The IPP gene is assigned to human chromosome 1p32-1p22

Differential DNA methylation of steatosis and non-alcoholic fatty liver disease in adolescence.

Hepatology international·2023

[Efficacy of selective bronchial occlusion in the treatment of biliary bronchial fistula].

Zhonghua yi xue za zhi·2022

Comparison of the cardiometabolic profiles of adolescents conceived through ART with those of a non-ART cohort.

Human reproduction (Oxford, England)·2022

DNA methylation patterns within whole blood of adolescents born from assisted reproductive technology are not different from adolescents born from natural conception.

Human reproduction (Oxford, England)·2021

Adiposity associated DNA methylation signatures in adolescents are related to leptin and perinatal factors.

Epigenetics·2021

Machine learning and clinical epigenetics: a review of challenges for diagnosis and classification.

Clinical epigenetics·2020

Charting host structural variations in cervical cancer by long-read sequencing pinpoints a functional deletion in PIAS1.

Genomics·2026

Exploring differences across pangenome-graph representations using Escherichia coli O157:H7 as a model.

Genomics·2026

Comprehensive analysis of differentially expressed mRNAs, lncRNAs, and miRNAs involved in ovarian differentiation and development in Qihe gibel carp (Carassius gibelio var. Qihe).

Genomics·2026

Genome-wide association and selective sweep analyses reveal genetic loci for teat number trait in pigs.

Genomics·2026

Effects of domestication on the body morphology and genetic diversity of the yellowfin seabream (Acanthopagrus latus).

Genomics·2026

A muskrat tissue atlas of small non-coding RNAs and their regulatory roles in muskrat musk secretion.

Genomics·2026

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

International journal of molecular sciences·2026

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Genes·2026

Site-Resolved Plasma-Protein Architecture of Infection Susceptibility: A Cis-pQTL Mendelian Randomization and Colocalization Study.

Genes·2026

Socioeconomic and Migration-Related Determinants of Newborn Metabolic Screening Uptake: A Case-Control Study in Urban Iran.

Journal of immigrant and minority health·2026

Generation of two induced pluripotent stem cell lines from Fabry disease patients carrying GLA mutations.

Stem cell research·2026

Variable Expressiveness of a Novel Pathogenic SETD1A Missense Variant Linked to FLOS Domain Haploinsufficiency in a Mexican Pedigree.

Diseases (Basel, Switzerland)·2026

Related Experiment Videos

The IPP gene is assigned to human chromosome 1p32-1p22

Related Concept Videos

Differential DNA methylation of steatosis and non-alcoholic fatty liver disease in adolescence.

[Efficacy of selective bronchial occlusion in the treatment of biliary bronchial fistula].

Comparison of the cardiometabolic profiles of adolescents conceived through ART with those of a non-ART cohort.

DNA methylation patterns within whole blood of adolescents born from assisted reproductive technology are not different from adolescents born from natural conception.

Adiposity associated DNA methylation signatures in adolescents are related to leptin and perinatal factors.

Machine learning and clinical epigenetics: a review of challenges for diagnosis and classification.

Charting host structural variations in cervical cancer by long-read sequencing pinpoints a functional deletion in PIAS1.

Exploring differences across pangenome-graph representations using Escherichia coli O157:H7 as a model.

Comprehensive analysis of differentially expressed mRNAs, lncRNAs, and miRNAs involved in ovarian differentiation and development in Qihe gibel carp (Carassius gibelio var. Qihe).

Genome-wide association and selective sweep analyses reveal genetic loci for teat number trait in pigs.

Effects of domestication on the body morphology and genetic diversity of the yellowfin seabream (Acanthopagrus latus).

A muskrat tissue atlas of small non-coding RNAs and their regulatory roles in muskrat musk secretion.

Genetic Modifiers of Cardiac Remodeling Severity in IVS4+919G>A-Associated Fabry Cardiomyopathy.

Dissecting Missing Heritability in Rare Inherited Macular Dystrophies.

Site-Resolved Plasma-Protein Architecture of Infection Susceptibility: A Cis-pQTL Mendelian Randomization and Colocalization Study.

Socioeconomic and Migration-Related Determinants of Newborn Metabolic Screening Uptake: A Case-Control Study in Urban Iran.

Generation of two induced pluripotent stem cell lines from Fabry disease patients carrying GLA mutations.

Variable Expressiveness of a Novel Pathogenic SETD1A Missense Variant Linked to FLOS Domain Haploinsufficiency in a Mexican Pedigree.

Related Experiment Videos

The IPP gene is assigned to human chromosome 1p32-1p22

Related Concept Videos

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