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Masculinization in affected individuals occurs gradually after puberty due to hormone changes.

ILC1-like cells can cause alopecia areata by themselves.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Abrocitinib at 100 mg and 200 mg daily may significantly improve moderate-to-severe atopic dermatitis in patients 12 years and older.

Hepatitis B virus alters steroid hormones in male mice, reducing dihydrotestosterone to inhibit viral replication.

The ALADIN score can predict how well patients with alopecia areata will respond to JAK inhibitor treatments.

The testes significantly contribute to vitamin D metabolism and may affect male reproductive health and conditions like hair loss.

Androgen receptor signaling causes early aging of cells important for hair growth by damaging their DNA.

AtZP1 protein stops root hair growth in plants by blocking certain genes.

Male pattern baldness is linked to specific genetic variations in the androgen receptor gene.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Impaired androgen production in 46,XY DSDs causes ambiguous genitalia and requires long-term care.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

CD8+ T cells expand significantly in alopecia areata, suggesting new treatment targets.

A new genetic model may improve treatment and diagnosis for certain inherited skin diseases.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

PRC1 is essential for proper skin development and stem cell formation by controlling gene activity.

Androgen receptors help prostate cancer cells grow and resist drugs.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

African American men with prostate cancer have more androgen receptor mutations, which may lead to more aggressive cancer compared to Caucasian American men.

Alpha-MSH affects mitochondrial function, and MC1R mutations may increase skin aging.

Protein tyrosine kinases are key in male pattern baldness, affecting skin structure, hair growth, and immune responses.

Androgen receptor inactivation delays skin cancer onset and reduces incidence in mice, with gender differences in susceptibility.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Researchers found a new gene area linked to male-pattern baldness, which, along with another gene, significantly increases the risk of hair loss in men.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.