Search

everythinglearnresearchcommunity

for

Search:↓

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Finasteride causes lasting fertility decrease in rats.

Minoxidil improves blood flow and vessel flexibility, potentially helping with vascular stiffness.

Testing for CAG repeat polymorphism in the androgen receptor gene is not currently recommended for managing hypogonadism.

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

ELL is crucial for gene transcription related to skin cell growth.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

Changing light exposure can affect hair growth timing in goats, possibly due to a key gene, CSDC2.

Mice without the IL-6 gene had more hair growth after injury due to higher activity of a related protein, Stat3.

Advanced therapies like gene, cell, and tissue engineering show promise for hair regrowth in alopecia, but their safety and effectiveness need more verification.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

Beard and scalp hair cells have different gene expressions, which may affect beard growth characteristics.

Removing a methyl group from the ITGAV gene speeds up bone formation in a specific type of bone disease model.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Cashmere and milk goats have different hair growth cycles and gene expressions, which could help improve wool production.

RCS-01 therapy is safe and may improve skin structure by affecting gene expression.

Hair follicles in the back of the rosette fancy mouse have reversed orientations due to a gene mutation.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

Minoxidil helps hair growth by activating the β-catenin pathway.

Wnt ligands are crucial for hair growth and repair.

Acne is caused by genetics, diet, hormones, and bacteria, with treatments not yet curative.

Different types of fibroblasts play various roles in both healthy and diseased tissues, and understanding them better could improve treatments for fibrotic diseases.

Kennedy's disease leads to muscle weakness without a cure, but exercise and managing symptoms may help patients live a normal lifespan.

A patient with a larger than usual genetic mutation had a broader range of symptoms for a muscle disease.

Hormones and genetics play key roles in male and female baldness, which can affect mental health and may be linked to other health issues.

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

Increased PPARGC1α relates to hair thinning in common baldness.