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LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

Lacking cyclin D3 reduces skin cancer growth without affecting normal skin cell growth.

Epigenetic factors play a crucial role in skin health and disease.

The research identifies genes linked to wool quality in sheep and provides insights to improve wool production.

The complement system might be involved in the development of alopecia areata and could lead to new treatments.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

The Wnt/β-catenin pathway is important for body functions and diseases, and targeting it may treat conditions like cancer, but with safety challenges.

Overexpressing thrombospondin-1 in mice skin prevents UVB-induced skin damage.

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

GPRC5D is linked to the formation of hair, nails, and certain tongue areas.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.

KAP7.1 and KAP8.2 genes are crucial for cashmere quality in goats.

Progerin affects cell shape but not hair or skin in mice.

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

Agouti protein affects melanocortin receptors through competitive antagonism and receptor down-regulation.

Canine hair follicles have stem cells similar to human hair follicles, useful for studying hair disorders.

Different types of cells in the eye express specific keratins at various stages of development.

Scientists successfully made a human growth factor in a plant, which could help with hair growth and bone development.

Bone marrow stem cells and their medium help hair regrowth.

The enzymes Tet2 and Tet3 are important for skin cell development and hair growth.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Activating the GDNF-GFRα1-RET signaling pathway could potentially promote skin and limb regeneration in humans and could be used to treat hair loss and promote wound healing.

Docetaxel often causes hair loss, with limited effective treatments and no cure for permanent hair loss.

Hydrogel composites have great potential in regenerative medicine, tissue engineering, and drug delivery.

Epigenetic mechanisms control skin development by regulating gene expression.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.

More research is needed to understand how testosterone is maintained in adult males.