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Using 17-hydroxyprogesterone levels to diagnose nonclassic congenital adrenal hyperplasia can result in many incorrect diagnoses.

Psoriasis involves immune and genetic factors, and understanding these can improve treatments.

The gene KAP22-1 affects wool yield and fiber shape in sheep.

The testes produce important hormones like testosterone and others that play key roles in male body functions.

Crossbreeding improves goat fiber quality, and specific genes affect hair traits and color.

Genetic variations affecting skin structure play a key role in severe acne.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

Certain genes and nutrients like vitamin D, zinc, and omega fatty acids affect COVID-19 severity and infection risk.

A mother's iron levels early in pregnancy can influence the DNA makeup of her child, potentially affecting the child's health.

The protein folliculin, involved in a rare disease, works with another protein to control how cells stick together and their organization, and changes in this interaction can lead to disease symptoms.

Testosterone is linked to cardiovascular risk factors and stroke, but its exact role is unclear.

PRP combined with minoxidil is the most effective treatment for hair growth in androgenetic alopecia.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The KRTAP21-1 gene affects wool yield and can help improve wool production.

The study concluded that the arachidonic acid pathway and the protein KRT79 play a role in determining the fineness of cashmere.

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

Keratins are important for skin cell health and their problems can cause diseases.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

pCLCA2 protein may help maintain skin structure and function.

Sphynx cats are hairless and Devon Rex cats have curly hair due to specific genetic mutations.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

New models predict male pattern baldness better than old ones but still need improvement.

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

Testosterone replacement therapy helps manage deficiency and has various methods, but requires careful monitoring to avoid side effects.

Changes in skin microbes play a role in some skin diseases and could lead to new treatments.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

Hair thinning causes stem cell loss through a process involving Piezo1, calcium, and TNF-α.

Trichoscopy is a useful, non-invasive way to diagnose different types of hair loss.

Hairlessness in mammals is due to complex genetic changes in both genes and regulatory regions.