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Lista de obras de Rhett P Ketterling

"Cryptic" dinucleotide polymorphism in the 3' region of the factor IX gene shows substantial variation among different populations

scientific article published on 01 March 1994

'Idiopathic' eosinophilia with an Occult T-cell clone: prevalence and clinical course

artículo científico publicado en 2006

A case of hairy cell leukemia with CCND1-IGH@ translocation: indolent non-nodal mantle cell lymphoma revisited

artículo científico publicado en 2011

A case of nonleukemic myeloid sarcoma with FIP1L1-PDGFRA rearrangement: an unusual presentation of a rare disease.

artículo científico publicado en 2013

A compendium of cytogenetic abnormalities in myelofibrosis: molecular and phenotypic correlates in 826 patients

artículo científico publicado en 2014

A leukemic presentation of a "triple-hit" lymphoma

artículo científico publicado en 2014

A novel report of cig-FISH and cytogenetics in POEMS syndrome.

artículo científico publicado en 2008

ALK-1 protein expression and ALK gene rearrangements aid in the diagnosis of inflammatory myofibroblastic tumors of the female genital tract

artículo científico publicado en 2012

ALK-negative anaplastic large cell lymphoma is a genetically heterogeneous disease with widely disparate clinical outcomes.

artículo científico publicado en 2014

ASXL1 and CBL mutations are independently predictive of inferior survival in advanced systemic mastocytosis

artículo científico publicado en 2015

ASXL1 and SETBP1 mutations and their prognostic contribution in chronic myelomonocytic leukemia: a two-center study of 466 patients.

artículo científico publicado en 2014

Abnormal FISH in patients with immunoglobulin light chain amyloidosis is a risk factor for cardiac involvement and for death.

artículo científico publicado en 2015

Absence of somatic mosaicism in 17 families with hemophilia B: an analysis with a sensitivity 10- to 1000-fold greater than that of sequencing gels.

artículo científico publicado en 1996

An MLL-SEPT9 fusion and t(11;17)(q23;q25) associated with de novo myelodysplastic syndrome.

artículo científico publicado en 2007

Analysis of HER2 gene amplification using an automated fluorescence in situ hybridization signal enumeration system.

artículo científico publicado en 2007

Analysis of genetic abnormalities provides insights into genetic evolution of hyperdiploid myeloma

article

Analysis of intratumoral heterogeneity and amplification status in breast carcinomas with equivocal (2+) HER-2 immunostaining

artículo científico publicado en 2005

Atypical generalized eruptive histiocytosis clonally related to chronic myelomonocytic leukemia with loss of Y chromosome

artículo científico publicado en 2013

Autologous transplantation gives encouraging results for young adults with favorable-risk acute myeloid leukemia, but is not improved with gemtuzumab ozogamicin ⬇️

artículo científico publicado el 17 de marzo de 2011

Automated Duet spot counting system and manual technologist scoring using dual-fusion fluorescence in situ hybridization (D-FISH) strategy: comparison and application to FISH minimal residual disease testing in patients with chronic myeloid leukemia

artículo científico publicado en 2007

Azacitidine with or without Entinostat for the treatment of therapy-related myeloid neoplasm: further results of the E1905 North American Leukemia Intergroup study.

artículo científico publicado en 2015

Blast transformation in chronic myelomonocytic leukemia: Risk factors, genetic features, survival, and treatment outcome

artículo científico publicado en 2015

Bone marrow JAK2V617F allele burden and clinical correlates in polycythemia vera

artículo científico publicado en 2007

C-MYC alterations and association with patient outcome in early-stage HER2-positive breast cancer from the north central cancer treatment group N9831 adjuvant trastuzumab trial.

artículo científico publicado en 2011

CALR and ASXL1 mutations-based molecular prognostication in primary myelofibrosis: an international study of 570 patients

artículo científico publicado en 2014

CALR vs JAK2 vs MPL-mutated or triple-negative myelofibrosis: clinical, cytogenetic and molecular comparisons

artículo científico publicado en 2014

CCND1 rearrangements and cyclin D1 overexpression in renal oncocytomas: frequency, clinicopathologic features, and utility in differentiation from chromophobe renal cell carcinoma

artículo científico publicado en 2009

CD36-positive B-lymphoblasts Predict Poor Outcome in Children With B-lymphoblastic Leukemia.

