Association of the ADAM33 gene with asthma and bronchial hyperresponsiveness

[1]  K. Yoshino,et al.  Identification and characterization of novel mouse and human ADAM33s with potential metalloprotease activity. , 2002, Gene.

[2]  R. Djukanović,et al.  The contribution of interleukin (IL)-4 and IL-13 to the epithelial-mesenchymal trophic unit in asthma. , 2001, American journal of respiratory cell and molecular biology.

[3]  J. Pelletier,et al.  Full-length cDNAs: more than just reaching the ends. , 2001, Physiological genomics.

[4]  P. Postmus,et al.  Asthma Genetics and Intermediate Phenotypes: A Review From Twin Studies , 2001, Twin Research.

[5]  L. Maquat.  The power of point mutations , 2001, Nature Genetics.

[6]  C. Blobel,et al.  Cloning and characterization of ADAM28: evidence for autocatalytic pro-domain removal and for cell surface localization of mature ADAM28. , 2000, The Biochemical journal.

[7]  S. Rose-John,et al.  The importance of shedding of membrane proteins for cytokine biology. , 2000, European cytokine network.

[8]  P. Primakoff,et al.  The ADAM gene family: surface proteins with adhesion and protease activity. , 2000, Trends in genetics : TIG.

[9]  P. Howarth,et al.  Epithelial-mesenchymal interactions in the pathogenesis of asthma , 2003 .

[10]  Gonçalo R. Abecasis,et al.  GOLD-Graphical Overview of Linkage Disequilibrium , 2000, Bioinform..

[11]  M. Overgaard,et al.  Regulation of Human ADAM 12 Protease by the Prodomain , 1999, The Journal of Biological Chemistry.

[12]  Michael R. Kroeger,et al.  Structure–Function Analysis of the ADAM Family of Disintegrin-Like and Metalloproteinase-Containing Proteins (Review) , 1999, Journal of protein chemistry.

[13]  D Siegmund,et al.  Statistical methods for mapping quantitative trait loci from a dense set of markers. , 1999, Genetics.

[14]  N. Morton,et al.  Linkage of asthma to markers on chromosome 12 in a sample of 240 families using quantitative phenotype scores. , 1998, Genomics.

[15]  R. Black,et al.  ADAMs: focus on the protease domain. , 1998, Current opinion in cell biology.

[16]  Matthias Wjst,et al.  An Internet linkage and mutation database for the complex phenotype asthma , 1998, Bioinform..

[17]  A. Gulsvik,et al.  Genes for asthma? An analysis of the European Community Respiratory Health Survey. , 1997, American journal of respiratory and critical care medicine.

[18]  Joseph B. Rayman,et al.  Methods for precise sizing, automated binning of alleles, and reduction of error rates in large-scale genotyping using fluorescently labeled dinucleotide markers. FUSION (Finland-U.S. Investigation of NIDDM Genetics) Study Group. , 1997, Genome research.

[19]  M. Lovett,et al.  Isolation of coding sequences from genomic regions using direct selection. , 1997, Methods in molecular biology.

[20]  L Kruglyak,et al.  Parametric and nonparametric linkage analysis: a unified multipoint approach. , 1996, American journal of human genetics.

[21]  Y. Nabeshima,et al.  A metalloprotease-disintegrin participating in myoblast fusion , 1995, Nature.

[22]  E. Lander,et al.  Quantitative locus analysis of airway hyperresponsiveness in A/J and C57BL/6J mice , 1995, Nature Genetics.

[23]  L. Excoffier,et al.  Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population. , 1995, Molecular biology and evolution.

[24]  E. Lander,et al.  Complete multipoint sib-pair analysis of qualitative and quantitative traits. , 1995, American journal of human genetics.

[25]  Aravinda Chakravarti,et al.  Automated construction of genetic linkage maps using an expert system (MultiMap): a human genome linkage map , 1994, Nature Genetics.

[26]  M. Soares.  CHAPTER SIXTEEN – Construction of Directionally Cloned cDNA Libraries in Phagemid Vectors , 1994 .

[27]  M. Adams,et al.  Automated DNA sequencing and analysis. , 1994 .

[28]  W. Ewens,et al.  Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). , 1993, American journal of human genetics.

[29]  Ada Hamosh,et al.  Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene , 1991, Nature.

[30]  M. Boehnke,et al.  Allele frequency estimation from data on relatives. , 1991, American journal of human genetics.

[31]  K. Lange,et al.  Programs for pedigree analysis: Mendel, Fisher, and dGene , 1988, Genetic epidemiology.

[32]  C. Blobel,et al.  Cloning and characterization of ADAM 28 : evidence for autocatalytic pro-domain removal and for cell surface localization of mature ADAM 28 , 2022 .