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A specific group of immune and skin cells may cause chronic inflammation in atopic dermatitis.

Genetic mutations that disrupt homocysteine breakdown lead to increased damage in mouse hair keratin.

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

Sensory neuron and Merkel-cell changes in the skin happen independently during normal skin maintenance.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

Anabolic steroids and inflammation can disrupt androgen metabolism, potentially causing health issues.

A new mouse mutation causes skin and hair defects due to a gene change.

Selenium deficiency worsens aging symptoms in mice.

Cell size controls when stem cells divide.

Claudin expression changes help the skin respond to injury.

A specific mutation in Kras causes abnormal tissue changes by making a cell signal continuously active, which disrupts normal cell coordination.

Adipose-derived stem cell exosomes can help reduce skin aging from UV exposure.

The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

Targeting mitochondria can improve skin health and slow aging.

Special gut cells help stem cells move to and fix injured areas by activating a specific signaling pathway.

Removing SIX1 in fat cells reduces skin fibrosis.

Fibroblast changes in systemic sclerosis may help understand disease severity and treatment.

Mutant stem cells adapt their metabolism differently to outcompete normal cells in the skin.

Seborrhea in Parkinson's disease may be linked to hormones, not autonomic impairment.

Endocrine disorders can cause various skin and hair issues.

Chronological age affects the mouse auditory cortex more than hearing loss, and the brain may be less sensitive to mitochondrial dysfunction.

A 7-year-old girl was diagnosed with trichothiodystrophy due to low sulfur levels in her hair.

Impaired autophagy may cause hair loss by triggering early catagen.

Cells communicate with neighbors to coordinate their development.

A gene mutation in mice causes skin defects and early death.

Faulty Notch signalling may cause hair follicle changes and inflammation in hidradenitis suppurativa.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

Lower proximal cup cells, not bulge stem cells, regenerate hair follicles after chemotherapy.

Impaired ABCA5 activity disrupts cholesterol balance in hair follicle cells, affecting hair growth.

Consider amyloidosis in patients with specific nail changes and check for systemic issues.