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Lista de obras de M J Calasanz

A new case of acute lymphoblastic leukemia B-cell type with chromosomal rearrangements involving the T-cell receptor breakpoint at band 14q11

artículo científico publicado en 1992

A new potential oncogenic mutation in the FERM domain of JAK2 in BCR/ABL1-negative and V617F-negative chronic myeloproliferative neoplasms revealed by a comprehensive screening of 17 tyrosine kinase coding genes.

artículo científico publicado en 2010

A variant t(14;17) in acute promyelocytic leukemia. Positive response to retinoic acid treatment

scientific article published on 01 April 1995

ASPP1, a common activator of TP53, is inactivated by aberrant methylation of its promoter in acute lymphoblastic leukemia.

artículo científico publicado en 2006

Aberrant DNA methylation profile of chronic and transformed classic Philadelphia-negative myeloproliferative neoplasms.

artículo científico publicado en 2013

Abnormalities on 1q and 7q are associated with poor outcome in sporadic Burkitt's lymphoma. A cytogenetic and comparative genomic hybridization study

artículo científico publicado en 2003

Additional chromosome abnormalities in patients with acute promyelocytic leukemia treated with all-trans retinoic acid and chemotherapy.

artículo científico publicado en 2009

Alpha CP-4, encoded by a putative tumor suppressor gene at 3p21, but not its alternative splice variant alpha CP-4a, is underexpressed in lung cancer.

artículo científico publicado en 2004

Amplification of ERBB2, RARA, and TOP2A genes in a myelodysplastic syndrome transforming to acute myeloid leukemia.

artículo científico publicado en 2001

Amplification of IGH/MYC fusion in clinically aggressive IGH/BCL2-positive germinal center B-cell lymphomas.

artículo científico publicado en 2005

Analysis of myelodysplastic syndromes with complex karyotypes by high-resolution comparative genomic hybridization and subtelomeric CGH array

artículo científico publicado en 2005

Array comparative genomic hybridization analysis of myelodysplastic syndromes with complex karyotypes. A technical evaluation

scientific article published on 01 July 2003

Assessment of Minimal Residual Disease by Next Generation Sequencing in Peripheral Blood as a Complementary Tool for Personalized Transplant Monitoring in Myeloid Neoplasms

scientific article published on 25 November 2020

Biallelic losses of 13q do not confer a poorer outcome in chronic lymphocytic leukaemia: analysis of 627 patients with isolated 13q deletion

article

CBL RING finger deletions are common in core-binding factor acute myeloid leukemias.

artículo científico publicado en 2012

CIP2A high expression is a poor prognostic factor in normal karyotype acute myeloid leukemia.

artículo científico publicado en 2015

Characterization and prognostic implication of 17 chromosome abnormalities in myelodysplastic syndrome.

artículo científico publicado en 2013

Chromatin modifications induced by the AML1-ETO fusion protein reversibly silence its genomic targets through AML1 and Sp1 binding motifs.

artículo científico publicado en 2012

Chromosomal abnormalities clustering in multiple myeloma reveals cytogenetic subgroups with nonrandom acquisition of chromosomal changes

artículo científico publicado en 2004

Clinical variability of patients with the t(6;8)(q27;p12) and FGFR1OP-FGFR1 fusion: two further cases.

artículo científico publicado en 2004

Coexistence of different clonal populations harboring the b3a2 (p210) and e1a2 (p190) BCR-ABL1 fusion transcripts in chronic myelogenous leukemia resistant to imatinib.

artículo científico publicado en 2005

Comparative genomic hybridization and amplotyping by arbitrarily primed PCR in stage A B-CLL

artículo científico publicado en 2001

Complex karyotype including 14q+ marker in a case of Waldenström's macroglobulinemia

scientific article published on 01 April 1994

Correlation of myelodysplastic syndromes with i(17)(q10) andTP53andSETBP1mutations

artículo científico publicado en 2015

CpG island methylator phenotype redefines the prognostic effect of t(12;21) in childhood acute lymphoblastic leukemia

scientific article published on 01 August 2006

Cryptic ins(2;11) with clonal evolution showing amplification of 11q23-q25 either on hsr(11) or on dmin, in a patient with AML-M2.

artículo científico publicado en 2004

Cytogenetic aberrations and their prognostic value in a series of 330 splenic marginal zone B-cell lymphomas: a multicenter study of the Splenic B-Cell Lymphoma Group.

artículo científico publicado en 2010

Cytogenetic and molecular characterization of a patient with simultaneous B-cell chronic lymphocytic leukemia and peripheral T-cell lymphoma

artículo científico publicado en 2001

Cytogenetic marker del(12p) in a case of acute myeloid leukemia M4 with eosinophilia and inv(16)

artículo científico publicado el 1 de abril de 1992

Cytogenetic patterns in 384 northern-Spanish patients with haematological disorders

artículo científico publicado en 1993

Cytogenetic profile of myelodysplastic syndromes with complex karyotypes: an analysis using spectral karyotyping

artículo científico publicado en 2004

Cytogenetic risk stratification in chronic myelomonocytic leukemia.

