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SASH1 gene mutations are linked to various inherited skin pigmentation disorders.

Targeting the TNFRSF1B gene may help treat hair loss.

A boy's hair turned red because of genetic mutations, not lack of zinc.

Mutations in hKAP1 genes may cause hereditary hair disorders.

ECM1-modified stem cells can effectively treat liver cirrhosis.

Arg1+ macrophages may play a role in causing alopecia areata.

HIF-1α in fibroblasts boosts hair growth and health.

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

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

A new mutation in the HJV gene was found in a young woman with juvenile hemochromatosis, causing unusual symptoms like secondary hypothyroidism.

Krtap11-1 is important for hair strength and structure.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

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

MX1 and AR genes are linked to milder COVID-19, while TMPRSS2 increases severe risk, especially in women.

Egfl6 is not needed for zebrafish face development.

Interleukin-1 increases keratin K6 production in skin cells.

FilaggrinHigh melanomas have active FGFR signaling and weak GNA14 and Th1 signatures.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

CNGA3, GLUD1, and SIRT1 are promising targets for treating aging and glioblastoma.

Aminoguanidine increases a specific growth signal in stored hair grafts, which may help them survive better after being transplanted.

Actin filaments help stabilize and reshape cell membranes.

WIF1 helps keep skin stem cells inactive to prevent excessive cell growth.

SIG-1451 could be a promising new treatment for atopic dermatitis.

Scientists found a gene in mice that causes early hearing loss.

Weak cell junctions disrupt hair follicle stem cell rest.

BcFLA1 protein is crucial for root hair growth in response to low phosphate in Brassica carinata.

SETDB1 is essential for controlling DNA methylation, silencing retrotransposons, and maintaining skin cell health, with its absence leading to skin inflammation and hair loss.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.