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Removing the ROBO4 gene in mice reduces skin inflammation and hair loss by affecting certain inflammation pathways and gene expression.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

Yak hair growth is influenced by genes and hormones, helping them adapt to alpine environments.

Personalized genomic interventions can effectively manage chronic hair loss.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

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

Hair treatments cause significant structural changes, especially with excessive heat, regardless of ethnicity.

Using special RNA to target a mutant gene fixed hair problems in mice.

The new bioreactor improves skin grafts by evenly stretching cells and monitoring conditions for better growth.

Laser microdissection helps get DNA from single hair follicles for better forensic analysis.

Monitoring TGF-β and linc-PINT expression may help identify and treat high-risk heart arrhythmia patients.

TGF-beta 1 and IGF-II mRNA have specific patterns in pig subcutaneous tissue, affecting fat and muscle development.

Key genes and pathways control sheep hair growth phases.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

Human head hair proteins can be typed into eight distinct patterns, useful for genetic and forensic investigations.

Recombinant thrombomodulin can effectively treat severe complications in Cronkhite-Canada syndrome.

miR-148a and miR-10a affect hair growth in Hu sheep.

Hair differentiation starts earlier than thought, involving multiple type-II keratins.

Immune activities and specific genes are important in male pattern baldness.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Researchers found 44 proteins that change during different hair growth stages and may be important for hair follicle function.

The scraggly mutation causes hair loss and skin defects in mice.

Chronic stress in mice changes skin metabolism and gene expression, leading to hair loss.

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

Most people have similar hair protein patterns, but a rare variant was found in two women.

The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.

The study identifies four distinct zones in the fetal vaginal epithelium, enhancing understanding for potential applications in women's health.

MFN2 mutations cause mitochondrial problems, leading to more upper body fat and lower leptin levels.

Biotinidase deficiency can mimic neuromyelitis optica and should be considered for accurate diagnosis and treatment.