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The analysis shows the U.S. leads in tissue expansion research, mainly for breast reconstruction, with a slightly higher complication rate when using acellular dermal matrix.

The new anti-dandruff shampoo with ketoconazole-coated zinc oxide nanoparticles is more effective against dandruff.

Women with greater androgen sensitivity respond better to finasteride for hair loss.

Longer GGN repeats in the androgen receptor gene are linked to polycystic ovary syndrome.

Researchers found that most genes affecting drug responses are not fully covered by commercial SNP chips, suggesting the need for more comprehensive tools to optimize drug selection based on genetics.

Longer CAG repeats in gene linked to more severe hair loss in females.

No significant link between CAG repeat numbers and female pattern hair loss in Han Chinese population.

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

Ageratum conyzoides L. extract may effectively and safely treat hair loss.

A genetic test can identify people at risk of male pattern baldness early, allowing for quicker treatment.

The genetic variant studied does not affect PCOS symptoms in Kashmiri women.

The research provides a gene-based framework for hair biology, highlighting the Hippo pathway's importance and suggesting links between hair disorders, cancer pathways, and the immune system.

The FDA approved the first gene therapy for a blood disorder after overcoming early challenges and demonstrating patient benefits.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Researchers used CRISPR/Cas9 to create a goat with a gene that increased cashmere production by 74.5% without affecting quality.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

The document concludes that specific hair and blood vessel abnormalities in infants with seizures and developmental issues may indicate Menkes disease, which lacks a cure and is often fatal by age 3.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The 39th Manfred Donike Workshop discussed methods for detecting misuse of steroids, gene doping, and the complexity of identifying drug residues in urine, highlighting the ongoing efforts to improve global anti-doping work.

The document concludes that computational methods using networks and various data can improve the process of finding new uses for existing drugs.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

M30 is a promising treatment for preventing hair loss during chemotherapy.

Leflunomide is effective for rheumatoid arthritis but has significant side effects.

JAK inhibitors help hair regrowth in alopecia areata but have a high risk of side effects.

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

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

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