Search

everythingexperts & clinicslearnresearchcommunity

for

Search:↓

A specific genetic trait in tumor cells is linked to longer survival without disease in certain lymphoma patients.

Researchers found a gene mutation responsible for a rare hair loss condition.

Blood type affects COVID-19 infection rates differently in Europe and Africa.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Genetic predictions of baldness in Europeans don't apply well to African men.

Hedgehog signaling controls hair follicle development and can affect skin cancer growth.

The N gene affects the protein makeup of mouse hair.

A specific gene mutation causes complete hair loss without other health issues.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.

Scientists identified and cloned specific keratin proteins in mouse hair.

Hair loss gene found on chromosome 3q26.

HLA can be linked to autoimmune hepatitis.

Six new genes linked to early hair loss were found, which also surprisingly connect to Parkinson's disease and lower fertility.

Major histocompatibility antigens are found in specific skin cells and structures, but not in sweat glands.

The Tru9I variant in the VDR gene may influence alopecia areata risk and vitamin D levels.

The research identified new skin traits in mice, some linked to human skin conditions.

Certain immune-related proteins are higher in people with alopecia and their healthy relatives, hinting at a genetic link.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

A specific mutation in PA-PLA1α causes abnormal hair growth.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

Hoxc13 regulates specific hair protein genes on mouse chromosome 16.

A new method can detect mutations in mice by observing changes in hair follicle cells.

A KRT32 gene variant causes loose anagen hair syndrome.

Mutations in the ABCB6 gene cause Dyschromatosis Universalis Hereditaria.

A specific gene mutation causes woolly hair and hair loss.

Higher PHGDH levels cause unusual melanin buildup in hair follicles.