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

A genetic mutation in a specific gene causes a salt-wasting condition in a Pakistani girl and her family.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

3-Deoxysappanchalcone helps human hair cells grow and stimulates hair growth in mice by affecting certain cell signaling pathways.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

Hsc70 protein may influence hair growth by responding to androgens.

VDUP1 is found in skin and hair follicles, interacts with sciellin, and may help regulate skin cell differentiation.

TSC2 is crucial for proper hair follicle development and patterning.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

ARHGEF3 is essential for proper hair follicle development in mice.

HSD3B1 gene variant and being overweight linked to hair loss in women with polycystic ovary syndrome.

Certain gene variations may protect against skin issues and oxidative stress in women with PCOS.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

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

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Retinoids increase steroid sulfatase activity in leukemia cells through RARα/RXR and involves certain pathways like phosphoinositide 3-kinase and ERK-MAP kinase.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Hox genes control hair follicle stem cell regeneration in different body regions.

Targeting the p300/AR axis may help treat polycystic ovary syndrome.

NFIB and STAT5 work together to control specific genetic programs in cells.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

Loss of TET2 increases the risk of skin and oral cancer.

Hereditary hyperplastic gingivitis in silver foxes may be linked to errors in the MAPK signaling pathway, influenced by androgens.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

GLI and EGF signalling affect Basal Cell Carcinoma development and could be therapeutic targets.

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