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Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

A gene variant increases the risk of a type of hair loss by affecting hair protein production.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

The document concludes that skin stem cells are important for hair growth and wound healing, and could be used in regenerative medicine.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

FoxN1 gene is essential for proper thymus structure and preventing hair loss.

Selective breeding caused the unique curly hair in Mangalitza pigs.

Newborn screening and gene therapy are expected to improve outcomes for Omenn syndrome patients.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

Hair follicle development is controlled by interactions between skin tissues and specific molecular signals.

Nerve signals are crucial for hair follicle stem cells to become skin stem cells and help in wound healing.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

The conclusion is that certain cell interactions and signals are crucial for hair growth and regeneration.

Stem cell offspring help control their parent stem cells, affecting tissue health, healing, and cancer.

Lactate production is important for activating hair growth stem cells.

The ZIP7 gene helps control zinc levels in cells by moving zinc from the Golgi apparatus to the cytoplasm.

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

Different types of skin cells have unique genetic markers that affect how likely they are to spread cancer.

Blood vessels and specific genes help turn cartilage into bone when bones heal.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Understanding hair growth involves complex interactions between molecules and could help treat hair disorders.

The WNT signaling pathway is important in many diseases and targeting it could offer new treatments.

Different types of stem cells with unique roles exist in blood, skin, and intestines, and this variety is important for tissue repair.

Adam10 enzyme is crucial for healthy skin and proper Notch signaling.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

PDGFA/AKT signaling is important for the growth and maintenance of certain skin fat cells.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.