Novel DNA sequence differences in the beta2-adrenergic receptor gene promoter region

Haematotoxicity of Craniospinal Radiochemotherapy for Metastatic Paediatric High-Grade Glioma.

Clinical oncology (Royal College of Radiologists (Great Britain))·2025

Neuroendocrine Deficits and Weight Development Before and After Proton Therapy in Children With Craniopharyngioma.

Clinical oncology (Royal College of Radiologists (Great Britain))·2025

Outcomes of Patients Treated in the UK Proton Overseas Programme: Non-central Nervous System Group.

Clinical oncology (Royal College of Radiologists (Great Britain))·2023

Deletion of Tbc1d4/As160 abrogates cardiac glucose uptake and increases myocardial damage after ischemia/reperfusion.

Cardiovascular diabetology·2023

The radiosensitizing effect of platinum nanoparticles in proton irradiations is not caused by an enhanced proton energy deposition at the macroscopic scale.

Physics in medicine and biology·2022

Can a ToF-PET photon attenuation reconstruction test stopping-power estimations in proton therapy? A phantom study.

Physics in medicine and biology·2021

Multiomic Investigation of Shared Genetic Pathways in Paediatric Congenital Heart Disease and Neurodevelopmental Disorders.

Human mutation·2026

Type III Osteogenesis Imperfecta and COL1A1 Pathological Variants Are Associated With Higher Incidence and Progression of Hearing Loss.

Human mutation·2026

A Study on the Clinical Phenotypes and Genetic Analysis of ENG Variants in Four Hereditary Hemorrhagic Telangiectasia Type 1 Families.

Human mutation·2026

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

Human mutation·2026

Bridging the Gap: High-Resolution RHCE Genotyping by Third-Generation Sequencing Enhances Serological Interpretation of Weak Variants.

Human mutation·2026

From Germline Variants to Tumor Outcome: GWAS-Based Functional Genomics Prioritizes Colorectal Cancer Susceptibility Genes and Links SMAD9 to Prognosis.

Human mutation·2026

Exploring the Causal Relationship Between Sex Hormones and Depression by Means of Two-Sample Mendelian Randomization Analysis.

Actas espanolas de psiquiatria·2026

Generation of 5 induced pluripotent stem cell lines with copy number variations in 22q11.2.

Stem cell research·2026

Whole-transcriptome profiling of the fat body identifies aae-miR-283-ApoLp-Ⅱ/Ⅰ regulation associated with lipid transport and ovarian development in Aedes aegypti.

Insect biochemistry and molecular biology·2026

Androgen signaling via sympathetic neurons regulates allergic pulmonary inflammation.

Science immunology·2026

VDR BsmI polymorphism and obesity in vitamin D deficiency among undergraduate students: a cross-sectional study.

Molecular biology reports·2026

Investigation of WNT2, DISC1, and DOCK4 polymorphisms in a Turkish autism spectrum disorder cohort: a case-control and bioinformatics analysis.

Molecular biology reports·2026

Related Experiment Videos

Novel DNA sequence differences in the beta2-adrenergic receptor gene promoter region

Related Concept Videos

Haematotoxicity of Craniospinal Radiochemotherapy for Metastatic Paediatric High-Grade Glioma.

Neuroendocrine Deficits and Weight Development Before and After Proton Therapy in Children With Craniopharyngioma.

Outcomes of Patients Treated in the UK Proton Overseas Programme: Non-central Nervous System Group.

Deletion of Tbc1d4/As160 abrogates cardiac glucose uptake and increases myocardial damage after ischemia/reperfusion.

The radiosensitizing effect of platinum nanoparticles in proton irradiations is not caused by an enhanced proton energy deposition at the macroscopic scale.

Can a ToF-PET photon attenuation reconstruction test stopping-power estimations in proton therapy? A phantom study.

Multiomic Investigation of Shared Genetic Pathways in Paediatric Congenital Heart Disease and Neurodevelopmental Disorders.

Type III Osteogenesis Imperfecta and COL1A1 Pathological Variants Are Associated With Higher Incidence and Progression of Hearing Loss.

A Study on the Clinical Phenotypes and Genetic Analysis of ENG Variants in Four Hereditary Hemorrhagic Telangiectasia Type 1 Families.

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

Bridging the Gap: High-Resolution RHCE Genotyping by Third-Generation Sequencing Enhances Serological Interpretation of Weak Variants.

From Germline Variants to Tumor Outcome: GWAS-Based Functional Genomics Prioritizes Colorectal Cancer Susceptibility Genes and Links SMAD9 to Prognosis.

Exploring the Causal Relationship Between Sex Hormones and Depression by Means of Two-Sample Mendelian Randomization Analysis.

Generation of 5 induced pluripotent stem cell lines with copy number variations in 22q11.2.

Whole-transcriptome profiling of the fat body identifies aae-miR-283-ApoLp-Ⅱ/Ⅰ regulation associated with lipid transport and ovarian development in Aedes aegypti.

Androgen signaling via sympathetic neurons regulates allergic pulmonary inflammation.

VDR BsmI polymorphism and obesity in vitamin D deficiency among undergraduate students: a cross-sectional study.

Investigation of WNT2, DISC1, and DOCK4 polymorphisms in a Turkish autism spectrum disorder cohort: a case-control and bioinformatics analysis.

Related Experiment Videos

Novel DNA sequence differences in the beta2-adrenergic receptor gene promoter region

Related Concept Videos

Related Articles