A citation-based method for searching scientific literature

K Takeda, T Kishimoto, S Akira. J Mol Med (Berl) 1997
Times Cited: 96







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



Times Cited
  Times     Co-cited
Similarity


Essential role of Stat6 in IL-4 signalling.
K Takeda, T Tanaka, W Shi, M Matsumoto, M Minami, S Kashiwamura, K Nakanishi, N Yoshida, T Kishimoto, S Akira. Nature 1996
41

Lack of IL-4-induced Th2 response and IgE class switching in mice with disrupted Stat6 gene.
K Shimoda, J van Deursen, M Y Sangster, S R Sarawar, R T Carson, R A Tripp, C Chu, F W Quelle, T Nosaka, D A Vignali,[...]. Nature 1996
36

Stat6 is required for mediating responses to IL-4 and for development of Th2 cells.
M H Kaplan, U Schindler, S T Smiley, M J Grusby. Immunity 1996
28

An interleukin-4-induced transcription factor: IL-4 Stat.
J Hou, U Schindler, W J Henzel, T C Ho, M Brasseur, S L McKnight. Science 1994
775
25

The association of atopy with a gain-of-function mutation in the alpha subunit of the interleukin-4 receptor.
G K Hershey, M F Friedrich, L A Esswein, M L Thomas, T A Chatila. N Engl J Med 1997
568
17


Human interleukin 4 receptor confers biological responsiveness and defines a novel receptor superfamily.
R L Idzerda, C J March, B Mosley, S D Lyman, T Vanden Bos, S D Gimpel, W S Din, K H Grabstein, M B Widmer, L S Park. J Exp Med 1990
432
15


Localization of the human stat6 gene to chromosome 12q13.3-q14.1, a region implicated in multiple solid tumors.
B K Patel, C L Keck, R S O'Leary, N C Popescu, W J LaRochelle. Genomics 1998
40
35

Ile50Val variant of IL4R alpha upregulates IgE synthesis and associates with atopic asthma.
H Mitsuyasu, K Izuhara, X Q Mao, P S Gao, Y Arinobu, T Enomoto, M Kawai, S Sasaki, Y Dake, N Hamasaki,[...]. Nat Genet 1998
289
12

Common polymorphisms in the coding part of the IL4-receptor gene.
K Deichmann, J Bardutzky, J Forster, A Heinzmann, J Kuehr. Biochem Biophys Res Commun 1997
104
12

Cutting edge: dominant effect of Ile50Val variant of the human IL-4 receptor alpha-chain in IgE synthesis.
H Mitsuyasu, Y Yanagihara, X Q Mao, P S Gao, Y Arinobu, K Ihara, A Takabayashi, T Hara, T Enomoto, S Sasaki,[...]. J Immunol 1999
137
12

Control of inflammation, cytokine expression, and germinal center formation by BCL-6.
A L Dent, A L Shaffer, X Yu, D Allman, L M Staudt. Science 1997
738
11

A genome-wide search for linkage to asthma. German Asthma Genetics Group.
M Wjst, G Fischer, T Immervoll, M Jung, K Saar, F Rueschendorf, A Reis, M Ulbrecht, M Gomolka, E H Weiss,[...]. Genomics 1999
289
11

Association between genetic variants of mast-cell chymase and eczema.
X Q Mao, T Shirakawa, T Yoshikawa, K Yoshikawa, M Kawai, S Sasaki, T Enomoto, T Hashimoto, J Furuyama, J M Hopkin,[...]. Lancet 1996
120
11

The interleukin-4 receptor gene (IL4R) maps to 16p11.2-16p12.1 in human and to the distal region of mouse chromosome 7.
M A Pritchard, E Baker, S A Whitmore, G R Sutherland, R L Idzerda, L S Park, D Cosman, N A Jenkins, D J Gilbert, N G Copeland. Genomics 1991
65
16

Atopy and asthma: genetic variants of IL-4 and IL-13 signalling.
I Shirakawa, K A Deichmann, I Izuhara, I Mao, C N Adra, J M Hopkin. Immunol Today 2000
211
11



Negative association between asthma and variants of CC16(CC10) on chromosome 11q13 in British and Japanese populations.
P S Gao, X Q Mao, M Kawai, T Enomoto, S Sasaki, O Tanabe, K Yoshimura, S R Shaldon, Y Dake, H Kitano,[...]. Hum Genet 1998
53
18

