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Ultrasound can help detect early signs and severity of hidradenitis suppurativa.

A new protein was made to detect specific skin cell growth receptors and worked in normal skin but not in skin cancer cells.

A new method can detect mutations in mice by observing changes in hair follicle cells.

Alopecia in these mice is caused by defective hair cycle communication due to missing vitamin D receptor function, not vitamin D levels.

Overexpression of the glucocorticoid receptor in mice causes developmental defects similar to ectodermal dysplasia.

A new DSG4 gene mutation causes hair defects in a young girl.

Hoxc13 is important for hair and tongue development by controlling hair keratin genes.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

3D bioprinting offers new ways to treat head and neck defects with bioinks that mimic natural tissues.

The study developed a method to detect minoxidil and its sulfate form, found that minoxidil sulfate is temperature-sensitive, and identified a way to potentially increase its stability for hair loss treatment.

P2X₃-IR fibers are widespread in rat skin and likely help detect pain.

A new method using special materials can help regrow hair by creating small wounds.

A new mouse mutation causes skin and hair defects due to a gene change.

Hoxc13 gene is essential for hair, nail, and papilla development.

Hair loss can indicate underlying systemic diseases and addressing these can sometimes reverse the hair loss.

The review suggests that other immune cells besides CD8+ T cells may contribute to alopecia areata and that targeting regulatory cell defects could improve treatment.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

Cysteine strengthens hair, and glutamine fuels hair growth.

Hair loss in certain mice is linked to changes in keratin-related genes.

Poodles' hair changes aren't always linked to calcium, and special staining is needed to detect true calcium deposits.

Scalp reconstruction uses different methods to restore hair and skin, depending on the defect size.

Sulphur, phosphorus, and metals are distributed differently in animal skin follicles, with variations in detection speed and location.

Different hair loss patterns may be linked to varying male hormone levels.

Genetic hair disorders can indicate other hidden health problems.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Disrupting the Sox21 gene in mice causes hair loss and regrowth cycles.

Hair greying is caused by oxidative stress damaging hair follicles and melanocytes.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

EGFR helps control how hair grows and forms without needing p53 protein.

Recent findings suggest that genetic factors, immune system issues, and skin cell defects might contribute to the development of hidradenitis suppurativa.