-
2
-
-
0030962735
-
Prevelence of allergic rhinitis in the United States
-
Nathan RA, Meltzer EO, Seiner JC, and Storms W. Prevelence of allergic rhinitis in the United States. J Allergy Clin Immunol 99(suppl):S808-S814, 1997.
-
(1997)
J Allergy Clin Immunol
, vol.99
, Issue.SUPPL.
-
-
Nathan, R.A.1
Meltzer, E.O.2
Seiner, J.C.3
Storms, W.4
-
3
-
-
0006072587
-
Worldwide variations in prevelance of symptoms of allergic rhinoconjunctivitis in children: The International Study of Asthma and Allergies in Childhood (ISAAC)
-
Strachan D, Sibbald B, Weiland S, et al. Worldwide variations in prevelance of symptoms of allergic rhinoconjunctivitis in children: The International Study of Asthma and Allergies in Childhood (ISAAC). Pediatr Allergy Immunol 8:161-176, 1997.
-
(1997)
Pediatr Allergy Immunol
, vol.8
, pp. 161-176
-
-
Strachan, D.1
Sibbald, B.2
Weiland, S.3
-
4
-
-
0028111223
-
Assessment of quality of life in patients with perennial rhinitis with the French version of the SF-36 Health Status Questionnaire
-
Bousquet J, Bullinger M, Fayol C, et al. Assessment of quality of life in patients with perennial rhinitis with the French version of the SF-36 Health Status Questionnaire. J Allergy Clin Immunol 94:182-188, 1994.
-
(1994)
J Allergy Clin Immunol
, vol.94
, pp. 182-188
-
-
Bousquet, J.1
Bullinger, M.2
Fayol, C.3
-
5
-
-
0035713154
-
Allergic rhinitis - A total genome scan for susceptibility genes suggests a locus on chromosome 4q24-q27
-
Haagerup A, Bjerke T, Schoitz PO, et al. Allergic rhinitis - A total genome scan for susceptibility genes suggests a locus on chromosome 4q24-q27. Eur J Hum Genet 9:945-952, 2001.
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 945-952
-
-
Haagerup, A.1
Bjerke, T.2
Schoitz, P.O.3
-
6
-
-
19944432535
-
A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3
-
Kurz T, Altmueller J, Strauch K, et al. A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3. Allergy 60:192-199, 2005.
-
(2005)
Allergy
, vol.60
, pp. 192-199
-
-
Kurz, T.1
Altmueller, J.2
Strauch, K.3
-
7
-
-
4644233904
-
DNA microarray analysis of chromosomal susceptibility regions to identify candidate genes for allergic disease: A pilot study
-
Benson M, Svensson PA, Adner M, et al. DNA microarray analysis of chromosomal susceptibility regions to identify candidate genes for allergic disease: A pilot study. Acta Otolaryngol 124:813-819, 2004.
-
(2004)
Acta Otolaryngol
, vol.124
, pp. 813-819
-
-
Benson, M.1
Svensson, P.A.2
Adner, M.3
-
8
-
-
7444228630
-
Inflammatory mediators in allergic rhinitis
-
Gelfand AW. Inflammatory mediators in allergic rhinitis. J Allergy Clin Immunol 114:S135-S137, 2004.
-
(2004)
J Allergy Clin Immunol
, vol.114
-
-
Gelfand, A.W.1
-
9
-
-
20444494431
-
The "united airways" require an holistic approach to management
-
Cruz AA. The "united airways" require an holistic approach to management. Allergy 60:871-874, 2005.
-
(2005)
Allergy
, vol.60
, pp. 871-874
-
-
Cruz, A.A.1
-
10
-
-
0038240988
-
Mucosal and systemic inflammatory changes in allergic rhinitis and asthma: A comparison between upper and lower airways
-
Braunstahl GJ, Fokkens WJ, Overbeek SE, et al. Mucosal and systemic inflammatory changes in allergic rhinitis and asthma: A comparison between upper and lower airways. Clin Exp Allergy 33:579-587, 2003.
-
(2003)
Clin Exp Allergy
, vol.33
, pp. 579-587
-
-
Braunstahl, G.J.1
Fokkens, W.J.2
Overbeek, S.E.3
-
12
-
-
30544439147
-
Microsatellite DNA instability in benign lung diseases
-
Samara K, Zervou M, Siafakas NM, and Tzortzaki EG. Microsatellite DNA instability in benign lung diseases. Respir Med 100:202-211, 2006.
