BglII polymorphism in the UNG gene in 4 populations

Mre11 exonuclease activity removes the chain-terminating nucleoside analog gemcitabine from the nascent strand during DNA replication.

Science advances·2020

The causal role of smoking on the risk of headache. A Mendelian randomization analysis in the HUNT study.

European journal of neurology·2018

The causal role of smoking on the risk of hip or knee replacement due to primary osteoarthritis: a Mendelian randomisation analysis of the HUNT study.

Osteoarthritis and cartilage·2017

The rare Arg181Cys mutation in the μ opioid receptor can abolish opioid responses.

Acta anaesthesiologica Scandinavica·2016

Nociceptive stimuli responses at different levels of general anaesthesia and genetic variability.

Acta anaesthesiologica Scandinavica·2012

The causal role of smoking in anxiety and depression: a Mendelian randomization analysis of the HUNT study.

Psychological medicine·2012

N-acetylcysteine suppresses retinal defects in Drosophila models of SNRNP200-associated retinitis pigmentosa.

Human molecular genetics·2026

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

[Recent Advances in the Classification and Treatment of Pediatric Gliomas].

No shinkei geka. Neurological surgery·2026

Integrated Analysis of SNPs and Structural Variations via High-depth Whole-genome Sequencing Reveals the Genetic Architecture and Optimizes Genomic Prediction in Chickens.

Poultry science·2026

Therapeutic challenge in a 5-year-old girl with Gorlin-Goltz syndrome and cardiac fibroma.

Annals of pediatric cardiology·2026

Integrative genomic and proteomic analyses identify candidate genetic loci and genetically supported proteins in age-related macular degeneration.

Eye and vision (London, England)·2026

Integrative Multi-omics Analysis for Prioritization of Candidate Genes in Polycystic Ovary Syndrome.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2026

Sequence analyses to accelerate the development of rapid resistance assays targeting the Neisseria gonorrhoeae gyrA gene.

European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology·2026

Related Experiment Videos

BglII polymorphism in the UNG gene in 4 populations

Related Concept Videos

Mre11 exonuclease activity removes the chain-terminating nucleoside analog gemcitabine from the nascent strand during DNA replication.

The causal role of smoking on the risk of headache. A Mendelian randomization analysis in the HUNT study.

The causal role of smoking on the risk of hip or knee replacement due to primary osteoarthritis: a Mendelian randomisation analysis of the HUNT study.

The rare Arg181Cys mutation in the μ opioid receptor can abolish opioid responses.

Nociceptive stimuli responses at different levels of general anaesthesia and genetic variability.

The causal role of smoking in anxiety and depression: a Mendelian randomization analysis of the HUNT study.

N-acetylcysteine suppresses retinal defects in Drosophila models of SNRNP200-associated retinitis pigmentosa.

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.

[Recent Advances in the Classification and Treatment of Pediatric Gliomas].

Integrated Analysis of SNPs and Structural Variations via High-depth Whole-genome Sequencing Reveals the Genetic Architecture and Optimizes Genomic Prediction in Chickens.

Therapeutic challenge in a 5-year-old girl with Gorlin-Goltz syndrome and cardiac fibroma.

Integrative genomic and proteomic analyses identify candidate genetic loci and genetically supported proteins in age-related macular degeneration.

Integrative Multi-omics Analysis for Prioritization of Candidate Genes in Polycystic Ovary Syndrome.

Sequence analyses to accelerate the development of rapid resistance assays targeting the Neisseria gonorrhoeae gyrA gene.

Related Experiment Videos

BglII polymorphism in the UNG gene in 4 populations

Related Concept Videos

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