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

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Hairless protein can both repress and activate vitamin D receptor functions, affecting gene regulation.

EBV infection increases a specific keratin variant in carcinoma cells, possibly affecting cell structure and cancer progression.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

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

DHHB from Platycladus orientalis L. promotes hair growth and could be a natural alternative to current treatments.

A new method creates valuable compounds for drug discovery by breaking traditional chemical rules.

A patient with Birt-Hogg-Dubé Syndrome also had choroidal melanoma, suggesting the need for careful eyelid exams in such patients.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

2,5-DBH shows promise for improving drugs in cancer, brain disorders, and infections.

Rushton's hyaline bodies form from hair keratin and blood substances.

Hydrocortisone 17-butyrate 21-propionate ointment caused reversible side effects like skin issues, weight gain, and organ changes in dogs.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

HLD10 can include increased body hair and Mongolian spots.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Growth hormone-releasing hormone (GHRH) boosts hair growth and human scalp hair follicles have their own growth hormone system.

A specific gene mutation causes vitamin D resistance, but certain vitamin D analogs might help.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

The new antibody, TYHF-1, specifically targets certain hair-related structures.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

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

Basal cell carcinomas may differentiate similarly to hair follicles and could be influenced by hair cycle-related treatments.

TGF-β1 increases androgen receptor activity in hair loss, but Hic-5/ARA55 can counter this effect.