(Q21261481)

Hildegard Kehrer-Sawatzki

17 August 2022

series ordinal

7

object named as

Hildegard Kehrer-Sawatzki

author given names

Hildegard

author last names

Kehrer-Sawatzki

1 reference

17 August 2022

6

Victor-Felix Mautner

Victor-Felix

Mautner

1 reference

17 August 2022

3

Josef Högel

Josef

Högel

1 reference

17 August 2022

2

Lan Kluwe

Lan

Kluwe

1 reference

17 August 2022

Tanja Mußotter

1

Tanja

Mußotter

1 reference

17 August 2022

Rosa Nguyen

series ordinal

4

author given names

Rosa

author last names

Nguyen

1 reference

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

17 August 2022

language of work or name

English

0 references

publication date

2012

0 references

published in

BMC Medical Genetics

0 references

volume

13

0 references

issue

1

0 references

page(s)

98

0 references

cites work

1 reference

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

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

19 March 2017

1 reference

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

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

19 March 2017

1 reference

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

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

19 March 2017

1 reference

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

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

19 March 2017

1 reference

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

Epigenetic silencing of tumour suppressor gene p15 by its antisense RNA

19 March 2017

1 reference

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

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

19 March 2017

1 reference

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

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

19 March 2017

1 reference

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

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

19 March 2017

1 reference

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

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

19 March 2017

1 reference

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

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

6 April 2017

1 reference

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

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

12 September 2017

1 reference

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

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

12 September 2017

1 reference

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

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

12 September 2017

1 reference

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

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

12 September 2017

1 reference

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

NF1 microdeletions in neurofibromatosis type 1: from genotype to phenotype

12 September 2017

1 reference

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

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

12 September 2017

1 reference

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

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

12 September 2017

1 reference

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

The regulation of INK4/ARF in cancer and aging

12 September 2017

1 reference

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

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

12 September 2017

1 reference

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

Elevated risk for MPNST in NF1 microdeletion patients

12 September 2017

1 reference

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

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

12 September 2017

1 reference

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

Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors

12 September 2017

1 reference

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

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

30 May 2018

1 reference

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

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

21 January 2018

1 reference

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

NF1 microdeletion breakpoints are clustered at flanking repetitive sequences

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

21 January 2018

1 reference

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

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

29 November 2018

1 reference

12 December 2020

Intelligence in individuals with a neurofibromatosis type 1 microdeletion

1 reference

12 December 2020

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

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Recombination hotspot in NF1 microdeletion patients

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

DOI

10.1186/1471-2350-13-98

0 references