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5-Bromo-3,4-dihydroxybenzaldehyde could potentially help hair growth by activating certain cell pathways and inhibiting others.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Mice with CBS deficiency are healthier on a low-methionine diet.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

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

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

A baby with maple syrup urine disease improved from skin problems by adjusting his diet to correct amino acid levels.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

Beta-trace protein may help diagnose and predict treatment response in certain nerve disorders.

Some people have a genetic variation that makes them less effective at breaking down drugs.

Vitamin D receptor is important for regulating hair growth and wound healing in mice.

Msx2 deficiency in mice leads to bone growth and organ development problems.

MOF controls skin development by regulating genes for mitochondria and cilia.

The Gsdma3 gene is essential for normal hair development in mice.

The BIOMAP glossary standardizes data to improve research on atopic dermatitis and psoriasis.

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

New mutations in the DSG4 gene cause a rare hair condition.

Smad4 is crucial for muscle repair, especially in aging, by promoting cell growth over differentiation.

Looser dietary restrictions can improve growth and reduce illness in methylmalonic acidemia patients.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Male-pattern baldness has a weak link to heart disease and some related health conditions.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

Deleting the BRD4 protein in certain skin cells causes hair loss and skin inflammation.

The ND1 gene of the Asian black bear Sichuan subspecies is similar to other bear species.

Some Greek melanoma patients have gene mutations linked to increased cancer risk, a new color feature helps diagnose melanoma, the incidence of a skin condition in the Netherlands is rare, and a gene possibly affects male-pattern baldness.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.