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AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

Certain genetic variants and pathways are linked to hair loss.

Steroidogenic isoenzymes may help improve treatments for common hair loss.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

Proteasome inhibitors are promising treatments for various cancers, autoimmune diseases, and other conditions.

Tabby mutations in mice affect hair follicle development and help study genetic mapping and certain medical conditions.

The Itpr3 gene causes a specific hair pattern in mice.

Blocking CYP17A1 enzyme may help improve certain brain function issues related to dopamine.

Mutations in the SNRPE gene cause hereditary hair loss.

IFN-γ production by CD4 T cells is crucial for causing alopecia areata.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

BTA safely and effectively treats hair loss, and works better with FNS.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Mice with human gene experienced hair loss when treated with DHT.

A specific metabolite, not a receptor protein, triggers the production of certain kidney enzymes, but this process is disrupted in mice with a mutation causing testicular feminization.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

GLABRA2 gene controls root-hair growth by regulating phospholipid signaling.

Trichohyalin is a versatile protein involved in hair and skin structure.

RNase L suppresses regeneration in mammals.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

TEDAR is crucial for skin cell differentiation and barrier formation.

The L412F variant of TLR3 is linked to skin infections, more viral infections, and autoimmune issues.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

Acute stress increases Y1 receptor gene expression in certain brain areas, but repeated stress does not.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.