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Some bacteria use arsenic compounds as antibiotics, and others have evolved resistance; a particular arsenic-based compound shows potential as a new antimalarial treatment.

CD3+ T-cell presence is a reliable marker to tell apart alopecia areata from pattern hair loss.

A second domain of high sulfur KAP genes on chromosome 21q23 is crucial for hair structure.

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

Alisertib was found to be an effective and tolerable treatment for children with recurrent brain tumors.

A new mutation in the CYP11B1 gene was found in a woman with mild hyperandrogenemia, a rare cause of non-classic congenital adrenal hyperplasia.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

New partnerships, clinical trials, and drug approvals marked progress in therapeutic delivery in July 2018.

Proteins from Tianshan red deer abomasum have strong anti-inflammatory, anti-tumor, and antioxidant effects.

Androgens like testosterone increase colon muscle contractions by affecting calcium pathways.

Certain gene variations increase the risk of alopecia areata in Koreans.

Mutations in iRhom2 affect hair and skin in mice and are linked to esophageal cancer, with ADAM17 playing a crucial role.

Combining ATRA with TPO-RA effectively stabilizes platelet counts in ITP patients.

Small molecule treatments improve the ability of human amniotic fluid stem cells to become different cell types.

A new method allows for controlled, long-lasting delivery of retinoic acid through the skin with less inflammation.

LGR5 mainly stays inside cells, moving to the trans-Golgi network, and this process is important for its role in cell signaling.

CCT128930 is a promising new drug that effectively targets and inhibits a cancer-related protein, showing potential for cancer treatment.

Kv1.3 blockers may help treat alopecia areata and promote hair regrowth.

Albumin and prednisone improved symptoms in a woman with Cronkhite-Canada syndrome, revealing potential genetic causes.

Long-read RNA sequencing can identify complex gene changes in IFAP syndrome.

A cluster of sulfur-rich hair protein genes was found on chromosome 17.

AQB reduces harmful skin changes in systemic sclerosis.

KSR1 is crucial for certain skin tumor formation and could be a cancer therapy target.

A deficiency in the TTC7A gene causes immune problems, gut issues, and hair loss.

CT60 polymorphism might increase the risk of Alopecia Areata.

A new genetic mutation in the hairless gene causes a rare hair loss disorder.

Recent advances show zebrafish can model anemia, Alx4 affects craniofacial and hair development, and mTORC1 is crucial for retinal development.

Vaccines and targeting TrxR variants can help prevent cancer and reduce metastasis.

A mutation in the Soat1 gene causes hair structure defects and other health issues in AKR/J mice.