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The research updated the skin cell profile, finding new skin cell markers and showing fibroblasts' key role in skin health.

Tsc2-deficient stem cells can help understand and treat TSC-related tumors.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

CRH in the skin acts like the body's stress response system, affecting cell behavior and immune activity.

KRT17 may be a new target for endometrial cancer treatment because it helps cancer cells move and form new blood vessels.

Removing SIX1 in fat cells reduces skin fibrosis.

Isotretinoin can raise CPK levels, so patients need monitoring, especially before surgery.

Kainar syndrome symptoms may be linked to nuclear test exposure effects.

Minoxidil sulfate and pinacidil promote hair growth likely by increasing blood flow, not by activating K channels.

PF-998425 is a new, effective, and non-phototoxic treatment for skin conditions related to androgens.

Different versions of the KRTAP6-2 gene in goats can lead to thinner cashmere fibers.

Radiesse is a versatile facial injectable used for cosmetic improvements and long-term collagen production, with careful dosing needed to prevent complications.

These methods help understand cell structures and reactions.

A new one-step test can quickly identify skin cancer during surgery.

The ABHRS has outlined its goals for the next year.

K6hf is a unique protein found only in a specific layer of hair follicles.

KRT81 gene variations in sheep affect wool weight but not fiber length or thickness.

Finasteride irreversibly affects human steroid 5α-reductase 2, providing insight into its catalytic mechanism and disease-related mutations.

Somatic BHD mutations are rare in Japanese renal tumors.

CRAC channels are crucial for the development and function of specialized immune cells, preventing severe inflammation and autoimmune diseases.

A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

PrrH sRNA controls pyochelin gene expression in Pseudomonas aeruginosa based on heme levels.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

A 36-year-old person with a female appearance but male chromosomes was diagnosed with a rare enzyme deficiency affecting sexual development.

Removing GRK2 in skin cells causes hair loss similar to immune-related alopecia.

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

Potassium cyanide treatment changes hair's disulfide bonds, making it more elastic.

AMPK activation may reduce melanoma risk in red-haired individuals.