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Chitosan-encapsulated Cordyceps militaris reduces lung cell damage from pollution.

Differences in cashmere quality between goat breeds are linked to specific genes affecting hair follicle development.

Human skin cells contain Protease Nexin-1, and male hormones can decrease its levels, potentially affecting hair growth.

TRPA1 is crucial for mechanical sensitivity in skin sensory neurons.

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

Hoxc13 gene expression and skin thickness change similarly during cashmere goat hair follicle development.

Cashmere quality differences between goat breeds are linked to specific genes and pathways.

CLE14 peptide promotes root hair growth in Arabidopsis.

Disrupting the Flcn gene in mice causes early kidney cysts and tumors, which can be treated with rapamycin.

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

Wnt/β-catenin signaling is crucial for heart development and could help improve heart repair.

The author now supports the JCCP's efforts to improve non-surgical aesthetic practices after initial skepticism.

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

Researchers found that certain RNA molecules might play a role in the growth of Cashmere goat hair.

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

ILC1-like cells can cause alopecia areata by affecting hair follicles.

Carbon dots from Cinnamomum burmannii leaves can promote hair growth and regeneration.

Traditional Chinese medicine may help relieve symptoms of Cronkhite-Canada syndrome.

Cinchonine Nanostructured Lipid Carriers serum safely and effectively stimulates hair growth and increases the number and size of hair follicles.

Cashmere quality differences are due to gene expression variations affecting hair development and adaptation to cold.

GPC1 is important for hair growth by helping blood vessels form around hair follicles.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

Black women with CCCA are more likely to have uterine fibroids.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

BCC can protect heart cells from damage caused by oxidative stress.

Ca_v1.2 affects hair growth and could be a target for hair loss treatments.

Two patients with Cronkhite-Canada syndrome achieved remission after treatment.

Certain long non-coding RNAs in cashmere goats affect hair growth when treated with a specific growth factor.

The Foxn1(-/-) phenotype disrupts hair growth and affects skin stem cells.