Search

everythinglearnresearchcommunity

for

Search:↓

Deleting the MAD2L1 gene in mice led to rapid tumor growth despite chromosomal instability.

The nano-carrier makes etoposide safer and more effective against lung cancer.

EDM is better for isolating and growing human foreskin fibroblasts, and PPP helps repair UVB damage.

Hydrogen sulfide disrupts protein function and root hair growth in plants by modifying proteins.

Mesenchymal stem cells in people with Hidradenitis Suppurativa are more inflammatory, possibly contributing to the disease.

The method reliably measures finasteride in human plasma.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

The topical inhibitor CUR61414 was not effective in treating basal cell carcinoma in human trials.

The method is effective and suitable for testing finasteride tablets.

Human pluripotent stem cells could be used to make platelets for medical use, but safety, effectiveness, and cost issues need to be resolved.

New mutations in MBTPS2 reduce its function and cause IFAP syndrome with unusual symptoms.

HDAC4 and HDAC7 are crucial for Th17 cell development and could be targeted to treat inflammatory diseases.

PCL nanoscaffold-based liver spheroids are effective for drug screening and studying liver toxicity.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

The early genes of a specific virus can cause abnormal skin cell growth and hair follicle changes.

Certain gene changes in osteopontin are linked to higher risk of atopic dermatitis and asthma.

A new gene mutation causes insulin resistance in a girl and her mother.

Mouse and human keratin 16 can both form filaments, with differences likely due to the tail domain, not the helical domain.

The method accurately measures cyproterone acetate in plasma, showing no significant difference between two formulations.

Disrupting the Hars2 gene in mice causes hearing loss due to mitochondrial problems and hair cell damage.

A rare gene variant causes sexual development issues in siblings, needing personalized treatment.

A reliable method was developed to measure Finasteride and Tadalafil together, showing they degrade under certain conditions.

Certain genetic variants reduce enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Squalene-based carriers improve delivery of a treatment to hair follicles for alopecia areata.

Genetic variations in hair keratin proteins exist but don't significantly affect hair structure.

The treatment was effective and tolerable for advanced gastric cancer.

Hair cortisol levels may not reliably indicate psychological distress.

Higher hs-CRP levels in Indian adolescent women with PCOS are more related to BMI than PCOS itself.