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Fibroblast growth factor receptor signaling controls cell development and repair, and its malfunction can cause disorders and cancer, but it also offers potential for targeted therapies.

The FAT1 gene and its variations can help improve wool quality in Chinese Merino sheep through selective breeding.

Runx genes are important for stem cell regulation and their roles in aging and disease need more research.

Sry may regulate fatty acid metabolism and shows different expression levels in rat tissues.

Researchers found a new gene, hacl-1, that is active in mouse hair follicles during hair growth and may be important for hair biology.

HoxC genes are crucial for normal hair and nail development.

ISX9 helps regrow hair by activating a specific cell signaling pathway.

RNA aptamers can specifically block FGF5-related cell growth, potentially treating related diseases or hair disorders.

Thymic transplantation normalized some T-cells but not others, maintaining immune function.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

FGF-5 promotes Cashmere goat hair growth by increasing keratin genes and reducing certain LncRNA and target genes.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

Foxp1 helps control hair stem cell growth and response to stress during hair growth cycles.

Two brothers from Bangladesh were diagnosed with X-linked adrenoleukodystrophy, showing neurological and adrenal symptoms.

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

New genetic mutations causing hair loss were found in a Chinese family.

Genetic factors play a major role in acne.

lncRNA XLOC_008679 and gene KRT35 affect cashmere fineness in goats.

Disrupting Acvr1b in mice causes severe hair loss and thicker skin.

HT-scCAT-seq helps understand gene regulation in embryonic skin development.

RXRα is crucial for hair growth and skin cell function.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

Foxn1 is important for fat development, metabolism, and wound healing in skin.

Long non-coding RNAs help regulate wool fineness in Gansu alpine fine-wool sheep.

AKR1D1 controls glucocorticoid levels and receptor activity in liver cells.

Runx1 is crucial for proper hair structure and development.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

Activin A and Follistatin affect how mouse hair follicles grow.

Frontal fibrosing alopecia is linked to increased immune system activity and reduced stem cells, suggesting early treatment targeting this pathway might prevent hair follicle damage.