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Foxp1 helps control hair stem cell growth and response to stress during hair growth cycles.

Alopecia areata has a complex genetic basis that was not fully understood as of 2001.

Hydroxychloroquine is ineffective for treating frontal fibrosing alopecia with lupus erythematosus.

Platelet Rich Plasma (PRP) shows promise for tissue repair and immune response, but more research is needed to fully understand it and optimize its use.

Boxer dogs may have a genetic skin condition that worsens seasonally and can be treated with certain medications.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Male pattern baldness is often genetic and linked to a hormone, with treatments like finasteride and minoxidil being effective for some men.

The conclusion is that certain genetic factors and blood types may affect COVID-19 severity, but changes in ACE2 and TMPRSS2 genes are not clearly linked to it.

Doxazosin mesylate and saw palmetto cause genetic changes in fruit flies.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Topical minoxidil helped an 8-year-old boy with a genetic hair disorder grow hair.

Men with thinner hair from genetic hair loss may be more likely to have an enlarged prostate.

D-OCT shows increased blood vessel growth in response to tissue damage in Frontal Fibrosing Alopecia and is useful for diagnosis and monitoring.

A woman's hyperandrogenism was caused by a genetic mutation leading to non-classic adrenogenital syndrome.

Chromosomal differences affect how muscle cells respond to testosterone.

Newly born mesenchymal cells quickly spread out in response to tissue tension during early development.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

A mother's diet at conception can cause lasting genetic changes in her child.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

Animals that change color with the seasons mainly do so in response to daylight changes, but climate change is causing camouflage problems that may require evolutionary changes.

Giving a special protein to dogs with a certain genetic disease improved their symptoms but didn't help with hair growth.

Stress can worsen skin conditions by affecting hormone levels and immune response.

Accurate diagnosis is key for treating different kinds of hair loss, and immune response variations may affect the condition and treatment results.

Finasteride reduces corpus cavernosum weight but doesn't affect erectile response in rats.

The HairCheck® device is effective for measuring hair loss and growth in people with alopecia.

A vitamin D receptor mutation causes rickets and affects immune responses.

High levels of male hormones and irregular periods best predict how well PCOS patients will respond to metformin treatment.

Chemotherapy may cause recurring hair loss due to an autoimmune response.