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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

Dermatologists should recognize diverse discoid lupus signs to avoid misdiagnosis.

A new gene mutation is linked to monilethrix in the studied family.

The spiny mouse regenerates ear tissue asymmetrically, with gene expression differences possibly explaining its unique healing abilities.

Heavy ions cause significant damage to rabbit forebrains, similar to other radiation effects.

Multiphoton microscopy can effectively assess breast cancer treatment responses without labels.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

Twins had rare skin cysts likely due to genetics.

Lupus erythematosus can mimic alopecia areata, and trichoscopy is key for accurate diagnosis and better patient outcomes.

Thorough history and examination are crucial for diagnosing genetic disorders like juvenile polyposis and hypomelanosis of Ito.

NBCCS and BFHS might be the same syndrome, helping better identify and manage cases.

LSD1 and HSP90 help heal skin wounds by changing hair follicle stem cells' metabolism.

ERK activation spreads between cells in mouse skin, linked to cell division and influenced by TPA and EGF receptors.

Killing specific cells in hair follicles can lead to hair growth problems in mice.

A girl with lupus had unusually long and thick eyelashes, a rare symptom of her condition.

Langerhans cells and melanocytes migrate to the skin and hair follicles during early human development.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

RCM and dermoscopy help identify different types of hair loss in children.

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.

Autofluorescence in hair follicle stem cells can interfere with studies but may help isolate these cells.

Overexpressing Merkel cell virus proteins in human hair follicles can create clusters of cells that resemble Merkel cell cancer.

Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

Hair follicle bumps with stem cells might contribute to permanent hair loss by getting disconnected due to scarring.

A rare hair regrowth pattern can occur in some people with alopecia areata.

A mutation in mice causes hair loss and skin issues due to a defect in a gene affecting cell adhesion.

Activating certain hair follicle cells could prevent hair loss from cancer treatments.

Mogamulizumab can cause hair loss, often linked to a better treatment response.

Mutations in the hairless gene cause a rare form of permanent hair loss.

Removing certain immune cells in mice causes their hair to enter the growth phase earlier than usual.

The pigment in black eyeliner can spread in the skin and may cause permanent eyelash loss.