-
(2006)
Respir Med
, vol.100
, pp. 202-211
-
-
Samara, K.1
Zervou, M.2
Siafakas, N.M.3
Tzortzaki, E.G.4
-
13
-
-
0028019398
-
Microsatellite instability marker of a mutator phenotype in cancer
-
Loeb LA. Microsatellite instability marker of a mutator phenotype in cancer. Cancer Res 54:5059-5063, 1994.
-
(1994)
Cancer Res
, vol.54
, pp. 5059-5063
-
-
Loeb, L.A.1
-
14
-
-
0029031294
-
Microsatellite instability in squamous cell carcinoma of the head and neck
-
Field JK, Kriaris H, Howard P, et al. Microsatellite instability in squamous cell carcinoma of the head and neck. Br J Cancer 75:1065-1069, 1995.
-
(1995)
Br J Cancer
, vol.75
, pp. 1065-1069
-
-
Field, J.K.1
Kriaris, H.2
Howard, P.3
-
15
-
-
0030071158
-
Multiple mutation in human cancer
-
Loeb LA, and Christian FC. Multiple mutation in human cancer. Mutat Res 350:279-286, 1996.
-
(1996)
Mutat Res
, vol.350
, pp. 279-286
-
-
Loeb, L.A.1
Christian, F.C.2
-
16
-
-
0346121625
-
Microsatellite DNA instability and loss of heterozygosity in bronchial asthma
-
Paraskakis E, Sourvinos G, Passam F, et al. Microsatellite DNA instability and loss of heterozygosity in bronchial asthma. Eur Respir J 22:951-955, 2003.
-
(2003)
Eur Respir J
, vol.22
, pp. 951-955
-
-
Paraskakis, E.1
Sourvinos, G.2
Passam, F.3
-
17
-
-
0029877849
-
Microsatellite instability in patients with chronic obstructive pulmonary disease
-
Spandidos DA, Ergazaki M, Hatzistamou J, et al. Microsatellite instability in patients with chronic obstructive pulmonary disease. Oncol Rep 3:489-491, 1996.
-
(1996)
Oncol Rep
, vol.3
, pp. 489-491
-
-
Spandidos, D.A.1
Ergazaki, M.2
Hatzistamou, J.3
-
19
-
-
33751264590
-
Differences in microsatellite DNA level between asthma and COPD
-
Zervou M, Tzortzaki EG, Makris D, et al. Differences in microsatellite DNA level between asthma and COPD. Eur Respir J 28(3)472-478, 2006.
-
(2006)
Eur Respir J
, vol.28
, Issue.3
, pp. 472-478
-
-
Zervou, M.1
Tzortzaki, E.G.2
Makris, D.3
-
20
-
-
0031761656
-
Joint Task Force summary statements on diagnosis and management of rhinitis
-
Dykewicz MS, Fineman S, and Skoner DP. Joint Task Force summary statements on diagnosis and management of rhinitis. Ann Allergy Asthma Immunol 81:474-477, 1998.
-
(1998)
Ann Allergy Asthma Immunol
, vol.81
, pp. 474-477
-
-
Dykewicz, M.S.1
Fineman, S.2
Skoner, D.P.3
-
21
-
-
0023676315
-
A brush method to harvest cells from the nasal mucosa for microscopic and biochemical analysis
-
Pipkorn U, Karlsson G, and Enerback L. A brush method to harvest cells from the nasal mucosa for microscopic and biochemical analysis. J Immunol Methods 112:37-42, 1988.
-
(1988)
J Immunol Methods
, vol.112
, pp. 37-42
-
-
Pipkorn, U.1
Karlsson, G.2
Enerback, L.3
-
23
-
-
0030867614
-
The candidate region approach to the genetics of asthma and allergy
-
Thomas NS, Wilkinson J, and Holgate ST. The candidate region approach to the genetics of asthma and allergy. Am J Respir Crit Care Med 15(suppl 4):144-151, 1997.
-
(1997)
Am J Respir Crit Care Med
, vol.15
, Issue.SUPPL. 4
, pp. 144-151
-
-
Thomas, N.S.1
Wilkinson, J.2
Holgate, S.T.3
-
24
-
-
0036331054
-
Asthma and atopy - A total genome scan for susceptibility genes
-
Haagerup A, Bjerke T, Schiotz PO, et al. Asthma and atopy - A total genome scan for susceptibility genes. Allergy 57:680-686, 2002.
