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An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

Alpha 6 + /MHCI - cells have stem cell traits and are similar to mouse hair follicle stem cells.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

HDMHG0401-10 treatment significantly improved hair count and was better than a placebo in reducing hair loss in men with hereditary hair loss, with no major side effects.

The gene GJA1 is important for regulating coarse hair density in goats.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

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

The fuzzy gene is crucial for controlling hair growth cycles.

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

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

A specific RNA can help hair growth in baldness by boosting stem cell activity.

The hedgehog signaling pathway is crucial for hair growth but not for the initial creation of hair follicles.

N‐AOHPA is a promising alternative to traditional surfactants for better hair conditioning.

The treatment improved hair growth in people with male pattern baldness.

Ultrasound shows 80% of Hidradenitis Suppurativa patients have abnormal hair tracts that may worsen the condition.

Hair follicle cells can help keep embryonic stem cells undifferentiated.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

ICP5249 helps hair grow by activating a specific cell pathway.

A combination of ixekizumab and tofacitinib successfully treated severe scalp cellulitis, leading to hair regrowth.

TACE/ADAM17 is essential for maintaining healthy hair and hair follicle stem cells.

Advancements in measuring chromatin accessibility at single-cell level improve understanding of gene regulation.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

Gasdermin A3 causes hair follicle stem cells to activate too early, leading to hair loss.

Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Tocilizumab treatment was associated with significant hair regrowth in one patient and temporary hair loss followed by regrowth in another.

hHbl gene is active in hair shaft cells and some pilomatricomas.

The condition is linked to chromosome 12, but no mutations were found in the known genes.