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

The study found that horizontal sections of scalp biopsies are better for analyzing hair loss, showing fewer hairs and more fine hairs in balding areas.

A gene called HDAC9 might be a new factor in male-pattern baldness.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

The new microrhizotron tool effectively observes and measures pepper plant roots non-destructively.

DNA can predict physical traits like eye and hair color accurately, especially in Europeans, but predicting other traits and in diverse populations needs more research.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The document concludes that the development of certain tumors is influenced by genetic background and that a specific gene modification can lead to tumor regression and reduced growth.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

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

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

CYLD mutations cause a variety of skin tumors with symptoms starting around age 16, and treatments are currently limited.

WAA-QOL measures impact of hair loss on women's well-being.

ARL15 is important for fat cell development and the release of the hormone adiponectin.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Melanocytes are crucial for skin pigmentation and can affect conditions like melanoma, vitiligo, and albinism, as well as hair color and hearing.

Mutations in Gasdermin A3 cause skin inflammation and hair loss by disrupting mitochondria.

Mutations in the hairless gene in mice affect its expression and lead to a range of developmental issues in multiple tissues.

Mice with human gene experienced hair loss when treated with DHT.

Genetic data can predict male-pattern baldness with moderate accuracy, especially for early-onset cases in some European men.

Hair can regrow in large wounds through a process similar to how hair forms in embryos, and understanding this could lead to new treatments for hair loss or scarring.

Researchers found a new mutation causing total hair loss from birth.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Using polyethylenimine-DNA to deliver the hTERT gene can stimulate hair growth and may be useful in treating hair loss, but there could be potential cancer risks.

Researchers found two genes that may explain why some Casertana pigs don't have hair.

Future work on macrolide antibiotic analysis will aim to enhance selectivity, sensitivity, and efficiency using advanced chromatographic methods.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.