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Certain genetic variations are linked to higher liver enzyme levels in patients treated for chronic hepatitis C with specific drugs.

The document reports findings on genetic research, including ethical concerns about genome editing, improved diagnosis of mitochondrial mutations, solving inherited eye diseases, confirming gene roles in epilepsy, linking a gene to aneurysms, and identifying genes associated with age-related macular degeneration.

The document concludes that autoimmune skin disorders are treated with corticosteroids and immunosuppressive drugs.

No clear link between specific gene and hair loss in Mexican brothers.

Most children with a common hemochromatosis genotype had elevated iron levels but no severe symptoms.

The document concludes that identifying the specific cells where skin cancers begin is important for creating better prevention, detection, and treatment methods.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

Young women in West Bengal, India, with PCOS often have estrogen resistance, leptin receptor issues, folate deficiency, T2DM, and acanthosis, commonly linked to obesity.

Recent selection on immune response genes was identified across seven ethnicities.

These specific gene polymorphisms are not linked to Alopecia Areata in Egyptians.

Lower PPARγ levels and specific gene variations are linked to more severe Frontal Fibrosing Alopecia.

The enzyme 5α-reductase is important for proper blood vessel development during the fertility-related transformation of the uterus lining.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

Azathioprine can cause severe blood issues and hair loss, needing careful monitoring and possible discontinuation.

Certain mutations in the KLHL24 gene cause a skin disorder by breaking down an important skin protein.

Eating a lot of fat increases PKCβ and inflammation in skin fat cells, which affects skin and hair health.

Researchers created a skin graft that senses blood glucose and could treat diabetes using CRISPR-edited stem cells.

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

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.

Dermatologists give better information on pathology forms, hypersensitivity vasculitis is a common skin issue, misdiagnoses can occur, and various skin conditions are linked to loss of elastin or genetic factors.

Male pattern hair loss may have evolved to promote younger fathers for offspring health and survival, encouraging monogamy and paternal nurturing.

Found new possible treatments for hair loss.

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

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Removing the ATR gene in adult mice causes rapid aging and stem cell loss.

DNA profiling in forensics has improved, but predicting physical traits and ancestry from DNA has limitations and requires ethical consideration.

The study found that in Latin America, ancestry varies by location, influences physical traits, and affects how people perceive their own heritage.

TGF-β is crucial for tissue repair and can cause diseases if not properly regulated.

Hair loss in women is genetic, diagnosed by examination and biopsy, and treated with minoxidil, finasteride, or transplantation.