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Lung and liver macrophages protect our tissues and their dysfunction can cause various diseases.

The study found that the hair loss condition in Cesky Fousek dogs is influenced by multiple genes affecting skin and muscle structure, fat metabolism, and immunity.

The document concluded that more research is needed to understand how estrogen affects the enzyme involved in hirsutism development.

FKBP10 and FBN2 are key proteins for hair growth in cashmere goats.

Hair RiseTM microemulsion effectively promotes hair growth and treats hair loss better than standard treatments.

Combination pharmacotherapy is generally more effective for treating keloids and hypertrophic scars.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

The conclusion is that accurately replicating the complexity of the extracellular matrix in the lab is crucial for creating realistic human tissue models.

Light therapy may improve eye conditions by stimulating cell activity and increasing oxygen availability.

JAM-A helps hair regrowth in alopecia areata by protecting VCAN in skin cells.

Certain SHBG gene variants, like rs727428, are linked to higher testosterone levels in women with PCOS.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

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

The research identified genes that explain why some sheep have curly wool and others have straight wool.

Future research on ectodysplasin should explore its role in diseases, stem cells, and evolution, and continue developing treatments for genetic disorders like hypohidrotic ectodermal dysplasia.

Blocking Wnt/β-catenin signaling with EGF receptor is necessary for proper hair growth.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

Elevated CO2 can lessen the negative impact of water shortage on soybean roots and affects specific genes.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Changing the diet of mice lacking the enzyme CBS can affect symptoms related to the genetic condition.

Eph receptors and ephrins may be promising targets for treating diseases, but more understanding is needed for effective and safe therapies.

Androgenetic alopecia is influenced by various factors and can be treated with medications, procedures, and non-drug methods.

Genetic changes in mice help understand skin and hair disorders, aiding treatment development for acne and hair loss.

Certain gene variants may contribute to high androgen levels in women with polycystic ovary syndrome.

The tropical legume Sesbania rostrata can form nodules in waterlogged conditions using a different method that involves plant hormones and specific genes.

A position effect on the TRPS1 gene causes excessive hair growth in humans and mice.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Certain genetic variations are linked to increased androgen levels in PCOS, but more research is needed to understand these connections fully.

TAF4 is important for skin cell growth and helps prevent skin cancer in mice.