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Immune checkpoint inhibitors used in cancer therapy can cause hair loss, and understanding this can help manage the side effect.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

MEF2C is crucial for normal hair cycle progression.

Blocking IL-12 can help treat alopecia areata by preventing hair follicle immune issues.

Upadacitinib is effective and safe for treating severe alopecia areata in teens.

The KRTAP13-3 gene affects wool fibre diameter variability in Chinese Tan sheep.

Blocking CISD1 reduces hearing loss from cisplatin in mice.

Silencing NtNCED3-2 gene in tobacco reduces drought tolerance and impairs growth.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

CLK1 is needed for skin cells to become epidermal cells but not sebocytes.

JAK inhibitors may help treat certain types of hair loss, but more research is needed.

KAP9.2 and Hoxc13 genes are important for cashmere growth and vary in activity during different stages.

PINK1 is important for controlling gut immune responses linked to early Parkinson's disease.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

High glycine–tyrosine keratin-associated proteins help make hair strong and maintain its shape.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

The article's correction clarifies scientific and methodological concerns about miR-200c-3p's role in alopecia areata.

Two drugs, ritlecitinib and brepocitinib, improved scalp hair loss condition markers.

Blocking certain proteins in mouse skin can reduce and shrink skin tumors.

TYK2 inhibition may help treat alopecia areata by promoting hair growth and reducing immune response.

NFATc1 controls hair stem cell activity, affecting hair growth and could be a target for hair loss treatments.

Higher CD8+ T cell levels are linked to Alopecia areata in Iraqi patients.

Lack of functional CYLD in mice leads to early aging and cancer.

Inhibiting ACE2 improves skin regeneration during tissue expansion.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

K6hf is a unique protein found only in a specific layer of hair follicles.

Expanded CD8+ T cells are linked to Alopecia Areata and may cause relapse after treatment.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.