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LncRNA MSTRG.14227.1 hinders hair follicle development in cashmere goats, affecting cashmere quality.

Twist1 helps maintain important features of cells crucial for hair growth by working with Tcf4 and β-catenin.

A new mutation in the KRT86 gene was found to cause the hair disorder monilethrix in a Han family.

A mutation in the VDR gene affects hair cycling without needing ligand binding.

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

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

5% topical minoxidil improves hair density and quality in monilethrix patients.

TTNPB helps turn stem cells into neural stem cells, improving depression-like behaviors in rats.

PCAT1 helps hair growth by controlling miR-329/Wnt10b.

Mutations in the desmoplakin gene can cause hair problems and deadly heart disease.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

Melanocyte pathology requires keratinocyte hyperplasia and regulation dysfunction.

Grafted human scalp samples on mice can produce human hair, useful for studying hair genetics.

K10 may not prevent tumors as previously thought and might increase benign tumor risk.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

Nitrogen mustard causes DNA damage and structural changes in mouse skin hair follicles, but some recovery occurs after 5 days.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

Notch signaling is crucial for specifying niche cells in Drosophila testis.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

The Gsdma3 gene is essential for normal hair development in mice.

Mutations in the KRT16 gene can cause skin and nail disorders.

Adding TERT and BMI1 to certain skin cells can improve their ability to create hair follicles in mice.

Mitochondrial Complex I reduces inflammation and increases bone breakdown by affecting certain immune cells.

The PML protein helps prevent skin cancer in mice.

Trps1 plays a key role in hair follicle development and cycling.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

The TGM3 gene's promoter region is key for skin and hair cell function and may aid gene therapy.