-7/7q- syndrome in myeloid-lineage hematopoietic malignancies: attempts to understand this complex disease entity

https://api.crossref.org/works/10.1038%2FONC.2014.196

Monosomy 7 and 7q- associated with myeloid malignancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Monosomy 7 and deletion 7q in children and adolescents with acute myeloid leukemia: an international retrospective study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Genetics of therapy-related myelodysplasia and acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Cytogenetic and genetic pathways in therapy-related acute myeloid leukemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Cytogenetic abnormalities in myelodysplastic syndrome: an overview

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Genetic analysis of dasatinib-treated chronic myeloid leukemia rapidly developing into acute myeloid leukemia with monosomy 7 in Philadelphia-negative cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Factors influencing a second myeloid malignancy in patients with Philadelphia-negative -7 or del(7q) clones during tyrosine kinase inhibitor therapy for chronic myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Refinement of the international prognostic scoring system (IPSS) by including LDH as an additional prognostic variable to improve risk assessment in patients with primary myelodysplastic syndromes (MDS).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Predicting survival of patients with hypocellular myelodysplastic syndrome: development of a disease-specific prognostic score system

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Structural aberrations of chromosome 7 revealed by a combination of molecular cytogenetic techniques in myeloid malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Evidence for two molecular steps in the pathogenesis of myeloid disorders associated with deletion of chromosome 7 long arm

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Molecular anatomy of chromosome 7q deletions in myeloid neoplasms: evidence for multiple critical loci

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Identification of a common microdeletion cluster in 7q21.3 subband among patients with myeloid leukemia and myelodysplastic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Identification of two critically deleted regions within chromosome segment 7q35-q36 in EVI1 deregulated myeloid leukemia cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Loss of heterozygosity in 7q myeloid disorders: clinical associations and genomic pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

CUX1 is a haploinsufficient tumor suppressor gene on chromosome 7 frequently inactivated in acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Role of histone H3 lysine 27 methylation in Polycomb-group silencing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Drosophila enhancer of Zeste/ESC complexes have a histone H3 methyltransferase activity that marks chromosomal Polycomb sites

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Histone methyltransferase activity of a Drosophila Polycomb group repressor complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

The Polycomb complex PRC2 and its mark in life

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Somatic mutations of the histone methyltransferase gene EZH2 in myelodysplastic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

EZH2 mutations are related to low blast percentage in bone marrow and -7/del(7q) in de novo acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Clinical effect of point mutations in myelodysplastic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Validation of a prognostic model and the impact of mutations in patients with lower-risk myelodysplastic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Prognostic relevance of integrated genetic profiling in acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

A key role for EZH2 and associated genes in mouse and human adult T-cell acute leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Concurrent loss of Ezh2 and Tet2 cooperates in the pathogenesis of myelodysplastic disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Coordinated activities of wild-type plus mutant EZH2 drive tumor-associated hypertrimethylation of lysine 27 on histone H3 (H3K27) in human B-cell lymphomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Somatic mutations at EZH2 Y641 act dominantly through a mechanism of selectively altered PRC2 catalytic activity, to increase H3K27 trimethylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Ectopic expression of the histone methyltransferase Ezh2 in haematopoietic stem cells causes myeloproliferative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Pharmacologic disruption of Polycomb-repressive complex 2-mediated gene repression selectively induces apoptosis in cancer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

EZH2 inhibition as a therapeutic strategy for lymphoma with EZH2-activating mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Human sterile alpha motif domain 9, a novel gene identified as down-regulated in aggressive fibromatosis, is absent in the mouse

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Haploinsufficiency of SAMD9L, an endosome fusion facilitator, causes myeloid malignancies in mice mimicking human diseases with monosomy 7

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

R-Ras regulates exocytosis by Rgl2/Rlf-mediated activation of RalA on endosomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Functional Characterization of SAMD9, a Protein Deficient in Normophosphatemic Familial Tumoral Calcinosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

