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Scientists made a mouse model of a serious skin cancer by changing skin cells with a virus and a specific gene, which is similar to the disease in humans.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

C/EBPalpha and C/EBPbeta are crucial for normal skin and oil gland cell development in adult mice.

The research identified key proteins and genes that may influence wool bending in goats.

Mice genetically modified to produce more CD109 in their skin had less inflammation and better healing with less scarring.

Cyclosporine A may help treat hair loss by blocking a protein that inhibits hair growth.

The congress highlighted new gene therapy techniques and cell transplantation methods for treating diseases.

Plant extracts may help prevent or reverse hair graying.

Removing Mediator 1 from certain mouse cells causes teeth to grow hair instead of enamel.

Fetal skin cells from a cell bank heal wounds faster and with less scarring than adult cells.

Involucrin helps strengthen the inner parts of human hair.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Food intake, not genetics, affects how the body processes tadalafil and finasteride.

The document is a detailed medical reference on skin and genetic disorders.

ZO-1 helps hair follicle stem cells renew better by changing their structure.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

Edelweiss extract can increase hair density and promote hair growth.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The zinc finger protein 3 in Arabidopsis thaliana reduces plant growth and root hair development.

Three specific genetic variants cause severe skin issues in children with EBS, highlighting the need for early genetic screening.

A protein from fat-derived stem cells, DKK1, is linked to hair loss and blocking it may help treat alopecia areata.

A rare type of skin cancer on the scalp can be mistaken for hair loss, causing delayed diagnosis and severe damage.

A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Wnt activation shows promise for regenerative medicine but requires selective targeting to minimize risks like cancer.

miR-29a-5p prevents the formation of early hair structures by targeting a gene important for hair growth and is regulated by a complex network involving lncRNA627.1.