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The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Blocking Hedgehog signaling offers new treatment options for advanced basal cell carcinoma.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

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

A woman with a rare hair loss condition developed skin cancer in the bald area.

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.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

Four genes are linked to alopecia areata, with two increasing risk and two offering protection.

The MBTPS2 gene variant c.970+5G>A is a common mutation causing IFAP syndrome.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

Male pattern baldness is linked to specific genetic variations in the androgen receptor gene.

The study found that pili bifurcati causes hair to intermittently split into two branches, each with its own outer layer.

PLAU and SerpinB2 affect cell death differently in various forms of leprosy and could be targets for new treatments.

Uncombable hair is inherited dominantly with complete penetrance.

Activating β-catenin in different skin stem cells causes various types of hair growth and skin tumors.

BTNL2 helps protect hair follicles from immune attacks, which could aid in treating alopecia areata.

Certain gene variations in PITX2 are linked to a higher risk of male pattern baldness in Indians.

E211 G>A gene linked to lower risk of severe prostate cancer and hair loss.

Estrogen and MLL enzymes work together to regulate genes important for hair growth and leukemia.

Selenium imbalance can cause hair loss and skin issues.

Basal cell carcinoma may originate from vellus hair cysts.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

A new mutation in the STING protein causes a disease with lupus-like symptoms and responds well to a specific inhibitor treatment.

ILC1-like cells can cause alopecia areata by themselves.

Safusidenib erbumine shows promise as a treatment for certain brain tumors, but mild side effects like hair loss need attention.

Upadacitinib successfully regrew hair in a child with alopecia universalis and specific genetic mutations.