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Scientists discovered a unique hair protein, KAP24.1, with a special structure, found only in the upper part of hair cuticles.

Sphingosine 1-phosphate affects inflammation and gene expression in different aorta cells.

Trps1 plays a key role in hair follicle development and cycling.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

NEDD4 and NEDD4L help control intestinal stem cells and prevent tumors by breaking down the LGR5 receptor.

The SYP123-VAMP727 complex is important for transporting materials that harden the root hair shank in Arabidopsis.

Epiprofin suppresses parathyroid hormone gene activity, helping regulate calcium levels and could be a treatment target for hyperparathyroidism.

FOXN1 gene variants cause low T cells and immune issues from birth.

Increasing XIAP and DDRGK1 can help prevent hearing loss from loud noise.

Lysophosphatidic acid affects sensory neurons and may cause neuropathic pain and itch.

A rare genetic variant linked to skin cysts was found in blood DNA, suggesting its role in cyst formation.

The POMP gene is active in various goat tissues and affects hair growth, with certain treatments influencing its expression.

Connexin mutations can cause various diseases like hearing loss and skin disorders.

ILC1-like cells can cause alopecia areata by themselves.

Type VII collagen absence helps skin development by allowing tissue remodeling.

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

Human dermal fibroblast proteins help restore nerves during healing.

Deleting podoplanin in mice promotes hair growth by enhancing cell migration.

Trichohyalin helps in hair and skin cell structure and function by binding calcium and linking proteins.

Nephronectin helps attach muscle cells to hair follicles.

The study found nine new hair protein genes in human hair follicles.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

CCC1 is crucial for pH balance in plant cells, affecting growth and stress tolerance.

Certain plasma proteins are linked to prostate cancer risk and could help in early detection and treatment.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

Basonuclin may help control ribosomal RNA gene activity in skin cells.

CENPV, a new partner of CYLD, helps regulate ciliary acetylated tubulin and is overexpressed in certain skin tumors.