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L-threonate may help prevent balding by blocking a key protein.

A new CDH3 gene mutation was found in a Spanish patient with sparse hair and eye issues.

Diagonal earlobe crease and lipoprotein(a) together help diagnose coronary heart disease.

The study found that a specific genetic variation in the TNFα gene is significantly linked to Alopecia Areata in the Jordanian Arab population.

Tribuloside can increase skin pigmentation by enhancing melanin production and distribution.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Corneodesmosin is essential for skin and hair health, and its dysfunction can lead to skin and hair disorders.

Dihydrotestosterone (DHT) doesn't affect rat skin cell growth, but it does change cell cycle, protein levels, and other cell functions, potentially shortening hair growth cycle.

Type II keratins are uniquely phosphorylated during stress and mitosis, affecting their structure and function.

PGD2 stops hair growth and is higher in bald men with AGA.

TCDD reduces EGF receptors in the liver, affecting growth and development.

Using DNase enzymes to break down harmful NETs could be a new treatment for Stevens-Johnson syndrome and toxic epidermal necrolysis.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

The study created a mouse model that survives longer and shows fewer symptoms of pemphigus vulgaris.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Anti-Desmocollin 3 antibodies can cause pemphigus-like symptoms in mice.

The DNN-DTIs method accurately predicts drug-target interactions and is useful for drug repositioning.

New mutations in the EBP gene cause CDPX2, affecting bones, skin, eyes, and hair, with females generally less affected than males.

ZPK helps skin cells mature and may affect skin health.

Deleting part of a gene in mice causes wavy hair and high pup loss.

All-trans retinoic acid helps amelanotic melanocytes in hair follicles develop and produce pigment while reducing their growth.

Four specific genes are linked to keloid formation and could be potential treatment targets.

VDAC2 promotes cell death in cashmere goat hair follicles through the P53 pathway.

Mouse high-glycine/tyrosine proteins have distinct patterns in hair follicles, peaking at specific hair cycle days.

Mutations in the SNRPE gene cause hereditary hair loss.

Angiopoietin-1 helps hair follicle cells survive and grow, potentially treating hair loss.