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Scientists made a mouse that shows how a specific protein in the skin changes and affects hair growth and shape.

Early regulatory T cells are crucial for normal skin pigmentation.

The mTOR signaling pathway is crucial for hair health and targeting it may lead to new hair loss treatments.

Certain changes in the SHBG gene may increase the risk of PCOS in Iraqi women.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

A new genetic change in the DSC3 gene is linked to a rare condition causing hair loss and skin blisters in a child.

The gene Tfap2b is essential for creating a type of stem cell in zebrafish that can become different pigment cells.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

New drugs for Alzheimer's and rheumatoid arthritis advanced, a Zika vaccine is in development, and there were business deals in anesthesia and oncology.

A specific DNA sequence caused hair loss in male mice by activating immune cells and increasing a certain immune signal.

Post-implantation erythema is a red skin condition after medical device implantation that sometimes goes away on its own.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Lower adrenal hormone levels may cause hair loss in postmenopausal women, certain patterns help diagnose nail cancer, and a gene variant linked to higher skin cancer risk in kidney transplant patients suggests monitoring folate levels.

The workshop highlighted the genetic links and psychological impacts of hair loss and skin disorders.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

Skin issues can indicate immune system problems.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

Baricitinib reduces inflammation and improves cell health in premature aging cells.

Ichthyosis with confetti is a genetic skin disorder with consistent ectodermal malformations and various KRT10 gene mutations.

A genetic mutation caused severe rickets and alopecia in an Indian patient, but high-dose calcium and phosphate treatment improved their condition.

IL16 gene variations may affect the risk of alopecia areata in Koreans.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Certain gene variations are linked to the thickness of cashmere goat hair.

Corneous beta-proteins evolved uniquely in reptiles and birds, forming scales, claws, beaks, and feathers.

Exosomes are crucial for protecting sensory hair cells in the inner ear.

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.