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

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Understanding snoRNA regulation may help slow skin aging.

Lateral plate mesoderm helps create skin and amnion-like tissues for studying development and therapies.

Activating Wnt in skin cells controls the number of hair follicles by directing cell movement and fate.

Ovol2 is important for proper skin healing and hair growth.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Lack of vitamin D receptor causes hair loss in mice by allowing certain genes to overactivate.

BMP signaling is essential for forming skin structures called rete ridges, aiding skin thickness and regeneration.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

The study mapped keratin 15 and 19 genes, aiding future genetic disorder research.

An 80-year-old man's deep beard infection was cured with oral terbinafine after identifying the fungus Trichophyton verrucosum.

Muscles and nerves that cause goosebumps also help control hair growth.

Fibroblasts can be turned into melanocytes for potential skin treatments.

Biotin helps regulate proteins in the blood, which may explain its role in hair growth.

The study identified key genes and pathways that influence goat wool quality and growth.

The gene Prss53 affects hair shape and bone development in rabbits.

Dutasteride and finasteride affect different cell types differently.

Sun-exposed skin shows different cell activity and gene expression, suggesting targets to prevent skin aging and cancer.

Staphylococcus levels may indicate hair loss in men and could help develop new treatments.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

A humanized CXCL12 antibody may delay and treat alopecia areata by altering the immune response.

The study found that different genes are active in cashmere goats' hair growth stages, which can help improve cashmere production.

Different types of fibroblasts play specific roles in wound healing and cancer, which could help improve treatments.

Different types of inactive melanocyte stem cells exist with unique characteristics and potential to develop into other cells.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Certain plasma proteins and genes are linked to obstructive sleep apnea, suggesting potential new treatments.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

Human stem cells were turned into cells similar to those that help grow hair and showed potential for hair follicle formation.