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FERONIA regulates plant growth, pollen interactions, and sugar signaling.

QSOX enzymes help form protein bonds in cells, especially in tissues with high secretory activity.

Kremen is crucial for proper development and preventing tumors by regulating Wnt signaling.

Keratin-associated proteins are crucial for hair strength and structure.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Sox2-positive cells determine specific hair follicle types in mammals.

The molecule Wise is involved in the development of various structures in chick embryos.

P-cadherin is important for hair growth and health, and its problems can cause hair and skin disorders.

Researchers created a new mouse model, G4, that mimics human PCOS symptoms and links the condition to a specific gene.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

EBF1 controls hair type and length.

Alpha-difluoromethylornithine prevents cancer in mice but causes hair loss.

The antibody 005-C04 blocks prolactin receptors, causing reversible infertility, impaired lactation, and hair regrowth in female mice.

ePUKs could be valuable for regenerative medicine due to their wound healing abilities.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.

Deleting the p63 gene in certain cells causes problems in thymus development and severe hair loss in mice.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

POMC-derived peptides are important for skin functions like immune response and stress management.

Hoxc genes control hair growth through Wnt signaling.

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

PDGF isoforms can promote and sustain hair growth.

A specific gene region can control targeted and responsive gene expression in mice, useful for skin disorder treatments.

PRC1 influences skin stem cell development by both turning genes on and off, affecting hair growth and skin cell types.

Mutations in the P2RY5 gene cause hereditary woolly hair.

A specific gene segment can make mouse skin cells glow, helping study hair growth and gene effects.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

CaBP1 and CaBP2 are important for maintaining hearing by supporting continuous calcium currents and nerve signaling in the ear.

Secreted inhibitors of Wnt and IGF signaling control hair and tooth development, creating species-specific patterns.