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Safusidenib erbumine shows promise as a treatment for certain brain tumors, but mild side effects like hair loss need attention.

Type 1/17 inflammation in psoriasis increases skin cell growth due to a molecule that could be a new treatment target.

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

A new mutation in the K6b gene caused a girl's late-appearing nail condition.

Keratin 19 forms less stable and shorter filaments than keratin 14, giving unique traits to certain skin cells.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Ethionine significantly inhibits wool growth in sheep but not hair growth in mice or rats.

Mutations in the enzyme don't significantly change how it binds to its specific substances.

ACKR2 helps prevent skin scarring and hair loss by controlling inflammation.

FTase and GGTase-I are essential for skin keratinocyte health.

Normal cells outcompete and remove mutant cells in the pancreas with the help of the EphA2 receptor.

The PTGER2 gene is highly active in Cashmere goat skin and its activity changes with the hair growth cycle.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

Blocking SEPT4 might help heal wounds and regrow hair faster.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Sebaceous glands can form new hair follicles when activated, but hair follicle bulges cannot.

BAF200 is essential for proper heart and coronary artery formation.

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

Some early COVID-19 mutations in patients predicted future common virus mutations.

KRT72 gene helps form hair.

LHX2, with other markers, can identify hair placodes in rats.

A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Overexpressing the human H-ferritin gene in mice causes mild growth delay and temporary hair loss.

A mutation in the iRhom2 gene causes hairless mice due to abnormal hair follicle development.

Egfl6 is not needed for zebrafish face development.