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A new MBTPS2 gene variant disrupts fat metabolism and collagen production, causing Osteogenesis imperfecta.

Systemic sclerosis skin shows varied gene patterns, suggesting potential for personalized treatment.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

LPAR6 has a unique way of binding and activating, which helps in designing treatments for hair loss and cancer.

Keratin K6irs is a marker for the inner root sheath of hair follicles in mice and humans.

The 3D structure of a key hair protein was modeled, revealing specific helical structures and stabilization features.

The study found a specific peptide that helps detect TGase 3 activity in skin and hair follicles.

Astrotactin2 affects hair follicle orientation and skin cell polarity.

A new method improves protein extraction from hair, helping identify potential biomarkers for fetal growth issues.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

The engineered yeast strain BLYAS can quickly and sensitively detect androgenic chemicals.

A mutation in the SREBF1 gene causes both hereditary mucoepithelial dysplasia and IFAP syndrome, which are related conditions.

A specific RNA helps increase the growth of skin cells in Liaoning cashmere goats by working with a protein to boost a growth-related gene.

Mice hair follicles take in the amino acid cystine.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

ARQ-234, a protein designed to treat atopic dermatitis, shows increased effectiveness in early testing.

SCD1 is important for hair growth by keeping the connection in skin cells where hair stem cells live stable.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

sPLA2-IIA increases growth in hair follicle stem cells and cancer cells, suggesting it could be targeted for hair growth and cancer treatment.

The research suggests that SFRP2 and PTGDS proteins might be indicators of female pattern hair loss and could contribute to hair loss.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

ILC1-like cells can cause alopecia areata by themselves.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

A substance called Compound 2g can strongly block STS (a hormone-related enzyme) without affecting estrogen levels, making it potentially good for treating breast cancer.

ATP-dependent chromatin-remodeling complexes are crucial for gene regulation, cell differentiation, and organ development in mammals.

A specific gene variant causes severe skin issues and increases infection risk, requiring careful medical monitoring.

The guideline offers current advice for diagnosing and treating Long- and Post-COVID symptoms.