MRTF-dependent cytoskeletal dynamics drive efficient cell cycle progression. [PDF]
Nielsen JC +5 more
europepmc +1 more source
Nickel-induced labial angioedema in a pediatric patient with orthodontic braces: a case report. [PDF]
Leone F +8 more
europepmc +1 more source
Cellular homeostatic responses to lysosomal damage. [PDF]
Jia J, Poolsup S, Salinas JE.
europepmc +1 more source
Recent Advances in Nanotechnology-Based Approaches for Ferroptosis Therapy and Imaging Diagnosis in Pancreatic Cancer. [PDF]
Yang X, Luo W, Wang Y, Du Y, Yu R.
europepmc +1 more source
Myoferlin-Mediated Lysosomal Exocytosis Regulates Cytotoxicity by Phagocytes
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Myoferlin Is a Yet Unknown Interactor of the Mitochondrial Dynamics’ Machinery in Pancreas Cancer Cells [PDF]
Pancreas ductal adenocarcinoma is one of the deadliest cancers where surgery remains the main survival factor. Mitochondria were described to be involved in tumor aggressiveness in several cancer types including pancreas cancer. We have previously reported that myoferlin controls mitochondrial structure and function, and demonstrated that myoferlin ...
Raphaël Peiffer +2 more
exaly +6 more sources
Expression of Myoferlin in Skeletal Muscles of Patients with Dysferlinopathy
Myoferlin is a novel protein of unknown function with high homology to dysferlin, the gene mutations of which cause limb girdle muscular dystrophy type 2B and Miyoshi myopathy. The myoferlin gene seems to be a candidate for the modifier, and because of the high homology to dysferlin myoferlin may work as a compensator for the absence of dysferlin in ...
Ichizo Nishino +2 more
exaly +4 more sources
Myoferlin plays a key role in VEGFA secretion and impacts tumor‐associated angiogenesis in human pancreas cancer [PDF]
peer reviewedPancreatic ductal adenocarcinoma is one of the most deadly forms of cancers with no satisfactory treatment to date. Recent studies have identified myoferlin, a ferlin family member, in human pancreas adenocarcinoma where its expression was ...
Paul Peixoto +2 more
exaly +2 more sources
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Myoferline gene mutation сan be associated with recurrent angioedema
Russian Journal of Allergy, 2023Hereditary angioedema is a rare genetically determined disease characterized by the recurrent angioedema of various localizations with no response to systemic glucocorticosteroids, antihistamines. In the majority of hereditary angioedema cases C1-inhibitor level or its functional activity is decreased due to a mutation in the SERPING1 gene.
Daria S. Fomina +5 more
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