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Results 131 to 140 of about 24,136 (236)

Human insulinoma: Clinical, cellular, and molecular aspects [PDF]

, 2018
Insulinoma is the most frequently encountered functioning endocrine pancreatic tumor in humans. In this overview we summarize morphological and clinical features of insulinomas, report about the proinsulin-insulin conversion in normal and neoplastic B ...
Heitz, Philipp, Komminoth, Paul, Roth, Jürgen +2 more
core

Table S3 from MEN1 Degradation Induced by Neddylation and the CUL4B–DCAF7 Axis Promotes Pancreatic Neuroendocrine Tumor Progression

, 2023
Junfeng Xu +16 more
openalex +2 more sources

Identification of MEN1 Mutations in Sporadic Enteropancreatic Neuroendocrine Tumors by Analysis of Paraffin-embedded Tissue [PDF]

, 1999
Matthew Mailman +5 more
openalex +1 more source

Inter-ethnic Partnerships: Key Characteristics, and What They Reveal about Successful Integration [PDF]

Partnerships between immigrants and native-born citizens are commonly viewed as the product of successful social integration, as well as a possible driving force of economic success.
Olga Nottmeyer
core

Is Surgery Beneficial for MEN1 Patients with Small (≤2 cm), Nonfunctioning Pancreaticoduodenal Endocrine Tumor? An Analysis of 65 Patients from the GTE [PDF]

, 2018
Background: The management of small, nonfunctioning pancreaticoduodenal endocrine tumors (NFPET) in multiple endocrine neoplasia type 1 (MEN1) patients is still controversial.
Bauters, Catherine +9 more
core

Novel MEN1-associated retroperitoneal pleomorphic liposarcoma

Rare Tumors
Soft tissue sarcomas are rarely associated with mutations of the MEN1 gene. We report a patient with a large retroperitoneal pleomorphic liposarcoma harboring a rare mutation of the MEN1 gene not previously reported to be associated with soft tissue ...
Christopher F McNicoll +3 more
doaj +1 more source

Microwave ablation for recurrent primary hyperparathyroidism in four patients with multiple endocrine neoplasia type 1: a case series report

International Journal of Hyperthermia
Multiple endocrine neoplasia type 1 (MEN1), a rare tumor syndrome, is inherited in an autosomal dominant pattern, mainly manifested as primary hyperparathyroidism (PHPT). Surgery is preferred for patients with MEN1 and PHPT.
Jie Tan +7 more
doaj +1 more source

Pasireotide Therapy of Multiple Endocrine Neoplasia Type 1–Associated Neuroendocrine Tumors in Female Mice Deleted for an Men1 Allele Improves Survival and Reduces Tumor Progression [PDF]