artículo científico publicado en 2017

CHIC2 deletion, a surrogate for FIP1L1-PDGFRA fusion, occurs in systemic mastocytosis associated with eosinophilia and predicts response to imatinib mesylate therapy

artículo científico publicado en 2003

CSF3R T618I is a highly prevalent and specific mutation in chronic neutrophilic leukemia.

artículo científico publicado en 2013

Change in Pattern of HER2 Fluorescent in Situ Hybridization (FISH) Results in Breast Cancers Submitted for FISH Testing: Experience of a Reference Laboratory Using US Food and Drug Administration Criteria and American Society of Clinical Oncology an

artículo científico publicado en 2016

Chromosomal rearrangements and copy number abnormalities of TP63 correlate with p63 protein expression in lung adenocarcinoma.

artículo científico publicado en 2014

Chromosomal rearrangements of 6p25.3 define a new subtype of lymphomatoid papulosis

artículo científico publicado en 2013

Chromosome 5q deletion: specific diagnoses and cytogenetic details among 358 consecutive cases from a single institution

artículo científico publicado en 2007

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

artículo científico publicado en 2009

Chronic lymphocytic leukemia with t(14;19)(q32;q13) is characterized by atypical morphologic and immunophenotypic features and distinctive genetic features.

artículo científico publicado en 2011

Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome

artículo científico publicado en 2015

Chronic myelomonocytic leukemia in younger patients: molecular and cytogenetic predictors of survival and treatment outcome

artículo científico publicado en 2015

Clinical characteristics and treatment outcomes of newly diagnosed multiple myeloma with chromosome 1q abnormalities

artículo científico publicado en 2020

Clinicopathologic and genetic characterization of follicular lymphomas presenting in the ovary reveals 2 distinct subgroups

artículo científico publicado en 2011

Clonal relationship between precursor B-cell acute lymphoblastic leukemia and histiocytic sarcoma: a case report and discussion in the context of similar cases

artículo científico publicado en 2009

Clonally related follicular lymphomas and Langerhans cell neoplasms: expanding the spectrum of transdifferentiation

artículo científico publicado en 2013

Comparison of fluorescence in situ hybridization, p57 immunostaining, flow cytometry, and digital image analysis for diagnosing molar and nonmolar products of conception.

artículo científico publicado en 2010

Concomitant myelodysplastic syndrome and chronic myeloid leukaemia: treatment outcomes with imatinib mesylate.

artículo científico publicado en 2003

Concurrent activating KIT mutations in systemic mastocytosis

artículo científico publicado en 2015

Conventional karyotyping and fluorescence in situ hybridization: an effective utilization strategy in diagnostic adult acute myeloid leukemia

artículo científico publicado en 2015

Correlation of CYP2B6, CYP2C19, ABCC4 and SOD2 genotype with outcomes in allogeneic blood and marrow transplant patients

artículo científico publicado en 2011

Cutaneous extramedullary plasmacytoma: clinical, prognostic, and interphase cytogenetic analysis.

artículo científico publicado en 2013

Cytogenetic abnormalities in essential thrombocythemia: prevalence and prognostic significance

artículo científico publicado en 2009

Cytogenetic abnormalities in multiple myeloma: association with disease characteristics and treatment response

artículo científico publicado en 2020

Cytogenetic studies at diagnosis in polycythemia vera: clinical and JAK2V617F allele burden correlates

artículo científico publicado en 2007

DNMT3A mutations are associated with inferior overall and leukemia-free survival in chronic myelomonocytic leukemia

artículo científico publicado en 2016

DUSP22 and TP63 rearrangements predict outcome of ALK-negative anaplastic large cell lymphoma: a Danish cohort study.

