Is scrapie solely a genetic disease?

An investigation of the clinical impact and therapeutic relevance of a DNA damage immune response (DDIR) signature in patients with advanced gastroesophageal adenocarcinoma.

ESMO open·2024

Progression free survival of myeloma patients who become IFE-negative correlates with the detection of residual monoclonal free light chain (FLC) by mass spectrometry.

Blood cancer journal·2024

Genetic factors influencing the risk of multiple myeloma bone disease.

Leukemia·2015

Small molecule kinase inhibitors as anti-cancer therapeutics.

Mini reviews in medicinal chemistry·2012

Muir-Torre Syndrome: expanding the genotype and phenotype--a further family with a MSH6 mutation.

Familial cancer·2008

The impact of two-dimensional versus three-dimensional ultrasound exposure on maternal-fetal attachment and maternal health behavior in pregnancy.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2006

Universal gates from braiding and fusing anyons on quantum hardware.

Nature·2026

People use fast and flat simulation to reason about new games.

Nature·2026

Rising dust pollution across Europe in a changing climate.

Nature·2026

Ammonia pressure controls colloidal metal nitride synthesis in molten salts.

Nature·2026

Programming fracture resistance in metamaterials via elastic instabilities.

Nature·2026

Selectivity Emerges from Indiscriminate Photoreduction.

Nature·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

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Is scrapie solely a genetic disease?

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An investigation of the clinical impact and therapeutic relevance of a DNA damage immune response (DDIR) signature in patients with advanced gastroesophageal adenocarcinoma.

Progression free survival of myeloma patients who become IFE-negative correlates with the detection of residual monoclonal free light chain (FLC) by mass spectrometry.

Genetic factors influencing the risk of multiple myeloma bone disease.

Small molecule kinase inhibitors as anti-cancer therapeutics.

Muir-Torre Syndrome: expanding the genotype and phenotype--a further family with a MSH6 mutation.

The impact of two-dimensional versus three-dimensional ultrasound exposure on maternal-fetal attachment and maternal health behavior in pregnancy.

Universal gates from braiding and fusing anyons on quantum hardware.

People use fast and flat simulation to reason about new games.

Rising dust pollution across Europe in a changing climate.

Ammonia pressure controls colloidal metal nitride synthesis in molten salts.

Programming fracture resistance in metamaterials via elastic instabilities.

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MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

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