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The nude gene causes skin cell overgrowth and improper development, leading to hair and urinary issues.

SDF-1/CXCL12 and its receptor CXCR4 are crucial for melanocyte movement in mouse hair follicles.

The enzyme 17β-HSD type 2 mainly performs oxidation in human sebaceous glands, which may help protect against acne.

Desmoglein 4 is controlled by specific proteins that affect hair growth.

Early onset hair loss linked to genetics and androgen levels.

Stump-tailed macaque best for researching hair loss causes and treatments.

Bioengineering can potentially treat hair loss by regenerating hair follicles and cloning hair, but the process is complex and needs more research.

Some mutant mice have hair with abnormal cross-linking, mainly in the cuticle, not affecting other hair parts.

Hair and skin can regenerate without bulge stem cells due to other compensating cells.

No single biomarker is reliable enough for diagnosing and assessing SLE.

Hibiscus micranthus leaf extract is safe and effective for antibacterial and wound healing.

Finasteride may improve sperm count in subfertile men with low sperm count.

The transgene likely activated an oncogene or interrupted a tumor suppressor gene, causing melanoma in mice.

Minoxidil 2% is more effective for female hair loss, but botanicals have fewer side effects.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Nonpalmoplantar skin cells can be made to express keratin 9 by interacting with palmoplantar fibroblasts.

Early diagnosis and a combination of treatments, including minoxidil and finasteride, are recommended for managing hair loss in India.

Discontinuing topical minoxidil can resolve headaches and dizziness.

Two mouse mutants have defective hair cuticle cross-linking.

Most women with excess hair growth have an underlying hormonal issue, often treated with medication and hair removal methods.

Hirsutism in women often indicates a hormonal imbalance and can be managed with a combination of hormonal treatments and hair removal methods.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

No consistent link between genotype and phenotype in 5-α-Reductase type 2 deficiency.

Certain DNA variants can predict straight hair in Europeans but are not highly specific.

Two sisters have rare hair disorders causing short, fragile, kinky hair.

Four-amino acid part makes enzyme sensitive to finasteride.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

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