Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

Disrupting a specific protein's function in hair follicle stem cells triggers their activation and a self-healing process.

The gene Prss53 affects hair shape and bone development in rabbits.

Tcf3 and Lef1 are key in deciding skin stem cell roles.

BTNL proteins help control inflammatory bowel disease by maintaining specific immune cells.

Three genes linked to the development of trichilemmal cysts were found.

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.

No treatment is clearly better for central serous chorioretinopathy, and more research is needed.

Periodontal ligament stem cells show promise for regrowing tissues but require more research for safe, effective use.

MPZL3 protein helps control the size of oil glands and the growth of oil-producing cells in both mice and humans.

Dexamethasone-primed stem cell media shows promise in treating lupus by reducing symptoms and inflammation.

A 70-year-old woman with a rare skin condition improved after treatment with topical steroids and acitretin.

Dermoscopy helped diagnose discoid lupus erythematosus in two patients without needing skin biopsies.

Dermoscopy helps diagnose and monitor treatment for hair loss from scarring conditions like discoid lupus and lichen planopilaris.

Tislelizumab can cause cutaneous lupus erythematosus.

Genetic factors, especially PADI3 gene variants, contribute to CCCA in women of African descent.

Most patients with cutaneous lupus erythematosus in Bangladesh are young women, with chronic forms and photosensitivity being common.

An artificial lipid barrier can restore hair growth in cases of SCD1 deficiency.

A method was found to accurately measure spironolactone and canrenone in blood samples using liquid chromatography-mass spectrometry.

The gene LRRC15 is more active in balding areas of the scalp compared to non-balding areas.

Lidocaine-loaded microparticles effectively relieve pain and fight bacteria in wounds.

Efficient enzyme function relies on specific residue interactions and structural coordination.

Targeted siRNA therapy may be a promising treatment for KID syndrome by reducing mutant gene expression and improving cell communication.

TCDD disrupts skin stem cells, causing skin issues like chloracne.

The Celsr1 gene is crucial for normal hair patterning in mice.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

EGM2 and SOX2 help form beige adipocytes by maintaining ASC immaturity and activating brown adipocytes.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

Genetic defects in the Wnt/PCP pathway may cause congenital yellow nail syndrome.