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Trichohyalin-like proteins are essential for the development of skin structures like hair, nails, and feathers.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

The document is a detailed medical reference on skin and genetic disorders.

A new ethical skin model using stem cells offers a reliable alternative for dermatological research.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

Overactive Wnt signaling in mouse skin stem cells causes acne-like cysts and shrinking oil glands, which some treatments can partially fix.

The document explains different types of hair loss, their causes, and treatments, and suggests future research areas.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

Ovol2 is crucial for hair growth and skin healing by controlling cell movement and growth.

EGFR helps control how hair grows and forms without needing p53 protein.

Vitamin D and its receptor regulate skin functions like cell growth, immunity, hair cycle, and tumor prevention.

Sweat gland development involves two unique skin cell programs and a temporary skin environment.

Bone marrow stem cells and their medium help hair regrowth.

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

The document concludes that more local research on African skin and hair is needed despite increased scientific output from Sub-Saharan Africa.

Some skin conditions may increase the risk of heart disease, but are not yet included in cardiovascular prevention guidelines.

The conclusion is that there's a link between high testosterone levels, insulin resistance, and certain skin conditions, regardless of obesity.

Meis1 is crucial for skin health and tumor development.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

The conclusion is that understanding how hair follicle stem cells live or die is important for maintaining healthy tissue and repairing injuries, and could help treat hair loss, but there are still challenges to overcome.

Intu gene is crucial for hair follicle formation by helping keratinocytes differentiate through primary cilia.

Different types of cell death affect skin health and inflammation, and understanding them could improve treatments for skin diseases.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.

Epigenetic changes control how adult stem cells work and can lead to diseases like cancer if they go wrong.

Hair loss in teenagers is hard to treat and lacks a cure, with some treatments available depending on the type of hair loss.

Filaggrin mutations are linked to atopic dermatitis and help explain how genetics and environment affect the disease.

Wnt ligands are crucial for hair growth and repair.

NK cells play a role in skin diseases like eczema and psoriasis.