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A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

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 more research is needed to reduce frequent hospital visits, addiction medicine education improves with specific training, early breast cancer surgery findings are emerging, nipple smears are not very accurate, surgery for older melanoma patients doesn't extend life, a genetic condition in infants can often be treated with one drug, doctors are inconsistent with blood clot medication, a certain gene may protect against cell damage, muscle gene overexpression affects many other genes, and some mitochondrial genes are less active in mice with tumors.

Cirrhosis affects quality of life with various symptoms, requiring a holistic, multidisciplinary approach for management.

A woman with childhood growth hormone deficiency had multiple hormone deficiencies and developed serious lung and kidney problems later in life.

Environmental factors and chemicals might affect hormone balance and contribute to common hair loss.

Men with androgenetic alopecia, or hair loss, often have abnormal blood flow in their small blood vessels, which might be linked to inflammation and stress.

Swiss Holstein cattle with curly, short hair carry genes from the Simmental breed.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

The most common skin problems in Indian children are infections and eczemas.

Different hair care practices and conditions affect African American hair and scalp health, requiring specialized knowledge for treatment.

Topical contact sensitizers can treat certain skin conditions but are rarely used in the U.K.

2011 dermatological research found new skin aging markers, hair loss causes, skin defense mechanisms, and potential for new treatments.

Hair changes can indicate systemic diseases or medication effects.

BFNB could be a promising treatment for hair growth.

Dermatology residents need thorough training in dermatosurgery for better patient outcomes.

RAPK is a rare skin disorder with pigmented spots, mainly on hands and feet, starting in youth.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

Recombinant human epidermal growth factor is versatile, effective, and safe for long-term skin and mucosal treatments.

Using radiation to make mice's hair turn gray helps study and find ways to prevent or reverse hair graying.

Alopecia X in dogs is a cosmetic issue, not a hormonal disorder, and harmful treatments should be avoided.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

The document concludes that better targeted treatments are needed for wound healing, and single-cell technologies may improve cell-based therapies.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

The conclusion is that recognizing hair growth cycles can improve the precision of dietary and health assessments from hair analysis.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Minoxidil helps hair regrowth in alopecia areata safely.