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Trichohyalin is a versatile protein involved in hair and skin structure.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Fz3 and Fz6 can partially replace each other in tissue polarity and axon guidance.

EZH1 and EZH2 are crucial for healthy hair growth and skin repair.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

Dermal EZH2 controls skin cell development and hair growth in mice.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

Blocking hair follicle development stops key gene signals needed for hair growth in mice.

Baricitinib reduces inflammation and improves cell health in premature aging cells.

A genetic marker linked to a type of hair loss was found in most patients studied.

HGF combined with ADA is highly accurate for diagnosing tuberculous pleural effusion, especially in younger females.

The development of breeding tubercles in male zebrafish relies on a specific enzyme that processes hormones.

Para-aminobenzoic acid in hair supplements can cause autoimmune hepatitis.

Secreted inhibitors of Wnt and IGF signaling control hair and tooth development, creating species-specific patterns.

Certain genes are linked to the risk of developing Alopecia Areata.

New genetic mutations causing hair loss were found in a Chinese family.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

FGF13 gene changes cause excessive hair growth in a rare condition.

Vitamin B6 may help activate dormant follicles.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Human hair follicle stem cells can become endothelial cells with certain growth factors, useful for vascular treatments.

The GPRC6A-Duox1 axis helps control hair growth and loss by affecting hydrogen peroxide production.

Researchers found a gene in hamsters that responds to male hormones and may be indirectly controlled by them.

A mouse gene mutation increases the risk of skin cancer.

ULBP3 levels are higher in Tinea capitis patients and may help predict the disease's severity.

C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

The GH-IGF-I axis is likely involved in the hormonal imbalances seen in non-obese women with functional hyperandrogenism.

High lactate dehydrogenase activity is not necessary for the growth of squamous cell carcinoma.