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Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Higher miR-34a levels and the A variant of the MIR-34A gene are linked to increased risk and severity of alopecia areata.

Hair follicle sampling is a practical method for measuring biomarkers in children with and without Fragile X syndrome.

HLA-DRB5 and other genes may be linked to alopecia universalis.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

Three specific mutations in the LIPH gene can cause hair loss by damaging the protein's structure and function.

Genetic testing confirmed a rare skin disorder in a young girl, which improved with zinc supplementation.

The Itpr3 gene causes a specific hair pattern in mice.

Skin cell types develop when specific genes are turned on by removing certain chemical tags from DNA.

Keratin 18 helps diagnose and predict cancer progression and affects cancer growth and spread.

The conclusion is that different blood diseases cause specific oral symptoms and require varied treatments to manage these symptoms and improve patient health.

Transplant success has improved with better immunosuppressive drugs and donor matching.

Miniaturized hairs stay connected to muscle in alopecia areata, allowing possible regrowth, but not in androgenetic alopecia.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Patients with advanced breast cancer and high hormone receptor levels who had surgery for ovarian/pelvic metastases lived longer, especially if they had high estrogen receptor levels.

Researchers found genes and microRNAs that control curly fleece in Chinese Tan sheep.

Children with darker skin tones can have specific skin conditions that need tailored treatments.

Hair shaft disorders, often due to genetics or environment, lack specific treatments but can be managed with gentle hair care and may improve with age or topical treatments.

Distinct β-catenin patterns are linked to cell growth, not cell death, in lung cancer.

Men and women get COVID-19 at similar rates, but men tend to get sicker and have a higher risk of dying, while women usually have stronger immune responses and vaccine reactions.

The SOSTDC1 gene is crucial for determining sheep wool type.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

Men may be more vulnerable to severe COVID-19 due to genetic and hormonal factors, but more research is needed.

Certain gene variations and irregular X chromosome activity may contribute to hair loss in women who can have children.

Rice bran oil extracted by supercritical CO2 is considered non-genotoxic.

The April 2014 issue of "Fertility and Sterility" discussed various reproductive health topics, including hormone therapy benefits, sperm and genetic factors in male infertility, and the link between PCOS and diabetes.