Lectin complement pathway gene profile of donor and recipient determine the risk of bacterial infections after orthotopic liver transplantation - Wikidata - wikimedia - TriplyDB

Lectin complement pathway gene profile of donor and recipient determine the risk of bacterial infections after orthotopic liver transplantation

Lectin complement pathway gene profile of donor and recipient determine the risk of bacterial infections after orthotopic liver transplantation

http://www.wikidata.org/entity/Q28286627

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Clinical immune-monitoring strategies for predicting infection risk in solid organ transplantation Genetic variants of innate immune receptors and infections after liver transplantation.Association of L-ficolin levels and FCN2 genotypes with chronic Chagas disease.Leprosy association with low MASP-2 levels generated by MASP2 haplotypes and polymorphisms flanking MAp19 exon 5 Recipient's genetic R702W NOD2 variant is associated with an increased risk of bacterial infections after orthotopic liver transplantation.The lectin pathway of complement and rheumatic heart disease.Circulating mannan-binding lectin, M-, L-, H-ficolin and collectin-liver-1 levels in patients with acute liver failure.Human L-ficolin (ficolin-2) and its clinical significance.Population pharmacokinetics and pharmacogenetics of once daily tacrolimus formulation in stable liver transplant recipients.C7 genotype of the donor may predict early bacterial infection after liver transplantation.Cost-effective procedures for genotyping of human FCN2 gene single nucleotide polymorphisms.Disease-causing mutations in genes of the complement system.The role of complement in the early immune response to transplantation.Mannose-Binding Lectin-Deficient Donors Increase the Risk of Bacterial Infection and Bacterial Infection-Related Mortality After Liver Transplantation.Fc-Gamma Receptor Polymorphisms Predispose Patients to Infectious Complications After Liver Transplantation.Risk of infection and sepsis in severely injured patients related to single nucleotide polymorphisms in the lectin pathway.Hypocomplementemia in kidney transplant recipients: impact on the risk of infectious complications.Genetic polymorphisms in innate immunity receptors do not predict the risk of bacterial and fungal infections and acute rejection after liver transplantation.Structural and functional diversity of collectins and ficolins and their relationship to disease.Ficolin-2 Gene rs7851696 Polymorphism is Associated with Delayed Graft Function and Acute Rejection in Kidney Allograft Recipients.High peak alanine aminotransferase determines extra risk for nonanastomotic biliary strictures after liver transplantation with donation after circulatory death.Circulating ficolin-2 and ficolin-3 in normal pregnancy and pre-eclampsia.

P2860

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P2860

Lectin complement pathway gene profile of donor and recipient determine the risk of bacterial infections after orthotopic liver transplantation

http://www.wikidata.org/entity/Q28286627

description

2010 nî lūn-bûn

@nan

2010 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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name

Lectin complement pathway gene ...... thotopic liver transplantation

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Lectin complement pathway gene ...... thotopic liver transplantation

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Lectin complement pathway gene ...... thotopic liver transplantation

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type

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Lectin complement pathway gene ...... thotopic liver transplantation

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Lectin complement pathway gene ...... thotopic liver transplantation

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Lectin complement pathway gene ...... thotopic liver transplantation

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Lectin complement pathway gene ...... thotopic liver transplantation

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Lectin complement pathway gene ...... thotopic liver transplantation

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Lectin complement pathway gene ...... thotopic liver transplantation

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Lectin complement pathway gene ...... thotopic liver transplantation

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P2093

Alexander F Schaapherder

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

Andrzej G Baranski

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

Anja Roos

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

Bart van Hoek

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

Bert-Jan F de Rooij

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

Bouke G Hepkema

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

Daniel W Hommes

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

Hein W Verspaget

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

Jan Ringers

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

Johan J van der Reijden

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

P2860

Natural substrates and inhibitors of mannan-binding lectin-associated serine protease-1 and -2: a study on recombinant catalytic fragments

Mannose-binding lectin-deficient mice are susceptible to infection with Staphylococcus aureus

L-ficolin specifically binds to lipoteichoic acid, a cell wall constituent of Gram-positive bacteria, and activates the lectin pathway of complement

A second serine protease associated with mannan-binding lectin that activates complement

Cutting edge: complement-activating complex of ficolin and mannose-binding lectin-associated serine protease

Bacterial resistance and overgrowth due to selective decontamination of the digestive tract.

Collections and ficolins: humoral lectins of the innate immune defense.

Activation of the classical complement pathway by mannose-binding protein in association with a novel C1s-like serine protease

Ficolins and the lectin complement pathway.

The structure of MBL-associated serine protease-2 reveals that identical substrate specificities of C1s and MASP-2 are realized through different sets of enzyme-substrate interactions.

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1100-10

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scholarly article

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2392068

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10.1002/HEP.23782

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3

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52

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2010-09-01T00:00:00Z

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44890178

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20593422

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liver transplantation