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Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

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

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.

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

Jumonji genes are important for development and their mutations can cause abnormalities, especially in the heart and brain.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

The HR protein's role as a repressor is essential for controlling hair growth.

New genetic mutations causing hair loss were found in a Chinese family.

A specific gene mutation causes congenital hair loss.

The Hairless gene is crucial for healthy skin and hair growth.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Hairless protein can block vitamin D activation in skin cells.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

The protein hairless is important for hair regrowth because it stops the protein wise from blocking the hair cycle.

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

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

Dermoscopy is useful for diagnosing Atrichia with Papular Lesions in children without needing a biopsy.

Hairless protein is crucial for healthy skin and hair, and its malfunction can cause hair loss.

Mutation in hairless gene may increase hair loss risk.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Mutation in hairless gene may increase hair loss risk.

Researchers found a new mutation causing total hair loss from birth.