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A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The protein aPKCλ is crucial for keeping hair follicle stem cells inactive and for hair growth and regeneration.

Vogt-Koyanagi-Harada disease can develop during interferon therapy for chronic hepatitis C.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Patients with lichen planus should be tested for hepatitis C.

Laser therapy on human skin affects the HERC6 gene and related genes, influencing many cell processes and requiring careful safety measures.

HHK can help restore skin structure.

Lymphatic vessels are essential for hair follicle regeneration and growth.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

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

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

Mutations in the KLHL24 gene cause skin blistering in epidermolysis bullosa simplex.

Impaired LEF1 activation speeds up skin cell development in Hutchinson-Gilford Progeria Syndrome.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

A genetic marker linked to a type of hair loss was found in most patients studied.

GHK-Cu liposome promotes hair growth in mice with alopecia.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

hHb1, hHb3, and hHb6 mRNAs start expressing at the same time in hair follicles.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

A genetic mutation in the LIPH gene causes hair loss and growth defects.

Monilethrix severity varies and may be influenced by other genetic or environmental factors.

A unique gene mutation was found in a family with monilethrix.

Dkk4 is necessary for the initial development and arrangement of hair follicles.

Four specific keratins in hair follicles help understand hair structure and function.