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A substance from Caulerpa racemosa seaweed may protect against skin damage caused by air pollution by reducing oxidative stress and cell death.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

Krt6a-Cre transgenic mice help study gene effects on hair follicle development and tumor suppression.

Trichorhinophalangeal syndrome causes hair, facial, and bone issues, with no specific treatment beyond gentle care.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

A KRT32 gene variant causes loose anagen hair syndrome.

Scientists created cell lines to study a genetic skin disorder using CRISPR technology.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Small bowel lesions in Cronkhite-Canada syndrome persist despite steroid treatment.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

Ketoconazole's structure and dynamics are linked, aiding antifungal drug development.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

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

A cluster of 21 keratin-associated protein genes important for hair growth was found on human chromosome 21.

Human hair keratin genes have unique simple sequence repeats that may help track genetic variations.

The hair keratin gene KRT81 is found in both normal and breast cancer cells and helps them invade surrounding tissues.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

The HCR gene contributes to psoriasis risk.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

TB and BCC tumors show similar follicular differentiation patterns.

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

An 80-year-old woman with Cronkhite-Canada syndrome had multiple polyps and symptoms like diarrhea, hair loss, nail issues, and dark skin.

Secang wood extract hair tonic promotes hair growth and meets quality standards.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Cromakalim relaxes various blood vessels, while minoxidil sulphate is more selective; they likely act on different potassium channels.