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Injecting specific cells into the skin can help improve skin structure and reduce blisters in a genetic skin disorder.

Perming and bleaching damage hair differently, with bleached hair having more cysteic acid in the cuticle.

A new gene mutation causes a rare type of hair loss.

Using enzymes to break down scalp hair follicles gets more stem cells for skin and hair growth than the old method.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Sweat hypersensitivity can cause severe skin issues in horses.

Transglutaminase does not modify human hair.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

The human keratin 6a gene's specific sequences trigger expression in skin layers after injury.

A young cat had a rare fungal infection caused by Microsporum gypseum.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

GCN reduces lung inflammation and damage from air pollution in mice.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A hair serum with 3% keratin from chicken feathers made hair smoother, shinier, and more elastic.

Defective protein folding due to a mutation is key in ANE syndrome.

Transglutaminase can repair damaged hair, making it stronger and shinier.

The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.

Hair proteins change location and structure as hair cells mature.

Overexpression of PTHrP in chondrocytes causes short-limbed dwarfism and delayed bone formation in mice.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Human hair keratin has a 40% α-helix structure that changes to a random coil in 8 M urea.

Multiple mouse desmoglein 1 isoforms have distinct roles in skin and hair development.

New compounds similar to cromakalim were less effective at inhibiting insulin release but improved in solubility and one acted as a calcium entry blocker, not a potassium channel opener.

People with ectodermal dysplasias often have reduced saliva production and should get saliva tests.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Diseased horse foot skin shows increased keratin expression, similar to wound healing in mammals.