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The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

In vivo lineage labelling is better than in vitro methods for identifying and understanding stem cells.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

Wnt7a protein is crucial for development and tissue maintenance and plays varying roles in diseases and potential treatments.

Certain genetic markers linked to reproductive potential were identified by their impact on a protein's ability to bind to genes.

The study suggests certain ACE gene variations are more common in women with PCOS and may be linked to increased insulin resistance.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Men with more vanadium in their blood and who drink less soy milk are more likely to have hair loss.

Some skin diseases and their treatments can negatively affect male fertility.

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

The document explains that hirsutism, often caused by hormonal issues, can be managed with treatment to improve both physical appearance and mental health.

Certain genetic variations in OCT1 may improve insulin sensitivity with metformin in women with PCOS.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

A certain genetic variation in the IL1A gene may lower the risk of a hair loss condition in Chinese people.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Ptprq has multiple forms that change during inner ear development.

Estrogens are key for bone growth spurts in both boys and girls and affect growth into adulthood.

A mutation in the KRT71 gene causes a hair disorder by disrupting hair follicle structure and texture.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

The document suggests a rare skin condition might be caused by a genetic phenomenon.

Mutation in hairless gene may increase hair loss risk.

The best animal model for studying male-pattern baldness is the stumptailed macaque, not rats or mice.

Hair loss can indicate or worsen with systemic diseases, and treating the underlying condition is important.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

Celsr1 is crucial for skin cell alignment, while Celsr2 has little effect on this process.

Both classical and L-type atypical BSE from cattle can infect goats with different incubation times, and tests can distinguish between the two strains.

Acne in dark skin is influenced by environmental factors and can lead to hyperpigmentation, with various treatment options available.

Genetic defects in testosterone production can cause hormonal and developmental disorders, and more research is needed to understand androgen regulation and develop safer treatments.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.