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A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

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 PP2A-B55α protein is essential for brain and skin development in embryos.

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Tmem30b is essential for hearing by maintaining hair cell structure in the ear.

A new gene, JMJD1C, may affect testosterone levels in men.

DNMT1 helps turn hair follicle stem cells into fat cells by blocking a specific microRNA.

The research identified and described a gene important for hormone conversion in endangered catfish, which varies in activity during different reproductive stages and after hormone treatment.

A new genetic tool improves the study of hair growth and potential hair disorder treatments.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

PSAT1 is key for hair growth and stem cell function in cashmere goats.

Brg1 is crucial for hair growth and skin repair by maintaining stem cells and promoting regeneration.

FGF5 spliceosomes inhibit rabbit hair growth by affecting gene expression.

A mutation in the MAP2 gene causes reduced hair follicle density, leading to hairlessness.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Mutations in the HEPHL1 gene cause abnormal hair and cognitive issues.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

CXXC5 can both suppress and promote cancer, making it a complex target for treatment.

A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A genetic variant linked to hair thinning in Japanese women was found.

A gene variation is linked to hair thickness in Asians.

KRTAP28-1 gene can help breed sheep with finer wool.

Increased methylation of the Filip1l gene may contribute to aggressive skin cancer.

Researchers identified a new variant of the FGF5 gene in sheep that affects hair length.