scispace - formally typeset
A

Ali A. Aghdassi

Researcher at Greifswald University Hospital

Publications -  99
Citations -  3498

Ali A. Aghdassi is an academic researcher from Greifswald University Hospital. The author has contributed to research in topics: Pancreatitis & Acute pancreatitis. The author has an hindex of 25, co-authored 80 publications receiving 2635 citations. Previous affiliations of Ali A. Aghdassi include University of Minnesota & University of Greifswald.

Papers
More filters
Journal ArticleDOI

European evidence-based guidelines on pancreatic cystic neoplasms

Marco Del Chiaro, +88 more
- 01 May 2018 - 
TL;DR: A conservative approach is recommended for asymptomatic MCN and IPMN, and Lifelong follow-up of IPMN is recommended in patients who are fit for surgery.
Journal ArticleDOI

Retinoic acid receptor antagonists inhibit miR-10a expression and block metastatic behavior of pancreatic cancer.

TL;DR: It is suggested that miR-10a is a key mediator of metastatic behavior in pancreatic cancer, which regulates metastasis via suppression of HOXB1 andHOXB3.
Journal ArticleDOI

Heat shock protein 70 increases tumorigenicity and inhibits apoptosis in pancreatic adenocarcinoma.

TL;DR: It is indicated that Hsp70 plays an important role in apoptosis and that selective HSp70 knockdown can be used to induce apoptosis in pancreatic cancer cells.
Journal ArticleDOI

Recruitment of histone deacetylases HDAC1 and HDAC2 by the transcriptional repressor ZEB1 downregulates E-cadherin expression in pancreatic cancer

TL;DR: An important role for histone deacetylation in the downregulation of E-cadherin in human pancreatic cancer is implied and inhibition of HDACs may be a promising antitumour therapy for Pancreatic cancer.
Journal ArticleDOI

Tumour necrosis factor α secretion induces protease activation and acinar cell necrosis in acute experimental pancreatitis in mice

TL;DR: The soluble inflammatory cell mediator TNFα directly induces premature protease activation and necrosis in pancreatic acinar cells and is suggested to be an effective treatment strategy that directly addresses the cellular causes of pancreatitis.