Single base polymorphism at -511 in the human interleukin-1 beta gene (IL1 beta)

Genetic Obesity and Bariatric Surgery Outcome in 1014 Patients with Morbid Obesity.

Obesity surgery·2019

Patient stratification for preventive care in dentistry.

Journal of dental research·2013

IL-1 receptor antagonist gene as a predictive biomarker of progression of knee osteoarthritis in a population cohort.

Osteoarthritis and cartilage·2013

Personalized medicine: will dentistry ride the wave or watch from the beach?

Journal of dental research·2012

Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.

Cytogenetic and genome research·2009

A nonsynonymous substitution of cystatin A, a cysteine protease inhibitor of house dust mite protease, leads to decreased mRNA stability and shows a significant association with atopic dermatitis.

Allergy·2007

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Human molecular genetics·2026

Mucolipidosis II: novel variants, clinical variation and assessment of HAP1 cells as a disease model.

Human molecular genetics·2026

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Human molecular genetics·2026

A patient-derived mouse model reproduces molecular, neurological, and sleep symptoms of SHINE syndrome.

Human molecular genetics·2026

The potential regulatory relationship between hsa_circ_0000973 and MBOAT2 in hypertriglyceridemia with abnormal glucose metabolism.

Human molecular genetics·2026

Clinical genome sequencing in neurodegenerative diseases-outcome in the first 500 patients.

Human molecular genetics·2026

Influenza A(H1N1) triggered atypical hemolytic uremic syndrome in a child with homozygous CD46 variant successfully treated with ravulizumab: a case report.

CEN case reports·2026

The first complete genome sequence of iris yellow spot virus from South America and comparative analysis with isolates of different geographic origin.

Archives of virology·2026

Optimizing antifungal management in immunocompromised paediatric patients: current gaps and future directions.

Current opinion in infectious diseases·2026

Subcutaneous immunoglobulin for chronic inflammatory demyelinating polyradiculoneuropathy.

The Cochrane database of systematic reviews·2026

Periampullary GIST in a neurofibromatosis type 1 patient with idiopathic thrombocytopenic purpura - a rare case report at a tertiary care center in Bangladesh.

International journal of surgery case reports·2026

Multidisciplinary genomic evaluation reveals adult inborn errors of immunity with rheumatic features.

Journal of human immunity·2026

Related Experiment Videos

Single base polymorphism at -511 in the human interleukin-1 beta gene (IL1 beta)

Related Concept Videos

Genetic Obesity and Bariatric Surgery Outcome in 1014 Patients with Morbid Obesity.

Patient stratification for preventive care in dentistry.

IL-1 receptor antagonist gene as a predictive biomarker of progression of knee osteoarthritis in a population cohort.

Personalized medicine: will dentistry ride the wave or watch from the beach?

Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.

A nonsynonymous substitution of cystatin A, a cysteine protease inhibitor of house dust mite protease, leads to decreased mRNA stability and shows a significant association with atopic dermatitis.

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Mucolipidosis II: novel variants, clinical variation and assessment of HAP1 cells as a disease model.

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

A patient-derived mouse model reproduces molecular, neurological, and sleep symptoms of SHINE syndrome.

The potential regulatory relationship between hsa_circ_0000973 and MBOAT2 in hypertriglyceridemia with abnormal glucose metabolism.

Clinical genome sequencing in neurodegenerative diseases-outcome in the first 500 patients.

Influenza A(H1N1) triggered atypical hemolytic uremic syndrome in a child with homozygous CD46 variant successfully treated with ravulizumab: a case report.

The first complete genome sequence of iris yellow spot virus from South America and comparative analysis with isolates of different geographic origin.

Optimizing antifungal management in immunocompromised paediatric patients: current gaps and future directions.

Subcutaneous immunoglobulin for chronic inflammatory demyelinating polyradiculoneuropathy.

Periampullary GIST in a neurofibromatosis type 1 patient with idiopathic thrombocytopenic purpura - a rare case report at a tertiary care center in Bangladesh.

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Related Experiment Videos

Single base polymorphism at -511 in the human interleukin-1 beta gene (IL1 beta)

Related Concept Videos

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