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The document concludes that ongoing research using animal models is crucial for better understanding and treating Alopecia Areata.

The Notch signaling pathway helps in mouse hair development through a noncanonical mechanism that does not rely on RBPj or transcription.

Combining skin tissue pathology with genetics has greatly improved the diagnosis and understanding of certain skin diseases.

A gene mutation causes early keratinocyte maturation leading to hair loss in Olmsted syndrome.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Eclipta alba extract may work as an anticancer agent and help reverse drug resistance.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Advancements in nanoformulations for CRISPR-Cas9 genome editing can respond to specific triggers for controlled gene editing, showing promise in treating incurable diseases, but challenges like precision and system design complexity still need to be addressed.

Bald thigh syndrome in sighthounds is caused by structural defects in hair shafts due to downregulated genes and proteins.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Inhibiting ALOX12 can help hair cuticle maturation by increasing S100A3 citrullination.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Different amounts of daylight affect cashmere growth in goats by changing the activity of certain genes and molecules.

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

Lipase H is important for hair follicle function and shaping hair fibers.

Peps help Arabidopsis plants grow more root hairs by affecting specific genes and calcium signaling.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Certain bacteria can enhance skin regeneration.

New treatments for skin and hair repair show promise, but further improvements are needed.

The meeting highlighted the genetic basis of female pattern hair loss and various skin health insights.

The CAP1 gene helps control ammonium levels and is necessary for the proper growth of root hairs in Arabidopsis.

Genes linked to fibrosis are more active in people with central centrifugal cicatricial alopecia.

Betacoronaviruses, like COVID-19, may cause hormone system dysfunction and affect disease susceptibility and severity.

Human nails and hair follicles have similar gene activity, especially in the cells that contribute to their growth and development.

A faulty KLHL24 gene leads to hair loss by damaging hair follicle stem cells.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Editing the FGF5 gene in sheep increases fine wool growth.

A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.