IL-22(+)CD4(+) T cells promote colorectal cancer stemness via STAT3 transcription factor activation and induction of the methyltransferase DOT1L (Q33655332)

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English	IL-22(+)CD4(+) T cells promote colorectal cancer stemness via STAT3 transcription factor activation and induction of the methyltransferase DOT1L	scientific article

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scholarly article

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PubMed publication ID

28 July 2017

IL-22(+)CD4(+) T cells promote colorectal cancer stemness via STAT3 transcription factor activation and induction of the methyltransferase DOT1L (English)

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Europe PubMed Central

PubMed publication ID

28 July 2017

colorectal cancer

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based on heuristic

inferred from title

colorectal carcinoma

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based on heuristic

inferred from title

Witold Zgodzinski

object named as

Witold Zgodzinski

11

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Emina Huang

15

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1

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Ilona Kryczek

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Europe PubMed Central

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28 July 2017

Grzegorz Wallner

13

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Grzegorz Wallner

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28 July 2017

author name string

Yanwei Lin

2

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28 July 2017

Nisha Nagarsheth

3

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28 July 2017

Dongjun Peng

4

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28 July 2017

Lili Zhao

5

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28 July 2017

Ende Zhao

6

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28 July 2017

Linda Vatan

7

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28 July 2017

Wojciech Szeliga

8

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28 July 2017

Yali Dou

9

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28 July 2017

Scott Owens

10

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28 July 2017

Marek Majewski

12

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28 July 2017

Jingyuan Fang

14

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28 July 2017

Weiping Zou

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28 July 2017

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publication date

8 May 2014

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28 July 2017

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28 July 2017

40

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28 July 2017

5

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28 July 2017

772-784

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Europe PubMed Central

PubMed publication ID

28 July 2017

Myeloid-derived suppressor cells enhance stemness of cancer cells by inducing microRNA101 and suppressing the corepressor CtBP2.

1 reference

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1 reference

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Catalytic site remodelling of the DOT1L methyltransferase by selective inhibitors

1 reference

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Requirement for Dot1l in murine postnatal hematopoiesis and leukemogenesis by MLL translocation.

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Linking H3K79 trimethylation to Wnt signaling through a novel Dot1-containing complex (DotCom)

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30 October 2018

Identifiers

10.1016/J.IMMUNI.2014.03.010

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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