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Two specific genetic markers increase the risk of hair loss in Asian populations.

mrp/plf-mRNA can indicate tumor-promoting effects in skin.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

A new enzyme, BSSP, is found in high amounts in the hair follicles of nude mice.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

The PER3 rs772027021 SNP may cause mild skin pigmentation changes in a new subtype of dyschromatosis universalis hereditaria.

Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

Overexpressing thrombospondin-1 in mice skin prevents UVB-induced skin damage.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

PTCH gene mutations contribute to basal cell carcinoma development.

Seven genetic variations in sheep's DSG4 gene are linked and affect wool traits.

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

A new gene mutation linked to Olmsted syndrome may increase cancer risk, suggesting the need for ongoing patient monitoring.

The research linked PLCD1 gene variants to the development of trichilemmal cysts.

Researchers found a new genetic mutation linked to a hair condition in a Japanese boy.

The SNP rs6457452 is linked to a higher risk of alopecia areata in Koreans.

Hutchinson-Gilford Progeria Syndrome caused rapid aging due to a genetic mutation, with treatments to manage symptoms.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

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

Chronic T. gondii infection may harm male fertility.

Gp₄G promotes hair growth and improves skin health.

Tgm2 helps stabilize dying cells and aids fibroblast attachment to the extracellular matrix.

GSH-T levels in hair follicles are similar in smokers and non-smokers and don't increase with certain treatments.

GLI2 activates GLI1, promoting skin tumor growth and hair development.

Sheep cells were successfully modified to include a spider silk protein gene.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.