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Heat-treated Limosilactobacillus fermentum with menthol, salicylic acid, and panthenol promotes hair growth and balances scalp microbiome in people with androgenetic alopecia.

The DiLiCre mouse model is an effective tool for precise genome editing using light.

A gene deletion in DSG4 causes sparse hair in some Pakistani families.

GLP-1 medications can cause skin and muscle issues, but treatments like ultrasound and PRP can help.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Topical glycopyrrolate lotion helped reduce excessive sweating from eating in a diabetic man.

Lower GPX4 mRNA levels are linked to higher disease activity and symptoms in lupus patients.

The study found that thioglycolic acid breaks down hair bonds more consistently than l-cysteine, which is less damaging to hair.

CT60 polymorphism might increase the risk of Alopecia Areata.

Pranlukast and mirabegron may work as new diabetes drugs.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

High glucocorticoids cause pancreatic malfunction and malabsorption, reversible with enzyme supplements.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

KAP6 genes are conserved across species and active in hair follicles.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Removing myelin protein zero-like 3 in mice leads to better metabolism and resistance to obesity.

VYN201 shows promise as a safe and effective treatment for non-segmental vitiligo.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

HLA can be linked to autoimmune hepatitis.

Altering SSAT affects fat metabolism and body fat in mice.

Hair-straightening products with glyoxylic acid can cause kidney damage.

Double-stranded RNA activates a pathway that causes a skin protein to be expressed in the wrong place.

Pyrene excimer nucleic acid probes are promising for detecting biomolecules accurately with potential for biological research and drug screening.

Enhanced stem cells from the placenta can help treat Graves' eye disease by stopping fat cell growth.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

LustrivaTM improves hair thickness and reduces facial wrinkles safely.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.