-
(2002)
Allergy
, vol.57
, pp. 680-686
-
-
Haagerup, A.1
Bjerke, T.2
Schiotz, P.O.3
-
25
-
-
0842265605
-
Fine-scale mapping of type I allergy candidate loci suggests central susceptibility genes on chromosomes 3q, 4q and Xp
-
Haagerup A, Borglum AD, Binderup AG, and Kruse TA. Fine-scale mapping of type I allergy candidate loci suggests central susceptibility genes on chromosomes 3q, 4q and Xp. Allergy 59:88-94, 2004.
-
(2004)
Allergy
, vol.59
, pp. 88-94
-
-
Haagerup, A.1
Borglum, A.D.2
Binderup, A.G.3
Kruse, T.A.4
-
26
-
-
0028788635
-
Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases
-
Jaworski A, Rosche WA, Gellibolian R, et al. Mismatch repair in Escherichia coli enhances instability of (CTG)n triplet repeats from human hereditary diseases. Proc Natl Acad Sci USA 92:11019-11023, 1995.
-
(1995)
Proc Natl Acad Sci USA
, vol.92
, pp. 11019-11023
-
-
Jaworski, A.1
Rosche, W.A.2
Gellibolian, R.3
-
27
-
-
0027342721
-
On the essence of "meaningless" simple repetitive DNA in eukaryote genomes. DNA fingerprinting: State of the science
-
Epplen C, Meimer G, Siedlaczck I, et al. On the essence of "meaningless" simple repetitive DNA in eukaryote genomes. DNA fingerprinting: State of the science. EXS 67:29-45, 1993.
-
(1993)
EXS
, vol.67
, pp. 29-45
-
-
Epplen, C.1
Meimer, G.2
Siedlaczck, I.3
-
28
-
-
0033951367
-
Selection against frame shift mutations limits microsatellite expansion in coding DNA
-
Metzgar D, Bytof J, and Wills C. Selection against frame shift mutations limits microsatellite expansion in coding DNA. Genome Res 10:72-80, 2000.
-
(2000)
Genome Res
, vol.10
, pp. 72-80
-
-
Metzgar, D.1
Bytof, J.2
Wills, C.3
-
29
-
-
0031837176
-
Epidemiology o rhinitis and asthma
-
Lundback B. Epidemiology o rhinitis and asthma. Clin Exp Allergy 2:3-10, 1998.
-
(1998)
Clin Exp Allergy
, vol.2
, pp. 3-10
-
-
Lundback, B.1
-
30
-
-
0032875421
-
Perennial rhinitis: An independent risk factor for asthma in nonatopic subjects: Results from the European Community Respiratory Health Survey
-
Leynaert B, Bousquet J, Neukirch C, et al. Perennial rhinitis: An independent risk factor for asthma in nonatopic subjects: Results from the European Community Respiratory Health Survey. J Allergy Clin Immunol 104:301-304, 1999.
-
(1999)
J Allergy Clin Immunol
, vol.104
, pp. 301-304
-
-
Leynaert, B.1
Bousquet, J.2
Neukirch, C.3
-
31
-
-
0037160539
-
Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains
-
Cal S, Obaya AJ, Llamazares M, et al. Cloning, expression analysis, and structural characterization of seven novel human ADAMTSs, a family of metalloproteinases with disintegrin and thrombospondin-1 domains. Gene 283:49-62, 2002.
-
(2002)
Gene
, vol.283
, pp. 49-62
-
-
Cal, S.1
Obaya, A.J.2
Llamazares, M.3
-
32
-
-
16944362967
-
Genetic heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21.23.2
-
Horwitz M, Benson KF, Li FQ, et al. Genetic heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21.23.2. Am J Hum Genet 61:873-881, 1997.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 873-881
-
-
Horwitz, M.1
Benson, K.F.2
Li, F.Q.3
-
33
-
-
0028784565
-
Allelic imbalance study of 16q in human primary breast carcinomas using microsatellite markers
-
Dorion-Bonnet M, Mautalen S, Hostein I, and Longy M. Allelic imbalance study of 16q in human primary breast carcinomas using microsatellite markers. Genes Chromosomes Cancer 14:171-181, 1995.
-
(1995)
Genes Chromosomes Cancer
, vol.14
, pp. 171-181
-
-
Dorion-Bonnet, M.1
Mautalen, S.2
Hostein, I.3
Longy, M.4
-
34
-
-
33745385612
-
Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseases
-
Brasch-Andersen C, Haagerup A, Borglum AD, et al. Highly significant linkage to chromosome 3q13.31 for rhinitis and related allergic diseases. J Med Genet 43:e10, 2006.
-
(2006)
J Med Genet
, vol.43
-
-
Brasch-Andersen, C.1
Haagerup, A.2
Borglum, A.D.3
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