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GALT5 and GALT2 are important for plant growth and development because they help with protein glycosylation.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Understanding how DHT works is important for diagnosing and treating hormone-related disorders.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Platelet-rich plasma (PRP) may help with various hair loss types, but more research is needed to find the best use method.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Follistatin and LIN28B together improve the ability of inner ear cells in mice to regenerate into hearing cells.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Scientists restored fertility in male mice lacking a key fertility gene by using a modified gene.

EGFR helps control how hair grows and forms without needing p53 protein.

Sox2 controls hair color by affecting pigment production in hair follicles.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

A special receptor in sensory nerve endings helps control how they respond to stretching.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

AIRE deficiency causes hair loss similar to alopecia areata in mice.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The study concludes that regulating apoptosis could lead to new treatments for various skin and hair conditions.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Dermal factors are crucial in regulating melanin production in skin.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

A gene mutation in Lama3 is linked to a common type of hair loss.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

Genes and epigenetic changes are important in the development of Polycystic Ovary Syndrome.

Field bean supplementation improved mohair growth and kid growth in Angora goats but didn't prevent weight loss after giving birth.

Mitochondrial reactive oxygen species are essential for skin and hair development.

Feather patterns form through genetic and epigenetic controls, with cells self-organizing into periodic patterns.