(Q34433808)

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Delineation of the minimal commonly deleted segment and identification of candidate tumor-suppressor genes in del(9q) acute myeloid leukemia

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scholarly article

1 reference

Europe PubMed Central

2 August 2017

Delineation of the minimal commonly deleted segment and identification of candidate tumor-suppressor genes in del(9q) acute myeloid leukemia (English)

1 reference

Europe PubMed Central

2 August 2017

David A. Sweetser

object named as

David A Sweetser

1

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Jacqueline Boultwood

object named as

Jacqueline Boultwood

10

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Elisabeth Paietta

12

object named as

Elisabeth Paietta

1 reference

Europe PubMed Central

2 August 2017

9

object named as

Nyla A Heerema

1 reference

Europe PubMed Central

2 August 2017

Cheryl L. Willman

14

object named as

Cheryl L Willman

1 reference

Europe PubMed Central

2 August 2017

author name string

Andrew J Peniket

2

1 reference

Europe PubMed Central

2 August 2017

Christina Haaland

3

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Europe PubMed Central

2 August 2017

Adam A Blomberg

4

1 reference

Europe PubMed Central

2 August 2017

Yuntian Zhang

5

1 reference

Europe PubMed Central

2 August 2017

Syed Tanweer Zaidi

6

1 reference

Europe PubMed Central

2 August 2017

Farshid Dayyani

7

1 reference

Europe PubMed Central

2 August 2017

Zheng Zhao

8

1 reference

Europe PubMed Central

2 August 2017

Gordon W Dewald

11

1 reference

Europe PubMed Central

2 August 2017

Marilyn L Slovak

13

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Europe PubMed Central

2 August 2017

James S Wainscoat

15

1 reference

Europe PubMed Central

2 August 2017

Irwin D Bernstein

16

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Europe PubMed Central

2 August 2017

Sarah B Daly

17

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Europe PubMed Central

2 August 2017

publication date

1 November 2005

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Europe PubMed Central

2 August 2017

Genes, Chromosomes and Cancer

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Europe PubMed Central

2 August 2017

44

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Europe PubMed Central

2 August 2017

279-291

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Europe PubMed Central

2 August 2017

3

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Europe PubMed Central

2 August 2017

Expression of the retinoblastoma tumor suppressor gene (RB-1) in acute leukemia

1 reference

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Molecular analysis of nonrandom 8q12 deletions in acute lymphoblastic leukemia: identification of two candidate genes.

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Evolution of neoplastic cell lineages in Barrett oesophagus

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

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Narrowing and genomic annotation of the commonly deleted region of the 5q- syndrome

1 reference

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7 January 2021

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A PMLRARalpha transgene initiates murine acute promyelocytic leukemia

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Expression of constitutively active nuclear-kappa B RelA transcription factor in blasts of acute myeloid leukemia

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The fusion gene Cbfb-MYH11 blocks myeloid differentiation and predisposes mice to acute myelomonocytic leukaemia

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Mutations with loss of heterozygosity of p53 are common in therapy-related myelodysplasia and acute myeloid leukemia after exposure to alkylating agents and significantly associated with deletion or loss of 5q, a complex karyotype, and a poor progno

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Cooperativity between mutations in tyrosine kinases and in hematopoietic transcription factors in AML.

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Review of alterations of the cyclin-dependent kinase inhibitor INK4 family genes p15, p16, p18 and p19 in human leukemia-lymphoma cells

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Transgenic expression of PML/RARalpha impairs myelopoiesis

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A genetic model for colorectal tumorigenesis

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The murine gene p27Kip1 is haplo-insufficient for tumour suppression

1 reference

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A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma

1 reference

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7 January 2021

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The predictive value of hierarchical cytogenetic classification in older adults with acute myeloid leukemia (AML): analysis of 1065 patients entered into the United Kingdom Medical Research Council AML11 trial

1 reference

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7 January 2021

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An activated receptor tyrosine kinase, TEL/PDGFbetaR, cooperates with AML1/ETO to induce acute myeloid leukemia in mice

1 reference

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Nuclear factor-kappaB is constitutively activated in primitive human acute myelogenous leukemia cells

1 reference

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Acute leukemia with promyelocytic features in PML/RARalpha transgenic mice

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

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TLE, the Human Homolog of Groucho, Interacts with AML1 and Acts as a Repressor of AML1-Induced Transactivation

1 reference

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7 January 2021

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PML/RARalpha and FLT3-ITD induce an APL-like disease in a mouse model

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

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

1 reference

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Altered expression of retinoblastoma (RB) protein in acute myelogenous leukemia does not result from methylation of the Rb promotor

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

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Analysis of the p53 gene mutations in acute myelogenous leukemia: the p53 gene mutations associated with a deletion of chromosome 17

1 reference

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7 January 2021

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Transcriptional repression by AML1 and LEF-1 is mediated by the TLE/Groucho corepressors

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

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Rearrangement of the p53 gene in human osteogenic sarcomas

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

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All kinesin superfamily protein, KIF, genes in mouse and human

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

based on heuristic

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Acute leukemia in children

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

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A role for Wnt signalling in self-renewal of haematopoietic stem cells

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

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Acute myeloid leukemia induced by graded reduction of a lineage-specific transcription factor, PU.1.

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

based on heuristic

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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/10.1002%2FGCC.20236

7 January 2021

based on heuristic

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Identification of RUNX1/AML1 as a classical tumor suppressor gene

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

based on heuristic

inferred from DOI database lookup

Core-binding factors in haematopoiesis and leukaemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

based on heuristic

inferred from DOI database lookup

Loss of heterozygosity in childhood de novo acute myelogenous leukemia

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

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Inhibition of nuclear factor-kappaB-mediated transcription by association with the amino-terminal enhancer of split, a Groucho-related protein lacking WD40 repeats

1 reference

https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

based on heuristic

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Is p53 haploinsufficient for tumor suppression? Implications for the p53+/- mouse model in carcinogenicity testing

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https://api.crossref.org/works/10.1002%2FGCC.20236

7 January 2021

based on heuristic

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Genetic alterations during colorectal-tumor development

1 reference

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7 January 2021

based on heuristic

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Deletion 9q as the sole karyotypic abnormality in myelocytic disorders: a new case of myelodysplastic syndrome and its prognostic implications in acute myelocytic leukemia

1 reference

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

1 reference

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Wnt proteins are lipid-modified and can act as stem cell growth factors

1 reference

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7 January 2021

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AML1-ETO expression is directly involved in the development of acute myeloid leukemia in the presence of additional mutations

1 reference

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7 January 2021

based on heuristic

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Identifiers

10.1002/GCC.20236

1 reference

Europe PubMed Central

2 August 2017

1 reference

Europe PubMed Central

2 August 2017

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