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Scientists found a new type of skin cell that could help with skin repair and these cells work better with a certain protein.

Endoglin is important for proper hair growth cycles and stem cell activation in hair follicles.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

A new method helps grow skin stem cells better, which could improve skin grafts for burn victims.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

Lrig1 marks a unique group of stem cells in mouse skin that can become different skin cell types.

GLI and EGF signalling affect Basal Cell Carcinoma development and could be therapeutic targets.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Nestin-expressing cells turn into a specific type of skin cell in hair follicles during development and in adults.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

TGM3 is important for skin and hair structure and may help diagnose cancer.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

EZH1 and EZH2 are crucial for healthy hair growth and skin repair.

GTL1 is needed to control root hair growth and prevent problems when there are too many nutrients.

Nestin marks cells that can become a specific type of skin cell in hair follicles of both developing and adult mice.

LncRNA RP11-818O24.3 may help treat hair loss by boosting hair follicle stem cell growth and differentiation.

Certain gene variations in EGF and EGFR may increase the risk of alopecia areata in Koreans.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

A unique enzyme in guinea pig hair follicles helps form protein cross-links in hair.

A novel CLDN1 mutation in a 2-month-old with NISCH showed improvement with symptom management.

A severe form of Netherton syndrome caused by a specific gene mutation led to neonatal deaths in a family.

Necl2 affects skin cell behavior and slows wound healing.

Laminin α5 is essential for skin communication and health.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

Researchers found two new genetic variants linked to Alzheimer's disease.

EGFR deficiency in skin causes hair follicle issues and inflammation.

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

GLABRA2 represses root hair formation by inhibiting a specific gene.

GFRα2 is essential for controlling neuron size but not for target innervation in certain sensory neurons.