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A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

This enzyme helps metabolize fatty acids and isoleucine, and could be key in treating neurological diseases and certain cancers.

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

Targeting ornithine decarboxylase can help prevent skin cancer.

Cathepsin E is crucial for normal skin cell differentiation and development.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

UVB exposure increases appetite by activating p53 in skin cells.

Two cases of hairy elbows syndrome were described, with normal skin texture and symmetrical hair growth.

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.

Different parts of cells interact at specific areas to control cell functions like energy production and fat storage.

Two specific genes are more active during hair growth in mice.

Cantú syndrome is caused by mutations in the ABCC9 gene.

The UHS promoter is specific to mouse hair follicles.

ILC1-like cells can cause alopecia areata by themselves.

OXI1 kinase is essential for plant defense and root hair growth in Arabidopsis.

UVB exposure increases skin proteins for retinoic acid synthesis and shifts their location, possibly affecting skin repair.

A specific enzyme is crucial for the bean plant's relationship with certain beneficial soil bacteria and fungi.

Involucrin is crucial for skin cell maturation and protection.

Enzymes are classified into six types and are essential for many biological processes, with only a few targeted by drugs.

Reconstructed skin models are useful for studying how skin processes certain chemicals.

Upadacitinib helped regrow hair and maintain ulcerative colitis remission.

A new protein linked to hair strength was identified, aiding in understanding brittle hair conditions.

Cathepsin L deficiency causes large, abnormal cell structures and health issues in mice.

ACBP is crucial for healthy skin in mice.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

WWP2 is crucial for tooth development in mice.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

AIRE protein, defective in APECED patients, is found in skin and hair cells and interacts with cytokeratin 17.

Metabolite 7 is a strong inhibitor for Alzheimer's disease management.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.