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Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

Genetic variants can affect valproic acid's effectiveness, side effects, and levels in epilepsy treatment.

Modified HDL can better deliver drugs and genes, potentially improving treatments and reducing side effects.

COVID-19 and vaccines cause various skin reactions and highlight the need for dermatologists in managing these issues and addressing vaccine distribution disparities.

Kidney transplant patients often have skin issues, mainly infections.

Vav2 changes how hair follicle stem cells' genes work as they age, which might improve regeneration but also raise cancer risk.

Both genes and environmental factors like chemicals may contribute to the increase in hypospadias, but the exact causes are still unclear.

Cantú syndrome may be linked to pituitary adenomas.

Taking 5-Alpha Reductase Inhibitors before bladder removal surgery might make high-grade bladder tumors less aggressive.

Researchers identified genes linked to coat color, body size, cashmere production, and high altitude adaptation in goats.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

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

The document concludes that PCOS has a strong genetic component, but more research is needed to fully understand the specific genes involved.

The document concludes that various findings in rheumatology offer insights into disease severity, treatment responses, and potential risks in medication, with some limitations due to unspecified participant numbers.

The document explains what healthy skin, nails, and hair look like on an ultrasound.

Some women with PCOS have rare genetic variants linked to the condition.

The TRPV3 gene variant may cause the long-haired suri alpaca coat.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Women with PCOS have lower adiponectin hormone levels and are more likely to have insulin resistance.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

A mutation in the IKZF1 gene causes immune system overactivity, linked to autoimmune diseases like lupus.

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

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

Zouboulis syndrome is a rare condition that helps diagnose monosomy 18p early.

A genetic duplication on chromosome 5 was linked to a woman's unique combination of medical conditions.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

Combining genetic and physical trait analysis improves diagnosis accuracy for monogenic diabetes.

Alopecia Areata has no cure, treatments are limited, and the condition often recurs, but new therapies like JAK inhibitors show promise.

Teriflunomide helps reduce multiple sclerosis symptoms and is safe for most patients.

Creating stronger blockers for skin enzymes might lead to better treatment for conditions like acne and excessive hair growth.