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Keloid skin disorder involves abnormal fibroblast activation and immune response, linked to a group of genes including FGF11.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

The genetic variation in the KAP13-3 gene may affect cashmere fiber traits in Liaoning goats.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

Human nails contain both skin and hair keratins, each needing different extraction methods.

Sox21 is crucial for tooth development and enamel formation by preventing cells from changing into a different type.

Proteomics combined with other technologies can lead to a better understanding of skin diseases.

Goat genes show adaptation to environments and traits like body development, with differences among cashmere, feral, and milk-producing goats.

Removing Mediator 1 from certain mouse cells causes teeth to grow hair instead of enamel.

Fibroblast growth factors could be a better, safer treatment for hair loss than current options.

Early detection and a multidisciplinary approach are crucial for improving gastric cancer survival rates.

Cactus extract from Notocactus ottonis may help promote hair growth.

A new mRNA variant of the SCF gene in sheep skin produces a shorter, different protein.

FGF-1 causes spiral ganglion neurites to branch more.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Gasdermin A3 causes hair follicle stem cells to activate too early, leading to hair loss.

A mutation in the KRT75 gene causes frizzle feathers in chickens.

The improved genome of the African spiny mouse helps study its tissue regeneration.

All five human steroid 5α-reductase enzymes are found in the endoplasmic reticulum.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

FOL-005 peptide may help treat excessive hair growth safely.

The Wave complex controls skin growth by suppressing certain signals.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

CNGA3, GLUD1, and SIRT1 are promising targets for treating aging and glioblastoma.

The model improves understanding of androgen interactions by focusing on signal intensity and system capacity.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

PP405 may help hair growth by activating hair follicle stem cells.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

Researchers created a genetic library from a cashmere goat's skin and found new genes linked to hair growth.