Linkage and allelic association of atopy and markers flanking the IL4-receptor gene.
K A Deichmann, A Heinzmann, J Forster, S Dischinger, C Mehl, E Brueggenolte, F Hildebrandt, M Moseler, J Kuehr. Clin Exp Allergy 1998
115
10

Maternal uniparental disomy 7 in Silver-Russell syndrome.
M A Preece, S M Price, V Davies, L Clough, P Stanier, R C Trembath, G E Moore. J Med Genet 1997
137
10


Alterations of a zinc finger-encoding gene, BCL-6, in diffuse large-cell lymphoma.
B H Ye, F Lista, F Lo Coco, D M Knowles, K Offit, R S Chaganti, R Dalla-Favera. Science 1993
597
10

Variants of B cell lymphoma 6 (BCL6) and marked atopy.
C N Adra, P S Gao, X Q Mao, B W Baron, S Pauker, T Miki, T Shirakawa, J M Hopkin. Clin Genet 1998
20
50

Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma.
C Ober, N J Cox, M Abney, A Di Rienzo, E S Lander, B Changyaleket, H Gidley, B Kurtz, J Lee, M Nance,[...]. Hum Mol Genet 1998
312
10


Cloning of murine Stat6 and human Stat6, Stat proteins that are tyrosine phosphorylated in responses to IL-4 and IL-3 but are not required for mitogenesis.
F W Quelle, K Shimoda, W Thierfelder, C Fischer, A Kim, S M Ruben, J L Cleveland, J H Pierce, A D Keegan, K Nelms. Mol Cell Biol 1995
299
9



Association of the FcepsilonRIbeta gene with bronchial hyper-responsiveness in an Italian population.
E Trabetti, V Cusin, G Malerba, L C Martinati, A Casartelli, A L Boner, P F Pignatti. J Med Genet 1998
33
27

Hearing loss in Townes-Brocks syndrome.
D R Rossmiller, T R Pasic. Otolaryngol Head Neck Surg 1994
27
33



Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene.
B Burwinkel, L Amat, R G Gray, N Matsuo, K Muroya, K Narisawa, R J Sokol, M A Vilaseca, M W Kilimann. Hum Genet 1998
46
19

Evidence that WT1 mutations in Denys-Drash syndrome patients may act in a dominant-negative fashion.
M H Little, K A Williamson, M Mannens, A Kelsey, C Gosden, N D Hastie, V van Heyningen. Hum Mol Genet 1993
127
9


Townes-Brocks syndrome in two mentally retarded youngsters.
T H Cameron, A M Lachiewicz, A S Aylsworth. Am J Med Genet 1991
31
29


p53 abnormalities in B-cell prolymphocytic leukemia.
D Lens, P J De Schouwer, R A Hamoudi, M Abdul-Rauf, N Farahat, E Matutes, T Crook, M J Dyer, D Catovsky. Blood 1997
77
11


Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters.
U Suter, G J Snipes, R Schoener-Scott, A A Welcher, S Pareek, J R Lupski, R A Murphy, E M Shooter, P I Patel. J Biol Chem 1994
170
9



Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene.
B B Roa, C A Garcia, U Suter, D A Kulpa, C A Wise, J Mueller, A A Welcher, G J Snipes, E M Shooter, P I Patel,[...]. N Engl J Med 1993
327
9

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism.
E M Rinchik, S J Bultman, B Horsthemke, S T Lee, K M Strunk, R A Spritz, K M Avidano, M T Jong, R D Nicholls. Nature 1993
322
9

Phosphorylase b kinase deficiency glycogenosis with cirrhosis of the liver.
A F Kagalwalla, Y A Kagalwalla, S al Ajaji, W Gorka, M A Ali. J Pediatr 1995
20
45

Smith-Lemli-Opitz syndrome: a variable clinical and biochemical phenotype.
A K Ryan, K Bartlett, P Clayton, S Eaton, L Mills, D Donnai, R M Winter, J Burn. J Med Genet 1998
173
9

Molecular and clinical study of 61 Angelman syndrome patients.
S Saitoh, N Harada, Y Jinno, K Hashimoto, K Imaizumi, Y Kuroki, Y Fukushima, T Sugimoto, M Renedo, J Wagstaff. Am J Med Genet 1994
72
12

Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR.
A Martínez-Mir, E Paloma, R Allikmets, C Ayuso, T del Rio, M Dean, L Vilageliu, R Gonzàlez-Duarte, S Balcells. Nat Genet 1998
328
9


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.