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The 1298CC genotype in RA patients leads to higher methotrexate toxicity, while the 1298AA genotype results in better treatment response.

Mutations in the Whn gene affect hair keratin gene expression differently.

RALF22 is essential for root hair growth in response to fungal emissions in Arabidopsis.

The research helps improve wool quality and aids human hair research.

RORA may help regulate hair growth by affecting hair follicle stem cells.

rPanglaoDB helps study rare cell types by merging RNA data, confirming fibrocytes' role in healing.

The LncRNA AC010789.1 slows down hair loss by promoting hair follicle growth and interacting with miR-21 and the Wnt/β-catenin pathway.

A new gene mutation causes insulin resistance in a girl and her mother.

A specific gene mutation causes long hair in Angora rabbits.

The C-allele and CC-genotype in the PTPN22 gene lower the risk of alopecia areata.

Genetic analysis of rabbits identified key genes for traits like coat color, body size, and fertility.

The lncRNA LOXL1-AS1 may help diagnose and treat androgenic alopecia.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

Altering the keratin 17 gene in mice hair follicles caused temporary hair issues, but changes were minimal and short-lived.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Changes in the HR gene have influenced hair growth and may lead to hair loss conditions in humans.

Researchers found a gene mutation responsible for a rare hair loss condition.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

Mutations in the P2RY5 gene cause autosomal recessive woolly hair.

RXRa is crucial for Th2 immune cell development and may link nutrition to immune health.

Certain gene combinations improve cashmere quality and production in Liaoning goats.

RXR and RAR proteins in skin may help with cell growth, hair growth, and gland function.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

CDKN2AIP gene is less active in nevus sebaceous, affecting related RNA networks.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

Certain genetic markers can indicate higher or lower risk for systemic lupus erythematosus.

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

A new genetic region, 17q21.31, is linked to higher ovarian cancer risk.

Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Researchers created a model to understand heart aging, highlighting key genes and pathways, and suggesting miR-208a as a potential heart attack biomarker.