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Patients with a specific genetic variant have more severe alopecia areata and higher recurrence rates.

New genetic mutations causing hair loss were found in a Chinese family.

Trichohyalin in sheep hair follicles may help with structure and calcium binding.

Type 3 acromegaly patients have more health issues and higher death risk.

A new gene mutation causes a rare type of hair loss.

Early diagnosis of trachyonychia improves treatment and reduces psychological and cosmetic issues.

Different hair follicles in the skin are innervated by unique combinations of mechanosensory neurons, crucial for touch sensation.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Using a certain drug on the skin can help prevent hair loss caused by pulling on the hair.

Inflammation damages sweat ducts, causing sweat gland injury.

Rat skin has a linear system of nerve fibers linked to hair follicles and muscles.

Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

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

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Correcting EDA fibronectin organization and YAP translocation can improve wound healing in fibrotic conditions.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

Frontal Fibrosing Alopecia involves disrupted cholesterol pathways, fibrosis, and increased mast cells.

Trichilemmal keratinization is a unique process in hair follicles where the outer root sheath turns into keratin without a specific layer.

Trichohyalin may trigger the immune response causing alopecia areata.

Trichohyalin, a hair follicle protein, has a part with repeating patterns of 23 amino acids.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Two people had unusual ring-shaped hair loss due to an autoimmune disorder.

Trichoscopy is effective for diagnosing scalp ACC in darker skin tones.

Two sisters had rare, widespread cysts and complete hair loss, suggesting a genetic link.

The patient with Ankylosing Spondylitis had shoulder joint damage and bone changes.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Trichohyalin is also found in the outer layers of normal human skin.

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

Disruption of glycinergic circuits increases pain sensitivity, suggesting new pain treatment options.