Characterization of the human beta-catenin gene

Multi-disciplinary support of infant feeding choice for parents living with HIV: experience across a guideline change.

Frontiers in reproductive health·2026

Chewing analysis of horses consuming bermudagrass hay in different styles of slow feeders as compared to loose hay.

Journal of equine veterinary science·2024

Real-world clinical profile, treatment patterns and patient-reported outcomes in a subset of HR+/HER2- advanced breast cancer patients with poor prognostic factors: data from an international study.

ESMO open·2021

Staff and participant perceptions of optimal recruitment and retention strategies for biomedical cohort studies in the Caribbean.

Cancer causes & control : CCC·2021

Objective and subjective rapid frailty screening tools in people with HIV.

HIV medicine·2020

Oxytocin reduces post-stress sweet snack intake in women without attenuating salivary cortisol.

Physiology & behavior·2019

ZDHHC5 may regulate the function of NKT cells and the immune response in Meniere's disease.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Genome-wide meta-analysis with 1,590,596 individuals identifies 12 novel risk loci for systemic lupus erythematosus.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Screening for candidate genes and cell populations associated with atherosclerotic calcification using single-cell RNA sequencing.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Multi-omics analysis of HLTF context-dependent regulation across TCGA cohorts revealed its potential as new biomarker in tumour.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

The future objectives of the International Mouse Phenotyping Consortium (IMPC): functional evaluation of human disease-relevant cis-regulatory elements in the mouse genome.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Draft nuclear and complete mitochondrial genome assemblies of the flare-horned markhor (Capra falconeri): genomic resources for conservation and phylogenetics.

Mammalian genome : official journal of the International Mammalian Genome Society·2026

Newborn screening and biobanking for preventable genetic disorders in Mongolia: A developing country perspective.

Regenerative therapy·2026

Whole-genome resequencing with multidimensional annotation revealed pathogenic networks in sirenomelia.

Italian journal of pediatrics·2026

Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Diabetes·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

Related Experiment Videos

Characterization of the human beta-catenin gene

Related Concept Videos

Multi-disciplinary support of infant feeding choice for parents living with HIV: experience across a guideline change.

Chewing analysis of horses consuming bermudagrass hay in different styles of slow feeders as compared to loose hay.

Real-world clinical profile, treatment patterns and patient-reported outcomes in a subset of HR+/HER2- advanced breast cancer patients with poor prognostic factors: data from an international study.

Staff and participant perceptions of optimal recruitment and retention strategies for biomedical cohort studies in the Caribbean.

Objective and subjective rapid frailty screening tools in people with HIV.

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Draft nuclear and complete mitochondrial genome assemblies of the flare-horned markhor (Capra falconeri): genomic resources for conservation and phylogenetics.

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Human Loss-of-Function ZNRF3 Mutation Impairs Adipose Thermogenesis and Drives Subcutaneous Fat Expansion.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

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Related Experiment Videos

Characterization of the human beta-catenin gene

Related Concept Videos

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