These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

259 related articles for article (PubMed ID: 9837814)

  • 1. Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.
    Honsho M; Tamura S; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
    Am J Hum Genet; 1998 Dec; 63(6):1622-30. PubMed ID: 9837814
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.
    Okumoto K; Itoh R; Shimozawa N; Suzuki Y; Tamura S; Kondo N; Fujiki Y
    Hum Mol Genet; 1998 Sep; 7(9):1399-405. PubMed ID: 9700193
    [TBL] [Abstract][Full Text] [Related]  

  • 3. PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.
    Ghaedi K; Honsho M; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
    Am J Hum Genet; 2000 Oct; 67(4):976-81. PubMed ID: 10968777
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I.
    Tamura S; Okumoto K; Toyama R; Shimozawa N; Tsukamoto T; Suzuki Y; Osumi T; Kondo N; Fujiki Y
    Proc Natl Acad Sci U S A; 1998 Apr; 95(8):4350-5. PubMed ID: 9539740
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly.
    Matsuzono Y; Kinoshita N; Tamura S; Shimozawa N; Hamasaki M; Ghaedi K; Wanders RJ; Suzuki Y; Kondo N; Fujiki Y
    Proc Natl Acad Sci U S A; 1999 Mar; 96(5):2116-21. PubMed ID: 10051604
    [TBL] [Abstract][Full Text] [Related]  

  • 6. PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p.
    Okumoto K; Shimozawa N; Kawai A; Tamura S; Tsukamoto T; Osumi T; Moser H; Wanders RJ; Suzuki Y; Kondo N; Fujiki Y
    Mol Cell Biol; 1998 Jul; 18(7):4324-36. PubMed ID: 9632816
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.
    Tamura S; Matsumoto N; Imamura A; Shimozawa N; Suzuki Y; Kondo N; Fujiki Y
    Biochem J; 2001 Jul; 357(Pt 2):417-26. PubMed ID: 11439091
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.
    Shimozawa N; Suzuki Y; Zhang Z; Imamura A; Toyama R; Mukai S; Fujiki Y; Tsukamoto T; Osumi T; Orii T; Wanders RJ; Kondo N
    Hum Mol Genet; 1999 Jun; 8(6):1077-83. PubMed ID: 10332040
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Molecular biology of peroxisome biogenesis].
    Fujiki Y
    Nihon Rinsho; 1993 Sep; 51(9):2336-42. PubMed ID: 8411711
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome.
    Shimozawa N; Nagase T; Takemoto Y; Suzuki Y; Fujiki Y; Wanders RJ; Kondo N
    Biochem Biophys Res Commun; 2002 Mar; 292(1):109-12. PubMed ID: 11890679
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Enlarged peroxisomes are present in oleic acid-grown Yarrowia lipolytica overexpressing the PEX16 gene encoding an intraperoxisomal peripheral membrane peroxin.
    Eitzen GA; Szilard RK; Rachubinski RA
    J Cell Biol; 1997 Jun; 137(6):1265-78. PubMed ID: 9182661
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Drosophila carrying pex3 or pex16 mutations are models of Zellweger syndrome that reflect its symptoms associated with the absence of peroxisomes.
    Nakayama M; Sato H; Okuda T; Fujisawa N; Kono N; Arai H; Suzuki E; Umeda M; Ishikawa HO; Matsuno K
    PLoS One; 2011; 6(8):e22984. PubMed ID: 21826223
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.
    Matsumoto N; Tamura S; Furuki S; Miyata N; Moser A; Shimozawa N; Moser HW; Suzuki Y; Kondo N; Fujiki Y
    Am J Hum Genet; 2003 Aug; 73(2):233-46. PubMed ID: 12851857
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Human peroxisome-deficient disorders and pathogenic gene].
    Fujiki Y
    Rinsho Shinkeigaku; 1994 Dec; 34(12):1219-21. PubMed ID: 7539728
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Peroxisome synthesis in the absence of preexisting peroxisomes.
    South ST; Gould SJ
    J Cell Biol; 1999 Jan; 144(2):255-66. PubMed ID: 9922452
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly.
    Honsho M; Hiroshige T; Fujiki Y
    J Biol Chem; 2002 Nov; 277(46):44513-24. PubMed ID: 12223482
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A human gene responsible for Zellweger syndrome that affects peroxisome assembly.
    Shimozawa N; Tsukamoto T; Suzuki Y; Orii T; Shirayoshi Y; Mori T; Fujiki Y
    Science; 1992 Feb; 255(5048):1132-4. PubMed ID: 1546315
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans.
    Fukuda S; Shimozawa N; Suzuki Y; Zhang Z; Tomatsu S; Tsukamoto T; Hashiguchi N; Osumi T; Masuno M; Imaizumi K; Kuroki Y; Fujiki Y; Orii T; Kondo N
    Am J Hum Genet; 1996 Dec; 59(6):1210-20. PubMed ID: 8940266
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Defective peroxisome membrane synthesis due to mutations in human PEX3 causes Zellweger syndrome, complementation group G.
    Muntau AC; Mayerhofer PU; Paton BC; Kammerer S; Roscher AA
    Am J Hum Genet; 2000 Oct; 67(4):967-75. PubMed ID: 10958759
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders.
    Imamura A; Tamura S; Shimozawa N; Suzuki Y; Zhang Z; Tsukamoto T; Orii T; Kondo N; Osumi T; Fujiki Y
    Hum Mol Genet; 1998 Dec; 7(13):2089-94. PubMed ID: 9817926
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.