(Q42166567)

English

Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11.

scientific article published on 12 March 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Genome-wide single-nucleotide polymorphism analysis in juvenile myelomonocytic leukemia identifies uniparental disomy surrounding the NF1 locus in cases associated with neurofibromatosis but not in cases with mutant RAS or PTPN11. (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

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based on heuristic

inferred from title

juvenile myelomonocytic leukemia

1 reference

based on heuristic

inferred from title

Charles G. Mullighan

3

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

author name string

Flotho C

1

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Steinemann D

2

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Neale G

4

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Mayer K

5

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Kratz CP

6

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Schlegelberger B

7

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Downing JR

8

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Niemeyer CM

9

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

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publication date

12 March 2007

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Europe PubMed Central

PubMed publication ID

17 October 2017

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

26

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Europe PubMed Central

PubMed publication ID

17 October 2017

39

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Europe PubMed Central

PubMed publication ID

17 October 2017

5816-5821

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

https://scigraph.springernature.com/pub.10.1038/sj.onc.1210361

0 references

Recent advances in neurofibromatosis type 1.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

Neurofibromatosis 1: closing the GAP between mice and men.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

Using high-throughput SNP technologies to study cancer

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

Targeting RAS signaling pathways in juvenile myelomonocytic leukemia

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

RAS mutations and clonality analysis in children with juvenile myelomonocytic leukemia (JMML)

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

A microRNA polycistron as a potential human oncogene

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

Analysis of array CGH data: from signal ratio to gain and loss of DNA regions

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

Inherited predispositions and hyperactive Ras in myeloid leukemogenesis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

dChipSNP: significance curve and clustering of SNP-array-based loss-of-heterozygosity data

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

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/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of candidate tumor-suppressor genes in 6q27 by combined deletion mapping and electronic expression profiling in lymphoid neoplasms

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

Clonal chromosomal aberrations in bone marrow cells of Fanconi anemia patients: gains of the chromosomal segment 3q26q29 as an adverse risk factor.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

An integrated view of copy number and allelic alterations in the cancer genome using single nucleotide polymorphism arrays

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of chromosomal imbalances in retinoblastoma by matrix-based comparative genomic hybridization

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210361

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.ONC.1210361

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 October 2017

ResearchGate publication ID

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