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Increased ODC activity leads to skin tumors by recruiting stem cells, not by toxic byproducts.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Lack of cystatin M/E causes thin hair and dry skin.

Dual TCR Treg cells are common in various mouse tissues and show diverse characteristics.

Phospholipase C-δ1 is crucial for normal hair development.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

MAA beads improved wound healing in male mice by activating the Shh pathway, but not in females.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

The oncoprotein causes abnormal hair growth without increasing skin cancer risk.

TNF alpha in skin cells causes weight loss, hair and fat issues, and skin inflammation in mice.

Bmpr2 and Acvr2a receptors are crucial for hair retention and color.

Mutations in specific genes cause certain congenital defects in dogs, aiding in understanding similar human diseases.

ACBP is crucial for healthy skin in mice.

The system allows precise control of gene expression in mouse skin, useful for studying skin biology.

BST2 is a key marker for hair loss disease alopecia areata.

Mice with autoimmune hair loss showed signs of heart problems.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Egfl6 is not needed for zebrafish face development.

Half-siblings with a rare skin condition improved with treatment for a fungal infection, but hair loss remained.

Activated protein C helps protect mice from long-term radiation damage.

BKN-1 antibody targets specific keratin in basal cell epithelioma and normal skin basal cells.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

17β-estradiol lowers polyamine oxidase levels in breast cancer cells through estrogen receptor 2.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.