Isolation and fine mapping of (CA)n repeats from the Xp11.23 and Xp11.4 region

Children with unilateral molar-incisor hypomineralisation (MIH) may exhibit contralateral temporalis and masseter muscle hyperactivity: a cross-sectional study.

European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry·2025

Analysis of the stomatognathic system functions and mastication muscles in children affected by molar hypomineralization (MH): a cross-sectional study.

European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry·2024

Association of dental hypersensitivity and anxiety in children with molar-incisor hypomineralisation (MIH).

European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry·2023

Epidemiological, clinical and laboratory aspects of Angiostrongylus cantonensis infection: an integrative review.

Brazilian journal of biology = Revista brasleira de biologia·2022

Modulation of inflammation by anti-TNF α mAb-dendrimer nanoparticles loaded in tyramine-modified gellan gum hydrogels in a cartilage-on-a-chip model.

Journal of materials chemistry. B·2021

Dynamics of lipid droplets in the endometrium and fatty acids and oxylipins in the uterine lumen, blood, and milk of lactating cows during diestrus.

Journal of dairy science·2021

Cell-type-specific dysregulated gene expression in the frontal cortex of an Angelman syndrome pig model.

Human molecular genetics·2026

Coding, modifier, and regulatory effects shape circulating APOL1 levels.

Human molecular genetics·2026

CaMKIIβ Signaling drives expression of metabolic and stress response genes in skeletal muscle, and its loss contributes to the LGMDR1 phenotype.

Human molecular genetics·2026

Genetic and epigenetic contributors to cleft laterality: evidence from monozygotic mirror twins and replication cohorts.

Human molecular genetics·2026

Molecular analysis of individuals with suspected 46,XY differences of sex development in a homogenous and understudied population.

Human molecular genetics·2026

Prevalence and mechanistic origins of genome-wide ploidy abnormalities in ICSI derived human preimplantation embryos.

Human molecular genetics·2026

Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

Medicine·2026

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Medicine·2026

Genetic evidence for CTSH as a potential therapeutic target in sepsis: A Mendelian randomization and colocalization study.

Medicine·2026

Genetic and clinical spectrum of progressive familial intrahepatic cholestasis type 1: novel ATP8B1 variants and genotype-phenotype correlations.

European journal of pediatrics·2026

Genetically supported targets and drug repurposing for sleep disorders: a Mendelian randomization systematic study.

Naunyn-Schmiedeberg's archives of pharmacology·2026

Yeast Knockout Strain Collection: Driving Functional Genomics, Biotechnological Applications and Human Disease Research.

Yeast (Chichester, England)·2026

Related Experiment Videos

Isolation and fine mapping of (CA)n repeats from the Xp11.23 and Xp11.4 region

Related Concept Videos

Children with unilateral molar-incisor hypomineralisation (MIH) may exhibit contralateral temporalis and masseter muscle hyperactivity: a cross-sectional study.

Analysis of the stomatognathic system functions and mastication muscles in children affected by molar hypomineralization (MH): a cross-sectional study.

Association of dental hypersensitivity and anxiety in children with molar-incisor hypomineralisation (MIH).

Epidemiological, clinical and laboratory aspects of Angiostrongylus cantonensis infection: an integrative review.

Modulation of inflammation by anti-TNF α mAb-dendrimer nanoparticles loaded in tyramine-modified gellan gum hydrogels in a cartilage-on-a-chip model.

Dynamics of lipid droplets in the endometrium and fatty acids and oxylipins in the uterine lumen, blood, and milk of lactating cows during diestrus.

Cell-type-specific dysregulated gene expression in the frontal cortex of an Angelman syndrome pig model.

Coding, modifier, and regulatory effects shape circulating APOL1 levels.

CaMKIIβ Signaling drives expression of metabolic and stress response genes in skeletal muscle, and its loss contributes to the LGMDR1 phenotype.

Genetic and epigenetic contributors to cleft laterality: evidence from monozygotic mirror twins and replication cohorts.

Molecular analysis of individuals with suspected 46,XY differences of sex development in a homogenous and understudied population.

Prevalence and mechanistic origins of genome-wide ploidy abnormalities in ICSI derived human preimplantation embryos.

Bidirectional associations between brain functional networks and sleep disorders: A bidirectional Mendelian randomization study.

Duodenal fluid analysis of 13 patients with progressive familial intrahepatic cholestasis type 2 from a single institution.

Genetic evidence for CTSH as a potential therapeutic target in sepsis: A Mendelian randomization and colocalization study.

Genetic and clinical spectrum of progressive familial intrahepatic cholestasis type 1: novel ATP8B1 variants and genotype-phenotype correlations.

Genetically supported targets and drug repurposing for sleep disorders: a Mendelian randomization systematic study.

Yeast Knockout Strain Collection: Driving Functional Genomics, Biotechnological Applications and Human Disease Research.

Related Experiment Videos

Isolation and fine mapping of (CA)n repeats from the Xp11.23 and Xp11.4 region

Related Concept Videos

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