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First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

Canine hair follicle cells show stem cell properties, aiding hair growth.

Long-term use of calcineurin inhibitors in transplant patients can cause hormone issues that can be managed with proper care.

AKN might be a skin marker for metabolic syndrome.

NKCC1 transporters help control neuron excitability and inhibition.

Nexin 1 may help control hair growth.

Mutations in the KRT16 gene can cause skin and nail disorders.

The calcineurin/NFAT pathway plays a significant role in the development and growth of a type of skin cancer called cutaneous squamous cell carcinoma.

Deleting the CDSN gene causes severe skin and hair problems, leading to death.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

KY19382 speeds up wound healing by activating a specific cell signaling pathway.

Some CKD patients' kidney function remains stable over time.

HOXC13 is essential for hair and nail development by regulating Foxn1.

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

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

Noncoding RNAs help determine cashmere quality in goats.

Poromas are related to sweat duct cells, and CK patterns help distinguish apocrine poromas from other neoplasms.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Blocking DKK1 with siRNA can improve hair growth.

DKK4 can be used to improve wool quality in Zhexi Angora rabbits.

Type I keratin genes are closely linked to the rex locus on mouse chromosome 11, affecting hair development.

DS-2325a is safe and well-tolerated, supporting further development for Netherton Syndrome treatment.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Krtap11-1 is important for hair strength and structure.

Certain genetic changes in the KRT82 gene may cause patchy skin in New Zealand rabbits.

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