Search

everythinglearnresearchcommunity

for

Search:↓

Hair loss in men treated best with early medication or transplant, new treatments researched.

AR polyglycine repeat doesn't cause baldness.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

Barn owls with smaller black spots have higher testosterone levels, which might be due to genetic effects on hormone regulation rather than hormone effects on coloration.

Female mice with disrupted 5α-reductase 1 had significant metabolic issues, including stress response problems, insulin resistance, liver fat buildup, and obesity.

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.

NSG mice had the most mites, and genetic factors affect immune response and susceptibility.

Scientists developed tools to observe hair regeneration in real time and assess skin health, using glowing mice and light-controlled genes.

The document concludes that hair transplantation and gene therapy may be important for future hair loss treatment.

Changes in skin microbes play a role in some skin diseases and could lead to new treatments.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

Testosterone therapy improved physical and social health in a male with 49,XXXXY syndrome.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

A man with both Klinefelter syndrome and primary hyperparathyroidism showed a rare combination of symptoms and genetic patterns.

Gender affects hair and scalp characteristics, with differences in hormone responses, graying patterns, and trace metals.

Different scalp and hair disorders are more common in certain ethnic groups, with the most common being androgenetic alopecia, which is treated with medications like minoxidil and finasteride.

The conclusion is that understanding how patterns form in biology is crucial for advancing research and medical science.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

The conclusion is that PCOS is caused by ovarian sensitivity to hormones and disrupted hormone control, possibly due to ovarian factors, and more research is needed.

Mutations in the PADI3 gene are linked to a higher risk of scarring hair loss in women of African descent.

Genetics and hormones play a role in male and female hair loss, but more research is needed to fully understand it.

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

Hormones and genetics affect hair growth and patterns, with some changes reversible and others not.

Understanding and tracking our body's natural daily rhythms could help improve heart health.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

The document concludes that veterinary dermatologists need more experience and a better approach to treating skin diseases in nonhuman primates.

Children's hairlines change shape as they grow, with women often developing a widow's peak and men's hairlines becoming more convex and possibly balding at the temples, influenced by genetics and hormones.

Alopecia Areata is an autoimmune hair loss condition that needs more research for better treatments.