artículo científico publicado en 2017

Deletion 5q is frequent in myelodysplastic syndrome (MDS) patients diagnosed with interstitial lung diseases (ILD): Mayo Clinic experience

artículo científico publicado en 2016

Deletions with inversions: report of a mutation and review of the literature.

artículo científico publicado en 1993

Desmoplastic small round cell tumor of the central nervous system: report of two cases and review of the literature

artículo científico publicado en 2009

Development of a D-FISH method to detect DEK/CAN fusion resulting from t(6;9)(p23;q34) in patients with acute myelogenous leukemia.

artículo científico

Development of a dual-color, double fusion FISH assay to detect RPN1/EVI1 gene fusion associated with inv(3), t(3;3), and ins(3;3) in patients with myelodysplasia and acute myeloid leukemia

artículo científico publicado en 2010

Development of an NPM1/MLF1 D-FISH probe set for the detection of t(3;5)(q25;q35) identified in patients with acute myeloid leukemia

artículo científico publicado en 2014

Development of five dual-color, double-fusion fluorescence in situ hybridization assays for the detection of common MLL translocation partners

artículo científico publicado en 2010

Diagnosis and Management of Waldenström Macroglobulinemia: Mayo Stratification of Macroglobulinemia and Risk-Adapted Therapy (mSMART) Guidelines 2016.

artículo científico publicado en 2017

Differences in the distribution of cytogenetic subtypes between multiple myeloma patients with and without a family history of monoclonal gammopathy and multiple myeloma

artículo científico publicado en 2013

Differential prognostic effect of IDH1 versus IDH2 mutations in myelodysplastic syndromes: a Mayo Clinic Study of 277 patients ⬇️

artículo científico publicado el 28 de octubre de 2011

Dysgranulopoiesis is an independent adverse prognostic factor in chronic myeloid disorders with an isolated interstitial deletion of chromosome 5q

artículo científico publicado en 2008

Epidemiology of adult acute myeloid leukemia: Impact of exposures on clinical phenotypes and outcomes after therapy

artículo científico publicado en 2015

Establishment and characterization of a novel Waldenstrom macroglobulinemia cell line, MWCL-1.

artículo científico publicado en 2011

Evaluation of a commercially available focused aCGH platform for the detection of constitutional chromosome anomalies

artículo científico publicado en 2007

Evaluation of revised IPSS cytogenetic risk stratification and prognostic impact of monosomal karyotype in 783 patients with primary myelodysplastic syndromes

artículo científico publicado en 2013

Evidence for cytogenetic and fluorescence in situ hybridization risk stratification of newly diagnosed multiple myeloma in the era of novel therapie

artículo científico publicado en 2010

Expression of p63 protein in anaplastic large cell lymphoma: implications for genetic subtyping

artículo científico publicado en 2017

Expression of the chemokine receptor gene, CCR8, is associated With DUSP22 rearrangements in anaplastic large cell lymphoma

artículo científico publicado en 2014

Extending Jak2V617F and MplW515 mutation analysis to single hematopoietic colonies and B and T lymphocytes

artículo científico publicado en 2007

FISH identifies a KAT6A/CREBBP fusion caused by a cryptic insertional t(8;16) in a case of spontaneously remitting congenital acute myeloid leukemia with a normal karyotype

artículo científico publicado en 2017

Failure of front-line autologous transplant in anaplastic lymphoma kinase-positive diffuse large B-cell lymphoma

artículo científico publicado en 2010

Familial 22q11.2 deletions in DiGeorge/velocardiofacial syndrome are predominantly smaller than the commonly observed 3Mb

artículo científico publicado en 2004

Functioning Paraganglioma and Gastrointestinal Stromal Tumor of the Jejunum in Three Women

article

Gender and survival in essential thrombocythemia: A two-center study of 1,494 patients

artículo científico

Genome-wide analysis reveals recurrent structural abnormalities of TP63 and other p53-related genes in peripheral T-cell lymphomas.

artículo científico publicado en 2012

Germline mutations in the factor IX gene: a comparison of the pattern in Caucasians and non-Caucasians.

