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A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

IL-1β inhibits human hair follicle growth.

TNF alpha in skin cells causes weight loss, hair and fat issues, and skin inflammation in mice.

Two new gene clusters important for hair formation were found on human chromosome 11.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

Congenital adrenal hyperplasia may be linked to adrenal myelolipoma.

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

CYB5R1 and IL1A genes may be linked to different types of acne scars.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Variation in the TCHH gene affects wool curliness in sheep.

The arrector pili muscle attaches to the extracellular matrix using α5β1 integrin and connects muscle cells using α1β1 integrin.

CCCA is a common, progressive hair loss condition that may not always be linked to hair care practices and requires a biopsy for diagnosis.

The OVOL1-OVOL2 axis is important for hair follicle differentiation and can help diagnose certain hair-related tumors.

Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

A 56-year-old man was diagnosed with Cronkhite-Canada Syndrome after showing symptoms like diarrhea, weight loss, and skin changes.

CCCA can affect both genders and all ages, and it has a genetic component.

A bull with a gene mutation was asymptomatic, synthetic retinoids cause hair loss, and new therapeutic targets were identified for skin diseases.

Ficus carica leaf extract may help treat skin disorders by reducing inflammation and androgen effects in skin cells.

Alkaline ceramidase 1 is crucial for healthy skin and energy balance.

A mutation in the hHb3 gene is linked to the hair disorder monilethrix.

A gene mutation causes monilethrix in a Chinese family.

MCHR2 gene duplications may be linked to alopecia areata.

Inhibiting ALOX12 can help hair cuticle maturation by increasing S100A3 citrullination.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Twist1 is crucial for UVB-induced skin cancer development.

CCN1 may aid wound healing, but more research with larger samples is needed.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.