(Q28249125)

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Somatic deletions of genes regulating MSH2 protein stability cause DNA mismatch repair deficiency and drug resistance in human leukemia cells

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21946537%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

Somatic deletions of genes regulating MSH2 protein stability cause DNA mismatch repair deficiency and drug resistance in human leukemia cells (English)

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21946537%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

1 reference

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DNA mismatch repair

1 reference

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inferred from title

Meyling H Cheok

5

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21946537%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

Charles G. Mullighan

13

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13 February 2020

17

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Mary V Relling

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13 February 2020

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Barthelemy Diouf

1

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13 February 2020

Qing Cheng

2

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13 February 2020

Natalia F Krynetskaia

3

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13 February 2020

Wenjian Yang

4

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Europe PubMed Central

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13 February 2020

Deqing Pei

6

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13 February 2020

Yiping Fan

7

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13 February 2020

Cheng Cheng

8

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13 February 2020

Evgeny Y Krynetskiy

9

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13 February 2020

Hui Geng

10

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13 February 2020

Siying Chen

11

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13 February 2020

William E Thierfelder

12

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13 February 2020

James R Downing

14

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13 February 2020

Peggy Hsieh

15

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13 February 2020

William E Evans

18

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13 February 2020

Ching-Hon Pui

16

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13 February 2020

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25 September 2011

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13 February 2020

Nature Medicine

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21946537%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

17

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21946537%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

10

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21946537%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

1298-1303

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21946537%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

Molecular origins of cancer: Molecular basis of colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

20 March 2017

CDK8 is a colorectal cancer oncogene that regulates beta-catenin activity

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

20 March 2017

Role of class II phosphoinositide 3-kinase in cell signalling

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

20 March 2017

A mutation creating a potential illegitimate microRNA target site in the myostatin gene affects muscularity in sheep

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

20 March 2017

hMutS alpha is protected from ubiquitin-proteasome-dependent degradation by atypical protein kinase C zeta phosphorylation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

20 March 2017

Regulation of mTOR function in response to hypoxia by REDD1 and the TSC1/TSC2 tumor suppressor complex

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

20 March 2017

Mismatch repair deficiency associated with overexpression of the MSH3 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

20 March 2017

The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

20 March 2017

Mouse models for hereditary nonpolyposis colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

20 March 2017

Modulation of mismatch repair and genomic stability by miR-155

1 reference

https://api.crossref.org/works/10.1038/NM.2430

22 April 2017

Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

7 April 2017

Regulation of translation initiation by FRAP/mTOR

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

7 April 2017

Hereditary ovarian carcinoma: heterogeneity, molecular genetics, pathology, and management

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Microdeletions are a general feature of adult and adolescent acute lymphoblastic leukemia: Unexpected similarities with pediatric disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

DNA repair alterations in common pediatric malignancies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Thiopurines in current medical practice: molecular mechanisms and contributions to therapy-related cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Constitutive deficiency in DNA mismatch repair

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

TSC1 stabilizes TSC2 by inhibiting the interaction between TSC2 and the HERC1 ubiquitin ligase.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Inherited susceptibility to colorectal cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Degadration of mismatch repair hMutSalpha heterodimer by the ubiquitin-proteasome pathway

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Functional interactions and signaling properties of mammalian DNA mismatch repair proteins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

TSC1 and TSC2 tumor suppressors antagonize insulin signaling in cell growth

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Evidence for Msh2 haploinsufficiency in mice revealed by MNU-induced sister-chromatid exchange analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Epigenetic phenotypes distinguish microsatellite-stable and -unstable colorectal cancers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Mouse embryonic stem cells carrying one or two defective Msh2 alleles respond abnormally to oxidative stress inflicted by low-level radiation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Protein phosphatase 2A is a critical regulator of protein kinase C zeta signaling targeted by SV40 small t to promote cell growth and NF-kappaB activation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

The role of DNA mismatch repair in platinum drug resistance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Defective mismatch binding and a mutator phenotype in cells tolerant to DNA damage

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

29 September 2017

Induction of two DNA mismatch repair proteins, MSH2 and MSH6, in differentiated human neuroblastoma SH-SY5Y cells exposed to doxorubicin.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3192247

2 June 2018

Msh2 deficiency attenuates but does not abolish thiopurine hematopoietic toxicity in msh2-/- mice

1 reference

https://api.crossref.org/works/10.1038%2FNM.2430

21 January 2018

Role of postreplicative DNA mismatch repair in the cytotoxic action of thioguanine.

1 reference

https://api.crossref.org/works/10.1038%2FNM.2430

21 January 2018

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3' exons of TACSTD1.

1 reference

https://api.crossref.org/works/10.1038%2FNM.2430

21 January 2018

Mismatch G-T binding activity and MSH2 expression is quantitatively related to sensitivity of cells to methylating agents.

1 reference

https://api.crossref.org/works/10.1038%2FNM.2430

21 January 2018

Acute lymphoblastic leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21946537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microsatellite instability and p53 mutations are associated with abnormal expression of the MSH2 gene in adult acute leukemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/21946537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expression of DNA mismatch repair proteins in acute lymphoblastic leukaemia and normal bone marrow

1 reference

https://pubmed.ncbi.nlm.nih.gov/21946537

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/NM.2430

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

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13 February 2020

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PMC publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21946537%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

PubMed publication ID

2 references

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21946537%20AND%20SRC:MED&resulttype=core&format=json

13 February 2020

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