CUX1 transcription factors: from biochemical activities and cell-based assays to mouse models and human diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

The multiple roles of CUX1: insights from mouse models and cell-based assays

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

CUTL1 is a target of TGF(beta) signaling that enhances cancer cell motility and invasiveness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

WNT5A--target of CUTL1 and potent modulator of tumor cell migration and invasion in pancreatic cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Transcription factor CUTL1 is a negative regulator of drug resistance in gastric cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Transgenic mice expressing the p75 CCAAT-displacement protein/Cut homeobox isoform develop a myeloproliferative disease-like myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Mouse mammary tumor virus p75 and p110 CUX1 transgenic mice develop mammary tumors of various histologic types

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Lymphoid apoptosis and myeloid hyperplasia in CCAAT displacement protein mutant mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Regional localization of the CCAAT displacement protein gene (CUTL1) to 7q22 by analysis of somatic cell hybrids

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Assignment of the human homologue of the Drosophila Cut homeobox gene (CUTL1) to band 7q22 by fluorescence in situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Inactivating CUX1 mutations promote tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Mixed lineage leukemia: roles in gene expression, hormone signaling and mRNA processing.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Enhancer malfunction in cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

High-resolution genomic profiling of adult and pediatric core-binding factor acute myeloid leukemia reveals new recurrent genomic alterations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Frequent mutations of chromatin remodeling genes in transitional cell carcinoma of the bladder

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

The genetic landscape of the childhood cancer medulloblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Identification of genomic alterations in oesophageal squamous cell cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

MLL3, a new human member of the TRX/MLL gene family, maps to 7q36, a chromosome region frequently deleted in myeloid leukaemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

MLL3 is a haploinsufficient 7q tumor suppressor in acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Hierarchical maintenance of MLL myeloid leukemia stem cells employs a transcriptional program shared with embryonic rather than adult stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Deregulated gene expression pathways in myelodysplastic syndrome hematopoietic stem cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Epigenetics in clinical practice: the examples of azacitidine and decitabine in myelodysplasia and acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Aberrant epigenetic and genetic marks are seen in myelodysplastic leukocytes and reveal Dock4 as a candidate pathogenic gene on chromosome 7q

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

DOCK4, a GTPase activator, is disrupted during tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Candidate gene isolation and comparative analysis of a commonly deleted segment of 7q22 implicated in myeloid malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Genomic structure of the PIK3CG gene on chromosome band 7q22 and evaluation as a candidate myeloid tumor suppressor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

MLL5, a homolog of Drosophila trithorax located within a segment of chromosome band 7q22 implicated in myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Isolation and analysis of candidate myeloid tumor suppressor genes from a commonly deleted segment of 7q22.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

The human Penumbra gene is mapped to a region on chromosome 7 frequently deleted in myeloid malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Putative RNA-splicing gene LUC7L2 on 7q34 represents a candidate gene in pathogenesis of myeloid malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Frequent pathway mutations of splicing machinery in myelodysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Cytogenetic abnormalities in a series of 1,029 patients with primary myelodysplastic syndromes: a report from the US with a focus on some undefined single chromosomal abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Better prognosis for patients with del(7q) than for patients with monosomy 7 in myelodysplastic syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Revised international prognostic scoring system for myelodysplastic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Does MDS with der(1;7)(q10;p10) constitute a distinct risk group? A retrospective single institutional analysis of clinical/pathologic features compared to -7/del(7q) MDS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

EVI1 and hematopoietic disorders: history and perspectives

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

The oncogene and developmental regulator EVI1: expression, biochemical properties, and biological functions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Evi1 forms a bridge between the epigenetic machinery and signaling pathways.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

The role of EVI1 in myeloid malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Retroviral activation of a novel gene encoding a zinc finger protein in IL-3-dependent myeloid leukemia cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

