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Nestin marks cells that can become a specific type of skin cell in hair follicles of both developing and adult mice.

N-Cadherin is crucial in scar formation, offering potential for scar prevention therapies.

Stress increases a factor in mice that leads to hair loss, and blocking this factor may prevent it.

PBX1 reduces aging and cell death in stem cells by boosting SIRT1 and lowering PARP1.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

Certain proteins and their receptors are more active during the growth phase of human hair and could be targeted to treat hair disorders.

Loss of Rap1 protein speeds up heart aging in mice.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Different gene mutations cause different types of ichthyosis, with some new mutations found.

An 8-year-old boy with neurofibromatosis type one also has rare hair and eye disorders.

Fibrosing alopecia in a pattern distribution is a unique hair loss condition with inflammation and scarring, resembling but distinct from common balding.

miR-214-3p helps nerve repair and recovery.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A specific mutation in the TRPV3 gene causes hair follicle cells to develop improperly, leading to hair loss.

Human dermal fibroblast proteins help restore nerves during healing.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

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

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

The study created special nanoparticles that effectively deliver an anti-inflammatory drug to treat skin inflammation in psoriasis.

Non-coding RNAs help control hair growth in cashmere goats.

Deleting the PTEN gene in mice causes nerve cells to grow larger and heal better after injury, but may cause overgrowth and hair loss in older mice.

A new genetic mutation linked to Hutchinson-Gilford progeria syndrome was found in China.

IVIG and dupilumab effectively improved symptoms in a child with Netherton syndrome.

ASLNC168501 can help treat hair loss by restoring hair follicle stem cell function.

Lipin-1 is important for skin cell differentiation and skin barrier function.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

DPP4 is important for scarring and skin regeneration, and managing its activity could improve skin healing treatments.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

ICAM-1 helps regulate hair growth cycles and skin remodeling.