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L-cysteine slows down the breaking of bonds in hair due to electrostatic interactions.

Cyproterone acetate treatment is safe and causes mild feminization, which increases with added estrogen.

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

Cal/BD aerosol foam effectively treats scalp psoriasis, improving symptoms and patient satisfaction.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

CLASI is a valid tool for assessing skin activity and damage in lupus patients.

CD90 is abundantly present on stem-like cells in dog hair follicles.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Different keratins have unique expression patterns in mouse skin cells.

CGRP-IR axons may help maintain and renew tissues.

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

Blocking CXXC5 speeds up diabetic wound healing by improving blood vessel growth and skin repair.

Hair steroid measurement is an effective method to diagnose and monitor CAH in developing countries.

Calcium fatty acid deposits found in human hair can change its appearance and feel.

AtCSLD3 and GhCSLD3 genes enhance root growth and cell elongation in plants.

Cyclosporin promotes hair growth by boosting cell growth and reducing cell death.

Caspases do more than kill cells; they also help in cell growth and disease, and targeting them could lead to new treatments.

Consider rare forms of CAH for accurate diagnosis and treatment.

CK15 is not a reliable marker for stem cells in damaged hair follicles from patients with CCCA.

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

SCD1 is important for hair growth by keeping the connection in skin cells where hair stem cells live stable.

High ornithine decarboxylase levels may lead to hair loss and cancer by increasing CK2 activity in the nucleus.

Lysophosphatidic acid boosts stem cell growth and movement by creating reactive oxygen species.

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

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

A Chinese man with KID syndrome had a new mutation in the GJB2 gene.

A specific gene mutation causes sparse, brittle hair in a family.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.