RTCGD: retroviral tagged cancer gene database

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Both AML1 and EVI1 oncogenic components are required for the cooperation of AML1/MDS1/EVI1 with BCR/ABL in the induction of acute myelogenous leukemia in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

High EVI1 expression predicts poor survival in acute myeloid leukemia: a study of 319 de novo AML patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

EVI1 overexpression in distinct subtypes of pediatric acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

A novel interaction between the proto-oncogene Evi1 and histone methyltransferases, SUV39H1 and G9a

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

EVI1 recruits the histone methyltransferase SUV39H1 for transcription repression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Regulation of the INK4b-ARF-INK4a tumour suppressor locus: all for one or one for all.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

p15Ink4b Functions in determining hematopoietic cell fates: implications for its role as a tumor suppressor

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Cyclin D-dependent kinases, INK4 inhibitors and cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Limited overlapping roles of P15(INK4b) and P18(INK4c) cell cycle inhibitors in proliferation and tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Loss of p16Ink4a confers susceptibility to metastatic melanoma in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Loss of p16Ink4a with retention of p19Arf predisposes mice to tumorigenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

p15Ink4b is a critical tumour suppressor in the absence of p16Ink4a

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Methylation of p15INK4B is common, is associated with deletion of genes on chromosome arm 7q and predicts a poor prognosis in therapy-related myelodysplasia and acute myeloid leukemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

p15INK4b methylation correlates with thrombocytopenia, blast percentage, and survival in myelodysplastic syndromes in a dose dependent manner: quantitation using pyrosequencing study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Epigenetic changes in therapy-related MDS/AML.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

The RUNX genes: gain or loss of function in cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Normal and transforming functions of RUNX1: a perspective

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

RUNX genes in development and cancer: regulation of viral gene expression and the discovery of RUNX family genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

A role for RUNX1 in hematopoiesis and myeloid leukemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Oncogenic potential of the RUNX gene family: 'overview'.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

AML1, the target of multiple chromosomal translocations in human leukemia, is essential for normal fetal liver hematopoiesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Disruption of the Cbfa2 gene causes necrosis and hemorrhaging in the central nervous system and blocks definitive hematopoiesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

AML1(-/-) embryos do not express certain hematopoiesis-related gene transcripts including those of the PU.1 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

RUNX1 Translocations and Fusion Genes in Malignant Hemopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Point mutations in the RUNX1/AML1 gene: another actor in RUNX leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Expression of a conditional AML1-ETO oncogene bypasses embryonic lethality and establishes a murine model of human t(8;21) acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

AML1 mutations induced MDS and MDS/AML in a mouse BMT model

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Mutations of AML1 are common in therapy-related myelodysplasia following therapy with alkylating agents and are significantly associated with deletion or loss of chromosome arm 7q and with subsequent leukemic transformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Hyperactivation of the RAS signaling pathway in myelodysplastic syndrome with AML1/RUNX1 point mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

AML1/RUNX1 gene point mutations in childhood myeloid malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

RUNX1 Mutations in Acute Myeloid Leukemia: Results From a Comprehensive Genetic and Clinical Analysis From the AML Study Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

RAS, FLT3, and TP53 mutations in therapy-related myeloid malignancies with abnormalities of chromosomes 5 and 7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Cooperation of activating Ras/rtk signal transduction pathway mutations and inactivating myeloid differentiation gene mutations in M0 AML: a study of 45 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Mutations in PTPN11 implicate the SHP-2 phosphatase in leukemogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

SETBP1 overexpression is a novel leukemogenic mechanism that predicts adverse outcome in elderly patients with acute myeloid leukemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

SETBP1 mutations in 658 patients with myelodysplastic syndromes, chronic myelomonocytic leukemia and secondary acute myeloid leukemias.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

