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

Keratin gene expression helps understand different types of skin cells and their development, and should be used carefully as biological markers.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

The conference presented findings on how vitamin D levels, genetic factors, and lifestyle choices like smoking and yoga affect various health conditions and diseases.

Keratin genes change gradually during skin cell development and should be used carefully as biomarkers.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

The study found that genetic differences related to hair growth and other traits help cashmere goats adapt to high-altitude environments.

Topical ceramide treatment partially improves the skin condition in Jack Russell Terriers with a genetic skin disorder.

Two mutations in KRT74 and EDAR genes cause sheep to have finer wool.

People with atopic dermatitis have different skin bacteria, and targeting these bacteria might help treat the condition.

A 14-year-old girl with no menstrual period was diagnosed with Swyer Syndrome and treated for a related cancer risk.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

Enhancers and super-enhancers are key in controlling specific gene activity and can play a role in cancer development.

New single-cell analysis techniques are improving our understanding of stem cells and could help in treating diseases.

Genetic defects in the glucocorticoid receptor gene can cause conditions with abnormal sensitivity to stress hormones, and other factors may also affect this sensitivity.

The research found genes that change during cashmere goat hair growth and could help determine the best time to harvest cashmere.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Alopecia areata involves complex immune and genetic factors, with potential treatment targets identified, but more research is needed.

Researchers found two new genetic variants linked to Alzheimer's disease.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

A gene in Sebekia benihana, CYP-sb21, is needed for a specific reaction on the drug Cyclosporine A, which could be important for hair growth without affecting the immune system.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

Genomic research can help improve the quality and production of natural fibers in animals.

Higher levels of β-carotene and vitamin E may help prevent certain types of hair loss.

The BUZZ gene is important for root hair growth and overall root structure in the plant Brachypodium distachyon.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

The research confirms that Hidradenitis Suppurativa is characterized by increased inflammation, disrupted skin cell organization, and abnormal metabolic processes.

New treatments and diagnostic methods for various animal skin conditions showed promising results.