(Q74789117)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9669834%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

review article

1 reference

title

Molecular features of primary MDS with cytogenetic changes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9669834%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

author name string

C Mecucci

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9669834%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

publication date

1 April 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9669834%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9669834%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

volume

22

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9669834%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9669834%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

page(s)

293-302

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9669834%20AND%20SRC:MED&resulttype=core&format=json

Defining tumour-suppressor genes

13 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Distinct haematological disorder with deletion of long arm of no. 5 chromosome

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

1 reference

7 January 2021

Mosaicism of the 5q deletion as assessed by interphase FISH is a common phenomenon in MDS and restricted to myeloid cells

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Possible evidence for genomic imprinting in childhood acute myeloblastic leukaemia associated with monosomy for chromosome 7

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Somatic mutations in the neurofibromatosis 1 gene in human tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Homozygous inactivation of the NF1 gene in bone marrow cells from children with neurofibromatosis type 1 and malignant myeloid disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Prolonged extreme thrombocytosis associated with neurofibromatosis type 1.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Hematologic manifestations associated with deletions of the long arm of chromosome 20

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Deletions of chromosome 20q and the pathogenesis of myeloproliferative disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Inactivation of the retinoblastoma gene appears to be very uncommon in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

11q-chromosome is associated with abnormal iron stores in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

A yeast artificial chromosome contig and NotI restriction map that spans the tumor suppressor gene(s) locus, 11q22.2-q23.3.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Do terminal deletions of 11q23 exist? Identification of undetected translocations with fluorescence in situ hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Myelodysplasia in a patient with pre-existing paroxysmal nocturnal haemoglobinuria: a clonal disease originating from within a clonal disease

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Trisomy 13 in a patient with a myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Characterization and molecular analysis of nondisjunction in 18 cases of trisomy 21 and leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

KRAS2 oncogene overexpression in myelodysplastic syndrome with translocation 5;12

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Myelodysplastic syndrome associated with increased bone marrow fibrosis and translocation (5;12)(q33;p12.3)

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

t(5;12)(q31;p12). A clinical entity with features of both myeloid leukemia and chronic myelomonocytic leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Fusion of PDGF receptor beta to a novel ets-like gene, tel, in chronic myelomonocytic leukemia with t(5;12) chromosomal translocation

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

ETV6 gene rearrangements in hematopoietic malignant disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Yolk sac angiogenic defect and intra-embryonic apoptosis in mice lacking the Ets-related factor TEL

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

The ETV6, CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberration in different hematological malignancies

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

A translocation involving a specific breakpoint (q35) on chromosome 5 is characteristic of anaplastic large cell lymphoma ('Ki-1 lymphoma').

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Dicentric (1;15) in myeloid disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Translocation (Y;1)(q12;q12) in hematologic malignancies. Report on two new cases, FISH characterization, and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Derivative (y)t(Y;1)(q12;q12),+9 in a patient with polycythemia vera during transition into myelodysplasia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Der(16)t(1;16)(q11;q11) in myelodysplastic syndromes: a new non-random abnormality characterized by cytogenic and fluorescence in situ hybridization studies

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Chromosome 11q23 abnormalities in leukaemia.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Involvement of erythrocytic and granulomonocytic lineages by trisomy 11 in two cases of acute myelomonocytic leukemia with trilineage myelodysplasia. An interphase cytogenetic study

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Refractory thrombocytopenia with chromosome 11q23 abnormality.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Agnogenic myeloid metaplasia preceded by repeated leukemoid reactions and persistent acquired Pelger-Huët anomaly of granulocytes: case report with review of acquired Pelger-Huët anomaly

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Chromosome characteristics of therapy-related acute non-lymphocytic leukemia and preleukemia: possible implications for pathogenesis of the disease

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

TP53 mutations in myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Monosomy X as a recurring sole cytogenetic abnormality associated with myelodysplastic diseases.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Twenty-six patients with hematologic disorders and X chromosome abnormalities. Frequent idic(X)(q13) chromosomes and Xq13 anomalies associated with pathologic ringed sideroblasts

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Characterization by chromosome painting of balanced and unbalanced X chromosome translocations in myelodysplastic syndromes.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

t(8;21) myelodysplasia, an early presentation of M2 AML

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Identification of chromosome changes in acute myeloid leukemia (AML-M2) by molecular cytogenetics

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Three cases of the myelodysplastic syndrome with pericentric inversion of chromosome 16

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

p190bcr/abl rearrangement in myelodysplastic syndromes: two reports and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Cytogenetic and molecular studies of the Philadelphia translocation in myelodysplastic syndromes. Report of two cases and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Three new cases of chromosome 3 rearrangement in bands q21 and q26 with abnormal thrombopoiesis bring further evidence to the existence of a 3q21q26 syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Expression of the Evi-1 zinc finger gene in 32Dc13 myeloid cells blocks granulocytic differentiation in response to granulocyte colony-stimulating factor

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

c-myc amplification in a preleukemia patient with trisomy 4 and double minutes: review of the unique coexistence of these two chromosome abnormalities in acute myelogenous leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Double-minute chromosomes appearing in a patient with myelodysplastic syndrome with disease evolution

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Expression of the multidrug resistance gene product (P-glycoprotein) in myelodysplasia is associated with a stem cell phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Modulation of activity of the promoter of the human MDR1 gene by Ras and p53.

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Evidence for the involvement of GM-CSF and FMS in the deletion (5q) in myeloid disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Mutation of CDKN2 is infrequently detected in myelodysplastic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Expression of the DCC gene in myelodysplastic syndromes and overt leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Abnormal regional hypermethylation of the calcitonin gene in myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Idiopathic macrocytic anaemia in the aged: molecular and cytogenetic findings

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

Evolution of the myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0145-2126%2897%2900193-8

7 January 2021

10.1016/S0145-2126(97)00193-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9669834%20AND%20SRC:MED&resulttype=core&format=json

13 November 2019

1 reference