SETBP1 mutations occur in 9% of MDS/MPN and in 4% of MPN cases and are strongly associated with atypical CML, monosomy 7, isochromosome i(17)(q10), ASXL1 and CBL mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Clinical implications of the SETBP1 mutation in patients with primary myelodysplastic syndrome and its stability during disease progression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Validation of the revised international prognostic scoring system (IPSS-R) in patients with myelodysplastic syndrome: a multicenter study.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Refractory anemia in childhood: a retrospective analysis of 67 patients with particular reference to monosomy 7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Analysis of risk factors influencing outcome in children with myelodysplastic syndrome after unrelated cord blood transplantation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Results of treatment of children with refractory anaemia with excess blasts (RAEB) and RAEB in transformation (RAEBt) in Great Britain 1990-99.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Hematopoietic stem cell transplantation in children and young adults with secondary myelodysplastic syndrome and acute myelogenous leukemia after aplastic anemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Analysis of risk factors influencing outcomes after cord blood transplantation in children with juvenile myelomonocytic leukemia: a EUROCORD, EBMT, EWOG-MDS, CIBMTR study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Reduced intensity hematopoietic stem-cell transplantation across human leukocyte antigen barriers in a patient with congenital amegakaryocytic thrombocytopenia and monosomy 7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Childhood monosomy 7 revisited.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Epigenetic targets in hematopoietic malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Epigenetics of myelodysplastic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Decitabine improves patient outcomes in myelodysplastic syndromes: results of a phase III randomized study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Efficacy of azacitidine compared with that of conventional care regimens in the treatment of higher-risk myelodysplastic syndromes: a randomised, open-label, phase III study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Prolonged survival with improved tolerability in higher-risk myelodysplastic syndromes: azacitidine compared with low dose ara-C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Low-dose decitabine versus best supportive care in elderly patients with intermediate- or high-risk myelodysplastic syndrome (MDS) ineligible for intensive chemotherapy: final results of the randomized phase III study of the European Organisation fo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

In vivo effects of decitabine in myelodysplasia and acute myeloid leukemia: review of cytogenetic and molecular studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Recurrent retroviral vector integration at the Mds1/Evi1 locus in nonhuman primate hematopoietic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Demethylation of a hypermethylated P15/INK4B gene in patients with myelodysplastic syndrome by 5-Aza-2'-deoxycytidine (decitabine) treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Results of a randomized study of 3 schedules of low-dose decitabine in higher-risk myelodysplastic syndrome and chronic myelomonocytic leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Phase 1/2 study of the combination of 5-aza-2'-deoxycytidine with valproic acid in patients with leukemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Epigenetic therapies in MDS and AML

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Genomic impact of transient low-dose decitabine treatment on primary AML cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Recovery of cells with a normal karyotype in a refractory anaemia patient with monosomy 7‐positive cells after long‐term administration of cyclosporin a

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Pancytopenia presenting with monosomy 7 which disappeared after immunosuppressive therapy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Treatment of children with refractory anemia: the Japanese Childhood MDS Study Group trial (MDS99).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Directed therapy for patients with myelodysplastic syndromes (MDS) by suppression of cyclin D1 with ON 01910.Na

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Treatment of higher risk myelodysplastic syndrome patients unresponsive to hypomethylating agents with ON 01910.Na

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Interleukin-1 in the pathogenesis and treatment of inflammatory diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Inhibition of BET recruitment to chromatin as an effective treatment for MLL-fusion leukaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

RNAi screen identifies Brd4 as a therapeutic target in acute myeloid leukaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

How I treat newly diagnosed chronic phase CML

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Pushing the limits of targeted therapy in chronic myeloid leukaemia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Tyrosine kinase targeted treatment of chronic myelogenous leukemia and other myeloproliferative neoplasms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Allelic imbalance in 1p, 7q, 9p, 11p, 12q and 16q regions in non-small cell lung carcinoma and its clinical association: a pilot study

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Identifying the molecular signature of the interstitial deletion 7q subgroup of uterine leiomyomata using a paired analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Mutation and cancer: statistical study of retinoblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Haploinsufficiency for tumor suppression: the hazards of being single and living a long time

