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An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

HB-EGF boosts the hair growth ability of stem cells, making it a potential hair loss treatment.

BMI1 is essential for preventing hair greying and maintaining hair color.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

MRI can effectively image skin structures noninvasively.

A girl had rickets due to a gene mutation affecting vitamin D response.

Early skin biopsy is crucial for diagnosing Conradi-Hünermann-Happle syndrome.

PRO-C22 can help diagnose and monitor the severity of hidradenitis suppurativa.

The assay effectively detects hormonal activity of certain chemicals.

Combining Proton Minibeam with FLASH Radiotherapy may improve cancer treatment by reducing side effects and increasing effectiveness.

Researchers successfully made new compounds for hormone level tests, but one attempt led to an unexpected product, correcting a past error.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Copper treatments increase copper in all tissues, but brindled female mice accumulate much more copper in their kidneys without clinical effects, unlike brindled male mice where brain copper deficiency is clinically significant.

A unique gene mutation was found in a family with monilethrix.

A higher calcium to magnesium ratio in hair is linked to lower insulin sensitivity.

The mFG score is effective for diagnosing hirsutism.

Biotin treatment improves symptoms of biotinidase deficiency, but some neurological damage may be permanent.

Functional nutrition evaluations can improve personalized wellness programs and help prevent chronic diseases.

Mouse hair keratins mHa1 and mHb4 can't form a strong network on their own in cells.

The mutation causing Hutchinson-Gilford progeria syndrome leads to severe skin problems and early death in mice.

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Human hair keratin may help repair injured spinal cord tissue in rats.

Major histocompatibility antigens are found in specific skin cells and structures, but not in sweat glands.

The Cell Membrane Complex in hair has both water-attracting and water-repelling layers.

The ABHRS held a test in Capri, Italy.

S100A4 and NMIIA promote tumor growth in glioblastoma by enhancing blood vessel functions.