbor chromosome 7 abnormalities.
|
Academic Article
|
Myelodysplastic syndrome with t(6;9)(p22;q34.1)/DEK-NUP214 better classified as acute myeloid leukemia? A multicenter study of 107 cases.
|
Academic Article
|
Concurrent TP53 Mutation and Deletion in Refractory Low-grade Follicular Lymphoma.
|
Academic Article
|
Analytical and clinical performance of chromosomal microarrays compared with FISH panel and conventional karyotyping in patients with chronic lymphocytic leukemia.
|
Academic Article
|
3'CBFB deletion in CBFB-rearranged acute myeloid leukemia retains morphological features associated with inv(16), but patients have higher risk of relapse and may require stem cell transplant.
|