artículo científico publicado en 1993

Haemophilia B Brandenberg-type promoter mutation.

artículo científico publicado en 1999

High hyperdiploidy among adolescents and adults with acute lymphoblastic leukaemia (ALL): cytogenetic features, clinical characteristics and outcome.

artículo científico publicado en 2013

Histiocytoid Sweet syndrome may indicate leukemia cutis: a novel application of fluorescence in situ hybridization

scientific article published on 14 March 2014

Histologic and immunohistochemical study of bone marrow monocytic nodules in 21 cases with myelodysplasia

artículo científico publicado en 2003

How precisely can data from transgenic mouse mutation-detection systems be extrapolated to humans?: lesions from the human factor IX gene.

artículo científico publicado en 1994

IDH mutations and trisomy 8 in myelodysplastic syndromes and acute myeloid leukemia ⬇️

artículo científico publicado el 23 de septiembre de 2010

Image analysis of HER2 immunohistochemical staining. Reproducibility and concordance with fluorescence in situ hybridization of a laboratory-validated scoring technique

artículo científico publicado en 2012

Impact of Alemtuzumab Therapy and Route of Administration in T-Prolymphocytic Leukemia: A Single-Center Experience.

artículo científico publicado en 2015

Impact of American Society of Clinical Oncology/College of American Pathologists guideline recommendations on HER2 interpretation in breast cancer

artículo científico publicado en 2009

Impact of acquired del(17p) in multiple myeloma

artículo científico publicado en 2019

Implications of MYC Rearrangements in Newly Diagnosed Multiple Myeloma

artículo científico publicado en 2020

Interphase FISH to detect PBX1/E2A fusion resulting from the der(19)t(1;19)(q23;p13.3) or t(1;19)(q23;p13.3) in paediatric patients with acute lymphoblastic leukaemia

artículo científico publicado en 2005

Interphase fluorescence in situ hybridization in untreated AL amyloidosis has an independent prognostic impact by abnormality type and treatment category

artículo científico publicado en 2016

Intralymphatic cutaneous anaplastic large cell lymphoma/lymphomatoid papulosis: expanding the spectrum of CD30-positive lymphoproliferative disorders.

artículo científico publicado en 2014

Is It Time for a New Gold Standard? FISH vs Cytogenetics in AML Diagnosis.

artículo científico publicado en 2016

Isochromosome 12p and polysomy 12 in primary central nervous system germ cell tumors: frequency and association with clinicopathologic features

artículo científico publicado en 2009

Isolated del(5q) in myeloid malignancies: clinicopathologic and molecular features in 143 consecutive patients.

artículo científico publicado en 2011

Isolated trisomy 15: a clonal chromosome abnormality in bone marrow with doubtful hematologic significance.

artículo científico publicado en 2008

Karyotype complements the International Prognostic Scoring System for primary myelofibrosis

artículo científico publicado en 2008

LMO2 Is a Specific Marker of T-Lymphoblastic Leukemia/Lymphoma.

artículo científico publicado en 2016

Lenalidomide therapy in del(5)(q31)-associated myelofibrosis: cytogenetic and JAK2V617F molecular remissions

artículo científico publicado en 2007

Lenalidomide therapy in myelofibrosis with myeloid metaplasia

artículo científico publicado en 2006

Leukemic transformation in myelofibrosis with myeloid metaplasia: a single-institution experience with 91 cases

artículo científico publicado en 2004

Long-term follow-up of FIP1L1-PDGFRA-mutated patients with eosinophilia: survival and clinical outcome.

