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Results 1 - 10 of 144 for Pathogenesis
  1. HLA-B gene 
    ... The role of HLA-B*51 in the pathogenesis of Behcet's disease. Clin Exp Immunol. 2018 ... 1111/cei.13102. Citation on PubMed Gul A. Pathogenesis of Behcet's disease: autoinflammatory features and beyond. ...
    https://medlineplus.gov/genetics/gene/hla-b - Genetics
  2. DMPK gene 
    ... protein kinase (DMPK) and its role in the pathogenesis of myotonic dystrophy 1. Cell Signal. 2008 Nov; ... Central Ranum LP, Day JW. Myotonic dystrophy: RNA pathogenesis comes into focus. Am J Hum Genet. 2004 ...
    https://medlineplus.gov/genetics/gene/dmpk - Genetics
  3. VCP gene 
    ... JP, Forman MS. Valosin-containing protein and the pathogenesis of frontotemporal dementia associated with inclusion body myopathy. ... Impaired protein aggregate handling and clearance underlie the pathogenesis of p97/VCP-associated disease. J Biol Chem. ...
    https://medlineplus.gov/genetics/gene/vcp - Genetics
  4. SNCA gene 
    ... system atrophy: the application of genetics in understanding etiology. Clin Auton Res. 2015 Feb;25(1):19- ... Theuns J, Cruts M, Van Broeckhoven C. Genetic etiology of Parkinson disease associated with mutations in the ...
    https://medlineplus.gov/genetics/gene/snca - Genetics
  5. NF1 gene 
    ... suppressor mutations and growth factor signaling in the pathogenesis of NF1-associated peripheral nerve sheath tumors. I. ... suppressor mutations and growth factor signaling in the pathogenesis of NF1-associated peripheral nerve sheath tumors: II. ...
    https://medlineplus.gov/genetics/gene/nf1 - Genetics
  6. DHCR7 gene 
    ... Bianconi SE, Cross JL, Wassif CA, Porter FD. Pathogenesis, Epidemiology, Diagnosis and Clinical Aspects of Smith-Lemli- ... WE, Labelle EF. A membrane defect in the pathogenesis of the Smith-Lemli-Opitz syndrome. J Lipid ...
    https://medlineplus.gov/genetics/gene/dhcr7 - Genetics
  7. GNE gene 
    ... Carrillo N, Malicdan MC, Huizing M. GNE Myopathy: Etiology, Diagnosis, and Therapeutic Challenges. Neurotherapeutics. 2018 Oct;15( ... J, Alrasheed K, Mozaffar T. GNE myopathy: History, etiology, and treatment trials. Front Neurol. 2022 Oct 18; ...
    https://medlineplus.gov/genetics/gene/gne - Genetics
  8. MFN2 gene 
    ... Milbrandt J. Altered axonal mitochondrial transport in the pathogenesis of Charcot-Marie-Tooth disease from mitofusin 2 ... Corti S. MFN2-related neuropathies: Clinical features, molecular pathogenesis and therapeutic perspectives. J Neurol Sci. 2015 Sep ...
    https://medlineplus.gov/genetics/gene/mfn2 - Genetics
  9. KRIT1 gene 
    ... is required for arterial morphogenesis: implications for the etiology of human cavernous malformations. Development. 2004 Mar;131( ... in cell signaling: implications for cerebral cavernous malformations pathogenesis. Hum Mol Genet. 2005 Sep 1;14(17): ...
    https://medlineplus.gov/genetics/gene/krit1 - Genetics
  10. PARK7 gene 
    ... to neurodegeneration offers novel insights for understanding the pathogenesis of Parkinson's disease. J Mol Med (Berl). ... Theuns J, Cruts M, Van Broeckhoven C. Genetic etiology of Parkinson disease associated with mutations in the ...
    https://medlineplus.gov/genetics/gene/park7 - Genetics
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