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Plucked hairs can be used instead of skin biopsies to study hair traits because they contain specific cells related to hair.

Runx1 helps control the KAP5 gene in human hair follicles.

Pashmina goats produce long hair-fiber due to specific gene expressions related to hair growth.

Camellia japonica extract may improve scalp health and promote hair growth.

Botryococcus terribilis and its compounds may promote hair growth and improve hair health.

Keratin 75 is important for fast wound healing and works with SOX2 and the LINC complex to help skin cells move and repair damage.

Keratin 79 is linked to liver damage and may help diagnose liver diseases.

The NF-κB effector p65/RelA activates hair keratin genes, aiding hair formation.

Keratin 17 is linked to various diseases, including cancer and skin conditions, and may be a target for diagnosis and treatment.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

New gene mutations linked to skin conditions were found, bacteria and chemicals may worsen acne, a dog mutation could exist in humans, virus-like elements might be involved in psoriasis, and a vitamin D3 treatment doesn't prevent chemotherapy-related hair loss.

The Foxn1 gene is essential for normal nail and hair development.

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

The study concluded that a protein important for hair strength is regulated by certain molecular processes and is affected by growth phases.

Scientists found 53 keratin genes in yaks that are important for hair growth and share similarities with those in other animals.

Mongolian gerbils heal wounds differently than mice, with unique protein levels and gene expression that affect skin repair.

Mice with human gene experienced hair loss when treated with DHT.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Removing a specific gene in certain skin cells causes hair loss in mice by disrupting hair follicle development.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

The Gsdma3 gene is essential for normal hair development in mice.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

Some cells may slow melanoma growth, a protein could affect skin pigmentation, a gene-silencing method might treat hair defects, skin bacteria changes likely result from eczema, and a defensin protein could help treat multiple sclerosis.

Mutations in the p63 gene affect skin adhesion, barrier integrity, and hair growth.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.