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Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

A substance called DKK-1 increases in balding areas and causes hair cells to die when exposed to DHT.

KGF-1 135 is a stable and effective alternative for treating oral mucositis.

The gene Prss53 affects hair shape and bone development in rabbits.

CIPK13 and CIPK18 genes are crucial for root hair growth in plants.

Blocking casein kinase 1 in skin cells can help melanocyte precursors move better, potentially helping with conditions like vitiligo or gray hair.

ATP-sensitive potassium channels are important for hair growth.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Rhodamin B stain is inconsistent for keratin in skin samples.

UC.145 may be a new biomarker for predicting gastric cancer.

BRG1 is essential for skin cells to move and heal wounds properly.

LRIG1 protein affects hair growth by regulating skin receptors, leading to hair loss when overexpressed.

Prostasin has two roles in skin: one for normal skin development without needing activation, and another for proper hair growth that requires activation.

Activating PKCα in skin causes cell death and inflammation through different pathways.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

The condition is linked to chromosome 12, but no mutations were found in the known genes.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

A family got a fungal infection from a boy who had contact with rabbits, but they all recovered with treatment.

The study revealed the detailed structure of a keratin dimer, aiding understanding of how intermediate filament proteins function.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

TRPS1 loss in balding scalp areas contributes to hair loss in androgenic alopecia.

A specific hair protein variant increases the spread of breast cancer and is linked to worse survival rates.

Hoxc13 is essential for hair growth and follicle development.

The new keratin film without KAPs stains better and could help study keratin functions.