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Hair stem cells produce a protein called COL17A1 that plays a key role in their development and is linked to hair thinning and baldness.

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

C-reactive protein helps monocytes stick to blood vessel cells by causing oxidative stress.

Collagen VI and Semaphorin 3C are important for hair pigmentation and could help treat pigmentation disorders.

The document reports a rare case of ECCL with a new association with optic disc colobomas.

The enzyme for activating vitamin D is found in many body tissues, not just the kidneys.

High amphiregulin in the skin is a bad sign for acute graft-versus-host disease.

A new mutation in the hHb1 keratin gene is linked to the hair disorder monilethrix.

Ritlecitinib reduces alopecia areata symptoms by blocking JAK3/TEC signaling and T-cell activity.

CS12192 effectively treats alopecia areata with better safety than current options.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

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

HOXC13 is crucial for regulating hair keratin genes in hair follicles.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

THH and PAD type III appear together early in hair growth, but deiminated THH appears later, suggesting another factor is involved.

Skin tumors with CYLD cutaneous syndrome show more NF-κB activity and less organized collagen.

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

Tongue cancer cells show more plectin-1 than non-cancer cells, but both have similar levels of trichohyalin.

GRHL3 is important for controlling gene activity in skin cells during different stages of their development.

The hair defect is due to abnormal inner root sheath keratinization.

Mast cells may significantly contribute to central centrifugal cicatricial alopecia.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

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

Collagen XVII is crucial for preventing hair and pigmentation loss by maintaining melanocyte stem cells.