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Folliculin deficiency causes problems with cell division and positioning due to disrupted RhoA signaling and interaction with p0071.

CDP is crucial for lung and hair follicle cell development.

Tofacitinib is a promising treatment for children with rheumatic diseases.

Overexpressing CtBP1 in skin cells causes skin and hair problems.

Arabidopsis Formin 2 stabilizes actin filaments to aid cell-to-cell trafficking.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

PlncRNA-1 helps hair follicle stem cells grow and develop by controlling a specific cell signaling pathway.

CXXC5 is a protein that controls cell growth and healing processes, and changes in its activity can lead to diseases like cancer and hair loss.

Integrin β1 is crucial for liver structure and function, preventing fibrosis.

Lack of TrkC receptor delays hair follicle development.

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

Human thymus has stem cells that can self-renew and maintain their identity.

Tebentafusp-tebn improves survival rates in uveal melanoma patients but has common side effects like rash and fatigue.

The HtrA1L364P mutation causes brain dysfunction and blood vessel damage.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

miR-140-y helps control feather growth in geese by affecting the Wnt signaling pathway.

Foxn1 helps skin cells mature by controlling a specific protein's activity.

TGF-β and FGF pathways are crucial for skin development and regeneration.

NFATc1 is crucial for keeping hair follicle stem cells inactive.

A mutant FERONIA gene affects root hair growth at high temperatures.

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

Special immune cells called Tregs can help prevent lung scarring by blocking a specific growth factor.

Special immune cells called Treg cells are important for maintaining and regenerating hair by activating a specific growth signal in hair stem cells.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

Foxc1 helps keep hair follicle stem cells inactive, preventing hair loss.

The protein FLCN is involved in cellular cleanup and is regulated by ULK1.

TFC-loaded microneedles effectively promote hair regrowth in androgenetic alopecia.

Claudin-1 is important for the barrier function and growth of hair.