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The peach gene CTG134 helps control the interaction between auxin and ethylene, which could lead to new agricultural chemicals.

A gene called Gk5 controls lipid production in the skin and affects hair growth.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Researchers found a non-functional sheep keratin gene due to mutations.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A new gene mutation is linked to monilethrix in the studied family.

GSDMA deficiency slows skin cancer growth.

Human hair keratin genes hHa2 and hHb1 are located on chromosomes 17 and 12.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Faulty LEF1 activation causes faster skin cell differentiation in premature aging syndrome.

The BMP2 gene is more active in the early growth phase of Cashmere goat hair and may affect hair regeneration and textile production.

GLABRA2 represses root hair formation by inhibiting a specific gene.

Gorab deficiency speeds up skin aging by disrupting protein regulation and reducing collagen.

Gasdermin A3 overexpression in skin causes inflammation and hair loss.

A new DSG4 gene mutation causes hair defects in a young girl.

The gp130 receptor helps in tissue regeneration and disease progression, and manipulating it could improve healing and prevent disease.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.

The hr gene is linked to hair loss in Valle del Belice sheep.

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

Keratinocytes can reverse the effects of the GNAQ oncogene, inhibiting melanoma cell growth.