The first signs of danger

Crystal structures of the components of the Staphylococcus aureus leukotoxin ED.

Acta crystallographica. Section D, Structural biology·2016

Phylogenetic analysis reveals multiple introductions of Cynodon species in Australia.

Molecular phylogenetics and evolution·2012

Crystal structure of the novel PaiA N-acetyltransferase from Thermoplasma acidophilum involved in the negative control of sporulation and degradative enzyme production.

Proteins·2011

Risk of breast cancer according to clinicopathologic features among long-term survivors of Hodgkin's lymphoma treated with radiotherapy.

British journal of cancer·2010

Structural genomics and drug discovery for infectious diseases.

Infectious disorders drug targets·2009

Reproduction of Meloidogyne spp. on Resistant Peanut Genotypes from Three Breeding Programs.

Journal of nematology·2009

Real-World Data from a Single-Center, Large Academic Centralized Manufacturing of CD19 CAR T Cells in an Industry Partnership.

Human gene therapy·2026

Streamlining Genetically Modified Organism Regulatory Classification in UK Gene Therapy Clinical Trials: A UK Pharmacy Perspective.

Human gene therapy·2026

Physiologically Regulated Frataxin Gene Replacement Restores Neurological Function in a Mouse Model of Friedreich Ataxia.

Human gene therapy·2026

Suppression of AAV-Delivered Transgene Expression Using Artificial MicroRNAs Delivered by an Alternative AAV Serotype.

Human gene therapy·2026

Safety, Tolerability, and Efficacy of a Prophylactic Sirolimus Protocol for Patients Receiving Delandistrogene Moxeparvovec-Rokl Gene Therapy.

Human gene therapy·2026

Accelerating Translation of NK Cell Therapies to the Clinic: A European Perspective.

Human gene therapy·2026

A Novel de Novo WAC Frameshift Variant in DeSanto-Shinawi Syndrome With Temporo-Occipital Epileptiform Activity and Congenital Cardiac Anomalies.

American journal of medical genetics. Part A·2026

PLCG2 downregulation impairs synaptic function and increases Alzheimer's disease hallmarks in neuronal cultures.

Nature genetics·2026

A Young Child With Global Developmental Delay and Epilepsy Secondary to a Novel Variant of KBG Syndrome.

Cureus·2026

Comprehensive Evaluation of Clinical, Developmental, Genetic, and Reproductive Characteristics of 133 Patients with Klinefelter Syndrome.

Molecular syndromology·2026

Deficiency in circulating T cells in four core genotypes mice with Sry translocation.

Journal of immunology (Baltimore, Md. : 1950)·2026

When to think of genetic causes for rhabdomyolysis? A Brazilian single-center exploratory study.

Arquivos de neuro-psiquiatria·2026

Related Experiment Videos

The first signs of danger

Related Concept Videos

Crystal structures of the components of the Staphylococcus aureus leukotoxin ED.

Phylogenetic analysis reveals multiple introductions of Cynodon species in Australia.

Crystal structure of the novel PaiA N-acetyltransferase from Thermoplasma acidophilum involved in the negative control of sporulation and degradative enzyme production.

Risk of breast cancer according to clinicopathologic features among long-term survivors of Hodgkin's lymphoma treated with radiotherapy.

Structural genomics and drug discovery for infectious diseases.

Reproduction of Meloidogyne spp. on Resistant Peanut Genotypes from Three Breeding Programs.

Real-World Data from a Single-Center, Large Academic Centralized Manufacturing of CD19 CAR T Cells in an Industry Partnership.

Streamlining Genetically Modified Organism Regulatory Classification in UK Gene Therapy Clinical Trials: A UK Pharmacy Perspective.

Physiologically Regulated Frataxin Gene Replacement Restores Neurological Function in a Mouse Model of Friedreich Ataxia.

Suppression of AAV-Delivered Transgene Expression Using Artificial MicroRNAs Delivered by an Alternative AAV Serotype.

Safety, Tolerability, and Efficacy of a Prophylactic Sirolimus Protocol for Patients Receiving Delandistrogene Moxeparvovec-Rokl Gene Therapy.

Accelerating Translation of NK Cell Therapies to the Clinic: A European Perspective.

A Novel de Novo WAC Frameshift Variant in DeSanto-Shinawi Syndrome With Temporo-Occipital Epileptiform Activity and Congenital Cardiac Anomalies.

PLCG2 downregulation impairs synaptic function and increases Alzheimer's disease hallmarks in neuronal cultures.

A Young Child With Global Developmental Delay and Epilepsy Secondary to a Novel Variant of KBG Syndrome.

Comprehensive Evaluation of Clinical, Developmental, Genetic, and Reproductive Characteristics of 133 Patients with Klinefelter Syndrome.

Deficiency in circulating T cells in four core genotypes mice with Sry translocation.

When to think of genetic causes for rhabdomyolysis? A Brazilian single-center exploratory study.

Related Experiment Videos

The first signs of danger

Related Concept Videos

Related Articles