Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations (Q34160516)

31 July 2017

title

Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations (English)

1 reference

31 July 2017

1 reference

P C Johannesma

1 reference

31 July 2017

H M van der Klift

1 reference

31 July 2017

N C T van Grieken

1 reference

31 July 2017

D Troost

1 reference

31 July 2017

H Te Riele

1 reference

31 July 2017

M A J M Jacobs

1 reference

31 July 2017

T J Postma

1 reference

31 July 2017

D A M Heideman

1 reference

31 July 2017

C M J Tops

1 reference

31 July 2017

J T Wijnen

1 reference

31 July 2017

F H Menko

1 reference

31 July 2017

publication date

20 February 2011

1 reference

31 July 2017

1 reference

31 July 2017

1 reference

31 July 2017

1 reference

31 July 2017

page(s)

243-255

1 reference

Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

31 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Management of extracolonic tumours in patients with Lynch syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Molecular models for the tissue specificity of DNA mismatch repair-deficient carcinogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Syndrome of early onset colon cancers, hematologic malignancies & features of neurofibromatosis in HNPCC families with homozygous mismatch repair gene mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Constitutive deficiency in DNA mismatch repair

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

The 2007 WHO classification of tumours of the central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Targeting brain cancer: advances in the molecular pathology of malignant glioma and medulloblastoma

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Exciting new advances in neuro-oncology: the avenue to a cure for malignant glioma

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

High-grade malignant glioma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

The multifaceted mismatch-repair system

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Loss of the mismatch repair protein MSH6 in human glioblastomas is associated with tumor progression during temozolomide treatment

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Mismatch repair-dependent processing of methylation damage gives rise to persistent single-stranded gaps in newly replicated DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Triazene compounds: mechanism of action and related DNA repair systems.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Medulloblastoma, acute myelocytic leukemia and colonic carcinomas in a child with biallelic MSH6 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Papillary glioneuronal tumor: a new variant of mixed neuronal-glial neoplasm

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Papillary glioneuronal tumor: a case report and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Aggressive variant of a papillary glioneuronal tumor. Report of 2 cases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Microsatellite instability in cancer of the proximal colon

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Two modes of microsatellite instability in human cancer: differential connection of defective DNA mismatch repair to dinucleotide repeat instability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Type A microsatellite instability in pediatric gliomas as an indicator of Turcot syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Mismatch repair deficiency is an uncommon mechanism of alkylator resistance in pediatric malignant gliomas: a report from the Children's Oncology Group

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

PMS2 mutations in childhood cancer

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Biallelic PMS2 mutations and a distinctive childhood cancer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Human PMS2 deficiency is associated with impaired immunoglobulin class switch recombination

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

MSH6 mutations arise in glioblastomas during temozolomide therapy and mediate temozolomide resistance.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

DNA mismatch repair and the DNA damage response to ionizing radiation: making sense of apparently conflicting data

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Biallelic mutation of MSH2 in primary human cells is associated with sensitivity to irradiation and altered RAD51 foci kinetics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Cerebral primitive neuroectodermal tumor in an adult with a heterozygous MSH2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Genetic instability influences drug response in cancer cells.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

The molecular basis of Turcot's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

The hPMS2 exon 5 mutation and malignant glioma. Case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Novel PMS2 pseudogenes can conceal recessive mutations causing a distinctive childhood cancer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Drastic genetic instability of tumors and normal tissues in Turcot syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Café-au-lait spots and early onset colorectal neoplasia: a variant of HNPCC?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Two PMS2 mutations in a Turcot syndrome family with small bowel cancers.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Hypothesis: Possible role of retinoic acid therapy in patients with biallelic mismatch repair gene defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Multifocal anaplastic astrocytoma in a patient with hereditary colorectal cancer, transcobalamin II deficiency, agenesis of the corpus callosum, mental retardation, and inherited PMS2 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Pediatric duodenal cancer and biallelic mismatch repair gene mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

A homozygote splice site PMS2 mutation as cause of Turcot syndrome gives rise to two different abnormal transcripts

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Mutational targets in colorectal cancer cells with microsatellite instability.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Early onset brain tumor and lymphoma in MSH2-deficient children

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

A homozygous mutation in MSH6 causes Turcot syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

Biallelic germline mutations of mismatch-repair genes: a possible cause for multiple pediatric malignancies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01635.X

10.1111/J.1399-0004.2011.01635.X

21 January 2018

Identifiers

DOI

1 reference

31 July 2017

1 reference