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The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

The KAP 7 gene affects wool traits in Rambouillet sheep, with the BB genotype showing the best wool characteristics.

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

CCCA affects Black men too, with a genetic link found in the PADI3 gene.

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

Alopecia areata greatly affects quality of life, needing psychological support.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

The scant hair in snthr-1Bao mice is likely caused by a deletion affecting the Plcd1 gene.

A certain gene variation can affect protein production and is linked to male pattern baldness.

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

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

Genetic factors, especially PADI3 gene variants, contribute to CCCA in women of African descent.

Blocking the CXCR3 receptor reduces T cell accumulation in the skin and prevents hair loss in mice.

Ptprq has multiple forms that change during inner ear development.

CARASIL can cause different symptoms even with the same genetic mutation.

Certain genetic variants are linked to frontal fibrosing alopecia in Spanish patients.

PolyQ repeats in neural proteins evolve together, affecting brain function and disease.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

Keratinocytes can reduce the survival of certain melanoma cells, suggesting new therapy paths.

A specific gene variant may increase the risk of developing Alopecia Areata.

MOF controls key genes for skin development by regulating mitochondrial and ciliary functions.

Certain HSD3B1 gene types are linked to worse prostate cancer outcomes and affect treatment response and other health conditions.

A gene called HDAC9 might be a new factor in male-pattern baldness.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

CLEC4D gene variants may increase the risk of alopecia areata in Jordanians.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

Upadacitinib improved both Crohn's ileitis and alopecia universalis in a patient.