(Q30666811)

26 June 2017

1 reference

title

Myelodysplastic syndrome: review of the cytogenetic and molecular data (English)

1 reference

26 June 2017

myelodysplastic syndrome

1 reference

Mhawech P

1

1 reference

PubMed ID

11738946

26 June 2017

Saleem A

series ordinal

2

1 reference

26 June 2017

1 December 2001

1 reference

Critical Reviews in Oncology Hematology

26 June 2017

1 reference

26 June 2017

40

1 reference

26 June 2017

3

1 reference

26 June 2017

229-238

1 reference

Proposals for the classification of the myelodysplastic syndromes

26 June 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Familial MDS with 5q- abnormality

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Anti-oncogenic and oncogenic potentials of interferon regulatory factors-1 and -2

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Molecular Mapping of Uncharacteristically Small 5q Deletions in Two Patients with the 5q- Syndrome: Delineation of the Critical Region on 5q and Identification of a 5q- Breakpoint

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Evidence implicating heterozygous deletion of chromosome 7 in the pathogenesis of familial leukemia associated with monosomy 7.

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Chromosomal localization of human genes required for G1 progression in mammalian cells

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Possible co-existence of RAS activation and monosomy 7 in the leukaemic transformation of myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Loss of the normal NF1 allele from the bone marrow of children with type 1 neurofibromatosis and malignant myeloid disorders

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Nf1 deficiency causes Ras-mediated granulocyte/macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Cancer. p53, guardian of the genome

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Mutation and cancer: statistical study of retinoblastoma

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

MDS and AML with trisomy 8 as the sole chromosome aberration show different sex ratios and prognostic profiles: a study of 115 published cases

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic, and molecular data on three cases

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Constitutional trisomy 8 mosaicism evolving to primary myelodysplastic syndrome: a new subset of biologically related patients?

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Trisomy 8 may not be related to the pathogenesis of myelodysplastic syndromes: disappearance of trisomy 8 in a patient with refractory anaemia without haematological improvement

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Trisomy of chromosome 8 in myelodysplastic syndrome. Significance of the fluctuating trisomy 8 population

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Incidence, characterization and prognostic significance of chromosomal abnormalities in 640 patients with primary myelodysplastic syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Fourth International Workshop on Chromosomes in Leukemia 1982: Translocation (8;21)(q22;q22) in acute nonlymphocytic leukemia

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Clinical significance of Y chromosome loss in hematologic disease

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Loss of the Y chromosome in acute myelogenous leukemia: a report of 13 patients

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

p27, a novel inhibitor of G1 cyclin-Cdk protein kinase activity, is related to p21

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Reduced expression of p27/Kip1 is associated with the development of pulmonary adenocarcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

The TEL/platelet-derived growth factor beta receptor (PDGF beta R) fusion in chronic myelomonocytic leukemia is a transforming protein that self-associates and activates PDGF beta R kinase-dependent signaling pathways

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

A novel translocation t(3;22)(q21;q11) involving 3q21 in myelodysplastic syndrome-derived overt leukemia with thrombocytosis

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

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%2FS1040-8428%2801%2900101-9

7 January 2021

Nuclear protein CBP is a coactivator for the transcription factor CREB

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

Isodicentric (X)(q13) in haematological malignancies: presentation of five new cases, application of fluorescence in situ hybridization (FISH) and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

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%2FS1040-8428%2801%2900101-9

7 January 2021

Acute leukemic transformation of myelodysplastic syndrome--immunophenotypic, genotypic, and cytogenetic studies

1 reference

https://api.crossref.org/works/10.1016%2FS1040-8428%2801%2900101-9

7 January 2021

10.1016/S1040-8428(01)00101-9

Identifiers

DOI

1 reference

26 June 2017

1 reference

PubMed ID

11738946