A chromosome 10p11.2 Gt-dinucleotide repeat polymorphism at the GLUDP5 gene locus

Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia.

Molecular psychiatry·2011

Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies.

Clinical genetics·2008

Inflammasomes and rheumatic diseases: evolving concepts.

Annals of the rheumatic diseases·2007

A novel Gypsy founder mutation, p.Arg1109X in the CMT4C gene, causes variable peripheral neuropathy phenotypes.

Journal of medical genetics·2005

The DNA sequence and comparative analysis of human chromosome 10.

Nature·2004

Phospholipase D1 and potential targets of its hydrolysis product, phosphatidic acid.

Biochemical Society transactions·2003

Zebrafish knockout models of atxn1a, atxn1b, and atxn1l reveal distinct and shared phenotypic and transcriptomic alterations.

Human molecular genetics·2026

PONG 2.0: allele imputation for the killer cell immunoglobulin-like receptors.

Human molecular genetics·2026

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

NOVEL GENETICALLY DRIVEN OA RISK SCORE REQUIRES ONLY PELVIC RADIOGRAPHS: A LONGITUDINAL MULTICOHORT STUDY.

Osteoarthritis imaging·2026

Transgenerational epigenetic inheritance: a critical perspective.

Frontiers in epigenetics and epigenomics·2026

Effects of Obstructive Sleep Apnea on Personality and Temperament: A Cohort and Mendelian Randomization Study.

World journal of otorhinolaryngology - head and neck surgery·2026

Serum Orexin A Levels and Heart Rate Variability Parameters in Newly Diagnosed, Treatment-Naïve Type 2 Diabetes Mellitus: A Case-Control Study.

Cureus·2026

Seven reasons why threatened species managers must consider genetic health.

Bioscience·2026

Exome sequencing and metabolite profiling identifies genetic variants associated with altered metabolism in early-onset schizophrenia.

iScience·2026

Related Experiment Videos

A chromosome 10p11.2 Gt-dinucleotide repeat polymorphism at the GLUDP5 gene locus

Related Concept Videos

Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia.

Genetic heterogeneity and minor CYP1B1 involvement in the molecular basis of primary congenital glaucoma in Gypsies.

Inflammasomes and rheumatic diseases: evolving concepts.

A novel Gypsy founder mutation, p.Arg1109X in the CMT4C gene, causes variable peripheral neuropathy phenotypes.

The DNA sequence and comparative analysis of human chromosome 10.

Phospholipase D1 and potential targets of its hydrolysis product, phosphatidic acid.

Zebrafish knockout models of atxn1a, atxn1b, and atxn1l reveal distinct and shared phenotypic and transcriptomic alterations.

PONG 2.0: allele imputation for the killer cell immunoglobulin-like receptors.

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

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

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

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.

NOVEL GENETICALLY DRIVEN OA RISK SCORE REQUIRES ONLY PELVIC RADIOGRAPHS: A LONGITUDINAL MULTICOHORT STUDY.

Transgenerational epigenetic inheritance: a critical perspective.

Effects of Obstructive Sleep Apnea on Personality and Temperament: A Cohort and Mendelian Randomization Study.

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Related Experiment Videos

A chromosome 10p11.2 Gt-dinucleotide repeat polymorphism at the GLUDP5 gene locus

Related Concept Videos

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