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Personalized thiopurine dosing based on NUDT15 genotyping can improve long-term outcomes for ulcerative colitis and Crohn's disease patients.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

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

Adverse events in lung cancer treatments increase fear, anxiety, and depression, with newer therapies causing fewer side effects.

Researchers found that certain RNA sequences play a role in yak hair growth and these sequences are somewhat similar to those in cashmere goats.

People with pattern hair loss have higher polyamine levels in the top of their head compared to the back.

Targeted therapy with Ustekinumab significantly improved a skin condition called ILVEN, which is caused by mutations in the CARD14 gene.

Specialized ribosomes affect aging in human skin cells.

Lichen Planopilaris is a hair loss condition best treated early with various medications, including hydroxychloroquine, to prevent permanent baldness.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Genetic mutations can affect female sexual development, requiring personalized medical care.

The conclusion is that adult males with muscle weakness and hormonal imbalances should be tested for Kennedy's disease.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

The study suggests that a specific gene variation and higher gene activity are linked to increased baldness in Egyptian men.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

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

Male hormones may play a role in the development of heart disease, and more research is needed to understand their effects.

Human skin can make serotonin and melatonin, which help protect and maintain it.

Lgr5 is a marker for active, self-renewing stem cells in the intestine and skin, important for tissue maintenance.

Increasing mir-302 turns human hair cells into stem cells by changing gene regulation and demethylation.

Removing part of the vitamin D receptor stops vitamin D from working properly.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Exposure to too much androgen before birth might cause polycystic ovary syndrome later in life.

The immune system plays a key role in tissue repair, affecting both healing quality and regenerative ability.

Human skin can make serotonin and melatonin.

Ectodin integrates BMP, SHH, and FGF signals in developing ectodermal organs.

Understanding where cancer cells come from helps create better prevention and treatment methods.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

Most women with excess hair growth have an underlying hormonal issue, often treated with medication and hair removal methods.