(Q48227977)

9 February 2018

title

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

1 reference

9 February 2018

1 reference

1 reference

10

1 reference

9 February 2018

author name string

Sven Gottschling

1

1 reference

9 February 2018

Harald Reinhard

2

1 reference

9 February 2018

Constanze Pagenstecher

3

1 reference

9 February 2018

Stefan Krüger

4

1 reference

9 February 2018

Jochen Raedle

5

1 reference

9 February 2018

Guido Plotz

6

1 reference

9 February 2018

Wolfram Henn

7

1 reference

9 February 2018

Reinhard Buettner

8

1 reference

9 February 2018

Sascha Meyer

9

1 reference

9 February 2018

publication date

27 March 2007

1 reference

9 February 2018

European Journal of Pediatrics

published in

1 reference

9 February 2018

volume

167

1 reference

9 February 2018

issue

2

1 reference

9 February 2018

page(s)

225-229

1 reference

9 February 2018

https://scigraph.springernature.com/pub.10.1007/s00431-007-0474-3

exact match

0 references

cites work

Analysis of the quaternary structure of the MutL C-terminal domain

1 reference

12 December 2020

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

1 reference

12 December 2020

Retinoids and cancer: antitumor effect of ATRA and of a new derivative of retinoic acid, IIF, on colon carcinoma cell lines CaCo-2 and HT-29.

1 reference

12 December 2020

Mismatch repair gene PMS2: disease-causing germline mutations are frequent in patients whose tumors stain negative for PMS2 protein, but paralogous genes obscure mutation detection and interpretation

1 reference

12 December 2020

Familial mutations in PMS2 can cause autosomal dominant hereditary nonpolyposis colorectal cancer

1 reference

12 December 2020

Contributions by MutL homologues Mlh3 and Pms2 to DNA mismatch repair and tumor suppression in the mouse

1 reference

12 December 2020

Interaction of mismatch repair protein PMS2 and the p53-related transcription factor p73 in apoptosis response to cisplatin

1 reference

12 December 2020

Phenotype associated with recessively inherited mutations in DNA mismatch repair (MMR) genes.

1 reference

12 December 2020

N-terminus of hMLH1 confers interaction of hMutLalpha and hMutLbeta with hMutSalpha

1 reference

12 December 2020

Long-time survival of a patient with glioblastoma and Turcot's syndrome

1 reference

12 December 2020

Retinoic acid increases the expression of p53 and proapoptotic caspases and sensitizes keratinocytes to apoptosis: a possible explanation for tumor preventive action of retinoids

1 reference

12 December 2020

Treatment of recurrent malignant gliomas with high-dose 13-cis-retinoic acid.

1 reference

12 December 2020

Characterization of the nuclear import of human MutLalpha

1 reference

12 December 2020

PMS2 mutations in childhood cancer

1 reference

12 December 2020

The molecular basis of Turcot's syndrome

1 reference

12 December 2020

Germline PMS2 mutations: one hit or two?

1 reference

12 December 2020

Immunohistochemical analysis reveals high frequency of PMS2 defects in colorectal cancer

1 reference

12 December 2020

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00431-007-0474-3

Identifiers

DOI

1 reference

9 February 2018

1 reference

9 February 2018