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Tet2 and Tet3 enzymes are essential for controlling hair growth by affecting DNA demethylation and gene expression in mice.

Scientists have found specific genes linked to different hair loss conditions, which could lead to new treatments.

The document concludes that the human keratin gene cluster is complex, with a need for updated naming to reflect over 50 functional genes important for hair and skin biology.

A mutation in the KRT82 gene is significantly associated with Alopecia Areata.

Melatonin treatment increases a specific RNA in goat cells that boosts cashmere growth.

A gene variant causes patched hair loss in mice, similar to alopecia areata in humans.

Rare changes in the KRT82 gene are linked to a higher risk of Alopecia Areata.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

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

New research has found 14 genes linked to the risk of developing alopecia areata, improving understanding and treatment options.

The document concludes that understanding the genes and pathways involved in hair growth is crucial for developing treatments for hair diseases.

Alopecia areata is an autoimmune condition causing hair loss, linked to genetic factors and immune system issues, with no cure yet.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

The gene Foxn1 is important for hair growth, and understanding it may lead to new alopecia treatments.

S100A3 protein is crucial for hair shaft formation in mice.

Hair loss involves immune responses, inflammation, and disrupted signaling pathways.

A gene variant in KRT71 causes the curly fur in Selkirk Rex cats.

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.

The HoxC gene cluster and its enhancers are essential for developing hair and nails in mammals.

A WNT10A gene mutation leads to ectodermal dysplasia by disrupting cell growth and differentiation.

The nucleus is key in controlling skin growth and repair by coordinating signals, gene regulators, and epigenetic changes.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

5% topical minoxidil improves hair density and quality in monilethrix patients.

The PCR technique can identify genetic differences in a wool-related gene among different sheep breeds, which may help improve wool and pelt quality.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Alopecia areata involves immune activation in the scalp, suggesting treatments targeting TH1, TH2, and IL-23 pathways.

Explosions don't stop hair proteins from being used to identify people.

Researchers found four genes that could help diagnose severe alopecia areata early.

The document concludes that stem cells and their environments are crucial for skin and hair health and have potential for medical treatments.