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Results 1 - 10 of 310 for z -"4-propenylphenol"
  1. Prostate cancer 
    ... CE, Bangma CH, Bjartell A, Catto JW, Culig Z, Gronberg H, Luo J, Visakorpi T, Rubin MA. ... M, Al Olama AA, Easton D, Kote-Jarai Z. The genetic epidemiology of prostate cancer and its ...
    https://medlineplus.gov/genetics/condition/prostate-cancer - Genetics
  2. Primary familial brain calcification 
    ... PubMed or Free article on PubMed Central Cen Z, Chen Y, Chen S, Wang H, Yang D, ... brain/awz392. Citation on PubMed Chen S, Cen Z, Fu F, Chen Y, Chen X, Yang D, ...
    https://medlineplus.gov/.../primary-familial-brain-calcification - Genetics
  3. Hypermethioninemia 
    ... ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY PubMed Augoustides-Savvopoulou P, Luka Z, Karyda S, Stabler SP, Allen RH, Patsiaoura K, ... 7192(03)00066-0. Citation on PubMed Luka Z, Capdevila A, Mato JM, Wagner C. A glycine ...
    https://medlineplus.gov/genetics/condition/hypermethioninemia - Genetics
  4. Mitochondrial trifunctional protein deficiency 
    ... Jul 24. Citation on PubMed Spiekerkoetter U, Khuchua Z, Yue Z, Bennett MJ, Strauss AW. General mitochondrial trifunctional protein ( ... Citation on PubMed Spiekerkoetter U, Sun B, Khuchua Z, Bennett MJ, Strauss AW. Molecular and phenotypic heterogeneity ...
    https://medlineplus.gov/...hondrial-trifunctional-protein-deficiency - Genetics
  5. Alpha-1 antitrypsin deficiency 
    ... moderately low levels of this protein, and the Z allele produces very little alpha-1 antitrypsin. Individuals with two copies of the Z allele (ZZ) in each cell have a high ...
    https://medlineplus.gov/.../condition/alpha-1-antitrypsin-deficiency - Genetics
  6. DLG4-related synaptopathy 
    ... MRD62 PubMed Levy AM, Gomez-Puertas P, Tumer Z. Neurodevelopmental Disorders Associated with PSD-95 and Its ... Savatt JM, Schluter A, Schonewolf-Greulich B, Shad Z, Shaw-Smith C, Shieh JT, Shohat M, Spranger ...
    https://medlineplus.gov/genetics/condition/dlg4-related-synaptopathy - Genetics
  7. Neuromyelitis optica 
    ... D, Trauninger A, Bors L, Rozsa C, Nagy Z, Jobbagy Z, Eizler K, Prohaszka Z, Varga L, Illes Z. A systematic analysis of the complement pathways in ...
    https://medlineplus.gov/genetics/condition/neuromyelitis-optica - Genetics
  8. X-linked infantile nystagmus 
    ... LINKED; NYS1 PubMed He X, Gu F, Wang Z, Wang C, Tong Y, Wang Y, Yang J, ... van Genderen MM, McLean RJ, Hisaund M, Tu Z, Hertle RW, Gronskov K, Bai D, Wei A, ...
    https://medlineplus.gov/.../condition/x-linked-infantile-nystagmus - Genetics
  9. Dowling-Degos disease 
    ... H, Yang L, Li C, Jiao Q, Lu Z, He J, Ji J, Shen Z, Li C, Hao F, Yu H, Yao Z. Mutations in POFUT1, encoding protein O-fucosyltransferase 1, ... on PubMed Central Zhang J, Li M, Yao Z. Updated review of genetic reticulate pigmentary disorders. Br ...
    https://medlineplus.gov/genetics/condition/dowling-degos-disease - Genetics
  10. STING-associated vasculopathy with onset in infancy 
    ... J, Ishikawa H, Gutman D, Barber G, Qin Z, Jiang Z. Activation of STAT6 by STING is critical for ... Free article on PubMed Central Ishikawa H, Ma Z, Barber GN. STING regulates intracellular DNA-mediated, type ...
    https://medlineplus.gov/...ciated-vasculopathy-with-onset-in-infancy - Genetics
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