Dinucleotide repeat polymorphism adjacent to the ANT1 gene on 4q35

Synergy between culturomics and metagenomics of health status-associated gut bacteria originating from non-IBD and IBD populations.

Scientific reports·2025

Gut feelings: the relations between depression, anxiety, psychotropic drugs and the gut microbiome.

Gut microbes·2023

Environmental factors shaping the gut microbiome in a Dutch population.

Nature·2022

A combination of fecal calprotectin and human beta-defensin 2 facilitates diagnosis and monitoring of inflammatory bowel disease.

Gut microbes·2021

A systems genomics approach identifies SIGLEC15 as a susceptibility factor in recurrent vulvovaginal candidiasis.

Science translational medicine·2019

A GWAS meta-analysis from 5 population-based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndrome.

Neurogastroenterology and motility·2018

iHaptenAb: an integrated hapten-antibody database for rational hapten design and antibody discovery.

Nucleic acids research·2026

Sparsomycin inhibits translation through a conserved mechanism across all domains of life.

Nucleic acids research·2026

Crystal structures of type T archaeal ribonuclease P Rpp30, Rpp30/Pop5, and L7Ae provide insights into a reduced RNase P.

Nucleic acids research·2026

Partitioning of parental histones between leading and lagging strands is modulated by DNA polymerase dosage.

Nucleic acids research·2026

RNase E resolves toxic condensates by counteracting phase separation of Type II RhlB helicases.

Nucleic acids research·2026

A CRISPR/Cas9-induced blunt-end telomere system in S. pombe reveals RNase H2-dependent RNA primer removal at the terminal Okazaki fragment of lagging telomeres.

Nucleic acids research·2026

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

American journal of medical genetics. Part A·2026

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

International journal of molecular sciences·2026

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

International journal of molecular sciences·2026

4-Phenylbutyrate Rescue in GABRA1 Variants Associated with Developmental Epileptic Encephalopathies: From Cell and Mouse Models to Humans.

Cells·2026

BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

Journal of medical genetics·2026

Ultrasound-guided renal artery administration of angiopoietin-1 RNA therapy slows the progression of preclinical WT1 glomerular disease.

Science translational medicine·2026

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Dinucleotide repeat polymorphism adjacent to the ANT1 gene on 4q35

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Synergy between culturomics and metagenomics of health status-associated gut bacteria originating from non-IBD and IBD populations.

Gut feelings: the relations between depression, anxiety, psychotropic drugs and the gut microbiome.

Environmental factors shaping the gut microbiome in a Dutch population.

A combination of fecal calprotectin and human beta-defensin 2 facilitates diagnosis and monitoring of inflammatory bowel disease.

A systems genomics approach identifies SIGLEC15 as a susceptibility factor in recurrent vulvovaginal candidiasis.

A GWAS meta-analysis from 5 population-based cohorts implicates ion channel genes in the pathogenesis of irritable bowel syndrome.

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Sparsomycin inhibits translation through a conserved mechanism across all domains of life.

Crystal structures of type T archaeal ribonuclease P Rpp30, Rpp30/Pop5, and L7Ae provide insights into a reduced RNase P.

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RNase E resolves toxic condensates by counteracting phase separation of Type II RhlB helicases.

A CRISPR/Cas9-induced blunt-end telomere system in S. pombe reveals RNase H2-dependent RNA primer removal at the terminal Okazaki fragment of lagging telomeres.

Identifying the Potential Role of Missense KIRREL3 Variants in Neurodevelopmental Phenotypes: A Case Series.

Delineating the CTBP1-Related Phenotypic Spectrum: A Review of HADDTS and Atypical Variants.

Association Study Between NOTCH2 Gene and Idiopathic Central Precocious Puberty in Korean Girls.

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BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

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Dinucleotide repeat polymorphism adjacent to the ANT1 gene on 4q35

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