Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies (Q35849015)

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21 January 2020

title

Interstitial uniparental isodisomy at clustered breakpoint intervals is a frequent mechanism of NF1 inactivation in myeloid malignancies (English)

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21 January 2020

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5

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21 January 2020

6

Michelle M Le Beau

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21 January 2020

author name string

Karen Stephens

1

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21 January 2020

Molly Weaver

2

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21 January 2020

Kathleen A Leppig

3

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21 January 2020

Kyoko Maruyama

4

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21 January 2020

Kevin M Shannon

7

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21 January 2020

language of work or name

English

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publication date

11 May 2006

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21 January 2020

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21 January 2020

volume

108

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21 January 2020

issue

5

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21 January 2020

page(s)

1684-1689

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Progress in concurrent analysis of loss of heterozygosity and comparative genomic hybridization utilizing high density single nucleotide polymorphism arrays

21 January 2020

cites work

1 reference

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A gain-of-function mutation of JAK2 in myeloproliferative disorders

27 July 2018

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Activating mutation in the tyrosine kinase JAK2 in polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis

27 July 2018

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A unique clonal JAK2 mutation leading to constitutive signalling causes polycythaemia vera

27 July 2018

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Acquired mutation of the tyrosine kinase JAK2 in human myeloproliferative disorders

27 July 2018

1 reference

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Whole genome DNA copy number changes identified by high density oligonucleotide arrays

27 July 2018

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Amplification and overexpression of genes in 17p11.2 ~ p12 in osteosarcoma

27 July 2018

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Concurrent analysis of loss of heterozygosity (LOH) and copy number abnormality (CNA) for oral premalignancy progression using the Affymetrix 10K SNP mapping array

27 July 2018

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High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 gene

27 July 2018

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Estimating the rate of gene conversion on human chromosome 21.

27 July 2018

1 reference

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Intense and highly localized gene conversion activity in human meiotic crossover hot spots

27 July 2018

1 reference

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Neurofibromatosis 1: closing the GAP between mice and men.

27 July 2018

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A 76-kb duplicon maps close to the BCR gene on chromosome 22 and the ABL gene on chromosome 9: possible involvement in the genesis of the Philadelphia chromosome translocation

27 July 2018

1 reference

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GTPase activating proteins: critical regulators of intracellular signaling

27 July 2018

1 reference

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NF1 tumor suppressor gene function: narrowing the GAP

27 July 2018

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Myeloid malignancies induced by alkylating agents in Nf1 mice

27 July 2018

1 reference

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Human Cancer Syndromes: Clues to the Origin and Nature of Cancer

27 July 2018

1 reference

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"Mistakes happen": somatic mutation and disease

27 July 2018

1 reference

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Loss of heterozygosity or: how I learned to stop worrying and love mitotic recombination

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1895516

Juvenile myelomonocytic leukemia: molecular understanding and prospects for therapy

27 July 2018

1 reference

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Patterns of hematopoietic lineage involvement in children with neurofibromatosis type 1 and malignant myeloid disorders

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1895516

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1895516

The neurofibromatosis type 1 (NF1) tumor suppressor gene and myeloid leukemia.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1895516

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

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1895516

Proteins regulating Ras and its relatives

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1895516

Neurofibromatosis and childhood leukaemia/lymphoma: a population-based UKCCSG study

27 July 2018

1 reference

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Tumour predisposition in mice heterozygous for a targeted mutation in Nf1

27 July 2018

1 reference

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Childhood monosomy 7: epidemiology, biology, and mechanistic implications.

27 July 2018

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Expression of recessive alleles by chromosomal mechanisms in retinoblastoma

27 July 2018

1 reference

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Paternal origin of new mutations in von Recklinghausen neurofibromatosis.

27 July 2018

1 reference

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Acquired uniparental disomy of chromosome 9p is a frequent stem cell defect in polycythemia vera

27 July 2018

1 reference

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NF1 microdeletion breakpoints are clustered at flanking repetitive sequences

24 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1895516

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

24 September 2018

1 reference

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Genetic analysis is consistent with the hypothesis that NF1 limits myeloid cell growth through p21ras

24 September 2018

1 reference

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Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia

24 September 2018

1 reference

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Determination of Gene Dosage by a Quantitative Adaptation of the Polymerase Chain Reaction (gd-PCR): Rapid Detection of Deletions and Duplications of Gene Sequences

22 October 2018

1 reference

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Genome-wide single nucleotide polymorphism analysis reveals frequent partial uniparental disomy due to somatic recombination in acute myeloid leukemias

22 October 2018

1 reference

12 December 2020

The ratio of maternal to paternal UPD associated with recessive diseases

1 reference

12 December 2020

Interphase FISH screening for the LCR-mediated common rearrangement of isochromosome 17q in primary myelofibrosis

1 reference

12 December 2020

Frequent loss of heterozygosity without loss of genetic material in acute myeloid leukemia with a normal karyotype

1 reference

12 December 2020

Association between acquired uniparental disomy and homozygous gene mutation in acute myeloid leukemias

1 reference

12 December 2020

Molecular nature of in vivo mutations in human cells at the autosomal HLA-A locus

1 reference

12 December 2020

Preferential mutation of the neurofibromatosis type 1 gene in paternally derived chromosomes

1 reference

12 December 2020

The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridization

1 reference

12 December 2020

Juvenile myelomonocytic leukemia

1 reference

12 December 2020

10.1182/BLOOD-2005-11-011486

Identifiers

DOI

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16690971%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

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21 January 2020

PubMed publication ID

16690971

1 reference