Chromosomal assignment of human uracil-DNA glycosylase to chromosome 12

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

Science advances·2020

Proteolytically activated, recombinant anti-mullerian hormone inhibits androgen secretion, proliferation, and differentiation of spermatogonia in adult zebrafish testis organ cultures.

Endocrinology·2011

Different organization of base excision repair of uracil in DNA in nuclei and mitochondria and selective upregulation of mitochondrial uracil-DNA glycosylase after oxidative stress.

Neuroscience·2006

The 118 A > G polymorphism in the human mu-opioid receptor gene may increase morphine requirements in patients with pain caused by malignant disease.

Acta anaesthesiologica Scandinavica·2004

A gel electrophoresis method for detection of mitochondrial DNA mutation (3243 tRNA(Leu (UUR))) applied to a Norwegian family with diabetes mellitus and hearing loss.

Scandinavian journal of clinical and laboratory investigation·2004

A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemia.

The pharmacogenomics journal·2003

Molecular insights into how maternal investment shapes embryonic development for improving conservation breeding of the Chinese alligator (Alligator sinensis).

Genomics·2026

Integrated transcriptomic and WGCNA analyses identify RBP7 as a regulator of skeletal muscle development in chickens.

Genomics·2026

A novel tRNA-derived fragment, tRF-16-WSNKP9D promotes malignant progression of colorectal carcinoma through mediating PFN1.

Genomics·2026

Integrative profiling of multi-modal plasma cfRNA signatures enables detection and prognostic risk stratification in breast cancer.

Genomics·2026

Metabolomics and network pharmacology identify three key bioactive organic acid metabolites in Amomum tsao-ko.

Genomics·2026

New genomic and transposable element annotation of the microsporidian parasite Anncaliia algerae.

Genomics·2026

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study.

International journal of reproductive biomedicine·2026

Whole-Exome Sequencing Reveals the Genetic Landscape and Genotype-Phenotype Spectrum of Dystonia in a Chinese Cohort.

CNS neuroscience & therapeutics·2026

Genome-wide analysis of 439 mass spectrometry-based proteomic profiles in a population of 15,035 Scottish individuals.

Nature communications·2026

Generation of a human induced pluripotent stem cell line (PNUYHi004-A) from a patient with hereditary spastic paraplegia type 46 (SPG46) carrying compound heterozygous GBA2 variants.

Stem cell research·2026

Polygenic Risk Scores for Islet Autoantibody Positive Early-Stage Type 1 Diabetes Pre-Screening.

Diabetes, obesity & metabolism·2026

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

Clinical genetics·2026

Related Experiment Videos

Chromosomal assignment of human uracil-DNA glycosylase to chromosome 12

Related Concept Videos

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

Proteolytically activated, recombinant anti-mullerian hormone inhibits androgen secretion, proliferation, and differentiation of spermatogonia in adult zebrafish testis organ cultures.

Different organization of base excision repair of uracil in DNA in nuclei and mitochondria and selective upregulation of mitochondrial uracil-DNA glycosylase after oxidative stress.

The 118 A > G polymorphism in the human mu-opioid receptor gene may increase morphine requirements in patients with pain caused by malignant disease.

A gel electrophoresis method for detection of mitochondrial DNA mutation (3243 tRNA(Leu (UUR))) applied to a Norwegian family with diabetes mellitus and hearing loss.

A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemia.

Molecular insights into how maternal investment shapes embryonic development for improving conservation breeding of the Chinese alligator (Alligator sinensis).

Integrated transcriptomic and WGCNA analyses identify RBP7 as a regulator of skeletal muscle development in chickens.

A novel tRNA-derived fragment, tRF-16-WSNKP9D promotes malignant progression of colorectal carcinoma through mediating PFN1.

Integrative profiling of multi-modal plasma cfRNA signatures enables detection and prognostic risk stratification in breast cancer.

Metabolomics and network pharmacology identify three key bioactive organic acid metabolites in Amomum tsao-ko.

New genomic and transposable element annotation of the microsporidian parasite Anncaliia algerae.

Rare missense variants identified by whole-genome sequencing in men with oligoasthenoteratozoospermia: An experimental study.

Whole-Exome Sequencing Reveals the Genetic Landscape and Genotype-Phenotype Spectrum of Dystonia in a Chinese Cohort.

Genome-wide analysis of 439 mass spectrometry-based proteomic profiles in a population of 15,035 Scottish individuals.

Generation of a human induced pluripotent stem cell line (PNUYHi004-A) from a patient with hereditary spastic paraplegia type 46 (SPG46) carrying compound heterozygous GBA2 variants.

Polygenic Risk Scores for Islet Autoantibody Positive Early-Stage Type 1 Diabetes Pre-Screening.

Analysis of Genomic Testing of Congenital Heart Disease in a Cohort From a Consanguineous Population.

Related Experiment Videos

Chromosomal assignment of human uracil-DNA glycosylase to chromosome 12

Abstract:

Related Concept Videos

Related Articles