artículo científico publicado en 2010

De novo erythroleukemia chromosome features include multiple rearrangements, with special involvement of chromosomes 11 and 19.

artículo científico

Double minute chromosomes and monosomy 7 in a lymphatic blast crisis of chronic myeloid leukemia.

artículo científico publicado en 1990

Downregulation of DBC1 expression in acute lymphoblastic leukaemia is mediated by aberrant methylation of its promoter

artículo científico publicado en 2006

Downregulation of specific miRNAs in hyperdiploid multiple myeloma mimics the oncogenic effect of IgH translocations occurring in the non-hyperdiploid subtype.

artículo científico publicado en 2012

EVI1 controls proliferation in acute myeloid leukaemia through modulation of miR-1-2

artículo científico publicado en 2010

Epigenetic activation of SOX11 in lymphoid neoplasms by histone modifications.

artículo científico publicado en 2011

Exome sequencing reveals novel and recurrent mutations with clinical impact in blastic plasmacytoid dendritic cell neoplasm

artículo científico publicado en 2013

FISH analysis of hematological neoplasias with 1p36 rearrangements allows the definition of a cluster of 2.5 Mb included in the minimal region deleted in 1p36 deletion syndrome

artículo científico publicado en 2005

Fluorescencein situhybridization analysis does not increase detection rate for trisomy 8 in chronic myelomonocytic leukemia

artículo científico publicado en 2014

Frequent gain of chromosome 19 in megakaryoblastic leukemias detected by comparative genomic hybridization.

artículo científico publicado en 2001

Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia

article

Functional characterization of the promoter region of the human EVI1 gene in acute myeloid leukemia: RUNX1 and ELK1 directly regulate its transcription.

artículo científico publicado en 2012

Further characterization of complex chromosomal rearrangements in myeloid malignancies: spectral karyotyping adds precision in defining abnormalities associated with poor prognosis.

artículo científico publicado en 2001

Genomic imbalances detected by comparative genomic hybridization are prognostic markers in invasive ductal breast carcinomas.

artículo científico publicado en 2002

Geographic differences in the incidence of cytogenetic abnormalities of acute myelogenous leukemia (AML) in Spain

article

Heterogeneity of structural abnormalities in the 7q31.3∼q34 region in myeloid malignancies

artículo científico publicado en 2004

High-throughput sequencing analysis of the chromosome 7q32 deletion reveals IRF5 as a potential tumour suppressor in splenic marginal-zone lymphoma.

artículo científico publicado en 2012

Homeobox NKX2-3 promotes marginal-zone lymphomagenesis by activating B-cell receptor signalling and shaping lymphocyte dynamics

artículo científico publicado en 2016

Hypermethylation of the alternative AWT1 promoter in hematological malignancies is a highly specific marker for acute myeloid leukemias despite high expression levels.

artículo científico publicado en 2014

Hypodiploidy and 22q11 rearrangements at diagnosis are associated with poor prognosis in patients with multiple myeloma

artículo científico publicado en 1997

Identification of recurrent chromosomal breakpoints in multiple myeloma with complex karyotypes by combined G-banding, spectral karyotyping, and fluorescence in situ hybridization analyses

artículo científico publicado en 2006

Impact of adjunct cytogenetic abnormalities for prognostic stratification in patients with myelodysplastic syndrome and deletion 5q

artículo científico publicado en 2010

Incidence and prognostic impact of secondary cytogenetic aberrations in a series of 145 patients with mantle cell lymphoma.

artículo científico publicado en 2010

Interphase FISH assays for the detection of translocations with breakpoints in immunoglobulin light chain loci

artículo científico publicado en 2002

Interphase FISH for the detection of breakpoints in IG loci and chromosomal changes with adverse prognostic impact in multiple myeloma with normal karyotypes

artículo científico publicado en 2006

Interstitial 13q14 deletions detected in the karyotype and translocations with concomitant deletion at 13q14 in chronic lymphocytic leukemia: Different genetic mechanisms but equivalent poorer clinical outcome

artículo científico publicado en 2014

JAK2 V617F mutation in classic chronic myeloproliferative diseases: a report on a series of 349 patients

artículo científico publicado en 2006

JAK2-V617F activating mutation in acute myeloid leukemia: prognostic impact and association with other molecular markers

scientific article published on 21 June 2007

LMO2 expression reflects the different stages of blast maturation and genetic features in B-cell acute lymphoblastic leukemia and predicts clinical outcome.

artículo científico publicado en 2011

Lack of association of CYP3A4-V polymorphism with the risk of treatment-related leukemia

artículo científico publicado en 2005

Landscape of somatic mutations and clonal evolution in mantle cell lymphoma.

artículo científico publicado en 2013

Methylation of CpG dinucleotides and/or CCWGG motifs at the promoter of TP53 correlates with decreased gene expression in a subset of acute lymphoblastic leukemia patients

artículo científico publicado en 2003

Molecular characterization of a t(1;3)(p36;q21) in a patient with MDS. MEL1 is widely expressed in normal tissues, including bone marrow, and it is not overexpressed in the t(1;3) cells.

