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Mice with LSS deficiency showed hair loss and cataracts, similar to humans, and can help in understanding and treating this condition.

Women have a higher risk of blood clots from hormonal factors and need careful treatment, especially during pregnancy.

Trichoscopy helps diagnose hair and scalp disorders in dark-skinned people by identifying unique patterns.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Flightless I protein affects hair growth, with low levels delaying it and high levels increasing hair length in rodents.

Scientists developed a method to grow human fetal skin and digits in a lab for 3-4 weeks, which could help study skin features and understand genetic interactions in tissue formation.

The Mason gastric bypass is a better surgery for weight loss with fewer complications compared to other methods.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

The surgery effectively promoted and maintained weight loss in obese women during the first year.

The document concludes that quick referral and appropriate treatments are crucial for managing common skin conditions and preventing permanent damage.

The research found that postmortem root bands in hair are likely caused by the breakdown of a specific part of the hair's inner structure after death.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

The symposium concluded that understanding how different species repair tissue and how this changes with age can help advance regenerative medicine.

Substance abuse can cause various skin problems, including marks from injections, sores, premature aging, and increased cancer risk.

Outside factors like grooming, chemicals, and the environment can damage hair and cause disorders.

New antiscarring strategies show promise, including drugs, stem cells, and improved surgical techniques.

Using skin stem cells and certain molecules might lead to scar-free skin healing.

Operative hysteroscopy is still the main treatment for Asherman syndrome, but more research is needed on post-surgery methods.

Modified stem cells that overexpress a specific protein can improve hair growth and reduce hair abnormalities in mice.

Current research explores hair growth drugs, while future research aims for personalized treatments.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Keratin hydrogel from human hair helps rats recover better from spinal cord injuries.

The mini-lift is a less invasive face-lift for younger patients that is quicker, cheaper, and has a fast recovery, but is less effective for the midface and excessive neck skin.

Two mouse mutations cause similar hair loss despite different skin changes.

Horse skin diseases are complex to manage and often require a biopsy for accurate diagnosis and treatment.

Dynamic, light touch is sensed through a common mechanism involving Piezo2 channels in sensory axons.

The top research priorities for congenital ichthyosis include long-term side effects of oral retinoids, best topical treatments, and treatments for itch and hair loss.

Skin and hair changes in horses can indicate serious diseases, and recognizing these signs is important for treatment and management.

The skin has about 230,000 touch-sensitive nerve fibers, with high concentrations in the hands and face.

Use some skin medications with caution during pregnancy; avoid strong steroids, certain eczema treatments, and systemic retinoids, but many topical treatments and nasal sprays are safe.