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Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

A new gene mutation linked to a skin condition was found in a Spanish family.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Enterobacter sp. SA187 helps tomato plants grow better in salt and heat by boosting stress-related responses.

The KAP13-3 gene in sheep affects wool quality by influencing keratin assembly.

SLC3A2 is crucial for hair follicle stem cell function and hair growth.

Key proteins and pathways regulate wool fiber diameter in Alpine Merino sheep.

Oral Acitretin effectively resolved symptoms in a child with Netherton syndrome.

Researchers developed a cost-effective 66 K SNP chip for cashmere goats that is accurate and useful for genetic studies.

Snakes and worm lizards lost claw proteins due to similar evolutionary changes.

Msx2 deficiency in mice leads to bone growth and organ development problems.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Ptprq has multiple forms that change during inner ear development.

The cornified cell envelope forms a protective barrier in skin and hair, using specific proteins and lipids to maintain effectiveness.

Lotus corniculatus seed extract reduces oily skin by decreasing sebum production.

The research found that the properties of solid-state Electronic Circular Dichroism (ss-ECD) are influenced by the orientation of local crystals, which could help in examining and mapping chiral materials like pharmaceutical ingredients.

Vaccines work well in Netherton syndrome patients, similar to healthy people.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Certain genetic changes in the KAP22-1 gene are linked to better wool quality in Egyptian sheep.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

A 2-year-old girl had a hair disorder not shared by her identical twin.

The new particle system could be a promising treatment for diseases related to the 5-α reductase enzyme.

The KRTAP36-2 gene in sheep affects wool yield.

ATP-sensitive potassium channels are important for hair growth.