Checkpoint kinase 1 inhibition sensitises transformed cells to dihydroorotate dehydrogenase inhibition.

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Inhibiting checkpoint kinase 1 protects bone from bone resorption by mammary tumor in a mouse model.

P2860

Q54123047-6F163AFD-0216-4608-8546-6AD9C9E4D03E

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Checkpoint kinase 1 inhibition sensitises transformed cells to dihydroorotate dehydrogenase inhibition.

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http://www.wikidata.org/entity/Q47100853

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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name

Checkpoint kinase 1 inhibition ...... tate dehydrogenase inhibition.

@en

Checkpoint kinase 1 inhibition ...... tate dehydrogenase inhibition.

@nl

type

Item

label

Checkpoint kinase 1 inhibition ...... tate dehydrogenase inhibition.

@en

Checkpoint kinase 1 inhibition ...... tate dehydrogenase inhibition.

@nl

prefLabel

Checkpoint kinase 1 inhibition ...... tate dehydrogenase inhibition.

@en

Checkpoint kinase 1 inhibition ...... tate dehydrogenase inhibition.

@nl

P1476

Checkpoint kinase 1 inhibition ...... otate dehydrogenase inhibition

@en

P2093

Charles Vincent

http://www.w3.org/2001/XMLSchema#string

Charlène Berthet

http://www.w3.org/2001/XMLSchema#string

Claude Sardet

http://www.w3.org/2001/XMLSchema#string

Florence Bernex

http://www.w3.org/2001/XMLSchema#string

Geneviève Rodier

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Gisèle Matar

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Hélène Delpech

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Jean Yohan Noël

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Marta Jarlier

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Nelly Pirot

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P2860

Pyrimidine Nucleotide Biosynthesis in Animals: Genes, Enzymes, and Regulation of UMP Biosynthesis

Activation of mammalian Chk1 during DNA replication arrest: a role for Chk1 in the intra-S phase checkpoint monitoring replication origin firing

ATR-mediated checkpoint pathways regulate phosphorylation and activation of human Chk1

DHODH modulates transcriptional elongation in the neural crest and melanoma

Structure-based design, synthesis, and characterization of inhibitors of human and Plasmodium falciparum dihydroorotate dehydrogenases

Novel Inhibitors of Plasmodium falciparum Dihydroorotate Dehydrogenase with Anti-malarial Activity in the Mouse Model

Structure-Guided Lead Optimization of Triazolopyrimidine-Ring Substituents Identifies Potent Plasmodium falciparum Dihydroorotate Dehydrogenase Inhibitors with Clinical Candidate Potential

Mechanism of action for leflunomide in rheumatoid arthritis

On dihydroorotate dehydrogenases and their inhibitors and uses

Death by releasing the breaks: CHK1 inhibitors as cancer therapeutics

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95206-95222

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scholarly article

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10.18632/ONCOTARGET.19199

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P407

English

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http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Pierre-Olivier Vidalain

Charles Theillet

Yves L Janin

P577

2017-07-12T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29221122

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P932

5707016

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Checkpoint kinase 1 inhibition sensitises transformed cells to dihydroorotate dehydrogenase inhibition.

about

P2860

P2860

Checkpoint kinase 1 inhibition sensitises transformed cells to dihydroorotate dehydrogenase inhibition.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P932