A new family of interspersed repetitive DNA sequences in the mouse genome

Genotype-guided diagnostic reassessment after exome sequencing in neuromuscular disorders: experiences with a two-step approach.

European journal of neurology·2019

Homozygous XYLT2 variants as a cause of spondyloocular syndrome.

Clinical genetics·2017

Extension of the phenotype of biallelic loss-of-function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type I.

Clinical genetics·2017

Mitochondrial genetic variants identified to be associated with posttraumatic stress disorder.

Translational psychiatry·2015

Adolescent growth: genes, hormones and the peer group. Proceedings of the 20th Aschauer Soiree, held at Glücksburg castle, Germany, 15th to 17th November 2013.

Pediatric endocrinology reviews : PER·2014

A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila.

Molecular psychiatry·2011

HuKSA: A Machine-Learning-Based Framework for Predicting Human Kinome Selectivity and Polypharmacology.

Journal of molecular biology·2026

piRTarBase2: an updated C. elegans piRNA binding site database with extensive evidence for piRNA targeting events.

Journal of molecular biology·2026

Structural basis for HKU5‑CoV main protease inhibition by the clinical antivirals nirmatrelvir and ensitrelvir.

Journal of molecular biology·2026

Two heads are better than one: Single stranded DNA translocation of UvrD-family dimers vs. monomers.

Journal of molecular biology·2026

Missense3D: leveraging protein structures, including AlphaFold models, to understand the effect of missense variants.

Journal of molecular biology·2026

HandMol at MolecularWebXR.org: Immersive, Multiuser Visualization and Interactive Modeling with Natural Interactions, on the Web Across a Wide Range of Devices.

Journal of molecular biology·2026

Hierarchy-Aware AI Nuclear Phenotyping in Human iPSC-Derived Cardiomyocytes: A Preclinical Framework for Imaging Biomarker Development.

Life (Basel, Switzerland)·2026

Molecular Heterogeneity Within Normozoospermia: A Pilot Pooled Small RNA Sequencing Study.

Biomolecules·2026

Chloroplast Genome Assembly and Genetic Structure Analysis of Coffea arabica L. Based on Maternal Inheritance Markers.

Genes·2026

Clinical and Molecular Spectrum of 1q21.1 Copy Number Variations: A Case Series.

Genes·2026

Heritability of Memory Functions and Related Brain Volumes: A Schizophrenia Spectrum Study of 214 Twins.

Schizophrenia bulletin open·2026

Quantitative Assessment of Mesoscale Cellular Order and Organization in the Mouse Hippocampus.

Hippocampus·2026

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A new family of interspersed repetitive DNA sequences in the mouse genome

Related Concept Videos

Genotype-guided diagnostic reassessment after exome sequencing in neuromuscular disorders: experiences with a two-step approach.

Homozygous XYLT2 variants as a cause of spondyloocular syndrome.

Extension of the phenotype of biallelic loss-of-function mutations in SLC25A46 to the severe form of pontocerebellar hypoplasia type I.

Mitochondrial genetic variants identified to be associated with posttraumatic stress disorder.

Adolescent growth: genes, hormones and the peer group. Proceedings of the 20th Aschauer Soiree, held at Glücksburg castle, Germany, 15th to 17th November 2013.

A K(ATP) channel gene effect on sleep duration: from genome-wide association studies to function in Drosophila.

HuKSA: A Machine-Learning-Based Framework for Predicting Human Kinome Selectivity and Polypharmacology.

piRTarBase2: an updated C. elegans piRNA binding site database with extensive evidence for piRNA targeting events.

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Two heads are better than one: Single stranded DNA translocation of UvrD-family dimers vs. monomers.

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HandMol at MolecularWebXR.org: Immersive, Multiuser Visualization and Interactive Modeling with Natural Interactions, on the Web Across a Wide Range of Devices.

Hierarchy-Aware AI Nuclear Phenotyping in Human iPSC-Derived Cardiomyocytes: A Preclinical Framework for Imaging Biomarker Development.

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Chloroplast Genome Assembly and Genetic Structure Analysis of Coffea arabica L. Based on Maternal Inheritance Markers.

Clinical and Molecular Spectrum of 1q21.1 Copy Number Variations: A Case Series.

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A new family of interspersed repetitive DNA sequences in the mouse genome

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