Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The effect of the MBL2 gene rs1800450 variant on COVID-19 development in Turkish patients.

Nucleosides, nucleotides & nucleic acids - 1 Jan 2025

Capraz Mustafa, Tekcan Akin, Cihangiroglu Mustafa, Nursal Ayse Feyda, Capraz Aylin, Menekse Elif, Dortok Demir Hatice, Kuruca Nilufer, Yigit Serbulent

Abstract excerpt

The coronavirus disease 2019 (COVID-19) is a recent pandemic occurring worldwide due to the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus, spreading mainly through large respiratory droplets or maybe through other transmission routes. The human genome has the most varied immune response genes correlated with infectious diseases. Genetic variants of mannose-binding lectin 2 (MBL2), an...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Aged
Share to Case-Control Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to COVID-19

Share to Gene Frequency

Share to Mannose-Binding Lectin

Share to Polymorphism, Single Nucleotide

Share to SARS-CoV-2

Share to Turkey

Source

Identifiers

PMID: 39210720
DOI: 10.1080/15257770.2024.2395872

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The effect of the MBL2 gene rs1800450 variant on COVID-19 development in Turkish patients.PMID 39210720Read ↗

Mannose binding lectin gene 2 (rs1800450) missense variant may contribute to development and severity of COVID-19 infection.Semantic proximity Read ↗

Association between MASP2 gene polymorphisms and susceptibility to Covid-19 in Iranian patients: a case-control study.Semantic proximity Read ↗

Effect of VDR and TLR2 gene variants on the clinical course of patients with COVID-19 disease.Semantic proximity Read ↗

Association between mannose binding lectin gene polymorphisms and clinical severity of COVID-19 in children.Semantic proximity Read ↗

Mannose-binding lectin gene 2 variant DD (rs 5030737) is associated with susceptibility to COVID-19 infection in the urban population of Patna City (India).Semantic proximity Read ↗

Evaluating interleukin-6 levels and the rs1800795 variant in Turkish patients with COVID-19: a prospective cohort study.Semantic proximity Read ↗

HLA-G 14-bp insertion/deletion polymorphism and risk of coronavirus disease 2019 (COVID-19) among Iraqi patients.Semantic proximity Read ↗

MBL deficiency-causing B allele (rs1800450) as a risk factor for severe COVID-19.Semantic proximity Read ↗

The MBL2 genotype relates to COVID-19 severity and may help to select the optimal therapy.Semantic proximity Read ↗

Relationship Between IL-10 Single Nucleotide Polymorphisms (rs1800871, rs1800872, and rs1800896) and the Severity of COVID-19.Semantic proximity Read ↗

Complement lectin pathway activation is associated with COVID-19 disease severity, independent of MBL2 genotype subgroups.Semantic proximity Read ↗

Frequency of Interleukin-6 rs1800795 (-174G/C) and rs1800797 (-597G/A) Polymorphisms in COVID-19 Patients in Turkey Who Develop Macrophage Activation Syndrome.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.