DNA synthesis in nucleotide-permeable Escherichia coli cells. I. Preparation and properties of ether-treated cells

Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C gene.

Heart (British Cardiac Society)·2002

Genomic structure and fine mapping of the two human filamin gene paralogues FLNB and FLNC and comparative analysis of the filamin gene family.

Human genetics·2001

Apical hypertrophic cardiomyopathy due to a de novo mutation Arg719Trp of the beta-myosin heavy chain gene and cardiac arrest in childhood. A case report and family study.

Zeitschrift fur Kardiologie·2000

A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance.

Circulation·2000

[Genetic causes of hypertrophic cardiomyopathy].

Medizinische Klinik (Munich, Germany : 1983)·1998

A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated beta-myosin heavy chain genes.

Human genetics·1998

HuKSA: A Machine-Learning-Based Framework for Predicting Human Kinome Selectivity and Polypharmacology.

Journal of molecular biology·2026

piRTarBase2: an updated C. elegans piRNA binding site database with extensive evidence for piRNA targeting events.

Journal of molecular biology·2026

Structural basis for HKU5‑CoV main protease inhibition by the clinical antivirals nirmatrelvir and ensitrelvir.

Journal of molecular biology·2026

Two heads are better than one: Single stranded DNA translocation of UvrD-family dimers vs. monomers.

Journal of molecular biology·2026

Missense3D: leveraging protein structures, including AlphaFold models, to understand the effect of missense variants.

Journal of molecular biology·2026

HandMol at MolecularWebXR.org: Immersive, Multiuser Visualization and Interactive Modeling with Natural Interactions, on the Web Across a Wide Range of Devices.

Journal of molecular biology·2026

Unanticipated intermediates during isopenicillin N synthase catalysis identified by time-resolved X-ray free-electron laser studies.

Nature catalysis·2026

Unlocking the Latent Dienophile Reactivity of Neutral Ketimines through Ketimine-Enamine Tautomerism: A Diastereoselective Povarov Reaction between Two Neutral Imines.

Organic letters·2026

Kinetic Resolution of Racemic γ,γ-Disubstituted Cyclohexenones Enabled by Artificial Carboligase-Catalyzed Stereoselective Michael Addition.

Organic letters·2026

A Second-Shell Mutation Preorganizes HpnG for Broad-Scope Nucleoside Transglycosylation.

Organic letters·2026

Remote Generation of Pyramidalized N-N Axial Chirality via a Copper-Catalyzed Friedel-Crafts Reaction.

Organic letters·2026

Synergistic Substrate- and Condition-Controlled Switching between Alkene and Alkyne: A [4 + 2] Strategy for Diverse Isoindolinone Frameworks.

Organic letters·2026

Related Experiment Videos

DNA synthesis in nucleotide-permeable Escherichia coli cells. I. Preparation and properties of ether-treated cells

Related Concept Videos

Genetic polymorphisms in the renin-angiotensin-aldosterone system associated with expression of left ventricular hypertrophy in hypertrophic cardiomyopathy: a study of five polymorphic genes in a family with a disease causing mutation in the myosin binding protein C gene.

Genomic structure and fine mapping of the two human filamin gene paralogues FLNB and FLNC and comparative analysis of the filamin gene family.

Apical hypertrophic cardiomyopathy due to a de novo mutation Arg719Trp of the beta-myosin heavy chain gene and cardiac arrest in childhood. A case report and family study.

A newly created splice donor site in exon 25 of the MyBP-C gene is responsible for inherited hypertrophic cardiomyopathy with incomplete disease penetrance.

[Genetic causes of hypertrophic cardiomyopathy].

A high risk phenotype of hypertrophic cardiomyopathy associated with a compound genotype of two mutated beta-myosin heavy chain genes.

HuKSA: A Machine-Learning-Based Framework for Predicting Human Kinome Selectivity and Polypharmacology.

piRTarBase2: an updated C. elegans piRNA binding site database with extensive evidence for piRNA targeting events.

Structural basis for HKU5‑CoV main protease inhibition by the clinical antivirals nirmatrelvir and ensitrelvir.

Two heads are better than one: Single stranded DNA translocation of UvrD-family dimers vs. monomers.

Missense3D: leveraging protein structures, including AlphaFold models, to understand the effect of missense variants.

HandMol at MolecularWebXR.org: Immersive, Multiuser Visualization and Interactive Modeling with Natural Interactions, on the Web Across a Wide Range of Devices.

Unanticipated intermediates during isopenicillin N synthase catalysis identified by time-resolved X-ray free-electron laser studies.

Unlocking the Latent Dienophile Reactivity of Neutral Ketimines through Ketimine-Enamine Tautomerism: A Diastereoselective Povarov Reaction between Two Neutral Imines.

Kinetic Resolution of Racemic γ,γ-Disubstituted Cyclohexenones Enabled by Artificial Carboligase-Catalyzed Stereoselective Michael Addition.

A Second-Shell Mutation Preorganizes HpnG for Broad-Scope Nucleoside Transglycosylation.

Remote Generation of Pyramidalized N-N Axial Chirality via a Copper-Catalyzed Friedel-Crafts Reaction.

Synergistic Substrate- and Condition-Controlled Switching between Alkene and Alkyne: A [4 + 2] Strategy for Diverse Isoindolinone Frameworks.

Related Experiment Videos

DNA synthesis in nucleotide-permeable Escherichia coli cells. I. Preparation and properties of ether-treated cells

Related Concept Videos

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