结核性硬化症的遗传学

Higher rates of immune-related adverse events in circulating tumor DNA (ctDNA)-negative patients following adjuvant checkpoint inhibitor therapy.

ESMO open·2026

Circulating kidney injury molecule-1 (KIM-1) and association with outcome to adjuvant immunotherapy in renal cell carcinoma.

Annals of oncology : official journal of the European Society for Medical Oncology·2025

Moving the Needle Toward Fair Compensation in Pediatric Nephrology.

Frontiers in pediatrics·2022

Stress response after race and endurance training sessions and competitions in Arabian horses.

Preventive veterinary medicine·2021

Identifying avoidable switchboard delays in England's NHS hospitals: phase one of the national SWITCH project.

Acute medicine·2020

River Continuity Restoration and Diadromous Fishes: Much More than an Ecological Issue.

Environmental management·2018

Multivessel coronary artery bypass grafting via small thoracotomy versus sternotomy (MIST): an investigator-initiated, international, open-label, randomised controlled trial.

Lancet (London, England)·2026

Efficacy and safety of once-daily oral zenagamtide, a novel unimolecular GLP-1 and amylin receptor agonist, in adults with type 2 diabetes: a multicentre, randomised, parallel, double-blind, placebo-controlled, dose-finding, phase 2 trial.

Lancet (London, England)·2026

Psoriasis.

Lancet (London, England)·2026

Deramiocel heart-derived cellular therapy in advanced Duchenne muscular dystrophy (HOPE-3): a phase 3, randomised, double-blind, placebo-controlled trial.

Lancet (London, England)·2026

Genetic Susceptibility to Nephrolithiasis: A Genome-Phenome Approach with Polygenic Risk Score Analysis.

Kidney diseases (Basel, Switzerland)·2026

Germline Variants in Centromere Binding Protein 126 Predispose to Glioblastoma.

medRxiv : the preprint server for health sciences·2026

Association Between Rare Germline Variants in Cancer Susceptibility Genes and Lung Cancer Risk.

The Annals of thoracic surgery·2026

Integrating Optical Genome Mapping into the Genetic Diagnostic Algorithm: Clinical Utility in Unresolved Autosomal Recessive Disorders from a Large Cohort.

Cytogenetic and genome research·2026

An improved SMS p.Gly56Ser mouse model of Snyder-Robinson syndrome reveals phenotypic parallels with clinical features.

Disease models & mechanisms·2026

PALM3 and hearing loss: a potential dual diagnosis interfering with novel gene discovery.

European journal of human genetics : EJHG·2026

相关实验视频

结核性硬化症的遗传学

相关概念视频

Higher rates of immune-related adverse events in circulating tumor DNA (ctDNA)-negative patients following adjuvant checkpoint inhibitor therapy.

Circulating kidney injury molecule-1 (KIM-1) and association with outcome to adjuvant immunotherapy in renal cell carcinoma.

Moving the Needle Toward Fair Compensation in Pediatric Nephrology.

Stress response after race and endurance training sessions and competitions in Arabian horses.

Identifying avoidable switchboard delays in England's NHS hospitals: phase one of the national SWITCH project.

River Continuity Restoration and Diadromous Fishes: Much More than an Ecological Issue.

Multivessel coronary artery bypass grafting via small thoracotomy versus sternotomy (MIST): an investigator-initiated, international, open-label, randomised controlled trial.

Efficacy and safety of once-daily oral zenagamtide, a novel unimolecular GLP-1 and amylin receptor agonist, in adults with type 2 diabetes: a multicentre, randomised, parallel, double-blind, placebo-controlled, dose-finding, phase 2 trial.

Psoriasis.

Deramiocel heart-derived cellular therapy in advanced Duchenne muscular dystrophy (HOPE-3): a phase 3, randomised, double-blind, placebo-controlled trial.

Genetic Susceptibility to Nephrolithiasis: A Genome-Phenome Approach with Polygenic Risk Score Analysis.

Germline Variants in Centromere Binding Protein 126 Predispose to Glioblastoma.

Association Between Rare Germline Variants in Cancer Susceptibility Genes and Lung Cancer Risk.

Integrating Optical Genome Mapping into the Genetic Diagnostic Algorithm: Clinical Utility in Unresolved Autosomal Recessive Disorders from a Large Cohort.

An improved SMS p.Gly56Ser mouse model of Snyder-Robinson syndrome reveals phenotypic parallels with clinical features.

PALM3 and hearing loss: a potential dual diagnosis interfering with novel gene discovery.

相关实验视频

结核性硬化症的遗传学

相关概念视频

相关文章