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The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

The study found that a specific area of the hair follicle helps start hair growth by reducing the blocking effects on certain cells and controlling growth signals.

Gata6 is important for protecting hair growth cells from DNA damage and keeping normal hair growth.

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

Curcumin may help reverse aging by targeting specific genes.

Eating selenium-rich rice improved antioxidant activity and signs of aging in mice.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

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

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

Genomic research can help improve the quality and production of natural fibers in animals.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Thymosin β4 helps increase hair growth in Cashmere goats.

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

The article concludes that studying how skin forms is key to understanding skin diseases and improving regenerative medicine.

The study found that giant pandas have more melanin in black hair follicles than white, with gene expression differences that could affect hair color and skin health.

CD4+ skin cells may be precursors to basal cell carcinoma.

Heredity and hormones cause common hair loss, and topical minoxidil is the first recommended treatment.

Recent selection on immune response genes was identified across seven ethnicities.

FOL-026 peptide can help repair blood vessels and promote growth, offering potential treatment for vascular diseases.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

Trichophyton bullosum has been found causing severe skin infections in donkeys in North Africa for the first time since 1933.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

The hair follicle dermal sheath is essential for hair shedding and needs to communicate with the outer root sheath for normal hair growth cycles.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

The boy's severe skin disorder is caused by two new mutations in his TGM1 gene.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

The skin microbiome helps heal wounds and can be targeted to improve healing.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.