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The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

The CuCS/Cur wound dressing helps regenerate nerves and heal deep skin burns by rebuilding hair follicles.

Cepharanthine may help treat gastric cancer by causing cancer cell death and affecting energy use.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

HoxC genes are crucial for normal hair and nail development.

Androgens increase norepinephrine release, promoting smooth muscle growth in male sex organs, which may contribute to benign prostatic hypertrophy.

ILC1-like cells can cause alopecia areata by themselves.

A rare skin condition appeared on a 19-year-old woman's scalp.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

A new goat gene affects cashmere fiber thickness; certain variations can make the fibers coarser.

Non-coding RNAs help control hair growth in cashmere goats.

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

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

pCLCA2 protein may help maintain skin structure and function.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

Early diagnosis and multidisciplinary care are crucial for managing CNOT3 syndrome.

MPA increases cancer spread by boosting Eph A2 activity.

CCCA causes progressive hair loss in Black women, starting from a central scalp patch.

lncRNAs may help control cashmere goat hair growth by responding to light changes.

CXCL7 is essential for muscle repair by aiding early neutrophil infiltration.

Armadillo Repeat Only proteins are essential for proper plant growth and response by regulating calcium channels.

The cornified envelope is crucial for skin's barrier function and involves key proteins and genetic factors.

CCCA is a common hair loss condition in African American women, often inherited and influenced by hairstyling, with unique scalp features detectable by special tools.

Kir6.1 mutations in Cantú syndrome increase channel sensitivity and hyperpolarization, while SUR2B mutations do not.

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

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

Ketoconazole improved symptoms of ACTH-independent Cushing syndrome despite inconclusive initial scans.

CCCA may involve the PD1/PDL1 pathway and increased caspase 3, leading to permanent hair loss.

Corin helps control salt and sweat release in sweat glands.