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Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

Topical glucocorticoids thin the skin and change collagen structure.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

Dorper sheep's wool shedding is linked to specific genes and pathways, which may help understand human hair growth.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

Finding a positive nonsentinel lymph node in melanoma patients indicates a worse prognosis.

β-catenin in the dermal papilla is crucial for normal hair growth and repair.

Researchers found 19 genes important for root hair growth in a plant called Arabidopsis.

Early development of hair, teeth, and glands involves specific signaling pathways and cellular interactions.

The human type II 5α-reductase gene, linked to certain male health conditions, has a specific structure and low similarity to other related genes.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

An mFG score of 5 or more indicates above-normal hair growth in Southern Chinese women.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

Obesity increases the risk of developing polycystic ovary syndrome, and weight loss can improve the condition.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

The human type II 5α-reductase gene has a specific structure important for understanding certain medical conditions.

AR polyglycine repeat doesn't cause baldness.

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Macrophages are essential for successful skin growth in reconstructive surgery.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

Injecting alpha-melanocyte-stimulating hormone in mice improved skin healing and reduced scarring.

Researchers found genes that control hair color and growth change before the visible coat color changes in snowshoe hares.

South American camelids should be sheared early, fleece type affects fiber quality, and the S/P follicle ratio doesn't distinguish between Bolivian llama genotypes.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.