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Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Carboxytherapy may help increase hair growth in alopecia patients but requires ongoing treatment.

LEF-1 boosts cell growth in goat hair follicles, aiding cashmere production.

Nicotinic acid reduces excessive oil production in skin cells by activating a specific receptor, which could help treat acne.

C-reactive protein helps monocytes stick to blood vessel cells by causing oxidative stress.

Vitamin C derivative may promote hair growth by activating specific genes.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

pCLCA2 protein may help maintain skin structure and function.

Some children with methylmalonic and propionic acidaemias have skin problems related to their condition and diet.

Lysine carboxymethyl cysteinate (LCC) protects skin from UVB damage by activating autophagy.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

Caffeic acid helps protect rats from the harmful effects of acrylamide.

Human keratinocytes do not naturally respond to androgens.

A protein from fat-derived stem cells, DKK1, is linked to hair loss and blocking it may help treat alopecia areata.

Sebaceous glands help study fatty acid transporters and binding proteins.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

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

Keratoacanthoma is a common, usually non-dangerous skin tumor that looks like squamous cell carcinoma but rarely becomes severe.

CARI ONE helps start hair growth and makes hair follicles bigger and more numerous.

AMPK activation may reduce melanoma risk in red-haired individuals.

A gene mutation in mice causes hair loss, weak bones, and protein buildup, showing how protein processing issues can lead to diseases.

Cholesterol transport in hair follicles decreases from growth to regression phase.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Targeting ornithine decarboxylase can help prevent skin cancer.

ABCD1 gene mutations cause adrenomyeloneuropathy, leading to symptoms like limb weakness and spasticity, with management focusing on rehabilitation and spasticity treatment.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

Arg1+ macrophages may play a role in causing alopecia areata.