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ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

The UHS promoter is specific to mouse hair follicles.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

EX104 shows promise in treating hair loss by promoting hair growth and improving scalp health.

BLMP-1 is important for regular molting and gene expression cycles in worms.

UT-018 speeds up wound healing and boosts hair growth in mice.

Finasteride helps female-pattern hair loss.

Targeting a protein that blocks hair growth with microRNAs could lead to new hair loss treatments, but more research is needed.

A DNA aptamer helps promote hair growth by enhancing a key cell growth signal in hair follicle cells.

Scientists can mimic hair disorders by altering genes in lab-grown human hair follicles, but these follicles lack some features of natural ones.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

NDP-MSH protects brain cells and reduces inflammation in Parkinson's disease by activating MC1R and involving Tregs.

Telitacicept helped stabilize complement levels in a patient with lupus and thyroid cancer.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

TRα and CRABPII genes change their activity levels during goat fetal skin development.

RADA16-I can effectively deliver and release mangiferin, improving its solubility and bioavailability.

Enhanced stem cells from the placenta can reduce fat buildup in eye tissue for Graves' disease.

The study showed that a specific DNA sequence can control gene expression in hair growth areas of mice.

Non-coding RNAs help control hair growth in cashmere goats.

MicroRNAs could help assess and manage multiple chronic diseases.

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

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Targeting SIRT1 with antisense oligonucleotides could be a promising treatment for hair loss.

Zfp157 is active in many mouse tissues during development and in specific adult cells.

Researchers found a non-functional sheep keratin gene due to mutations.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

AP-1 and TGFß work together to drive resistance in basal cell carcinoma, suggesting new treatment options.

Pigs without the Hairless gene showed skin and thymus changes, useful for studying human hair disorders.