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Removing anthrax toxin receptor 1 in pigs prevents Senecavirus A infection and causes a rare disease similar to GAPO syndrome.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

A genetic marker linked to a type of hair loss was found in most patients studied.

A protein called GIS3 is important for the growth of root hairs in Arabidopsis by controlling two genes with the help of certain growth signals.

The MDR1 C3435T polymorphism does not significantly affect methotrexate response in rheumatoid arthritis patients.

Atelocollagen boosts collagen production and improves skin elasticity in aged skin.

Transamidases are present in the epidermis but their exact role is unclear.

Integrin α6 helps identify different neural crest cell types in the skin.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

The proteins transthyretin and megalin are more present in the growth phase of hair, suggesting they might affect hair health and growth.

Truncated hHb1 keratin may play a role in breast cancer cell transformation.

PRDX5 enzyme may contribute to alopecia areata by affecting oxidative stress and autoimmunity.

YAP and TAZ proteins are necessary for the development of two types of skin cancer.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Cell-based therapy using specific immune cells may help treat alopecia areata by promoting hair regrowth.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

Amotosalen-treated donor T-cells can prevent late CMV infection after bone marrow transplants.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

ODC expression in mouse skin and tumors is varied and can be inhibited by retinoic acid or cycloheximide.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

The research aims to better understand hair follicle regulation and find new treatments for hair loss.

A new gene mutation may cause cyclic thrombocytopenia by affecting platelet production.

The QuantAnts machines can find cancer markers and create CRISPR targets for them.

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

The hairless gene is crucial for hair health, and its mutations cause hair loss.

Activated protein C helps protect mice from radiation damage.

Extracellular ATP is crucial for plant root growth and signaling.

OR2AT4 helps reduce aging and cell damage in human skin cells.

The methylation of the HOXC8 gene's exon 1 affects cashmere fiber length in goats.