PGLS Antibody
- Known as:
- PGLS Antibody
- Catalog number:
- 34365
- Product Quantity:
- USD
- Category:
- -
- Supplier:
- Signalway
- Gene target:
- PGLS Antibody
Ask about this productRelated genes to: PGLS Antibody
- Gene:
- PGLS NIH gene
- Name:
- 6-phosphogluconolactonase
- Previous symbol:
- -
- Synonyms:
- 6PGL
- Chromosome:
- 19p13.2
- Locus Type:
- gene with protein product
- Date approved:
- 2000-01-20
- Date modifiied:
- 2015-08-25
Related products to: PGLS Antibody
Related articles to: PGLS Antibody
- Paragangliomas (PGLs) are uncommon neuroendocrine tumors most commonly found in the head and neck that originate from neural crest cells. Primary pancreatic paraganglioma is exceedingly rare and has largely been described in case reports and small case series. We present the case of a 79-year-old woman with an incidental pancreatic head lesion initially favored to represent a well-differentiated neuroendocrine tumor. Endoscopic ultrasound with rapid on-site cytopathologic evaluation demonstrated neoplastic cells with neuroendocrine features. Further immunohistochemical (IHC) workup demonstrated tumor cells negative for cytokeratins and positive for GATA-3, supporting a diagnosis of paraganglioma over a well-differentiated neuroendocrine tumor. Cytokeratin immunohistochemistry should be employed alongside neuroendocrine markers in the workup of neuroendocrine tumors to avoid misdiagnosis. - Source: PubMed
Publication date: 2026/07/01
Storozuk TannerVecchio Marc - This exploratory pilot study, employing a single-center and cross-sectional design, aimed to characterize urinary protein alterations associated with pediatric metabolic-associated fatty liver disease (MAFLD) and to identify preliminary candidate proteins associated with MAFLD status within a cohort of children with obesity. - Source: PubMed
Publication date: 2026/06/23
Zhang XiaohuiZhu ZhongyiZhou ZhaoxinLiu ChangDu LinaGuo ZiyunPu GuoweiHe QiangYang Yan - Paraganglioma (PGL) is a rare non-epithelial neuroendocrine neoplasm that can occur in multiple locations within the body. Most PGLs grow slowly and are benign, but some can metastasize to distant sites. Reports of brain metastatic PGL are relatively rare, particularly those with comprehensive case histories. - Source: PubMed
Publication date: 2026/06/18
Zhang HongweiQiao XiaolongWang ZixuanLi QinCheng Chuandong - Pheochromocytomas and paragangliomas, collectively known as paragangliomas (PGLs), are rare neuroendocrine tumors originating from chromaffin cells. Surgical resection is the treatment of choice, with preoperative α-adrenoceptor blockade being consistently used prior to any surgical intervention; however, this approach has recently been challenged. This comprehensive systematic review of the literature was conducted across PubMed, Embase, and the Cochrane Library up to December 2025 to address the necessity and potential indications of α-adrenoceptor blockade in the pre-, peri-, and postoperative phase of PGL management. Papers were categorized into guidelines/consensus, meta-analyses, and clinical studies. All international guidelines uniformly recommend preoperative α-adrenoceptor blockade for functional PGLs, albeit there is no substantial evidence to support abandoning this long-standing practice. Therefore, both for medicolegal considerations and for alignment with current clinical practice, the recommendation for preoperative α-adrenoceptor blockade is still widely utilized. However, recent meta-analyses and patient cohort studies indicate no significant benefits in terms of mortality, intraoperative, or postoperative outcomes using such agents in selective patient populations. The paucity of randomized controlled trials and the recent progress in clinical practice and surgical/anesthetic techniques underscore the need for a reevaluation of the routine use of α-adrenoceptor blockade during PGL surgical resections to resolve this issue. - Source: PubMed
Publication date: 2026/06/08
Angelousi AnnaMemi EleniZografos George NChatzellis EleftheriosKassi EvaKaltsas Gregory - The prognostic importance of tumor location in pheochromocytomas and paragangliomas (PPGLs) remains controversial. This study aimed to assess whether anatomic site independently influences survival in PPGLs. - Source: PubMed
Wu KanBai HexiangLiu XuZhu YuchunLi XiangLiu Zhihong