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CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

CRET therapy affects inflammation in skin cells by changing cytokine levels and activating certain proteins.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

CXXC5 is a protein that prevents hair growth and could be a target for hair loss treatment.

1α,25-dihydroxyvitamin D3 directly affects cartilage growth and development.

A mouse gene mutation increases the risk of skin cancer.

Severe CCCA may be biologically and clinically different from milder forms.

Mutations in the HOXC13 gene cause hair and nail development issues.

Blocking CCR5 can prevent and improve hair loss in alopecia areata.

Vitamin D receptor and hairless protein are essential for hair growth.

Cronkhite-Canada syndrome can sometimes show unusual colonic adenomatous polyps.

The Cashmere goat hair keratin gene is crucial for hair structure.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Genetic factors, especially PADI3 gene variants, contribute to CCCA in women of African descent.

CCCA in women of African ancestry may be caused by PADI3 gene mutations and intense hair grooming.

Lack of cystatin M/E causes thin hair and dry skin.

Shh and Dhh affect skin development and can cause tumors, while Ihh does not.

Chemical treatments damage hair more than UV exposure, making it thinner and less flexible.

Hair chromium levels reflect nutritional status after standard washing.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

Rituximab may be an effective treatment for Cronkhite-Canada syndrome with kidney disease.

Three genes linked to the development of trichilemmal cysts were found.

Cholecystokinin may help reduce skin inflammation in psoriasis.

μ-Crystallin may help hair growth by affecting thyroid hormone levels in mouse hair follicles.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

A man with Cronkhite-Canada syndrome improved significantly with immunosuppressive therapy.

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