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Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Genosomes are promising for safe and effective gene delivery in therapy.

A new gene variant causes glucocorticoid resistance in a mother and son.

New mutations in the DSG4 gene cause a rare hair condition.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

About 50% of 46, XY DSD cases lack a genetic diagnosis, but advanced sequencing methods improve detection.

The environment around the time of conception can change the VTRNA2-1 gene in a way that lasts for years and may affect disease risk.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Certain genes affect udder shape in Holstein cows, important for health and milk production.

Humans have ancient DNA from Neanderthals and other lineages in their chromosomes, affecting traits and evolution.

The research suggests that a specific skin gene can be controlled by signals within and between cells and is wrongly activated in certain skin diseases.

A genetic hair protein variant is more common in Japanese people and is inherited.

Haplogroup X found in Altaian population supports Amerindian origin.

Gene expression affects fur development in rex rabbits.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

FGF5 gene mutations cause long hair in domestic cats.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

Frontal fibrosing alopecia has occurred in two related male families.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Certain genes are linked to wool follicle structure and function, but not hair cycle regulation.