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A new sheep gene, KRTAP36-1, may help breed sheep with better wool by reducing prickle factor.

Glutamine metabolism affects hair stem cell maintenance and their ability to change back to stem cells.

Triple therapy with clobetasol, hydroxychloroquine, and N-acetylcysteine is recommended for better outcomes in treating lichen planopilaris.

Energy healing treatment improved L-cysteine's stability, solubility, bioavailability, and shelf-life.

Amino acid supplements may not be necessary for all women with chronic hair loss.

Four-amino acid part makes enzyme sensitive to finasteride.

A new mouse mutation causes skin and hair defects due to a gene change.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

Recessive X-linked ichthyosis involves a less efficient enzyme in hair follicles, suggesting two distinct enzymes.

Combining low-level laser therapy with topical corticosteroids effectively improved Lichen Planopilaris symptoms.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

LEKTI is crucial for skin barrier and immune function, affecting conditions like Netherton syndrome and atopic dermatitis.

A specific gene mutation in Japanese people can cause varying degrees of hair thinning in adulthood.

Chemical lumbar sympathectomy is an effective and safe treatment for idiopathic livedo reticularis.

Combining cetirizine and topical steroids can effectively manage severe lichen planus pilaris.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

The cream effectively reduced hair growth on forearms.

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.

Lykoi cats' unique sparse hair is linked to specific genetic variants in the Hairless gene.

Using special RNA to target a mutant gene fixed hair problems in mice.

CD8+ T cells attack hair follicle stem cells, causing scarring and hair loss.

Altering SSAT affects fat metabolism and body fat in mice.

Super-enhancers controlled by pioneer factors like SOX9 are crucial for stem cell adaptability and identity.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.

Cancer can hijack the body's cell repair system to promote tumor growth, and targeting this process may improve cancer treatments.

L-Carnitine-L-tartrate may help hair grow and prevent hair loss.

Blocking a specific receptor slows down hair loss in mice.