artículo científico publicado en 2004

Molecular cytogenetic characterization of breakpoints in 19 patients with hematologic malignancies and 12p unbalanced translocations

scientific article published on 01 April 2003

Molecular heterogeneity in AML/MDS patients with 3q21q26 rearrangements.

artículo científico publicado en 2004

Molecular profiling of immunoglobulin heavy-chain gene rearrangements unveils new potential prognostic markers for multiple myeloma patients

artículo científico publicado en 2020

Multiple myeloma primary cells show a highly rearranged unbalanced genome with amplifications and homozygous deletions irrespective of the presence of immunoglobulin-related chromosome translocations

artículo científico publicado en 2007

Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression.

artículo científico publicado en 2013

NIN, a gene encoding a CEP110-like centrosomal protein, is fused to PDGFRB in a patient with a t(5;14)(q33;q24) and an imatinib-responsive myeloproliferative disorder

artículo científico publicado en 2004

NPM1 gene deletions in myelodysplastic syndromes with 5q- and complex karyotype ⬇️

artículo científico publicado el 10 de marzo de 2011

Neurofibromatosis 1, and NotTP53, Seems to Be the Main Target of Chromosome 17 Deletions in De Novo Acute Myeloid Leukemia

artículo científico publicado en 2007

Nonclonal Chromosomal Aberrations Induced by Anti-Tumoral Regimens in Childhood Cancer

scientific article published on 01 August 2000

Novel dic(16;18)(q11;p11) in two cases of Philadelphia chromosome positive acute B-cell lymphoblastic leukemia

artículo científico publicado en 2002

Novel translocations that disrupt the platelet-derived growth factor receptor beta (PDGFRB) gene in BCR-ABL-negative chronic myeloproliferative disorders.

artículo científico publicado en 2003

Overexpression of GATA2 predicts an adverse prognosis for patients with acute myeloid leukemia and it is associated with distinct molecular abnormalities.

artículo científico publicado en 2011

PP2A impaired activity is a common event in acute myeloid leukemia and its activation by forskolin has a potent anti-leukemic effect.

artículo científico publicado en 2011

Preclinical activity of LBH589 alone or in combination with chemotherapy in a xenogeneic mouse model of human acute lymphoblastic leukemia.

artículo científico publicado en 2012

Profile of polymorphisms of drug-metabolising enzymes and the risk of therapy-related leukaemia

artículo científico publicado en 2007

Prognostic impact of chromosomal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemia patients. A study by the spanish group of myelodysplastic syndromes.

artículo científico publicado en 2015

Promoter hypermethylation of cancer-related genes: a strong independent prognostic factor in acute lymphoblastic leukemia.

artículo científico publicado en 2004

Reciprocal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemias: review of 5,654 patients with an evaluable karyotype.

artículo científico

Recurrent involvement of the REL and BCL11A loci in classical Hodgkin lymphoma.

artículo científico publicado en 2002

Relationship of disability prevention to patient health status and satisfaction with primary care provider

scientific article published on 01 August 2001

Response to lenalidomide in a patient with myelodysplastic syndrome with isolated del(5q) and JAK2 V617F mutation ⬇️

artículo científico publicado el 1 de octubre de 2010

Response to lenalidomide in myelodysplastic syndromes with del(5q): influence of cytogenetics and mutations.

artículo científico publicado en 2013

Role of MTHFR (677, 1298) haplotype in the risk of developing secondary leukemia after treatment of breast cancer and hematological malignancies

artículo científico publicado en 2007

Secondary myelodysplastic syndrome after treatment for promyelocytic leukemia

artículo científico publicado en 2003

Simultaneous translocations of FGFR3/MMSET and CCND1 into two different IGH alleles in multiple myeloma: lack of concurrent activation of both proto-oncogenes.

artículo científico

TP53is frequently altered by methylation, mutation, and/or deletion in acute lymphoblastic leukaemia

artículo científico publicado en 2003

Targeted resequencing analysis of 31 genes commonly mutated in myeloid disorders in serial samples from myelodysplastic syndrome patients showing disease progression.

artículo científico publicado en 2015

The Minnesota Health Partnership and coordinated health care and disability prevention: the implementation of an integrated benefits and medical care model

artículo científico publicado en 2002

The potential effect of gender in combination with common genetic polymorphisms of drug-metabolizing enzymes on the risk of developing acute leukemia

artículo científico publicado en 2007

The relationship of TP53 R72P polymorphism to disease outcome and TP53 mutation in myelodysplastic syndromes

artículo científico publicado en 2015

Use of human pharyngeal and palatine tonsils as a reservoir for the analysis of B-cell ontogeny in 10 paired samples

artículo científico publicado en 2016

Whole-epigenome analysis in multiple myeloma reveals DNA hypermethylation of B cell-specific enhancers.

artículo científico publicado en 2015

Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia

artículo científico publicado en 2013

p53 Aberrations do not predict individual response to fludarabine in patients with B-cell chronic lymphocytic leukaemia in advanced stages Rai III/IV.

artículo científico publicado en 2005

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