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A new mutation linked to partial Androgen Insensitivity Syndrome and prostate cancer was found in a patient unhappy with their female gender assignment.

A genetic variant in goats is linked to cashmere growth.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A new technology showed that the SOX9 gene might control heart scar formation after injury, suggesting new treatment possibilities.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

ISX-9 helps stem cells heal lung injury better by boosting growth factor secretion.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

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

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

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

The research helps in creating genetically modified animals to study hair growth.

The study concluded that specific proteins are necessary to maintain the structure that holds epithelial cells tightly together.

Non-coding RNA boosts retinoic acid production and signaling, aiding regeneration.

Hoxc8 gene helps start mammary gland development by controlling specific signals.

KRT85 gene variations can help improve wool traits in sheep through selective breeding.

XEDAR triggers a specific signaling pathway in cells.

The gene therapy showed significant wound healing and was safe for treating severe RDEB.

The Msx2 gene affects feather development in Hungarian white geese and a specific gene variation could indicate feather quality.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Key genes and RNA networks regulate hair growth and follicle density in Rex rabbits.

A new mouse mutation causes skin and hair defects due to a gene change.

Researchers found an RNA transcript that might help control a growth factor linked to tumor development.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

SOX18 helps sheep hair cells grow by activating a specific cell growth pathway.

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