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A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

Potent extracellular vesicles from cardiosphere-derived cells can improve heart health and other functions in aging.

WHV infection does not affect woodchuck skin anatomy.

Lizard claws have hair-like keratins similar to those in mammals.

Bioré Pore Perfect strips effectively and safely clean pores on the nose.

Mouse skin has special cells in the epidermis that decrease with age and are linked to keratinocyte stem cells.

A reliable model for screening type II 5α-reductase inhibitors was created and validated.

These ovarian conditions cause high testosterone levels.

A gene mutation causes monilethrix in a Chinese family.

Reliable, non-invasive tools are needed for better vitiligo diagnosis.

Trichoepithelioma and desmoplastic trichoepithelioma have distinct features that can be identified using reflectance confocal microscopy.

NCBP3, SDHA, and PTPRA are the best genes for normalizing goat skin experiments.

A new method helps detect androgen receptor movement in cells, aiding research on hair loss treatments.

Standard reference values for hair analysis in healthy Indian males were established.

A PEG-400/oleic acid mixture best improves drug delivery monitoring through hair follicles.

Degraded hair shafts resist contamination and can be easily cleaned.

Dermoscopy improves diagnosis and treatment planning for trichostasis spinulosa.

STK11 gene variations do not predict how well metformin will work for PCOS, but may affect hair loss and excess hair growth.

OCT can detect hidden hair follicles in alopecia areata, indicating potential hair regrowth.

Two specific hair keratin genes are active during hair growth and decline as hair transitions to rest.

Diagnosing oral ulcers can be complex and requires careful examination and follow-up.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

Scientists discovered two versions of a new human hair keratin gene.