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The BMP2 gene is more active in the early growth phase of Cashmere goat hair and may affect hair regeneration and textile production.

PRC2 is not essential for hair follicle stem cell maintenance or hair growth.

aPKCλ is crucial for keeping hair follicle stem cells inactive and maintaining normal hair growth.

Id proteins, especially Id2 and Id3, are crucial for hair follicle development and stem cell regulation.

Increasing Wnt5a in mice skin delays hair growth but doesn't stop it.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Human hair keratin genes are similar to mouse genes and are specifically expressed in hair follicles.

Keratin proteins in hair are complex and come from multiple gene families.

A new keratin, hK6irs1, is found in all layers of the hair follicle's inner root sheath.

Recognizing mild or atypical cases of ectodermal dysplasia is crucial for better treatment and future planning.

β-catenin is essential for stem cell activation and proliferation in hair follicles.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

The hr gene is linked to hair loss in Valle del Belice sheep.

Hairless protein and putrescine regulate each other, affecting hair growth and skin balance.

Hsc70 protein may influence hair growth by responding to androgens.

PBX1 helps reduce aging and cell death in hair follicle stem cells by decreasing DNA damage, not by improving DNA repair.

SOX2 is crucial for skin cell function and hair growth, and it plays a role in skin cancer and wound healing.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

Antizyme slows skin tumor growth by reducing cell growth in mice.

DKK2 and SOSTDC1 together are necessary for the normal timing of the first regression phase in the hair growth cycle.

Different processes create patterns in skin and things like hair and feathers.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

The protein RSL4 is crucial for making root hairs longer by controlling genes related to cell growth.

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

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Mutations in hKAP1 genes may cause hereditary hair disorders.

The Itpr3 gene causes a specific hair pattern in mice.