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Results 1 - 10 of 309 for Pathogenesis
  1. Congenital diaphragmatic hernia 
    ... G. Congenital diaphragmatic hernia: an overview of the etiology and current management. Acta Paediatr. 2009 Apr;98( ... Kantarci S, Donahoe PK. Congenital diaphragmatic hernia (CDH) etiology as revealed by pathway genetics. Am J Med ...
    https://medlineplus.gov/.../congenital-diaphragmatic-hernia - Genetics
  2. 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
  3. 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
  4. 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
  5. Prion disease 
    ... KURU, SUSCEPTIBILITY TO PubMed Aguzzi A, Heikenwalder M. Pathogenesis of prion diseases: current status and future outlook. ... of humans and farm animals: epidemiology, genetics, and pathogenesis. J Neurochem. 2006 Jun;97(6):1726-39. ...
    https://medlineplus.gov/genetics/condition/prion-disease - Genetics
  6. Hidradenitis suppurativa 
    ... Impaired Notch signalling: the unifying mechanism explaining the pathogenesis of hidradenitis suppurativa (acne inversa). Br J Dermatol. ... mutations in hidradenitis suppurativa: new insights into disease pathogenesis. J Invest Dermatol. 2013 Mar;133(3):601- ...
    https://medlineplus.gov/genetics/condition/hidradenitis-suppurativa - Genetics
  7. HLA-B gene 
    ... The role of HLA-B*51 in the pathogenesis of Behcet's disease. Clin Exp Immunol. 2018 ... 191(3):373. Citation on PubMed Gul A. Pathogenesis of Behcet's disease: autoinflammatory features and beyond. ...
    https://medlineplus.gov/genetics/gene/hla-b - Genetics
  8. 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
  9. Pelizaeus-Merzbacher disease 
    ... Garbern JY. Pelizaeus-Merzbacher disease: Genetic and cellular pathogenesis. Cell Mol Life Sci. 2007 Jan;64(1): ... Yamauchi J, Tanoue A. Pelizaeus-Merzbacher disease: cellular pathogenesis and pharmacologic therapy. Pediatr Int. 2014 Oct;56( ...
    https://medlineplus.gov/.../condition/pelizaeus-merzbacher-disease - Genetics
  10. 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
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