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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Botryococcus braunii's three chemical races should be reclassified as separate species.

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

Chinese domestic goats have unique genetic traits due to domestication and geographic isolation.

People with keratosis pilaris might be more likely to get a rare type of tinea versicolor.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Diagnosing and managing Glucocorticoid Resistance Syndrome is complex due to genetic differences and varied symptoms.

Scientists can make stem cells that can turn into any cell type.

Iron deficiency anemia can cause hair breakage.

The research identified new skin traits in mice, some linked to human skin conditions.

Trichoscopy can help diagnose Vitamin B12, Vitamin D3, and ferritin deficiencies without blood tests.

Eight blood metabolites are linked to causing allergic conjunctivitis, offering new ways to predict and treat it.

Sarcoptes scabiei caused mange in Goa goats, but they fully recovered with treatment.

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

Genetic analysis of Cashmere goats identified key genes for wool, reproduction, and high-altitude adaptation.

lncRNA MTC affects protein levels in goat skin cells, impacting hair growth.

Biliverdin IXβ and IXδ help Pseudomonas aeruginosa adapt to chronic infections.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

Scientists found a new gene in a bacterium that can modify an immunosuppressant drug, potentially helping to treat hair loss.

Anastrozole and cyproterone acetate treatment can help increase adult height in boys with testotoxicosis.

A 6-year-old girl was diagnosed with a rare hair disorder called monilethrix.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A new IL6ST gene variant may cause a unique form of hyper-IgE syndrome with skin abscesses and high IgE levels.

Identifying and manipulating key genes can improve wool quality and productivity in sheep.

The new formulation greatly improved quercetin absorption in rats.

Zinc supplementation effectively treats acrodermatitis enteropathica symptoms.

Tributyltin exposure causes sex changes, sterilization, and decline in the snail Ocinebrina aciculata, risking its extinction.

Ets2 gene is crucial for placental development in mice.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.