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The internet has accurate information on Polycystic Ovarian Syndrome, but it's not high quality or easy to read, so we need better, user-friendly resources.

Some families have a genetic condition where they are born with irregular scalp defects.

Trichilemmal carcinoma shares genetic changes with other skin cancers, suggesting similar causes and potential treatments.

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

Hairless mammals have genetic changes in both their protein-coding and regulatory sequences related to hair.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

Pangolins have lost some skin-related genes, but kept others, showing complex skin evolution.

Tandem repeats significantly influence hair color, especially darker shades, across different ancestries.

The most different genetic segment between Africans and East Asians is the EDA2R/AR region, with two main types influenced by population changes and natural selection, and linked to baldness.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Keratin mutations cause skin diseases and could lead to new treatments.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Researchers found genes linked to hair loss in male giant pandas.

The research identified key proteins that affect wool fiber thickness in Angora rabbits.

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

New method finds genetic links between Type 2 Diabetes and Prostate Cancer not seen before.

Some natural remedies may help with hair regrowth, but more research is needed to confirm their effectiveness and safety.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

Hair loss in Androgenetic alopecia (AGA) is due to altered cell sensitivity to hormones, not increased hormone levels. Hair growth periods shorten over time, causing hair to become thinner and shorter. This is linked to miscommunication between cell pathways in hair follicles. There's also a change in gene expression related to blood vessels and cell growth in balding hair follicles. The exact molecular causes of AGA are still unclear.

Antiandrogen therapy helps treat genetic hair loss.

The most effective treatments for hair loss are minoxidil, finasteride, PRP, and hair transplants, with steroids and immunosuppressants for autoimmune types.

Follicular Unit Extraction (FUE) is a popular hair transplant method with minimal scarring that can transplant many grafts quickly and improve appearance and psychological well-being.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.