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A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

The B2 genes are crucial for hair growth in rats.

Acid can block TRPV3 from outside the cell but boost its function from inside.

Integrin α6 helps identify different neural crest cell types in the skin.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Mutations in the hHb6 gene cause the hair disorder monilethrix.

Changing the 6-position on benzopyran molecules affects insulin release, with some compounds showing strong inhibitory effects.

848 genes related to fat and metabolism are less active in people with Central Centrifugal Cicatricial Alopecia.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

A girl with excessive hair growth had a genetic change on chromosome 17 that reduced the activity of two genes linked to hair growth.

S100A4 and S100A6 proteins may activate stem cells for hair follicle regeneration and could be potential targets for hair loss treatments.

The gene GJA1 is important for regulating coarse hair density in goats.

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

EAAT4 decreases with age, harming skin function and calcium balance.

Alkaline ceramidase 1 is crucial for healthy skin and energy balance.

Certain gene variations may increase the risk of hair loss in Egyptians.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

K6 gene expression can be controlled and manipulated in mice for studying skin disorders.

Acid inside cells speeds up aging and turns on aging signs in mice.

CaM7 and CNGC14 interaction controls root hair growth in Arabidopsis.

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

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.