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Short-term treatment with ROCKi increases skin cell growth without changing stem cell features.

Whn is essential for hair growth, and its malfunction causes hair loss.

ICAM-1 helps regulate hair growth cycles and skin remodeling.

Transferrin receptor 1 is essential for normal function in the intestines, pancreas, and skin.

PRP can improve hair growth in people with hair loss, but more research is needed.

Mutations in the Whn gene affect hair keratin gene expression differently.

A specific gene mutation in KRT86 is linked to hair disorder in a Chinese Han family.

Rac1 is crucial for normal hair structure and pigmentation.

NGAL may help maintain skin balance and is linked to skin disorders and cancers.

TRPV3 and TRPV6 channels change structure to regulate calcium and heat responses.

PBX1 helps hair stem cells grow and change by turning on certain cell signals and preventing cell death, which may be useful for hair regrowth treatments.

Nelfb is essential for dermal fat development and survival.

Nilotinib can cause skin issues like red bumps and hair loss.

Pachyonychia congenita is linked to a keratin gene on chromosome 17.

K39 and K40 are the last keratins expressed in hair development, completing the hair keratin catalog.

FOXN1 gene variants cause low T cells and immune issues from birth.

Keratinocyte growth factor significantly alters skin and tissue development.

Too much IKZF1 and Ikaros protein may cause alopecia areata.

Basonuclin helps identify and track hair follicle development and cycling in mice.

Neprilysin is important for hair growth regulation.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

IL-9 increases skin cell movement but decreases their ability to invade, and this effect is controlled by cell contractility, not by MMPs.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Higher Lnk protein levels in ovaries may lead to insulin resistance in women with PCOS.

Targeting NETs may help reduce fibrosis in Crohn's disease.

EGFR helps mouse hair follicles stop growing by reducing certain growth regulators.

Damaging mutations in NFKB2 cause a severe and distinct form of primary immunodeficiency with early-onset and often ACTH-deficiency.

Different ligands change the shape of the TRPV3 ion channel in unique ways.