A dinucleotide repeat polymorphism at the ribosomal protein S6 (RPS6) gene

Genetic susceptibility to temporomandibular joint involvement in juvenile idiopathic arthritis.

Journal of oral rehabilitation·2024

Genome-wide analysis of nuclear magnetic resonance metabolites revealed parent-of-origin effect on triglycerides in medium very low-density lipoprotein in PTPRD gene.

Biomarkers in medicine·2018

An epigenome-wide association study meta-analysis of educational attainment.

Molecular psychiatry·2017

Genetic risk scores and family history as predictors of schizophrenia in Nordic registers.

Psychological medicine·2017

Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies.

Clinical pharmacology and therapeutics·2016

Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia.

Hernia : the journal of hernias and abdominal wall surgery·2016

N-acetylcysteine suppresses retinal defects in Drosophila models of SNRNP200-associated retinitis pigmentosa.

Human molecular genetics·2026

Suppressive genetic interactions between haploinsufficient mitochondrial genes encoded in the 22q11.2 microdeletion locus define brain and cardiac phenotypes.

Human molecular genetics·2026

Mucolipidosis II: novel variants, clinical variation and assessment of HAP1 cells as a disease model.

Human molecular genetics·2026

CoCoRV-nf: a powerful and cost-effective tool for rare variant analysis leveraging external biobank sequence data identified new candidate predisposition genes in amyotrophic lateral sclerosis and neuroblastoma.

Human molecular genetics·2026

A patient-derived mouse model reproduces molecular, neurological, and sleep symptoms of SHINE syndrome.

Human molecular genetics·2026

The potential regulatory relationship between hsa_circ_0000973 and MBOAT2 in hypertriglyceridemia with abnormal glucose metabolism.

Human molecular genetics·2026

Comprehensive analysis of the Bombyx mori satellitome reveals evolutionary stability, dispersed chromosomal organization, and transposable element-related origins.

Heredity·2026

Behavioral and transcriptional divergence across rat strains differing in the nervous system excitability.

Neuroscience·2026

Tissue-level division of labor is coordinated across organs through universal programs and context-specific adaptations.

Cell reports·2026

Long non-coding RNA gene polymorphisms and risk of recurrent pregnancy loss: a meta-analysis.

Journal of assisted reproduction and genetics·2026

Systematic evaluation of the heterogeneity of topologically associating domain boundaries in a large genomic context in humans.

NAR genomics and bioinformatics·2026

Integrating heterogeneity into topologically associating domain boundary prediction in large genomic context in human.

NAR genomics and bioinformatics·2026

Related Experiment Videos

A dinucleotide repeat polymorphism at the ribosomal protein S6 (RPS6) gene

Related Concept Videos

Genetic susceptibility to temporomandibular joint involvement in juvenile idiopathic arthritis.

Genome-wide analysis of nuclear magnetic resonance metabolites revealed parent-of-origin effect on triglycerides in medium very low-density lipoprotein in PTPRD gene.

An epigenome-wide association study meta-analysis of educational attainment.

Genetic risk scores and family history as predictors of schizophrenia in Nordic registers.

Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies.

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N-acetylcysteine suppresses retinal defects in Drosophila models of SNRNP200-associated retinitis pigmentosa.

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Comprehensive analysis of the Bombyx mori satellitome reveals evolutionary stability, dispersed chromosomal organization, and transposable element-related origins.

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A dinucleotide repeat polymorphism at the ribosomal protein S6 (RPS6) gene

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