Nucleotide sequence of a glycine transfer RNA coded by bacteriophage T4

The genome of the simian and human malaria parasite Plasmodium knowlesi.

Nature·2008

SCP1, a 356,023 bp linear plasmid adapted to the ecology and developmental biology of its host, Streptomyces coelicolor A3(2).

Molecular microbiology·2004

The complete genome sequence and analysis of Corynebacterium diphtheriae NCTC13129.

Nucleic acids research·2003

Isolation of novel tRNA(Ala) mutants by library selection in a tRNA(Ala) knockout strain.

Biochimie·2002

Conservation of long-range synteny and microsynteny between the genomes of two distantly related nematodes.

Genome biology·2002

Sequence of Plasmodium falciparum chromosomes 1, 3-9 and 13.

Nature·2002

Partial depletion of plasminogen activator inhibitor-1 decreases subcutaneous fat cell hypertrophy and liver cholesterol in high-fat-fed female mice.

FEBS letters·2026

Ligand-dependent transcriptional heterogeneity in cell cycle gene expression delays G1/S entry.

FEBS letters·2026

The impact of aging on the gut-liver axis in health and disease.

FEBS letters·2026

Autophagy and mitophagy in pancreatic β-cell homeostasis and their involvement in diabetes pathophysiology.

FEBS letters·2026

Oxidative modification of the D1 residue 332H during photoinactivation drives photosystem II turnover.

FEBS letters·2026

Synergistic perspectives-How single-molecule biophysics complement biochemical understanding.

FEBS letters·2026

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Bioinformatics (Oxford, England)·2026

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Drug metabolism and personalized therapy·2026

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

Current medicinal chemistry·2026

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

American journal of medical genetics. Part A·2026

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

Human mutation·2026

Functional genomics in Xenopus identifies ARHGAP10 as a congenital heart disease and ciliopathy gene.

iScience·2026

Related Experiment Videos

Nucleotide sequence of a glycine transfer RNA coded by bacteriophage T4

Related Concept Videos

The genome of the simian and human malaria parasite Plasmodium knowlesi.

SCP1, a 356,023 bp linear plasmid adapted to the ecology and developmental biology of its host, Streptomyces coelicolor A3(2).

The complete genome sequence and analysis of Corynebacterium diphtheriae NCTC13129.

Isolation of novel tRNA(Ala) mutants by library selection in a tRNA(Ala) knockout strain.

Conservation of long-range synteny and microsynteny between the genomes of two distantly related nematodes.

Sequence of Plasmodium falciparum chromosomes 1, 3-9 and 13.

Partial depletion of plasminogen activator inhibitor-1 decreases subcutaneous fat cell hypertrophy and liver cholesterol in high-fat-fed female mice.

Ligand-dependent transcriptional heterogeneity in cell cycle gene expression delays G1/S entry.

The impact of aging on the gut-liver axis in health and disease.

Autophagy and mitophagy in pancreatic β-cell homeostasis and their involvement in diabetes pathophysiology.

Oxidative modification of the D1 residue 332H during photoinactivation drives photosystem II turnover.

Synergistic perspectives-How single-molecule biophysics complement biochemical understanding.

Network-based stratification of allele-specific expression reveals patient subgroups in Huntington's disease.

Association of HTR2A (rs6313) gene polymorphism with autism spectrum disorder in Jordanian children: a case-control study.

Single-cell Transcriptome-wide Mendelian Randomization and Colocalization Converge on Astrocytic TRIM66 as a Candidate Driver and Potential Therapeutic Target for Trigeminal Neuralgia.

A Novel Constitutional TUBB Variant Associated With Familial Malformations of Cortical Development.

Pathogenic Variants in PET Complex Encoding Genes TDRD12 and EXD1 Impair piRNA Biogenesis and Cause Male Infertility.

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Related Experiment Videos

Nucleotide sequence of a glycine transfer RNA coded by bacteriophage T4

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