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Hair and nail cells share similar proteins, indicating a common differentiation pathway.

Human skin makes sexual hormones that affect hair growth, skin health, and healing; too much can cause acne and hair loss, while treatments can manage these conditions.

The circadian clock affects skin stem cell behavior, impacting aging and cancer risk.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Ectodin integrates BMP, SHH, and FGF signals in developing ectodermal organs.

PGD2 stops hair growth and is higher in bald men with AGA.

Overexpression of activin A in mice skin causes skin thickening, fibrosis, and improved wound healing.

Lactate production is important for activating hair growth stem cells.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Androgens may cause hair loss by increasing TGF-beta1 from scalp cells, which inhibits hair cell growth.

Pectin biosynthesis is essential for the growth of cotton fibers and Arabidopsis root hairs.

CDP is crucial for lung and hair follicle cell development.

Cancer cells often have more copies of TERT and TERC genes, which helps them grow and could affect patient outcomes.

K6hf is a unique protein found only in a specific layer of hair follicles.

Prolactin contributes to hair loss by promoting hair follicle shrinkage and cell death.

Macrophages help regrow hair by activating stem cells using AKT/β-catenin and TNF.

Lowering testosterone speeds up wound healing in male mice.

Overexpressing Dsg3 in mice skin causes excessive cell growth and abnormal skin development.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Activating TRPV3 stops human hair growth.

MicroRNA-214 is important for skin and hair growth because it affects the Wnt pathway.

The study found that two enzymes linked to hair loss are located in different parts of the scalp, supporting a common treatment's effectiveness.

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

Androgens block hair growth by disrupting cell signals; targeting GSK-3 may help treat hair loss.

Fatty acid transport protein 4 is essential for skin and hair development.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

Cholesterol sulfate buildup due to a genetic mutation disrupts the skin barrier, leading to the scaling skin seen in X-linked ichthyosis.

The tumor suppressor gene FLCN affects mitochondrial function and energy use in cells.