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A new test more accurately detects citrulline in hair follicles and pilomatrixomas.

Type B Insulin Resistance Syndrome is rare, linked to lupus, and hard to treat due to severe insulin resistance.

A missing mK6irs1 gene causes hair loss in mice.

Cutaneous lupus patients have higher levels of certain immune cells in their blood and skin.

Trichoscopy helps accurately diagnose temporal triangular alopecia.

A woman with a skin disorder was found to have hepatitis C, which may be linked, and was safely treated with methotrexate.

Rac1 is vital for hair follicle health but not needed for skin maintenance.

The assay effectively identifies compounds that affect immune cell activation.

Inducing ferroptosis in hepatic stellate cells is crucial for treating liver fibrosis.

lncRNA MTC helps goat skin cells grow and may aid hair growth by controlling proteins linked to cell growth.

A special receptor in sensory nerve endings helps control how they respond to stretching.

Childhood hypertrichosis is excessive hair growth not linked to hormones, with types based on location and origin.

Ritlecitinib is effective and safe for treating alopecia areata, promoting significant hair regrowth.

Blocking mTORC1 activity could increase hair pigmentation and potentially reverse greying.

Skin organoids with NCSTN mutation show changes in hair follicle development and higher inflammation, key features of Hidradenitis Suppurativa.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

The research developed new fortilin protein constructs for potential heart disease treatments.

Human placenta extract reduces inflammation and symptoms in atopic dermatitis.

A new genetic mutation was found causing hair and eye issues in a boy.

A new DSG4 gene mutation causes hair defects in a young girl.

Aδ-LTMRs have complex synapses with glycine, while Aβ-LTMRs have simpler ones.

Natural α-hydroxyl acids cause skin exfoliation by activating TRPV3 channels.

Tranilast successfully treated a man's skin sarcoidosis when other treatments failed.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

Paneth cells help support stem cells and aid tissue regeneration after injury.

Targeting thyroid hormone receptor α in liver cells may help treat liver fibrosis.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

The fer-ts mutation in plants prevents root hair growth at high temperatures.

Baricitinib and its combination with lonafarnib improve fat cell formation in certain genetic disorders.