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Researchers found two genes that may explain why some Casertana pigs don't have hair.

A new model can predict drug-disease links well, helping drug research.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

Certain DNA regions in alpacas are linked to fiber diameter.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

Mutant mice help researchers understand hair growth and related genetic factors.

The document concludes that the androgen receptor's structure and function are complex, affecting how it regulates genes and is involved in diseases like prostate cancer.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

Genetic variations affecting skin structure play a key role in severe acne.

Keratin proteins are crucial for hair structure and strength.

Recent progress has been made in understanding inherited hair and nail disorders.

Understanding skin structure and development helps diagnose and treat skin disorders.

Genetic defects and UV radiation cause skin damage and aging.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Hair gets thinner, grayer, and changes texture with age due to genetics, environment, and cellular changes, affecting the growth cycle.

Asian hair is generally straight and thick, with unique disorders and properties, and more research is needed to understand it fully.

Hair follicle hyperplasia is common in both benign and malignant skin lymphoproliferative disorders, with a proposed new term "pseudolymphomatous adnexitis."

KAP genes show significant genetic variability, but its impact on hair traits is unclear.

The document concludes that mouse models are crucial for studying hair biology and that all mutant mice may have hair growth abnormalities that require detailed analysis to identify.

iPSCs can help treat genetic skin disorders by creating healthy skin cells from a small biopsy.

Self-perceived facial aging is linked to skin pigmentation, immune system, hair loss in men, and genes related to the skin's structure.

Afro-textured hair needs specialized care due to its unique genetic and structural properties.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.

Hairless mice lack fur due to a genetic mutation affecting skin response, not hormone issues.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Different hair growth problems are caused by genetic issues or changes in hair growth cycles, and new treatments are being developed.

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

Some hair loss disorders are caused by genetic mutations affecting hair growth.