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Type 2 diabetes in youth is increasing, with high treatment failure rates and more severe than Type 1; certain drugs can lower lipid levels effectively with varying side effects, and apples may benefit heart health like statins but with fewer side effects.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

Finasteride is effective for male hair loss, teledermatology is accurate and accepted, and cyclosporin helps treat toxic epidermal necrolysis.

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

Skin issues can indicate immune system problems.

TGFα gene mutation in mice causes abnormal skin, wavy hair, curly whiskers, and sometimes eye inflammation.

IL-4 gene variation may increase the risk of alopecia areata in Turkish people.

Biotin supplements significantly improved a young girl's uncombable hair.

The document concludes that recent research has improved understanding of skin diseases and the balance between cell growth and differentiation in the epidermis.

FGF5 gene mutations cause unusually long eyelashes by affecting hair growth regulation.

Ancient DNA blocks are still present in human genomes, possibly due to advantages they provide.

A mouse gene mutation increases the risk of skin cancer.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

The enzyme RDH12 plays a role in vision and retinal disease, with mutations leading to early onset visual loss and blindness, but the exact disease mechanism is unclear and there are no treatments yet.

A new therapy for a skin blistering condition has not been developed yet.

Testosterone undecanoate safely and effectively increased penis size in male children with 5-alpha-reductase deficiency.

Genes related to calcium signaling and lipid metabolism are important for curly hair in Mangalitza pigs.

Certain surgical methods are better than routine incision for hidradenitis suppurativa, topical clindamycin and acitretin are effective treatments, men with HS have a risk of skin cancer, HS patients are more likely to die from heart problems, and specific genetic markers are linked to treatment response.

Mutations in three genes cause Uncombable Hair Syndrome, leading to frizzy hair that can't be combed flat.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

The rhg mutation in mice affects the Oat gene, causing hair growth issues and other symptoms.

Genomic research can help improve the quality and production of natural fibers in animals.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Imaging helps detect adrenal gland issues and monitor treatment in congenital adrenal hyperplasia, and can identify tumors affecting fertility.

A certain mutation in the fetal alpha 5-reductase gene is linked to a higher risk of late miscarriage.