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A specific RNA modification in cashmere goats helps activate hair growth-related stem cells.

Early detection and multidisciplinary treatment are crucial for managing Papillon-Lefévre syndrome.

A specific genetic deletion in goats affects cashmere yield and thickness.

Mice with a Gsdma3 gene mutation have thicker skin and longer hair follicle openings due to increased β-catenin levels.

Researchers found genetic mutations causing hypohidrotic ectodermal dysplasia in 88% of studied patients and identified new mutations and genetic variations affecting the disease.

Early onset baldness in men may indicate a condition similar to PCOS, linked to heart disease, diabetes, and prostate issues.

A mutation in the FAM83G gene is linked to skin and hair abnormalities in two related individuals.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Keratin-associated proteins have ancient origins and were used for different purposes before being adapted for hair in mammals.

A new gene, JMJD1C, may affect testosterone levels in men.

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

The document concludes that recognizing and properly diagnosing lipodystrophy syndromes is crucial for effective management and treatment.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Eyebrow loss has many causes and requires accurate diagnosis for proper treatment.

The cause of alopecia areata is likely a mix of genetics, immune system issues, and environmental factors, with more research needed to understand it fully.

The we/we wal/wal mice have defects in hair growth and skin layer formation, causing hair loss, useful for understanding alopecia.

Frontal Fibrosing Alopecia might be an autoimmune disease.

Cell death shapes skin stem cell environments, affecting inflammation, repair, and cancer.

The document concludes that more research is needed to better understand and treat primary cicatricial alopecias, and suggests a possible reclassification based on molecular pathways.

Alopecia areata is an autoimmune disease causing patchy hair loss, often with other autoimmune disorders, but its exact causes are unknown.

Cytokeratin 19 and cytokeratin 15 are key markers for monitoring the quality and self-renewing potential of engineered skin.

Formyl-peptide receptor agonists could be new anti-inflammatory drugs.

Mice are useful for researching human hair loss and testing treatments, despite some differences between species.

GasderminA3 is important for normal hair cycle transitions by controlling Wnt signaling.

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

Inhibiting AP1 in mice skin causes structural changes and weakens the skin barrier.

The research identified genes that explain why some sheep have curly wool and others have straight wool.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.