Search

everythinglearnresearchcommunity

for

Search:↓

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.

IL-9 increases skin cell movement but decreases their ability to invade, and this effect is controlled by cell contractility, not by MMPs.

The conclusion is that a new method combining magnetic tweezers and traction force microscopy may help understand skin cell interactions and diseases.

Desmoglein 3 organization in cell connections changes without calcium, affecting cell adhesion.

Dsg1 is essential for maintaining a healthy skin barrier in mice.

Nonmelanoma skin cancers have higher levels of certain osteopontin variants than normal skin.

Skin changes throughout life, from development before birth to aging effects like wrinkles, influenced by both genetics and environment.

Pattern baldness is likely caused by a dominant gene influenced by testosterone levels, making it more common in men.

AGA is a common hair loss affecting both genders, treated with various therapies to promote regrowth and slow thinning.

PCOS is a complex condition with major health impacts, needing more research for better diagnosis and treatment.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

Removing part of the vitamin D receptor stops vitamin D from working properly.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

The document concludes that the fast-growing direct-to-consumer genetic testing market lacks sufficient regulation, posing risks to consumers due to questionable test quality and accuracy.

Insulin resistance and obesity are key factors in the development and worsening of polycystic ovary syndrome, and lifestyle changes are important for managing it.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

Pregnancy can cause various skin changes and diseases, with PUPPP being the most common skin condition specific to pregnancy.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Hair loss needs more research for better treatments.

Transplant success has improved with better immunosuppressive drugs and donor matching.

Adam10 enzyme is crucial for healthy skin and proper Notch signaling.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

The article concludes that the wool follicle is a valuable model for studying tissue interactions and has potential for genetic improvements in wool production.

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.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

The sebaceous gland has more roles than just producing sebum and contributing to acne, and new research could lead to better skin disease treatments.