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The conclusion is that genetic differences affect how the cochlea heals after hair cell loss, which may challenge the creation of hearing loss treatments.

Maxillariinae orchids contain 62 compounds with potential health benefits, including treating skin conditions and diseases like cancer and diabetes.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

A gene variation is linked to hair thickness in Asians.

A gene deletion causes the "hairless" trait in Iffa Credo rats.

A gene network led by RSL4 is crucial for early root hair growth in response to cold in Arabidopsis thaliana.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

A mutation in the Adam10 gene causes freckle-like spots on Hairless mice.

A new painless method to collect hair follicles helps study DNA damage and aging.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A protein called FERONIA helps control root hair growth in response to cold and low nitrogen by activating nutrient-sensing pathways in a plant called Arabidopsis.

SOX2 is crucial for skin cell function and hair growth, and it plays a role in skin cancer and wound healing.

Chitosan slows root hair growth and causes a buildup of callose at low concentrations, but at high concentrations, it only inhibits growth without callose buildup.

A group has developed therapies that show promise for treating cancer and various other conditions.

Hair follicle sampling is a feasible method to measure FMRP and FMR1 mRNA levels in children.

Trichoscopy is a useful tool for diagnosing hair disorders without pulling out hair.

Male hormones may play a role in the development of heart disease, and more research is needed to understand their effects.

Toxic epidermal necrolysis is a severe skin condition often caused by drugs, with complex treatment and a high risk of death, but survivors usually heal without scars.

The Itpr3 gene causes a specific hair pattern in mice.

UVB is good for a skin condition in Asian kids, a lotion works for head lice, a drug helps with a skin blistering disorder, a foam reduces itchiness in skin inflammation, birthmarks can be more widespread, and criteria for a neurocutaneous disorder were agreed upon.

Mutations in the DSG4 gene can cause a rare hair disorder similar to monilethrix.

Taking riboflavin and eating less lysine can help some people with a specific genetic disorder avoid brain damage.

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.