A citation-based method for searching scientific literature

A Imamura, N Shimozawa, Y Suzuki, Z Zhang, T Tsukamoto, T Orii, T Osumi, N Kondo. J Med Genet 2001
Times Cited: 3







List of co-cited articles
2 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels.
C Walter, J Gootjes, P A Mooijer, H Portsteffen, C Klein, H R Waterham, P G Barth, J T Epplen, W H Kunau, R J Wanders,[...]. Am J Hum Genet 2001
63
66

A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents.
Annick Raas-Rothschild, Ronald J A Wanders, Petra A W Mooijer, Jeannette Gootjes, Hans R Waterham, Alisa Gutman, Yasuyuki Suzuki, Nobuyuki Shimozawa, Naomi Kondo, Gideon Eshel,[...]. Am J Hum Genet 2002
50
66

Rapid stable isotope dilution analysis of very-long-chain fatty acids, pristanic acid and phytanic acid using gas chromatography-electron impact mass spectrometry.
P Vreken, A E van Lint, A H Bootsma, H Overmars, R J Wanders, A H van Gennip. J Chromatogr B Biomed Sci Appl 1998
67
33

Late onset white matter disease in peroxisome biogenesis disorder.
P G Barth, J Gootjes, H Bode, P Vreken, C B Majoie, R J Wanders. Neurology 2001
34
33


Immunoblot analysis of peroxisomal proteins in liver and fibroblasts from patients.
R J Wanders, C Dekker, R Ofman, R B Schutgens, P Mooijer. J Inherit Metab Dis 1995
27
33

Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.
B T Poll-The, J M Saudubray, H A Ogier, M Odièvre, J M Scotto, L Monnens, L C Govaerts, F Roels, A Cornelis, R B Schutgens. Eur J Pediatr 1987
97
33

Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis.
E G van Grunsven, E van Berkel, P A Mooijer, P A Watkins, H W Moser, Y Suzuki, L L Jiang, T Hashimoto, G Hoefler, J Adamski,[...]. Am J Hum Genet 1999
84
33

Analysis of very long-chain fatty acids using electrospray ionization mass spectrometry.
Fredoen Valianpour, Jacqueline J M Selhorst, Lia E M van Lint, Albert H van Gennip, Ronald J A Wanders, Stephan Kemp. Mol Genet Metab 2003
104
33

PEX1 mutations in complementation group 1 of Zellweger spectrum patients correlate with severity of disease.
Natalie Preuss, Ute Brosius, Martina Biermanns, Ania C Muntau, Ernst Conzelmann, Jutta Gartner. Pediatr Res 2002
40
33

Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans.
A Imamura, N Shimozawa, Y Suzuki, Z Zhang, T Tsukamoto, Y Fujiki, T Orii, T Osumi, N Kondo. Brain Dev 2000
15
33

Characterization of a novel component of the peroxisomal protein import apparatus using fluorescent peroxisomal proteins.
J E Kalish, G A Keller, J C Morrell, S J Mihalik, B Smith, J M Cregg, S J Gould. EMBO J 1996
64
33

Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders.
A Imamura, T Tsukamoto, N Shimozawa, Y Suzuki, Z Zhang, T Imanaka, Y Fujiki, T Orii, N Kondo, T Osumi. Am J Hum Genet 1998
38
33


Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient.
N Shimozawa, Z Zhang, A Imamura, Y Suzuki, Y Fujiki, T Tsukamoto, T Osumi, P Aubourg, R J Wanders, N Kondo. Biochem Biophys Res Commun 2000
16
33

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders.
B E Reuber, E Germain-Lee, C S Collins, J C Morrell, R Ameritunga, H W Moser, D Valle, S J Gould. Nat Genet 1997
174
33

Peroxisome biogenesis disorders with prolonged survival: phenotypic expression in a cohort of 31 patients.
Bwee Tien Poll-The, Jeannette Gootjes, Marinus Duran, Johannis B C De Klerk, Liesbeth J Maillette de Buy Wenniger-Prick, Ronald J C Admiraal, Hans R Waterham, Ronald J A Wanders, Peter G Barth. Am J Med Genet A 2004
58
33


Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.
N Shimozawa, Y Suzuki, Z Zhang, A Imamura, R Toyama, S Mukai, Y Fujiki, T Tsukamoto, T Osumi, T Orii,[...]. Hum Mol Genet 1999
62
33

A new variant of Zellweger syndrome with normal peroxisomal functions in cultured fibroblasts.
R B Schutgens, R J Wanders, C Jakobs, M Arslan-Kirchner, K Miller, P Wieacker, D Hunnemann, P Hurter, M von Schutz. J Inherit Metab Dis 1994
12
33


