Is the monocyte chemotactic protein-1 -2518 G allele a risk factor for severe acute pancreatitis? (Q54664671)

2 June 2018

title

Is the monocyte chemotactic protein-1 -2518 G allele a risk factor for severe acute pancreatitis? (English)

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2 June 2018

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6

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David C Whitcomb

8

object named as

David C Whitcomb

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2 June 2018

Janette Lamb

4

object named as

Janette Lamb

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2 June 2018

Adam Slivka

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object named as

Adam Slivka

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2 June 2018

author name string

Georgios I Papachristou

1

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2 June 2018

David A Sass

2

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Haritha Avula

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Anna Lokshin

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language of work or name

English

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publication date

1 May 2005

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2 June 2018

Clinical Gastroenterology and Hepatology

published in

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2 June 2018

volume

3

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2 June 2018

issue

5

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2 June 2018

page(s)

475-481

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2 June 2018

Natural history of acute pancreatitis and the role of infection

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The APACHE II score is unreliable to diagnose necrotizing pancreatitis on admission to hospital.

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Macrophage migration inhibitory factor is a critical mediator of severe acute pancreatitis

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CC-chemokine activation in acute pancreatitis: enhanced release of monocyte chemoattractant protein-1 in patients with local and systemic complications

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Chemokine gene expression in rat pancreatic acinar cells is an early event associated with acute pancreatitis

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Chemokines MCP-1 and RANTES in isolated rat pancreatic acinar cells treated with CCK and ethanol in vitro

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Chronic alcohol consumption accelerates fibrosis in response to cerulein-induced pancreatitis in rats

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Involvement of polymorphisms in the chemokine system in the susceptibility for coronary artery disease (CAD). Coincidence of elevated Lp(a) and MCP-1 -2518 G/G genotype in CAD patients

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Polymorphism in the gene regulatory region of MCP-1 is associated with asthma susceptibility and severity

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APACHE II: a severity of disease classification system

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APACHE-II score for assessment and monitoring of acute pancreatitis

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SPINK1/PSTI polymorphisms act as disease modifiers in familial and idiopathic chronic pancreatitis

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Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene

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Identifiers

DOI

1 reference

2 June 2018

PubMed ID

15880317

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2 June 2018