Two mutations, one novel and one frequently observed, in Japanese patients with McArdle's disease

Enhanced immunity in intradermal vaccination by novel hollow microneedles.

Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI)·2018

Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).

Muscle & nerve. Supplement·2013

Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses.

Muscle & nerve. Supplement·2013

Characterization of the Asian myopathy patients with VCP mutations.

European journal of neurology·2011

Difference in the nature of tannins on in vitro ruminal methane and volatile fatty acid production and on methanogenic archaea and protozoal populations.

Journal of dairy science·2009

Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.

Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology·2008

KATNAL2 dysfunction impairs microtubule dynamics and contributes to syndromic neurodevelopmental disease.

Human molecular genetics·2026

Immune-related DNA methylation signatures, age prediction, and cross-tissue assessment via biologically informed neural networks.

Human molecular genetics·2026

Droplet digital PCR as a first-line detection tool in the genetic diagnosis of vascular anomalies.

Human molecular genetics·2026

The monogenic forms of obesity in Saudi families.

Human molecular genetics·2026

VPS13C regulates triglyceride homeostasis and adipocyte differentiation.

Human molecular genetics·2026

Gene regulatory behaviors of mutant CRX proteins demonstrated with late-stage human retinal organoids.

Human molecular genetics·2026

Related Experiment Videos

Two mutations, one novel and one frequently observed, in Japanese patients with McArdle's disease

Related Concept Videos

Enhanced immunity in intradermal vaccination by novel hollow microneedles.

Cloning and mapping of a very short (10-kb) EcoRI fragment associated with facioscapulohumeral muscular dystrophy (FSHD).

Inflammatory response in facioscapulohumeral muscular dystrophy (FSHD): immunocytochemical and genetic analyses.

Characterization of the Asian myopathy patients with VCP mutations.

Difference in the nature of tannins on in vitro ruminal methane and volatile fatty acid production and on methanogenic archaea and protozoal populations.

Emerinopathy and laminopathy clinical, pathological and molecular features of muscular dystrophy with nuclear envelopathy in Japan.

KATNAL2 dysfunction impairs microtubule dynamics and contributes to syndromic neurodevelopmental disease.

Immune-related DNA methylation signatures, age prediction, and cross-tissue assessment via biologically informed neural networks.

Droplet digital PCR as a first-line detection tool in the genetic diagnosis of vascular anomalies.

The monogenic forms of obesity in Saudi families.

VPS13C regulates triglyceride homeostasis and adipocyte differentiation.

Gene regulatory behaviors of mutant CRX proteins demonstrated with late-stage human retinal organoids.

Related Experiment Videos

Two mutations, one novel and one frequently observed, in Japanese patients with McArdle's disease

Related Concept Videos

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