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Hearing decline in SAMP8 mice starts before outer hair cell loss and may be linked to other changes.

CD61 is important for mouse tooth cell growth and works through Lgr5.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

Mice with the naked gene have missing or abnormal hair cells.

Erythropoietin overexpression disrupts hair growth and fat formation in mice.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

Dermal EZH2 controls skin cell development and hair growth in mice.

IFN-γ production by CD4 T cells is crucial for causing alopecia areata.

A substance from hair follicle stem cells helps heal skin wounds in diabetic mice by promoting cell growth and preventing cell death.

Younger mice's hair-follicle stem cells are better at turning into heart cells than older mice's.

Mouse hair follicle stem cells can help prevent Type 1 Diabetes.

Tet1/2/3 enzymes affect hair follicle cell development by influencing BMP signaling.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

Controlled delivery of specific RNA and IL-4 restored hair growth in mice with autoimmune alopecia.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

Zinc deficiency in female rabbits causes poor health and reproductive issues.

Young C57BL/6 mice heal better than BALB/c mice, and older mice heal faster but regenerate worse.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Hair zinc levels don't reliably indicate overall zinc status in animals.

SkQ1 antioxidant improved health and lifespan in mice.

A boy's hair turned red because of genetic mutations, not lack of zinc.

Selenoproteins are crucial for healthy skin and hair.

Removing certain brain receptors in mice worsens seizure severity and response to treatment during hormone withdrawal.

A new genetic variant of Woodhouse-Sakati syndrome was found in two adult sisters in Russia.

Consider rare forms of CAH for accurate diagnosis and treatment.

Progeroid mouse models show signs of early aging similar to humans, helping us understand aging better.

Some people have genetic mutations that make them resistant to vitamin D, leading to rickets even with enough vitamin D intake.