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

Genetic factors affect hair loss, and molecular testing may help predict, diagnose, and treat it.

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.

CRISPR/Cas9 gene-editing shows promise for improving sheep and goat breeding but faces challenges with efficiency and accuracy.

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

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.

Men with genetic hair loss are more likely to have abnormal blood lipid levels, especially if the hair loss is severe.

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

A genetic change in the EDAR gene causes the unique hair traits found in East Asians.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

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

The conclusion is that androgen receptor gene polymorphism might be a marker for polycystic ovary syndrome, but more research is needed.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

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

Acne and other skin conditions can indicate internal diseases like Polycystic Ovary Syndrome (PCOS), and early treatment can prevent long-term issues.

Charnoly bodies could be a marker for cell damage, and certain nutrients and proteins might prevent them, potentially helping with brain diseases and cancer.

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

RDW can be a useful marker for inflammation in alopecia areata patients.

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

Lgr5 is a marker for active, long-lasting stem cells in mouse hair follicles.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

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

Androstanediol glucuronide is a reliable marker for hirsutism in women.