artículo científico publicado en 2012

Long-term survival and blast transformation in molecularly annotated essential thrombocythemia, polycythemia vera, and myelofibrosis

artículo científico publicado en 2014

Mantle cell lymphoma with a novel t(11;12)(q13;p11.2): a proposed alternative mechanism of CCND1 up-regulation

artículo científico publicado en 2017

Mayo prognostic model for WHO-defined chronic myelomonocytic leukemia: ASXL1 and spliceosome component mutations and outcomes ⬇️

artículo científico publicado el 27 de marzo de 2013

Metaphase cytogenetics and plasma cell proliferation index for risk stratification in newly diagnosed multiple myeloma

artículo científico publicado en 2020

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

artículo científico publicado en 2003

Microgranular variant of acute promyelocytic leukemia with normal conventional cytogenetics, negative PML/RARA FISH and positive PML/RARA transcripts by RT-PCR.

artículo científico publicado en 2011

Molecular and prognostic correlates of cytogenetic abnormalities in chronic myelomonocytic leukemia: a Mayo Clinic-French Consortium Study.

artículo científico publicado en 2014

Molecular correlates of anemia in primary myelofibrosis: a significant and independent association with U2AF1 mutations

artículo científico publicado en 2016

Monocytosis in polycythemia vera: Clinical and molecular correlates.

artículo científico publicado en 2017

Morphologic Features of ALK-negative Anaplastic Large Cell Lymphomas With DUSP22 Rearrangements

artículo científico publicado en 2015

Morphologically occult systemic mastocytosis in bone marrow: clinicopathologic features and an algorithmic approach to diagnosis

artículo científico publicado en 2015

Mutational analysis of candidate tumor-associated genes in acute megakaryoblastic leukemia

artículo científico publicado en 2009

Mutations and thrombosis in essential thrombocythemia: prognostic interaction with age and thrombosis history.

artículo científico publicado en 2014

Natural history of multiple myeloma with de novo del(17p)

scholarly article by Arjun Lakshman et al published 7 March 2019 in Blood Cancer Journal

Nearly identical near-haploid karyotype in a peritoneal mesothelioma and a retroperitoneal malignant peripheral nerve sheath tumor.

artículo científico publicado en 2010

New highly sensitive fluorescence in situ hybridization method to detect PML/RARA fusion in acute promyelocytic leukemia

artículo científico publicado en 2003

Novel FISH probes designed to detect IGK-MYC and IGL-MYC rearrangements in B-cell lineage malignancy identify a new breakpoint cluster region designated BVR2.

artículo científico

Nucleophosmin 1 (NPM1) mutations in chronic myelomonocytic leukemia and their prognostic relevance

artículo científico publicado en 2017

Occurrence and prognostic significance of cytogenetic evolution in patients with multiple myeloma

artículo científico publicado en 2016

Overexpression of IL-1 receptor accessory protein in stem and progenitor cells and outcome correlation in AML and MDS.

artículo científico publicado en 2012

Peripheral blood cytogenetic studies in hematological neoplasms: predictors of obtaining metaphases for analysis

artículo científico publicado en 2007

Peripheral blood cytogenetic studies in myelofibrosis: overall yield and comparison with bone marrow cytogenetic studies

artículo científico publicado en 2008

Philadelphia chromosome mosaicism at diagnosis in chronic myeloid leukemia: clinical correlates and effect on imatinib mesylate treatment outcome

artículo científico publicado en 2007

Pituitary blastoma

artículo científico publicado en 2008

Polyclonal immunoglobulin free light chain levels predict survival in myeloid neoplasms

artículo científico publicado en 2012

Preclinical validation of fluorescence in situ hybridization assays for clinical practice

artículo científico publicado en 2006

Predictors of survival in WHO-defined hypereosinophilic syndrome and idiopathic hypereosinophilia and the role of next-generation sequencing

artículo científico publicado en 2016

Prefibrotic versus overtly fibrotic primary myelofibrosis: clinical, cytogenetic, molecular and prognostic comparisons.

artículo científico publicado en 2017

Primary Myelodysplastic Syndromes: The Mayo Clinic Experience With 1000 Patients

artículo científico publicado en 2015

Primary myelodysplastic syndrome with normal cytogenetics: utility of 'FISH panel testing' and M-FISH.

