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MYB83 limits root hair growth and helps plants tolerate nutrient deficiencies.

A specific DNA region controls skin cell gene expression by working with certain proteins.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

Removing integrin α3β1 from hair stem cells lowers skin tumor growth by affecting CCN2 protein levels.

VEGF and VEGFR-2 genes influence feather maturity, and specific genetic markers can improve chicken breeding.

Exosomal miR-199a-3p from dermal papilla cells helps control hair color by affecting melanocytes.

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

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

Ephrin-A3 helps increase and speed up hair growth in baby mice.

KRT72 gene helps form hair.

PTHrP is important for bone formation and may be targeted for osteoporosis treatment and longevity therapies.

CRABP2 helps increase the growth of cells important for hair growth by activating a specific growth pathway.

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

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

PRSS35 enzyme may help start skin tumors and could be a target for cancer treatment.

The prolactin gene polymorphism doesn't affect cashmere quality in these goats.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

PDGFC gene may help select goats with desirable curly wool traits.

NCBP3, SDHA, and PTPRA are the best genes for accurate goat skin research.

BMP-2 activates the Dlx3 gene in mouse skin cells, important for hair and skin development.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

A new gene mutation linked to a skin condition was found in a Spanish family.

A deletion in the CDH3 gene causes a rare disorder with short hair and vision loss.

Spt4 and Spt6 are essential for fat cell development.

TIP39 and PTH2R help control calcium levels and skin cell development.

mEphA1 receptor tyrosine kinase is important for skin and hair development and may play a role in certain diseases.