Catalase-less peroxisomes. Implication in the milder forms of peroxisome biogenesis disorder.
C Fujiwara, A Imamura, N Hashiguchi, N Shimozawa, Y Suzuki, N Kondo, T Imanaka, T Tsukamoto, T Osumi. J Biol Chem 2000
14
33


Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders.
A Imamura, S Tamura, N Shimozawa, Y Suzuki, Z Zhang, T Tsukamoto, T Orii, N Kondo, T Osumi, Y Fujiki. Hum Mol Genet 1998
57
33

Novel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorder.
Jeannette Gootjes, Frank Schmohl, Hans R Waterham, Ronald J A Wanders. Eur J Hum Genet 2004
13
33

Measurement of peroxisomal fatty acid beta-oxidation in cultured human skin fibroblasts.
R J Wanders, S Denis, J P Ruiter, R B Schutgens, C W van Roermund, B S Jacobs. J Inherit Metab Dis 1995
81
33


Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1.
A Imamura, N Shimozawa, Y Suzuki, Z Zhang, T Tsukamoto, Y Fujiki, T Orii, T Osumi, R J Wanders, N Kondo. Pediatr Res 2000
18
33


Neonatal adrenoleukodystrophy: new cases, biochemical studies, and differentiation from Zellweger and related peroxisomal polydystrophy syndromes.
R I Kelley, N S Datta, W B Dobyns, A K Hajra, A B Moser, M J Noetzel, E H Zackai, H W Moser. Am J Med Genet 1986
172
33

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.
K Okumoto, N Shimozawa, A Kawai, S Tamura, T Tsukamoto, T Osumi, H Moser, R J Wanders, Y Suzuki, N Kondo,[...]. Mol Cell Biol 1998
92
33



Analysis of plasmenylethanolamines using electrospray tandem mass spectrometry and its application in screening for peroxisomal disorders.
P Vreken, F Valianpour, H Overmars, P G Barth, J J Selhorst, A H van Gennip, R J Wanders. J Inherit Metab Dis 2000
8
33

Peroxisome senescence in human fibroblasts.
Julie E Legakis, Jay I Koepke, Chris Jedeszko, Ferdous Barlaskar, Laura J Terlecky, Holly J Edwards, Paul A Walton, Stanley R Terlecky. Mol Biol Cell 2002
120
33

Peroxisomal disorders: a review.
R J Wanders, R B Schutgens, P G Barth. J Neuropathol Exp Neurol 1995
123
33

Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome).
H S Heymans, R B Schutgens, R Tan, H van den Bosch, P Borst. Nature 1983
261
33

Peroxisomal beta-oxidation--a metabolic pathway with multiple functions.
Yves Poirier, Vasily D Antonenkov, Tuomo Glumoff, J Kalervo Hiltunen. Biochim Biophys Acta 2006
285
33


Caenorhabditis elegans utilizes dauer pheromone biosynthesis to dispose of toxic peroxisomal fatty acids for cellular homoeostasis.
Hyoe-Jin Joo, Yong-Hyeon Yim, Pan-Young Jeong, You-Xun Jin, Jeong-Eui Lee, Heekyeong Kim, Seul-Ki Jeong, David J Chitwood, Young-Ki Paik. Biochem J 2009
56
33


A shortcut to identifying small molecule signals that regulate behavior and development in Caenorhabditis elegans.
Chirag Pungaliya, Jagan Srinivasan, Bennett W Fox, Rabia U Malik, Andreas H Ludewig, Paul W Sternberg, Frank C Schroeder. Proc Natl Acad Sci U S A 2009
155
33


Small-molecule pheromones that control dauer development in Caenorhabditis elegans.
Rebecca A Butcher, Masaki Fujita, Frank C Schroeder, Jon Clardy. Nat Chem Biol 2007
222
33

Molecular time-course and the metabolic basis of entry into dauer in Caenorhabditis elegans.
Pan-Young Jeong, Min-Seok Kwon, Hyoe-Jin Joo, Young-Ki Paik. PLoS One 2009
37
33

Modeling human peroxisome biogenesis disorders in the nematode Caenorhabditis elegans.
Heather Thieringer, Britta Moellers, Gabriele Dodt, Wolf-H Kunau, Monica Driscoll. J Cell Sci 2003
29
33



Chemical structure and biological activity of the Caenorhabditis elegans dauer-inducing pheromone.
Pan-Young Jeong, Mankil Jung, Yong-Hyeon Yim, Heekyeong Kim, Moonsoo Park, Eunmi Hong, Weontae Lee, Young Hwan Kim, Kun Kim, Young-Ki Paik. Nature 2005
239
33

Protein sensors for membrane sterols.
Joseph L Goldstein, Russell A DeBose-Boyd, Michael S Brown. Cell 2006
33


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.