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Finasteride side effects in young men may be linked to specific gene variations.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

XEDAR triggers a specific signaling pathway in cells.

Researchers found two new genetic variants linked to Alzheimer's disease.

GPC1 is important for hair growth by helping blood vessels form around hair follicles.

SRD5A2 gene variations affect PTSD symptoms differently in males and females.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

The scaffold improves wound healing and tissue regeneration.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

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

A JAK1 variant causes hair loss, skin issues, and thyroid disease, but treatment with a specific inhibitor can help.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

Lgr6+ cells are important for tissue repair and could be a target for treating cancer and other diseases.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

The HGCA tool helps identify genes that work together by analyzing their co-expression patterns.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

New ginseng compounds may help treat degenerative diseases.

Increasing SSAT makes skin more prone to cancer.

Neurosteroids are crucial for stress response, and targeting specific receptors may help treat certain disorders.

Presynaptic inhibition of certain nerve fibers in cats is mainly controlled by GABA and glycine.

The Thr1022Ala variant in the hairless gene is not a disease-causing mutation.

TEDAR is crucial for skin cell differentiation and barrier formation.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.

Researchers found a new mutation causing total hair loss from birth.

OsRopGEF3 is crucial for rice root hair growth and ROS production.