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Quercetin and kaempferol may be effective and safe natural treatments for hair loss.

A 22-year-old woman with a rare genetic condition was successfully treated to develop normal female characteristics and regular menstruation.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.

Keratins are crucial for cell structure, growth, and disease risk.

Activating TLR9 helps heal large wounds and regrow hair by involving a specific type of immune cell.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Quercetin and kaempferol may be effective and safe natural treatments for hair loss.

Bleach baths with 0.005% hypochlorite help manage atopic dermatitis by affecting skin cells and reducing itchiness.

The enzymes Tet1, Tet2, and Tet3 are important for the development of hair follicles and determining hair shape by controlling hair keratin genes.

Keratinocyte growth factor promotes hair growth and reduces hair loss from chemotherapy.

Glutamine helps macrophages reduce inflammation and improve wound healing.

C3G and Vitisin A may help prevent hair loss by blocking male hormones and stopping hair cell death.

TGM3 is important for skin and hair structure and may help diagnose cancer.

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

Hox proteins help maintain keratinocyte identity by regulating miRNA expression.

Specific keratin gene mutations can cause monilethrix.

A gene mutation in mice causes skin defects and early death.

TIP39 and PTH2R help control calcium levels and skin cell development.

The gene Endothelin 3 makes mice's fur darker by increasing pigment cells and pigment levels.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

Finasteride helps treat hair loss and prostate enlargement by blocking a specific enzyme.

11α-Hydroxyprogesterone is changed into different substances by certain enzymes and may play a role in prostate cancer.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Mutations in the androgen receptor gene cause different levels of androgen insensitivity, making it hard to create simple tests for the condition.

Progesterone protects rat brain cells by enhancing GABA A receptor activity.

Involucrin is crucial for skin cell maturation and protection.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.