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Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

The AIRE gene variant rs2075876 is linked to a higher risk of alopecia areata in males.

Wasabi leaf extract affects gene expression in skin cells.

New insights into cell communication in psoriasis suggest innovative drug treatments.

Black wool in Qira sheep is linked to specific gene mutations, especially in the TYRP1 gene.

Combining genetic models helps improve heat tolerance in beef cattle.

New genetic factors linked to acne risk were discovered, highlighting the role of certain pathways and genes.

Genetics play a major role in acne, but environmental factors and epigenetics also contribute.

Differences in gene expression and methylation patterns found in AGA patients suggest potential targets for future treatments.

Using micro skin tissue columns improves skin wound healing and reduces scarring.

Caffeine intake during pregnancy and lactation can cause skin lesions in mother rats and their babies, not linked to cortisol levels.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

A new mutation in the DCAF17 gene was found in a Chinese family, causing Woodhouse-Sakati syndrome and diabetes.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

A specific gene mutation causes a severe skin disorder in a family.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

CDP is crucial for lung and hair follicle cell development.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

A specific gene change in APCDD1 increases the risk of hair loss.

CCDC22 and CCDC93 are essential for root and root hair growth in Arabidopsis.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

Csdc2 helps hair growth in cashmere goats by regulating specific genes.