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

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

ATP-dependent chromatin remodeling is crucial for skin development and stem cell function.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

Genetic variants at 20p11 increase baldness risk in Chinese Han people.

Esrp1 is important for skin health by helping form and maintain the skin barrier.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Tudor-SN is important for immune cells, and polyamines can promote hair growth.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

HSD11b1 affects skin nerves and increases non-histaminergic itch.

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

Scalp hair follicle cells help protect and heal skin in certain skin conditions.

Dauricine may help treat certain brain cancers by reducing cancer cell growth and promoting cell death.

Blocking S100A8 can reduce chemotherapy-induced hair loss.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

New mutations in the DSG4 gene cause a rare hair condition.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

Notch-related genes play a key role in the development and cycling of hair follicles.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Vitamin D receptor is important for regulating hair growth and wound healing in mice.

Mutations in the Sgk3 gene cause fuzzy hair in mice.