Twelve species (including six new ones) of the spider wasp genus Gonaporus Ashmead, 1902 are revised. The composition of the genus is discussed. Six new species of Gonaporus are described: G. simulator Wahis & I. Zonstein, sp. nov. (♀ ♂, Egypt, Saudi Arabia, United Arab Emirates, Mauritania), G. emiratus I. Zonstein & Wahis, sp. nov. (♀ ♂, United Arab Emirates), G. jaziratensis Wahis & I. Zonstein, sp. nov. (♂, United Arab Emirates), G. mirabilis I. Zonstein & Wahis, sp. nov. (♀ ♂, United Arab Emirates, Pakistan), G. setitarsus I. Zonstein & Wahis, sp. nov. (♀ ♂, Pakistan), and G. spinosissimus Wahis & I. Zonstein, sp. nov. (♀ ♂, Oman). A new synonymy is proposed for G. ecbatanus Wolf, 1990 = G. flamingo S. Zonstein, 2001, syn. nov. Gonaporus israelicus (Wolf, 1990), comb. nov. is transferred from Micraporus Priesner, 1955. An emended diagnosis to genus and a key to species are provided. The Gonaporus species inhabit open arid sandy biotopes of the Mediterranean Region, Africa, Near East and Central Asia. The subgenus Stigmaporus S. Zonstein, 2001 is elevated to full generic rank, stat. nov. A new combination is proposed for S. centralasiaticus (Wolf, 1990), comb. nov., S. lystracantha (Wolf, 1988), comb. nov. and S. wolfi (S. Zonstein, 2001), comb. nov. (all are from genus Gonaporus).
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http://dx.doi.org/10.11646/zootaxa.4018.4.1 | DOI Listing |
Pol J Radiol
November 2024
Department of Surgery, Section of Vascular Surgery and Endovascular Therapy, Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran, Mexico City, Mexico.
Purpose: Monocyte chemoattractant protein-1 (MCP-1/CCL2) plays a key role for infiltration of monocytes/macrophages and studies have demonstrated that the MCP-1/C-C chemokine receptor 2 (CCR2) axis might be involved in the pathogenesis and progression of abdominal aortic aneurysms (AAA). Molecular imaging has shown potential for human clinical research studies. We evaluated the expression of CCR2 in patients with small AAA using single-photon emission computed tomography (SPECT) with the technetium-99m-6-hydrazinylnicotinoyl-C-C-chemokine receptor-2 ligand (Tc-HYNIC-CCR2-L).
View Article and Find Full Text PDFBiomolecules
November 2024
Klinik für Gefäßchirurgie und Endovaskuläre Chirurgie, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 420, 69120 Heidelberg, Germany.
There is currently no clinically valid biomarker for predicting the growth and prognosis of abdominal aortic aneurysms (AAA). The most promising candidates with the highest diagnostic values are plasma D-dimers and markers of activated neutrophils, i.e.
View Article and Find Full Text PDFExplor Target Antitumor Ther
November 2024
Oncology Institute of Southern Switzerland (IOSI), Ente Ospedaliero Cantonale (EOC), 6500 Bellinzona, Switzerland.
Advanced urothelial carcinoma (aUC) has a dismal prognosis, with a 5-year survival rate of approximately 10%. Platinum-based chemotherapy has been the backbone of the first-line treatment of aUC for over 40 years. Only in the last decade, the treatment of aUC has evolved and been enriched with new classes of drugs that demonstrated pivotal improvements in terms of oncological responses and, ultimately, survival.
View Article and Find Full Text PDFCardiovasc Ther
January 2025
Institute of Cardiovascular Science, Translational Medicine Institute, Xi'an Jiaotong University Health Science Center, Xi'an, Shaanxi 710061, China.
Cysteinyl leukotrienes (LTs) and their receptors are involved in the pathogenesis of abdominal aortic aneurysms (AAAs). However, whether CysLT1 receptor antagonists such as montelukast can influence experimental nondissecting AAA remains unclear. Nondissecting AAAs were induced in C57BL/6J mice by transient aortic luminal infusion of porcine pancreatic elastase (PPE).
View Article and Find Full Text PDFClin Genitourin Cancer
November 2024
Genitourinary Medical Oncology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Background: There is a lack of published data on real-world cabozantinib use in patients with advanced renal cell carcinoma after prior vascular endothelial growth factor (VEGF)-targeted therapy.
Methods: CASSIOPE was a real-world, prospective, multicenter, non-interventional postauthorization safety study of cabozantinib in adult patients with advanced renal cell carcinoma in Europe following prior VEGF-targeted treatment (NCT03419572). Endpoints included cabozantinib utilization (dose modifications due to adverse events [AEs; primary endpoint], dose, dose modifications, and treatment duration), safety, effectiveness (progression-free survival [PFS], overall survival [OS], best overall response [BOR]), and healthcare resource utilization.
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