Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1 microdeletions (Q21261481)

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Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1microdeletions

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English	Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1 microdeletions	scientific article	Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1microdeletions

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scholarly article

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Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1 microdeletions (English)

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David N. Cooper

object named as

David N Cooper

5

author given names

David N

author last names

Cooper

1 reference

Dimensions Publication ID

17 August 2022

Hildegard Kehrer-Sawatzki

7

object named as

Hildegard Kehrer-Sawatzki

author given names

Hildegard

author last names

Kehrer-Sawatzki

1 reference

Dimensions Publication ID

17 August 2022

Victor-Felix Mautner

6

object named as

Victor-Felix Mautner

author given names

Victor-Felix

author last names

Mautner

1 reference

Dimensions Publication ID

17 August 2022

3

object named as

Josef Högel

author given names

Josef

author last names

Högel

1 reference

Dimensions Publication ID

17 August 2022

2

object named as

Lan Kluwe

author given names

Lan

author last names

Kluwe

1 reference

Dimensions Publication ID

17 August 2022

author name string

Tanja Mußotter

1

author given names

Tanja

author last names

Mußotter

1 reference

Dimensions Publication ID

17 August 2022

Rosa Nguyen

4

author given names

Rosa

author last names

Nguyen

1 reference

Dimensions Publication ID

17 August 2022

language of work or name

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publication date

2012

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BMC Medical Genetics

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13

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1

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98

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https://scigraph.springernature.com/pub.10.1186/1471-2350-13-98

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The genetic basis of early T-cell precursor acute lymphoblastic leukaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

19 March 2017

Long non-coding RNA ANRIL is required for the PRC2 recruitment to and silencing of p15(INK4B) tumor suppressor gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

19 March 2017

Epigenetic regulation of the INK4b-ARF-INK4a locus: in sickness and in health

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

19 March 2017

Molecular interplay of the noncoding RNA ANRIL and methylated histone H3 lysine 27 by polycomb CBX7 in transcriptional silencing of INK4a

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

19 March 2017

Several distinct polycomb complexes regulate and co-localize on the INK4a tumor suppressor locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

19 March 2017

Epigenetic silencing of tumour suppressor gene p15 by its antisense RNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

19 March 2017

Connective tissue dysplasia in five new patients with NF1 microdeletions: further expansion of phenotype and review of the literature

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

19 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

19 March 2017

Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

19 March 2017

Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

6 April 2017

Genetic inactivation of the polycomb repressive complex 2 in T cell acute lymphoblastic leukemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

Frequent deletions of JARID2 in leukemic transformation of chronic myeloid malignancies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

Long noncoding RNA, polycomb, and the ghosts haunting INK4b-ARF-INK4a expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

Mortality in neurofibromatosis 1: in North West England: an assessment of actuarial survival in a region of the UK since 1989.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

Susceptible stages in Schwann cells for NF1-associated plexiform neurofibroma development

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

Unravelling the genetic basis of variable clinical expression in neurofibromatosis 1.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

The regulation of INK4/ARF in cancer and aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

Regulation of the INK4b-ARF-INK4a tumour suppressor locus: all for one or one for all.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

Elevated risk for MPNST in NF1 microdeletion patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

An analysis of variation in expression of neurofibromatosis (NF) type 1 (NF1): evidence for modifying genes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

12 September 2017

Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

30 May 2018

Role of noncoding RNA ANRIL in genesis of plexiform neurofibromas in neurofibromatosis type 1.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-98

21 January 2018

Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type-2 NF1 deletions.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-98

21 January 2018

NF1 microdeletion breakpoints are clustered at flanking repetitive sequences.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-98

21 January 2018

Inactivation of polycomb repressive complex 2 components in myeloproliferative and myelodysplastic/myeloproliferative neoplasms.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-98

21 January 2018

Somatic loss of wild type NF1 allele in neurofibromas: Comparison of NF1 microdeletion and non-microdeletion patients.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-98

21 January 2018

Copy number variations in the NF1 gene region are infrequent and do not predispose to recurrent type-1 deletions

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-13-98

21 January 2018

Mutation analysis of ASXL1, CBL, DNMT3A, IDH1, IDH2, JAK2, MPL, NF1, SF3B1, SUZ12, and TET2 in myeloproliferative neoplasms.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3500256

29 November 2018

Screening 500 unselected neurofibromatosis 1 patients for deletions of the NF1 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/23101500

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intelligence in individuals with a neurofibromatosis type 1 microdeletion

1 reference

https://pubmed.ncbi.nlm.nih.gov/23101500

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extensively high load of internal tumors determined by whole body MRI scanning in a patient with neurofibromatosis type 1 and a non-LCR-mediated 2-Mb deletion in 17q11.2

1 reference

https://pubmed.ncbi.nlm.nih.gov/23101500

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Absence of cutaneous neurofibromas in an NF1 patient with an atypical deletion partially overlapping the common 1.4 Mb microdeleted region

1 reference

https://pubmed.ncbi.nlm.nih.gov/23101500

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Plexiform neurofibromas in children with neurofibromatosis type 1: frequency and associated clinical deficits

1 reference

https://pubmed.ncbi.nlm.nih.gov/23101500

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recombination hotspot in NF1 microdeletion patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/23101500

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

p15INK4b, p14ARF, and p16INK4a inactivation in sporadic and neurofibromatosis type 1-related malignant peripheral nerve sheath tumors

1 reference

https://pubmed.ncbi.nlm.nih.gov/23101500

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Internal tumor burden in neurofibromatosis Type I patients with large NF1 deletions

1 reference

https://pubmed.ncbi.nlm.nih.gov/23101500

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/23101500

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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10.1186/1471-2350-13-98

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