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Gene network oscillations inside hair stem cells are key for hair growth regulation and could help treat hair loss.

ADM scaffolds help skin heal by promoting a healing-type immune response.

A specific microRNA, chi-miR-30b-5p, slows down the growth of hair-related cells by affecting the CaMKIIδ gene in cashmere goats.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Chemokine signaling is important for hair development.

Vitamin D boosts a specific gene activity in kidney cells that could improve heart and kidney function.

Different fish use the same genes to regrow teeth.

The enzyme CD73 helps control human hair growth and could be targeted to treat hair growth disorders.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

Finasteride improves heart function and repairs damage after heart attack in mice.

A circular RNA helps cashmere goat hair cells become hair follicles by blocking a molecule to boost a gene important for hair growth.

SP1 promotes and KROX20 inhibits hair cell growth by affecting the CUX1 gene.

STAT3 reduces FST gene activity and cell growth, affecting hair development and wool quality.

Hair growth phase and certain genes can speed up wound healing, while an inflammatory mediator can slow down new hair growth after a wound. Understanding these factors can improve tissue regeneration during wound healing.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Involucrin gene expression is controlled by specific proteins and signaling pathways.

The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

A gene in Arabidopsis thaliana, AtPRPL1, affects root hair length but not cell wall composition.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Ancient Chinese goats evolved cashmere-producing traits due to selective breeding, particularly in genes affecting hair growth.

The gene Msx2 is crucial for hair follicle regeneration during wound healing.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

A new mutation in the HR gene causes hair loss in a specific family.

Vitamin D receptor can control the hairless gene linked to hair loss even without vitamin D.

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

DNA methylation likely doesn't cause different lambskin patterns in Hu sheep.

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.