BanI and PvuII polymorphisms in intron 2 of selectin E (SELE)

Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration.

Scientific reports·2021

Assessing the effects of candidate genes on quantitative traits in primate populations.

American journal of primatology·2020

Common variants in the Na(+)-coupled bicarbonate transporter genes and salt sensitivity of blood pressure: the GenSalt study.

Journal of human hypertension·2015

Associations of epithelial sodium channel genes with blood pressure: the GenSalt study.

Journal of human hypertension·2014

The PPAR alpha gene is associated with triglyceride, low-density cholesterol and inflammation marker response to fenofibrate intervention: the GOLDN study.

The pharmacogenomics journal·2012

Genetic correlation of blood pressure responses to dietary sodium and potassium intervention and cold pressor test in Chinese population.

Journal of human hypertension·2010

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

Unveiling the Immune Mechanisms of Hypertension With Single-Cell Transcriptome-Wide Mendelian Randomization.

FASEB journal : official publication of the Federation of American Societies for Experimental Biology·2026

Case Report: Functional validation of a PKD1 c.7489 + 5G>A variant in an ADPKD family.

Frontiers in genetics·2026

An analysis of intestinal morphology and incretin-producing cells after sleeve gastrectomy in male mice.

Journal of molecular endocrinology·2026

MRI-based assessment of fetal brain gyrification: Reliability across two methods.

Neuroimage. Reports·2026

Transcriptome-wide splicing analysis reveals HuR-regulated post-transcriptional programs in osteocytes.

iScience·2026

Structural variants contribute substantially to complex trait heritability.

Research square·2026

Related Experiment Videos

BanI and PvuII polymorphisms in intron 2 of selectin E (SELE)

Related Concept Videos

Human myelomeningocele risk and ultra-rare deleterious variants in genes associated with cilium, WNT-signaling, ECM, cytoskeleton and cell migration.

Assessing the effects of candidate genes on quantitative traits in primate populations.

Common variants in the Na(+)-coupled bicarbonate transporter genes and salt sensitivity of blood pressure: the GenSalt study.

Associations of epithelial sodium channel genes with blood pressure: the GenSalt study.

The PPAR alpha gene is associated with triglyceride, low-density cholesterol and inflammation marker response to fenofibrate intervention: the GOLDN study.

Genetic correlation of blood pressure responses to dietary sodium and potassium intervention and cold pressor test in Chinese population.

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.

Unveiling the Immune Mechanisms of Hypertension With Single-Cell Transcriptome-Wide Mendelian Randomization.

Case Report: Functional validation of a PKD1 c.7489 + 5G>A variant in an ADPKD family.

An analysis of intestinal morphology and incretin-producing cells after sleeve gastrectomy in male mice.

MRI-based assessment of fetal brain gyrification: Reliability across two methods.

Transcriptome-wide splicing analysis reveals HuR-regulated post-transcriptional programs in osteocytes.

Structural variants contribute substantially to complex trait heritability.

Related Experiment Videos

BanI and PvuII polymorphisms in intron 2 of selectin E (SELE)

Related Concept Videos

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