NME7 maintains primary cilium assembly, ciliary microtubule stability, and Hedgehog signaling.

NME7 (nucleoside diphosphate kinase 7), a lesser studied member of the non-metastatic expressed (NME) family, has been reported as a potential subunit of the γ-tubulin ring complex (γTuRC). However, its role in the cilium assembly and function remains unclear. Our research demonstrated that NME7 is located at the centrosome, including at the spindle poles during metaphase and at the basal bodies during cilium assembly.

Total Percutaneous Transfemoral Endovascular Treatment of Non-A Non-B Aortic Dissection.

Although open repair remains the mainstream treatment for aortic arch dissection, its surgical complexity and perioperative complications are significant. We developed a novel stentgraft system for less-invasive endovascular aortic arch repair. We successfully performed a total percutaneous transfemoral endovascular repair of aortic arch dissection using a novel off-the-shelf endograft system.

The development of deep convolutional generative adversarial network to synthesize odontocetes' clicks.

Odontocetes are capable of dynamically changing their echolocation clicks to efficiently detect targets, and learning their clicking strategy can facilitate the design of man-made detecting signals. In this study, we developed deep convolutional generative adversarial networks guided by an acoustic feature vector (AF-DCGANs) to synthesize narrowband clicks of the finless porpoise (Neophocaena phocaenoides sunameri) and broadband clicks of the bottlenose dolphins (Tursiops truncatus). The average short-time objective intelligibility (STOI), spectral correlation coefficient (Spe-CORR), waveform correlation coefficient (Wave-CORR), and dynamic time warping distance (DTW-Distance) of the synthetic clicks were 0.

The efficacy and safety of induction chemotherapy combined with sintilimab followed by concurrent chemoradiotherapy plus sintilimab sequencing maintaining with sintilimab for patients with unresectable locally advanced esophageal squamous cell carcinoma.

Purpose: To evaluate the efficacy and safety of induction chemotherapy combined with programmed death protein 1 (PD-1) inhibitor (sintilimab) followed by concurrent chemoradiotherapy (CCRT) plus sintilimab, and subsequent maintenance with sintilimab (IC-ICCRT-IO) for patients with unresectable locally advanced esophageal squamous cell carcinoma (ESCC) in a retrospective study.

Methods: Data from patients with histologically confirmed, locally advanced, inoperable ESCC who received IC-ICCRT-IO were retrospectively analyzed. Treatment effects were evaluated after 2 cycles of induction therapy and after CCRT by contrast-enhanced CT scans and esophagograms, followed by subsequent evaluations every 3 months post-treatment.

Biological function and mechanism of NAT10 in cancer.

-acetyltransferase 10 (NAT10) is a nucleolar acetyltransferase with an acetylation catalytic function and can bind various protein and RNA molecules. As the N4-acetylcytidine (ac4C) "writer" enzyme, NAT10 is reportedly involved in a variety of physiological and pathological activities. Currently, the NAT10-related molecular mechanisms in various cancers are not fully understood.