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ALRN-6924 may prevent hair loss caused by chemotherapy.

HPV8 causes hair follicle stem cells to grow, leading to skin lesions.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive forestomach cancer.

LIPH mutations in Japan cause varying degrees of hair loss and woolly hair.

Acidic keratin genes are on CFA9 and basic keratin genes are on CFA27 in dogs.

Progerin affects cell shape but not hair or skin in mice.

Increasing PDCD4 protein may help prevent or treat some skin cancers.

Caspase-14 is important for skin and hair development in all mammals.

The study found that tight junctions reach the top layer of the skin's stratum granulosum, not just the second top layer as previously thought.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Frontal fibrosing alopecia is linked to four genetic areas, especially the HLA-B*07:02 allele.

CD73 may regulate hair growth and could be targeted for hair growth treatments.

Desmosomes are crucial for skin and heart development, and JNK may help regulate them.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

The study identified key genes and pathways linked to hair disorders, aiding precision medicine.

A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

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

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Screening for the NUDT15 gene variant can prevent severe side effects from thiopurine drugs in East-Asian people.

A new Wnt surrogate specifically targets the Frizzled7 receptor, promoting organoid formation and hair growth.

Researchers mapped and categorized specific keratin-associated protein genes on human chromosome 21q22.1.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Birt–Hogg–Dubé Syndrome requires genetic testing for accurate diagnosis due to its similarities with tuberous sclerosis.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Using human recombinant hyaluronidase in donor strip harvesting may improve the procedure.