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The new anti-acne treatment HA-P5 effectively reduces acne by targeting two key receptors and avoids an enzyme that can hinder treatment.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

Ayurveda treats hair problems like hair loss and dandruff by balancing body elements and using natural remedies like Indian Gooseberry and false Daisy.

Disrupted stem cell signals in hairpoor mice cause hair loss.

Certain bacteria from the Citrullus colocynthis plant may be a new source of antibiotics to fight drug-resistant diseases.

Premature balding in some men may be linked to altered hormones, but it's not the male equivalent to polycystic ovary syndrome or metabolic syndrome.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

The skin systems of jawed vertebrates evolved diverse appendages like hair and scales from a common structure over 420 million years ago.

Trichoscopy effectively diagnoses early female hair loss, but may need scalp biopsy for confirmation.

Tadalafil and Finasteride may help treat aggressive melanoma.

Increasing EGR1 levels makes hair root cells grow faster.

Genes affecting wool fiber thickness in Angora rabbits were identified, which could help breed finer wool.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Faulty inflammasome activation may lead to autoimmune skin diseases and could be a target for new treatments.

A rare genetic skin condition usually affecting males was found in a 9-year-old girl.

Behçet's Disease may be caused by genetic and environmental factors leading to abnormal immune responses, and stress management and new treatments could improve patient outcomes.

Intralesional triamcinolone acetonide is the most effective treatment for localized alopecia areata.

The case shows skin changes can indicate deeper health issues like insulin resistance, which are challenging to manage.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Maintaining healthy mitochondria may help treat hair loss.

PCOS is a major cause of infertility in women of childbearing age.

Men with early hair loss may have higher insulin resistance and should be checked for related health issues.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

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

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

The KRTAP36-2 gene in sheep affects wool yield.

Plucked hairs can be used instead of skin biopsies to study hair traits because they contain specific cells related to hair.