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The TRPV3 channel structure changes linked to severe itch and hyperkeratosis were identified using cryo-EM.

Geranium Sibiricum L extract may promote hair growth by increasing growth factors and decreasing inhibitory factors under stress.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

Somatic BHD mutations are rare in Japanese renal tumors.

Targeted cancer therapies can cause skin side effects, but activating SOS in the skin may help reduce them.

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

Pay attention to early warnings.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

Serenoa repens is mostly safe but has some risks, especially at high doses or when used with other products for over two weeks.

Lampreys have a functional vitamin D receptor that may help detoxify harmful substances.

Cudrania tricuspidata and Sargassum fusiforme extracts improved hair growth in mice by affecting growth-related genes.

A specific RNA in cashmere goats helps improve hair growth by interacting with certain molecules.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

New topical treatment using spherical nucleic acids shows promise in reducing psoriasis inflammation.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

The gene HDC is important for the development of hair follicles in newborn mice.

The study identified a key protein involved in producing underarm odor and found ways to inhibit it.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Stereotactic Radiosurgery is an effective non-invasive treatment for cerebral AVM, with successful outcomes and minimal side effects.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

KRT2.13 gene is similar to KRT2.9 but not expressed in hair follicles.

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