Genetic dissection of tyrosyl-tRNA synthetase

Indexing electron backscatter diffraction patterns with a refined template matching approach.

Ultramicroscopy·2019

Validation of an algorithm to reveal the U wave in atrial fibrillation.

Scientific reports·2018

Quantitative imaging of anti-phase domains by polarity sensitive orientation mapping using electron backscatter diffraction.

Scientific reports·2017

The dissolvable bead: A novel in vitro biofilm model for evaluating antimicrobial resistance.

Journal of microbiological methods·2017

Diffraction effects and inelastic electron transport in angle-resolved microscopic imaging applications.

Journal of microscopy·2017

Assessing the precision of strain measurements using electron backscatter diffraction--part 2: experimental demonstration.

Ultramicroscopy·2013

The molecular mechanisms of crista formation: how mitochondria give themselves breathing room.

Biochemical Society transactions·2026

Propionic acidemia as a framework for understanding the impact of disturbed propionyl-CoA on histone modifications.

Biochemical Society transactions·2026

Functional amyloids as molecular switches: emerging roles in diverse signalling pathways.

Biochemical Society transactions·2026

Fc-engineering for improved cancer immunotherapy.

Biochemical Society transactions·2026

Where metabolism and virulence meet-sulfoxide reductases as determinants of bacterial survival.

Biochemical Society transactions·2026

Molecular mechanisms of Kir channel gating.

Biochemical Society transactions·2026

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

Brain : a journal of neurology·2026

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics·2026

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Therapeutic advances in rare disease·2026

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Journal of human genetics·2026

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Science (New York, N.Y.)·2026

Related Experiment Videos

Genetic dissection of tyrosyl-tRNA synthetase

Related Concept Videos

Indexing electron backscatter diffraction patterns with a refined template matching approach.

Validation of an algorithm to reveal the U wave in atrial fibrillation.

Quantitative imaging of anti-phase domains by polarity sensitive orientation mapping using electron backscatter diffraction.

The dissolvable bead: A novel in vitro biofilm model for evaluating antimicrobial resistance.

Diffraction effects and inelastic electron transport in angle-resolved microscopic imaging applications.

Assessing the precision of strain measurements using electron backscatter diffraction--part 2: experimental demonstration.

The molecular mechanisms of crista formation: how mitochondria give themselves breathing room.

Propionic acidemia as a framework for understanding the impact of disturbed propionyl-CoA on histone modifications.

Functional amyloids as molecular switches: emerging roles in diverse signalling pathways.

Fc-engineering for improved cancer immunotherapy.

Where metabolism and virulence meet-sulfoxide reductases as determinants of bacterial survival.

Molecular mechanisms of Kir channel gating.

AGG repeat expansion and aggregation of BIN1 in multiple system atrophy.

[Optical genome mapping analysis of a Chinese pedigree with a complex balanced translocation involving four chromosomes].

[Pathogenicity analysis and prenatal genetic counseling for five Chinese pedigrees harboring a hemizygous c.-32C>G variant of FGF13 gene].

Interim analysis of an international multi-site prospective natural history study evaluating the clinical presentation and progression of Leigh syndrome spectrum disorders.

Systematic genotype-phenotype mapping and transcriptomic analyses highlight SEMA6A as a candidate for neuronal migration defects in 5q22-q23 deletions.

Autism mutations rewire protein interaction networks to drive neurodevelopmental pathology.

Related Experiment Videos

Genetic dissection of tyrosyl-tRNA synthetase

Related Concept Videos

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