artículo científico publicado en 2002

Primary myelofibrosis is the most frequent myeloproliferative neoplasm associated with del(5q): clinicopathologic comparison of del(5q)-positive and -negative cases

artículo científico publicado en 2008

Prognostic implications of abnormalities of chromosome 13 and the presence of multiple cytogenetic high-risk abnormalities in newly diagnosed multiple myeloma

artículo científico publicado en 2017

Prognostic irrelevance of ring sideroblast percentage in World Health Organization-defined myelodysplastic syndromes without excess blasts.

artículo científico publicado en 2012

Prognostic significance of interphase FISH in monoclonal gammopathy of undetermined significance

scientific article published on 30 January 2018

Prognostic value of chromosome 1q21 gain by fluorescent in situ hybridization and increase CKS1B expression in myeloma

artículo científico publicado en 2006

Prolonged administration of azacitidine with or without entinostat for myelodysplastic syndrome and acute myeloid leukemia with myelodysplasia-related changes: results of the US Leukemia Intergroup trial E1905.

artículo científico publicado en 2014

Racial differences in primary cytogenetic abnormalities in multiple myeloma: a multi-center study

artículo científico publicado en 2015

Racial differences in primary cytogenetic abnormalities in multiple myeloma: a multi-center study

scientific article published on 13 February 2015

Rapid assessment of hyperdiploidy in plasma cell disorders using a novel multi-parametric flow cytometry method

scientific article published on 08 January 2019

Rearrangements and amplification of IER3 (IEX-1) represent a novel and recurrent molecular abnormality in myelodysplastic syndromes.

artículo científico publicado en 2009

Reflex fluorescent in situ hybridization testing for unsuccessful product of conception cultures: a retrospective analysis of 5555 samples attempted by conventional cytogenetics and fluorescent in situ hybridization

artículo científico publicado en 2011

Relationship of patient survival and chromosome anomalies detected in metaphase and/or interphase cells at diagnosis of myeloma.

artículo científico publicado en 2005

Revisiting the need for bone marrow examination in chronic myeloid leukemia

artículo científico publicado en 2017

Risk factors and a prognostic model for postsplenectomy survival in myelofibrosis

artículo científico publicado en 2017

Rosette-forming glioneuronal tumor: report of a chiasmal-optic nerve example in neurofibromatosis type 1: special pathology report

artículo científico publicado en 2009

SETBP1 mutations in 415 patients with primary myelofibrosis or chronic myelomonocytic leukemia: independent prognostic impact in CMML ⬇️

artículo científico publicado el 5 de abril de 2013

SF3B1 mutations are prevalent in myelodysplastic syndromes with ring sideroblasts but do not hold independent prognostic value

artículo científico publicado en 2011

SF3B1 mutations in primary myelofibrosis: clinical, histopathology and genetic correlates among 155 patients

scientific article published on 08 November 2011

SRSF2 mutations in primary myelofibrosis: significant clustering with IDH mutations and independent association with inferior overall and leukemia-free survival

artículo científico publicado en 2012

Section E9 of the American College of Medical Genetics technical standards and guidelines: fluorescence in situ hybridization

artículo científico publicado en 2011

Somatic rearrangement of the TP63 gene preceding development of mycosis fungoides with aggressive clinical course.

artículo científico publicado en 2014

Spectrum of autoimmune diseases and systemic inflammatory syndromes in patients with chronic myelomonocytic leukemia

artículo científico publicado en 2016

Spliceosome mutations involving SRSF2, SF3B1, and U2AF35 in chronic myelomonocytic leukemia: prevalence, clinical correlates, and prognostic relevance

artículo científico publicado en 2013

Substratification of patients with newly diagnosed standard-risk multiple myeloma

scientific article published on 15 February 2019

Successful treatment of a child with T/myeloid acute bilineal leukemia associated with TLX3/BCL11B fusion and 9q deletion.

