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Plucked hairs can be used instead of skin biopsies to study hair traits because they contain specific cells related to hair.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

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

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

The KRT84 gene is linked to better wool quality in Gansu Alpine Fine-wool sheep.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

The ABCA4 gene protects hair follicle stem cells from toxic vitamin A byproducts.

New tools show that in fish, NPY increases feeding and somatostatin decreases it.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

The Foxn1 gene mutation causes hairlessness and immune system issues, and understanding it could lead to hair growth disorder treatments.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

FGF5 gene mutations cause long hair in domestic cats.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

FOXN1 gene variants cause low T cells and immune issues from birth.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Researchers found a gene mutation responsible for a rare hair loss condition.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

WNT7A gene expression is higher in early stages of androgenetic alopecia, showing the role of WNT pathway, apoptosis, and inflammation in the disorder.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Keratin protein production in cells is controlled by a complex system that changes with cell type, health, and conditions like injury or cancer.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

The SOSTDC1 gene is crucial for determining sheep wool type.