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Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

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The May issue discussed publishing agreements and four studies on cholesterol in hair, cancer cell changes, hormones in the uterus, and skin protein effects.

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

c-Maf positive macrophages help form hypertrophic scars by affecting fibroblasts and collagen production.

Research on HIV-1 capsid inhibitors has progressed significantly, with the U.S. leading in contributions.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

hHbl gene is active in hair shaft cells and some pilomatricomas.

MPZL3 is important for controlling the hair growth cycle in mice and humans.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

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A rare neck cyst in a 47-year-old man showed diverse skin cell types and was not linked to HPV.

Tinea capitis is a fungal infection of the scalp that mainly affects children and can cause symptoms from mild itching to severe inflammation.

Manipulating the catagen and telogen phases of hair growth could lead to treatments for hair disorders.

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A compound from brown algae boosts the production of a certain inflammatory substance in skin cells.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.

One child resisted treatment, while the other was successfully treated for scalp ringworm.

A man developed severe skin reactions after using a treatment for hair loss.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

Tinea capitis is a common scalp infection causing hair loss, mostly in young children.

The Hr protein binds to DNA, interacts with p53, and affects cell cycle genes.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

Topical patidegib gel effectively treats basal cell carcinoma in Gorlin syndrome patients without causing the side effects seen with oral treatments.

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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

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