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Botulinum toxin type A helps treat hair loss by stopping cell death in hair follicles through a process involving certain non-coding RNAs and a protein called Bax.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

TAGX-0003 protected hair follicles and reversed alopecia areata in a mouse model.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Androgenetic alopecia may be irreversible due to the detachment of a muscle from hair follicles.

The prototype for analyzing skin aging works technically and clinically.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Two gene areas linked to male pattern baldness found, more research needed.

The transporter protein SH1446 in Staphylococcus hominis is key to underarm odor production.

A gene called HDAC9 might be a new factor in male-pattern baldness.

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TRPV3 channels are involved in skin processes and are affected by shear stress, influencing itch and mechanotransduction.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Researchers created a new tool to measure the effects of alopecia areata from the patient's view, focusing on hair loss, daily life, and emotional health.

Different PADI isoforms help cells develop diverse functions.

KCNQ potassium channels help control the sensitivity of touch receptors in the skin.

A woman developed rare, unexplained curly hair on her scalp and eyelashes.

PGD2 increases androgen receptor activity in hair cells, which could be targeted to treat hair loss.

CRABP1 boosts hair cell growth in Hu sheep by affecting key genes.

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

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

BAP1 mutations are rare in pediatric melanocytic tumors and may develop later in life.

Human and mouse TGase3 enzymes are similar but differ near the activation site, crucial for their function in skin and hair development.

The two-step enzyme digestion method is the best for isolating axillary dermal papilla cells.

The arrector pili muscle attaches to the extracellular matrix using α5β1 integrin and connects muscle cells using α1β1 integrin.

Activated platelet-rich plasma is a safe and effective treatment for hair loss.

A gene mutation in Lama3 is linked to a common type of hair loss.

MCHR2 gene duplications may be linked to alopecia areata.

Poor air quality increases the risk of atopic dermatitis in Taiwan.