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Layer-by-Layer self-assembly is promising for biomedical uses like tissue engineering and cell therapy, but challenges remain in material safety and process optimization.

Effervescent cleansing tablets with Asiatic acid were successfully developed, showing good stability and cleansing effectiveness.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

C-scores can help predict gain-of-function and loss-of-function mutations.

Stopping valproate and using lactulose can quickly treat valproate-induced hyperammonemia.

Nanostructured lipid carriers can effectively deliver spironolactone to hair follicles for treating hair loss.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Cubosomes enhance antimicrobial peptide stability and effectiveness.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

Anti-DFS70 antibodies can help identify nonsystemic autoimmune conditions in SLE patients.

A rare ovarian tumor was found in a young woman with a genetic fat disorder.

A specific gene mutation causes sparse, brittle hair in a family.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

ODC1 gene mutations cause a neurodevelopmental disorder with large head size, hair loss, and facial abnormalities.

The drug TGU was ineffective against small cell lung cancer and caused significant bone marrow suppression.

The LEF-1 gene in cashmere goats was successfully cloned and analyzed, showing potential for improving cashmere production.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

Low-coverage sequencing is a cost-effective way to identify genes related to wool traits in rabbits.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

AtVPS29 is essential for proper plant growth by regulating gibberellin signaling.

TCF/Lef1 is essential for skin barrier function by regulating lipid metabolism.

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

The gene NM_026333 slows down aging by affecting the NCX1 pathway and could be targeted for anti-aging treatments.

Lidocaine-loaded microparticles effectively relieve pain and fight bacteria in wounds.

Cathepsin L is essential for normal hair growth and development.

CLE40 and CRN/CLV2 pathways have opposite effects on root growth in Arabidopsis.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.