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5α reductase type 2 enzyme mutation and oxidative stress may increase androgenetic alopecia risk in Egyptians.

A new EDA gene variant causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family.

The hr gene is linked to hair loss in Valle del Belice sheep.

Idiopathic hirsutism may be linked to increased enzyme activity.

A new compound that could treat various androgen-related conditions was created and analyzed.

Adrenomedullin 2 stops cell growth and causes cell death in human hair follicles.

Compound 7b is a promising candidate for treating benign prostatic hyperplasia and prostate cancer.

The enzyme DHHC13 is essential for healthy hair and skin, and its deficiency leads to hair loss and skin problems.

A child with a rare vitamin D-resistant condition improved with treatment.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Reduced AhR signaling in HS tunnels leads to persistent inflammation and microbial imbalance.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Different halogens on progesterone derivatives can either block or mimic male hormone effects, depending on their type and amount.

Minoxidil's crystal structure shows two different molecule shapes and nitrogen states.

A reliable method was created to measure dutasteride and related molecules in capsules.

DDAIP-HCl significantly increases minoxidil absorption into the skin.

A girl had rickets due to a gene mutation affecting vitamin D response.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Androstanediol glucuronide is a reliable marker for hirsutism in women.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Trichohyalin is modified by enzymes to form strong structures in hair cells.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

11α-Hydroxyprogesterone is changed into different substances by certain enzymes and may play a role in prostate cancer.

8-OHdG may help diagnose and assess alopecia areata.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

Retinoic acid can either maintain stem cells or make them specialize, depending on the cell type.