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The BMP2 gene is more active in the early growth phase of Cashmere goat hair and may affect hair regeneration and textile production.

Rat dermal papilla cells have unique genes crucial for hair growth.

Minoxidil foam helps hair growth by increasing good proteins and decreasing bad pathways in men with hair loss.

Key genes can rewire networks, changing skin appendage types.

Chilled ATPv-supplemented saline best preserves hair grafts' key genes.

Certain transcription factors are key in controlling skin stem cell behavior and could impact future treatments for skin repair and hair loss.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

Different types of skin stem cells can change and adapt, which is important for developing new treatments.

SH-MSCs gel reduced IL-6 and increased TGF-β, suggesting it could treat alopecia.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

Melatonin treatment increases a specific RNA in goat cells that boosts cashmere growth.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Some vitamin D analogs can thicken skin and reduce pore size like a common acne treatment, with one analog also affecting skin growth factors.

SH-MSCs gel can effectively treat alopecia by increasing IL-10 and decreasing TNF-α gene expression.

Wnt/ß-catenin signaling is crucial for regulating skin stem cells and hair growth, with the right levels and timing needed for proper function.

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

Changing light exposure can affect hair growth timing in goats, possibly due to a key gene, CSDC2.

Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

Hair pattern in androgenetic alopecia overlaps with scalp and bone demarcations, with distinct gene profiles affecting susceptibility.

Arrector pili muscle regulates hair follicle stem cells, DNA methylation needed for hair cycling, and Wnt/B-catenin signaling starts hair growth.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

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.

Wounds heal without scarring in early development but later result in scars, and studying Wnt signaling could help control scarring.

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

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

A new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.