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

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

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

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.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Genetic variations greatly affect individual metabolism and can impact health and disease risk.

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

Gut health affects skin diseases, and probiotics might help.

Organoids help study and treat genetic diseases, offering personalized medicine and therapy testing.

FKBP10 and FBN2 are key proteins for hair growth in cashmere goats.

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.

Trichohyalin-like proteins are essential for the development of skin structures like hair, nails, and feathers.

Different hair types in mammals are linked to variations in specific protein genes, with changes influenced by their living environments.

Certain genes in Iranian sheep are linked to wool production and heat adaptation.

Melanoma's complexity requires personalized treatments due to key genetic mutations and tumor-initiating cells.

A mouse gene mutation increases the risk of skin cancer.

New treatments for ichthyosis, like protein replacement and gene therapy, show promise and may become standard care.

Four new cases of Bachmann-Bupp syndrome suggest potential for targeted treatment.

A 70-year-old woman with bronchiectasis developed a rare immune disease due to a bacterial infection, requiring a difficult balance of treatments.

Different genes are active in dogs' hair growth and skin, similar to humans, which helps understand dog skin and hair diseases and can relate to human conditions.

The study found specific skin and cell changes in patients with monkeypox, helping diagnose and understand the disease.

Your skin is like an ecosystem, with its own community of microbes and substances that interact and affect its health.

Removing β-catenin in certain stem cells causes hair whitening and pigmentation issues.

Mushrooms offer benefits for food, energy, and water security, and have potential uses in health and environmental applications.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

The document concludes that individuals with a rare genetic disorder linked to the AEBP1 gene may experience a unique type of hair loss and should be monitored for heart issues.

Manipulating cell cleanup processes could help treat hair loss.

A COVID-19 infected patient with chronic kidney disease experienced worsened kidney function, hair loss, and unexpected wart clearance.