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A new DSG4 gene mutation causes hair defects in a young girl.

Maintaining DNA health in stem cells is key to preventing aging and tissue breakdown.

Gorab deficiency speeds up skin aging by disrupting protein regulation and reducing collagen.

Mutations in β1 integrins cause embryonic death but have milder effects on skin.

Men with androgenetic alopecia have lower levels of certain proteins and more cell damage.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

Ripretinib is effective and safe for treating advanced GIST in Chinese patients, particularly for non-gastric GISTs.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

Wnt ligands, produced by dermal papilla cells, are essential for adult hair growth and regeneration.

Excessive putrescine causes hair loss in transgenic mice by disrupting hair follicle development.

Mutant cells in hair follicles are influenced by their location and interactions with surrounding cells.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

Ponatinib can cause a rare skin reaction that resolves with topical treatment and temporary drug discontinuation.

Removing PLCg1 from skin cells caused thicker oil glands and less hair in mice.

miR-370-3p slows sheep hair cell growth by blocking SMAD4.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

Keratin 17 gene mutations cause both steatocystoma multiplex and pachyonychia congenita type 2.

Krt16-deficient mice help understand skin disorders like PC and FNEPPK.

Removing both KLK5 and KLK7 proteins can prevent death and skin issues in Netherton syndrome.

CXCR2 in skin cells promotes tumor growth.

A rare skin cancer on a man's elbow was successfully treated with surgery, showing no recurrence after one year.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Diphenylcyclopropenone treatment helps hair growth in alopecia areata by promoting blood vessel growth and cell survival.

Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

Lack of KSR1 stops certain skin tumors in mice.

A new gene mutation causes a rare type of hair loss.