MICHAEL  WANGLER  to  Membrane Proteins
                            
                            
                                This is a "connection" page, showing publications  MICHAEL  WANGLER  has written about  Membrane Proteins.
                            
                            
                            
                                
                                    
                                            
    
        
        
        
            Connection Strength
            
                
            
            1.086
         
        
        
     
 
    
        
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            Distinguishing PEX2 and PEX16 gene variant severity for mild, severe and atypical peroxisome biogenesis disorders. Dis Model Mech. 2025 Jul 01; 18(7).
            
            
                Score: 0.549
             
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            Drosophila models uncover substrate channeling effects on phospholipids and sphingolipids in peroxisomal biogenesis disorders. PLoS One. 2025; 20(6):e0324143.
            
            
                Score: 0.137
             
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            Dicarboxylic acylcarnitine biomarkers in peroxisome biogenesis disorders. Mol Genet Metab. 2023 11; 140(3):107680.
            
            
                Score: 0.120
             
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            A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkers. Genet Med. 2018 10; 20(10):1274-1283.
            
            
                Score: 0.082
             
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            Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse. PLoS Genet. 2017 Jun; 13(6):e1006825.
            
            
                Score: 0.079
             
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            Loss of the endoplasmic reticulum protein Tmem208 affects cell polarity, development, and viability. Proc Natl Acad Sci U S A. 2024 Feb 27; 121(9):e2322582121.
            
            
                Score: 0.031
             
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            De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movement. Am J Hum Genet. 2022 10 06; 109(10):1932-1943.
            
            
                Score: 0.028
             
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            Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders. Nat Commun. 2019 10 15; 10(1):4679.
            
            
                Score: 0.023
             
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            Lessons learned from additional research analyses of unsolved clinical exome cases. Genome Med. 2017 03 21; 9(1):26.
            
            
                Score: 0.019
             
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            Peroxisome biogenesis disorders in the Zellweger spectrum: An overview of current diagnosis, clinical manifestations, and treatment guidelines. Mol Genet Metab. 2016 Mar; 117(3):313-21.
            
            
                Score: 0.018