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

A new mutation in the Hairless gene causes hair loss in two Pakistani families.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Hairless protein affects hair follicle structure by regulating the Dlx3 gene.

The trichohyalin gene is located at chromosomal region 1q21 with other skin-related protein genes.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Vitamin D receptor and hairless protein are essential for hair growth.

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Brepocitinib reduces interferon signaling in hidradenitis suppurativa patients.

The skin of both rat strains showed similar lectin binding patterns.

Type I and Type II keratin chains can form heterodimers despite sequence differences.

Secukinumab treatment may cause HBV reactivation and hair discoloration.

Gene sequencing is crucial for diagnosing Junctional epidermolysis bullosa.

BBS7 is crucial for maintaining healthy periodontal ligaments by supporting Shh signaling.

Notch1 signaling is impaired in hidradenitis suppurativa, affecting skin and hair cells.

New mutations in the hairless gene may cause hair loss and affect bone development.

A mutation in the HOXC13 gene causes hair and nail problems in a Syrian family.

A new gene mutation causes vitamin D resistance and rickets, treatable with calcium therapy.

The hepatitis B vaccine did not cause hair loss in the tested mice.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Mutations in specific genes disrupt development of sweat glands, teeth, hair, skin, and nails in HED.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

A protein called HMGB1 helps hair grow by affecting prostaglandin metabolism.

Dab2 protein is crucial for hair follicle stem cell renewal and preventing early aging.