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Haploinsufficiency for tumour suppressor genes: when you don't need to go all the way.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Tumor suppressor genetics

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

A continuum model for tumour suppression

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Identification of RPS14 as a 5q- syndrome gene by RNA interference screen

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Advances in the 5q- syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Poly-ADP ribosylation of Miki by tankyrase-1 promotes centrosome maturation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Use of chromosome engineering to model a segmental deletion of chromosome band 7q22 found in myeloid malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

One-step generation of mice carrying mutations in multiple genes by CRISPR/Cas-mediated genome engineering

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

One-step generation of mice carrying reporter and conditional alleles by CRISPR/Cas-mediated genome engineering

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

The microcosmos of cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Non-coding RNAs in human disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Epigenetic regulation of microRNAs in cancer: An integrated review of literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy 7. European Working Group on MDS in Childhood (EWOG-MDS)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Sole abnormalities of chromosome 7 in myeloid malignancies: spectrum, histopathologic correlates, and prognostic implications

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Monosomy 7 with severe myelodysplasia developing during imatinib treatment of Philadelphia-positive chronic myeloid leukemia: Two cases with a different outcome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Letter: Deletions of chromosome 7 in haematological disorders

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Fourth International Workshop on Chromosomes in Leukemia 1982: Abnormalities of chromosome 7 resulting in monosomy 7 or in deletion of the long arm (7q-): review of translocations, breakpoints, and associated abnormalities.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Molecular characterization of the 7q deletion in myeloid disorders

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Recurrent genetic defects on chromosome 7q in myeloid neoplasms

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Mechanisms of polycomb gene silencing: knowns and unknowns

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Delineation of multiple deleted regions in 7q in myeloid disorders

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Commonly altered genomic regions in acute myeloid leukemia are enriched for somatic mutations involved in chromatin remodeling and splicing

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Exome sequencing of gastric adenocarcinoma identifies recurrent somatic mutations in cell adhesion and chromatin remodeling genes

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

DOCK4 deletion at 7q31.1 in a de novo acute myeloid leukemia with a normal karyotype

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Large-scale sequencing of two regions in human chromosome 7q22: analysis of 650 kb of genomic sequence around the EPO and CUTL1 loci reveals 17 genes

31 March 2020

2 references

https://api.crossref.org/works/10.1038%2FONC.2014.196

31 March 2020

12 December 2020

Evidence for a direct role of the disease modifier SCNM1 in splicing

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Refined mapping of the region of loss of heterozygosity on the long arm of chromosome 7 in human breast cancer defines the location of a second tumor suppressor gene at 7q22 in the region of the CUTL1 gene

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

New insights into the prognostic impact of the karyotype in MDS and correlation with subtypes: evidence from a core dataset of 2124 patients

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Complex karyotype newly defined: the strongest prognostic factor in advanced childhood myelodysplastic syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

EVI1 induces myelodysplastic syndrome in mice

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Clinical, molecular, and prognostic significance of WHO type inv(3)(q21q26.2)/t(3;3)(q21;q26.2) and various other 3q abnormalities in acute myeloid leukemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

High EVI1 expression predicts outcome in younger adult patients with acute myeloid leukemia and is associated with distinct cytogenetic abnormalities

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Methylation of the p15(INK4B) gene in myelodysplastic syndrome: it can be detected early at diagnosis or during disease progression and is highly associated with leukaemic transformation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Aberrant p15 gene promoter methylation in therapy-related myelodysplastic syndrome and acute myeloid leukaemia: clinicopathological and karyotypic associations

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

RUNX1 gene mutation in primary myelodysplastic syndrome--the mutation can be detected early at diagnosis or acquired during disease progression and is associated with poor outcome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

TP53 alterations in acute myeloid leukemia with complex karyotype correlate with specific copy number alterations, monosomal karyotype, and dismal outcome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Mutations of the PTPN11 gene in therapy-related MDS and AML with rare balanced chromosome translocations

