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Immortalized rat dermal papilla cells can still induce hair growth.

A specific DNA duplication in Polish chickens affects feather shape by altering gene expression.

Identical p53 gene mutations in different cancers suggest the need for careful treatment.

Foxp3 is crucial for regulatory T cell function, and targeting these cells may help treat immune disorders.

The PLP2 gene affects cashmere fiber quality in goats and is linked to hair growth and loss.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

A specific metabolite, not a receptor protein, triggers the production of certain kidney enzymes, but this process is disrupted in mice with a mutation causing testicular feminization.

Mice with extra sheep genes had hair that fell out and regrew in cycles.

Childhood and adult height, and early immune-related hospitalizations increase testicular cancer risk, while baldness, larger families, and sports reduce it.

The type of tumor suppressor gene lost affects the behavior of skin cancer.

Repetin is a protein involved in skin and hair development, binding calcium and compensating for other proteins when needed.

CREB, a protein that can promote cancer traits, is controlled by β-catenin in skin cancer cells.

Antizyme slows skin tumor growth by reducing cell growth in mice.

The KRTAP7-1 gene is very similar across different cattle and yak breeds and likely plays a role in hair strength and shape.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Mrp3 may aid in wound healing and hair growth.

A rare gene variant causes hair and nail issues in a family.

The protein STAT3 slows down cell growth by blocking the FST gene, which affects hair development in sheep.

Keratin 17 is important for skin's response to radiation, affecting many genes and cell division.

CRISPR/Cas9 and prime editing can potentially fix skin disorder genes safely and effectively.

p63 controls Satb1 to help skin develop properly.

TNF alpha in skin cells causes weight loss, hair and fat issues, and skin inflammation in mice.

TMPRSS2 affects COVID-19 severity and treatment options.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

ANE syndrome is caused by a mutation in the RBM28 protein that disrupts ribosome assembly.

Monilethrix is linked to the type II keratin gene on chromosome 12q13.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

Targeting the TNFRSF1B gene may help treat hair loss.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.