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

IL-9/IL-9R signaling can negatively affect human hair growth and may be a target for treating hair loss conditions.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

HAC and BAC improve skin targeting and reduce diffusion without causing irritation.

HAIRCARECUBE TM (HCC) helps hair products work better by getting active ingredients deeper into the hair.

Farudodstat may help treat alopecia areata by protecting hair follicles.

HASHA is a safe and effective option for chin augmentation.

Hirosaki hairless rats lack hair due to missing DNA with key keratin genes.

Patients with the same genetic mutation for vitamin D-resistant rickets showed different symptoms but all improved with treatment except for hair loss.

The hydrogel helps heal wounds and regrow hair by mimicking a baby's environment.

The Hair Cell Analysis Toolbox automates and improves the analysis of cochlear hair cells using machine learning.

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

A new mouse hair mutation, called hague, is semidominant and unstable, but the exact cause is unknown.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.

Hairless protein helps control hair growth by regulating vitamin D receptor activity.

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

Certain genetic markers, especially the MICA gene, are linked to alopecia areata.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Certain mutations in the hairless protein disrupt its ability to regulate the hair cycle.

Human placenta extract reduces inflammation and symptoms in atopic dermatitis.

16-MHA can restore the barrier and moisture of damaged hair, making it similar to undamaged hair.

Somatic BHD mutations are rare in Japanese renal tumors.

Tofacitinib helps improve skin conditions in people with Down syndrome, especially alopecia areata.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

16-MHA can restore damaged hair's protective barrier and moisture balance.

The 736T>A mutation in the LIPH gene is common in Japanese people with autosomal recessive woolly hair.