Irinotecan disrupts tight junction proteins within the gut : implications for chemotherapy-induced gut toxicity. (Q37591476)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24316664%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

title

Irinotecan disrupts tight junction proteins within the gut : implications for chemotherapy-induced gut toxicity (English)

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2 March 2020

1 reference

1 reference

1

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2 March 2020

Joanne Bowen

2

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2 March 2020

Emma Bateman

5

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2 March 2020

Romany Stansborough

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2 March 2020

Rachel J. Gibson

8

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2 March 2020

3

Noor Al-Dasooqi

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2 March 2020

7

Joseph Shirren

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2 March 2020

author name string

Masooma Sultani

4

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publication date

6 December 2013

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Cancer Biology and Therapy

2 March 2020

published in

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2 March 2020

volume

15

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2 March 2020

issue

2

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2 March 2020

page(s)

236-244

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Matrix metalloproteinase-9 mediates hypoxia-induced vascular leakage in the brain via tight junction rearrangement

2 March 2020

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Chemotherapy-induced gut toxicity: are alterations to intestinal tight junctions pivotal?

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1 September 2018

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1 September 2018

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1 September 2018

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1 September 2018

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1 September 2018

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Crossref

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21 January 2018

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12 December 2020

Effect of interleukin-11 on ameliorating intestinal damage after methotrexate treatment of breast cancer in rats

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12 December 2020

Effect of high-dose chemotherapy on intestinal permeability in humans

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12 December 2020

Selection of Housekeeping Genes for Gene Expression Studies in a Rat Model of Irinotecan-Induced Mucositis

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The expression and the cellular distribution of the tight junction proteins are altered in irritable bowel syndrome patients with differences according to the disease subtype

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Establishment of a Single-Dose Irinotecan Model of Gastrointestinal Mucositis

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12 December 2020

Identifiers

DOI

10.4161/CBT.27222

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24316664%20AND%20SRC:MED&resulttype=core&format=json

2 March 2020

1 reference

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2 March 2020

PubMed publication ID

24316664

1 reference

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