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Ludwig pattern hair loss in women results from varying sensitivity in hair follicles, causing fewer visible hairs.

Androgen receptor activity blocks Wnt/β-catenin signaling, affecting hair growth and skin cell balance.

Excessive hair growth can be assessed by history, exam, and blood tests, and treated with medication like dexamethasone, birth control pills, and spironolactone.

Beard and scalp hair cells have different gene expressions, which may affect beard growth characteristics.

The review concluded that keeping the hair-growing ability of human dermal papilla cells is key for hair development and growth.

Mice without certain skin proteins had abnormal skin and hair development.

The model suggests that scalp tension could lead to hair loss, with factors like blood vessel hardening, enlarged oil glands, and poor microcirculation also playing a role. It also hints at a possible link between skull shape and baldness pattern.

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

Fat under the skin releases HGF which helps hair grow and gain color.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

Researchers created a skin treatment that could effectively deliver medication into hair follicles.

Dying cells can help with faster healing and new hair growth by releasing a growth-promoting molecule.

Runx1 controls fat-related genes important for normal and cancer cell growth, affecting skin and hair cell behavior.

The environment around melanocyte stem cells is key for hair regeneration and color, with certain injuries affecting hair color and potential treatments for pigmentation disorders.

Hair thinning causes stem cell loss through a process involving Piezo1, calcium, and TNF-α.

Different sPLA2 enzymes affect immunity, skin and hair health, reproduction, and may be potential targets for therapy.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

MMP-9 is essential for proper hair canal formation.

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

Early diagnosis and aggressive treatment are key for managing rare scalp disorders that cause permanent hair loss.

Certain genes and pathways are crucial for high-quality brush hair in Yangtze River Delta White Goats.

Alopecia areata involves persistent gene abnormalities and immune activity, even in regrown hair, suggesting a risk of relapse.

Deleting the Far2 gene in mice causes sebaceous gland issues and patchy hair loss.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

An apple-based supplement was found to stimulate hair protein production, which may help with hair growth.

PRP therapy and minoxidil combo works best for male hair loss.

Twist1 helps maintain important features of cells crucial for hair growth by working with Tcf4 and β-catenin.

Different types of scarring alopecia may be stages of one disease, and accurate diagnosis is crucial to prevent permanent hair loss.

Non-coding RNAs are important for hair growth and could lead to new hair loss treatments, but more research is needed.