Search

everythinglearnresearchcommunity

for

Search:↓

The document concludes that managing non-classical congenital adrenal hyperplasia in females requires personalized treatment, genetic counseling, and a team of specialists.

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

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Genetic variants linked to ten skin diseases were found, showing both immune and non-immune factors play a role.

The study concluded that testing hormone levels after stimulation is not reliable for identifying carriers of 21-hydroxylase deficiency; genetic testing is necessary.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

No strong genetic link to other skin conditions was found, but some genetic factors may make people more likely to get seborrheic dermatitis.

Genetic mutation and carcinogen treatment are both needed for skin cancer to develop in these specific mice.

Certain genetic variants in the androgen receptor are linked to higher PSA levels, potentially affecting prostate cancer screening outcomes.

The Megsin-Cre transgene is a new tool for genetic manipulation in the skin and upper digestive tract.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

The conclusion is that certain physical signs in the body can indicate past acute and chronic stress, which may help in child abuse investigations.

Different human traits like skin color and hair type vary between populations due to genetic adaptations to the environment.

Women with nonclassical congenital adrenal hyperplasia may have a higher risk of fertility issues and miscarriages, and should get genetic counseling.

Certain genes may influence hair loss differently in men and women.

AGEs and their receptors play a significant role in hair loss by causing inflammation and oxidative stress.

Genetic risk for PCOS can affect children's growth, metabolism, and development from early life into adulthood.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.

Lack of Ctip2 in skin cells delays wound healing and disrupts hair follicle stem cell markers in mice.

Nellore cattle have genetic variations linked to their adaptation to tropical environments.

Certain genetic variations in the A2M gene are linked to better milk quality in Murrah buffaloes.

Enzymes involved in Vitamin A metabolism affect hair growth and type in mice.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Researchers found 15 new genetic links to skin traits in Japanese women.

Certain signals are important for reducing specific chemical markers on hair follicle stem cells during rest periods, which is necessary for healthy hair growth.

Antiandrogen therapy helps treat genetic hair loss.

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

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.