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Monosomy 7 associated with pediatric acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS): successful management by allogeneic hematopoietic stem cell transplant (HSCT)

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

A predictive model for the clinical response to low dose ara-C: a study of 102 patients with myelodysplastic syndromes or acute leukaemia

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Preferential cytogenetic response to continuous intravenous low-dose decitabine (DAC) administration in myelodysplastic syndrome with monosomy 7

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

CDKN2B methylation status and isolated chromosome 7 abnormalities predict responses to treatment with 5-azacytidine

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Combined DNA methyltransferase and histone deacetylase inhibition in the treatment of myeloid neoplasms

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Safety and clinical activity of the combination of 5-azacytidine, valproic acid, and all-trans retinoic acid in acute myeloid leukemia and myelodysplastic syndrome

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

Loss of heterozygosity analysis of a candidate gastric carcinoma tumor suppressor locus at 7q31

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

CUX1 in leukemia: dosage matters

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FONC.2014.196

The many faces of marginal zone lymphoma

31 March 2020

1 reference

12 December 2020

Homozygous loss of the cyclin-dependent kinase 4-inhibitor (p16) gene in human leukemias

1 reference

12 December 2020

Aberrant p15 promoter methylation in adult and childhood acute leukemias of nearly all morphologic subtypes: potential prognostic implications

1 reference

12 December 2020

Modulation of cell proliferation and cytokine production in acute myeloblastic leukemia by interleukin-1 receptor antagonist and lack of its expression by leukemic cells

1 reference

12 December 2020

Monosomy-7 in childhood hemopoietic disorders

1 reference

12 December 2020

Expression of EVI1 in myelodysplastic syndromes and other hematologic malignancies without 3q26 translocations

1 reference

12 December 2020

Molecular cytogenetic delineation of deletions and translocations involving chromosome band 7q22 in myeloid leukemias

1 reference

12 December 2020

p16 gene homozygous deletions in acute lymphoblastic leukemia

1 reference

12 December 2020

Classification of deletions and identification of cryptic translocations involving 7q by fluorescence in situ hybridization (FISH)

1 reference

12 December 2020

Cytogenetic and molecular delineation of a region of chromosome 7 commonly deleted in malignant myeloid diseases.

1 reference

12 December 2020

Hypermethylation of the p15INK4B gene in myelodysplastic syndromes

1 reference

12 December 2020

Molecular cytogenetic characterization of a critical region in bands 7q35-q36 commonly deleted in malignant myeloid disorders

1 reference

12 December 2020

The importance of diagnostic cytogenetics on outcome in AML: analysis of 1,612 patients entered into the MRC AML 10 trial. The Medical Research Council Adult and Children's Leukaemia Working Parties

1 reference

12 December 2020

Myelodysplastic and myeloproliferative disorders of childhood: a study of 167 patients.

1 reference

12 December 2020

Hypermethylation-associated inactivation indicates a tumor suppressor role for p15INK4B.

1 reference

12 December 2020

Mutations of the ras proto-oncogenes in childhood monosomy 7

1 reference

12 December 2020

Pediatric myelodysplasia: a study of 68 children and a new prognostic scoring system

1 reference

12 December 2020

Karyotypic analysis predicts outcome of preremission and postremission therapy in adult acute myeloid leukemia: a Southwest Oncology Group/Eastern Cooperative Oncology Group Study

1 reference

12 December 2020

Chromosome studies in preleukemia. I. Aneuploidy of group C chromosomes in three patients

1 reference

12 December 2020

International scoring system for evaluating prognosis in myelodysplastic syndromes

1 reference

12 December 2020

Molecular characterization of chromosome 7 long arm deletions in myeloid disorders

1 reference

12 December 2020

Methylation of the p15(INK4b) gene in myelodysplastic syndromes is frequent and acquired during disease progression

1 reference

12 December 2020