artículo científico publicado en 2010

Sustained remission in a patient with myelodysplastic syndrome and a complex karyotype after erythropoiesis-stimulating therapy followed by colonic T-cell lymphoblastic lymphoma

artículo científico publicado en 2012

T-cell acute lymphoblastic leukemia in adults: clinical features, immunophenotype, cytogenetics, and outcome from the large randomized prospective trial (UKALL XII/ECOG 2993)

artículo científico publicado en 2009

T296----M, a common mutation causing mild hemophilia B in the Amish and others: founder effect, variability in factor IX activity assays, and rapid carrier detection.

artículo científico publicado en 1991

TP53 mutations and polymorphisms in primary myelofibrosis

scientific article published on 04 November 2011

Targeted next generation sequencing and identification of risk factors in World Health Organization defined atypical chronic myeloid leukemia.

artículo científico publicado en 2017

Targeted next-generation sequencing in myelodysplastic syndromes and prognostic interaction between mutations and IPSS-R.

artículo científico publicado en 2017

Tetraploidy is associated with poor prognosis at diagnosis in multiple myeloma

scientific article published on 06 February 2019

The 2016 revised World Health Organization definition of 'myelodysplastic syndrome with isolated del(5q)'; prognostic implications of single versus double cytogenetic abnormalities

artículo científico publicado en 2017

The B cell antigen receptor in atypical chronic lymphocytic leukemia with t(14;19)(q32;q13) demonstrates remarkable stereotypy

scientific article published on 26 October 2010

The number of prognostically detrimental mutations and prognosis in primary myelofibrosis: an international study of 797 patients

scientific article published on 19 February 2014

The oncogenic transcription factor IRF4 is regulated by a novel CD30/NF-κB positive feedback loop in peripheral T-cell lymphoma

artículo científico publicado en 2015

Therapy related-chronic myelomonocytic leukemia (CMML): Molecular, cytogenetic, and clinical distinctions from de novo CMML.

artículo científico publicado en 2017

Translocation t(11;14) and survival of patients with light chain (AL) amyloidosis.

artículo científico publicado en 2009

Treatment-influenced associations of PML-RARα mutations, FLT3 mutations, and additional chromosome abnormalities in relapsed acute promyelocytic leukemia

artículo científico publicado en 2012

Trisomies in multiple myeloma: impact on survival in patients with high-risk cytogenetics

artículo científico publicado en 2012

Trisomy 11: prevalence among 22,403 unique patient cytogenetic studies and clinical correlates

artículo científico publicado en 2010

Two novel factor IX promoter mutations: incremental progress towards 'saturation in vivo mutagenesis' of a human promoter region.

artículo científico publicado en 1995

Type 1 versus Type 2 calreticulin mutations in essential thrombocythemia: a collaborative study of 1027 patients

artículo científico publicado en 2014

Type 1 vs type 2 calreticulin mutations in primary myelofibrosis: differences in phenotype and prognostic impact.

artículo científico publicado en 2014

Utility of ALK-1 protein expression and ALK rearrangements in distinguishing inflammatory myofibroblastic tumor from malignant spindle cell lesions of the urinary bladder

artículo científico publicado en 2007

Utility of peripheral blood dual color, double fusion fluorescent in situ hybridization for BCR/ABL fusion to assess cytogenetic remission status in chronic myeloid leukemia

artículo científico publicado en 2006

Utility of subtelomeric fluorescent DNA probes for detection of chromosome anomalies in 425 patients

artículo científico publicado en 2003

Validation of a new three-color fluorescence in situ hybridization (FISH) method to detect CHIC2 deletion, FIP1L1/PDGFRA fusion and PDGFRA translocations

artículo científico publicado en 2008

Vascular events and risk factors for thrombosis in refractory anemia with ring sideroblasts and thrombocytosis

artículo científico publicado en 2016

When are apparently non-clonal abnormalities in bone marrow chromosome studies actually clonal?

artículo científico publicado en 2012

Whole-exome analysis reveals novel somatic genomic alterations associated with outcome in immunochemotherapy-treated diffuse large B-cell lymphoma.

artículo científico publicado en 2015

t(8;9)(p22;p24)/PCM1-JAK2 activates SOCS2 and SOCS3 via STAT5.

artículo científico publicado en 2013

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