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Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.

Rapamycin and anti-EGFR antibody reduce LAM/TSC cell migration and blood vessel growth in the uterus.

Nonimmunogenic forms of keratins K71 and K31 can delay and prevent alopecia areata.

Expanding CD4+ Tregs can stop hair loss in alopecia areata.

The patient with autoimmune hypothyroidism improved after treatment for thyroid and associated conditions.

Recognizing eyebrow hair loss linked to a rare skin condition is crucial for proper treatment.

The MAGE3 hypothesis for alopecia areata did not lead to a significant breakthrough.

CD8+ virtual memory T cells may cause hair loss in alopecia areata.

CDH3-related disease causes worsening eye and hair issues.

A mouse model for studying scleroderma in chronic graft-versus-host disease was successfully created.

Trichoblastomas in aged house musk shrews show unique features and may involve serum amyloid A in inflammation.

Insulin therapy helped a man with autoimmune issues regrow his hair.

People with hair loss conditions may also have thyroid disorders, but more research is needed to understand the connection.

Congenital triangular alopecia is more common than thought and some treatments can be beneficial for appearance concerns.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Two boys developed a viral skin infection during chemotherapy, which resolved with improved immune function.

Matrigel supports cell growth and repair, and thymosin beta 4 aids tissue regeneration and healing.

A rare type of skin lymphoma was identified, affecting hair follicles and sweat glands.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Enhancing regulatory T cells may help treat autoimmune diseases like alopecia areata.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

Smad2 and Smad3 are essential for normal skin development, and their absence causes severe skin issues and cancer.

Adjusting the medication tacrolimus resolved a boy's red nail beds after a stem cell transplant.

Specific brain and bone imaging findings can help diagnose Trichothiodystrophy.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

Mice with autoimmune hair loss showed signs of heart problems.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

Genetic testing can identify causes of rare hair loss disorders in children, but no treatments exist.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.