1 |
Athma, P., R. Rappaport, and M. Swift. 1996. Molecular genotyping shows that ataxia telangiectasia heterozygotes are predisposed to breast cancer. Cancer Genet. Cytogenet. 92: 130-134
DOI
ScienceOn
|
2 |
Barnes, M. G., B. J. Aronow, L. K. Luyrink, M. B. Moroldo, P. Pavlidis, M. H. Passo, et al. 2004. Gene expression in juvenile arthritis and pondyloarthropathy: Pro-angiogenic ELR+ chemokine genes relate to course of arthritis. Rheumatology 43: 973-979
DOI
ScienceOn
|
3 |
Chen, S. L., C. P. Han, Y. P. Tsao, J. W. Lee, and C. S. Yin. 2006. Identification and typing of human papillomavirus in cervical cancers in Taiwan. Cancer 72: 1939-1945
DOI
ScienceOn
|
4 |
Collas, P. and J. A. Dahl. 2008. Chop it, ChIP it, check it: The current status of chromatin immunoprecipitation. Front. Biosci. 13: 929-943
DOI
|
5 |
Concannon, P. and R. A. Gatti. 1997. Diversity of ATM gene mutations detected in patients with ataxia-telangiectasia. Hum. Mutat. 10: 100-107
DOI
ScienceOn
|
6 |
Forbes, J. R. and D. W. Cox. 1998. Functional characterization of missense mutations in ATP7B: Wilson disease mutation or normal variant? Am. J. Hum. Genet. 63: 1663-1674
DOI
ScienceOn
|
7 |
Gilad, S., A. Bar-Shira, R. Harnik, D. Shkedy, Y. Ziv, R. Khosravi, et al. 1996. Ataxia-telangiectasia: Founder effect among North African Jews. Hum. Mol. Genet. 5: 2033-2037
DOI
ScienceOn
|
8 |
Liu, H. H., X. Cao, Y. Yang, M. G. Liu, and Y. F. Wang. 2006. Array-based nano-amplification technique was applied in detection of hepatitis E virus. J. Biochem. Mol. Biol. 39: 247-252
DOI
PUBMED
|
9 |
Morel, Y. and W. L. Miller. 1991. Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency. Adv. Hum. Genet. 20: 1-68
PUBMED
|
10 |
Mulligan, M. E., L. R. Peterson, R. Y. Kwok, C. R. Clabots, and D. N. Gerding. 1988. Immunoblots and plasmid fingerprints compared with serotyping and polyacrylamide gel electrophoresis for typing Clostridium difficile. J. Clin. Microbiol. 26: 41-46
PUBMED
|
11 |
Payne, A. S., E. J. Kelly, and J. D. Gitlin. 1998. Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation. Proc. Natl. Acad. Sci. USA 95: 10854-10859
DOI
ScienceOn
|
12 |
Swift, M., D. Morrell, R. B. Massey, and C. L. Chase. 1991. Incidence of cancer in 161 families affected by ataxiatelangiectasia. N. Engl. J. Med. 325: 1831-1836
DOI
PUBMED
ScienceOn
|
13 |
McNeil, M. M., S. L. Nash, R. A. Hajjeh, M. A. Phelan, L. A. Conn, B. D. Plikaytis, and D. W. Warnock. 2001. Trends in mortality due to invasive mycotic diseases in the United States, 1980-1997. Clin. Infect. Dis. 33: 641-647
DOI
ScienceOn
|
14 |
Thomas, G. R., P. C. Bull, E. A. Roberts, J. M. Walshe, and D. W. Cox. 1994. Haplotype studies in Wilson disease. Am. J. Hum. Genet. 54: 71-78
|
15 |
Wang, R. F., M. L. Beggs, L. H. Robertson, and C. E. Cerniglia. 2002. Design and evaluation of oligonucleotidemicroarray method for the detection of human intestinal bacteria in fecal samples. FEMS Microbiol. Lett. 213: 175-182
DOI
ScienceOn
|
16 |
Hamilton, A. J. 1998. Serodiagnosis of histoplasmosis, paracoccidioidomycosis and penicilliosis marneffei; current status and future trends. Med. Mycol. 36: 351-364
DOI
PUBMED
ScienceOn
|
17 |
Holland, E. J., S. M. Daya, E. M. Stone, R. Folberg, A. A. Dobler, J. D. Cameron, and D. J. Doughman. 1992. Avellino corneal dystrophy: Clinical manifestations and natural history. Ophthalmology 99: 1564-1568
DOI
PUBMED
ScienceOn
|
18 |
Anthony, R. M., T. J. Brown, and G. L. French. 2000. Rapid diagnosis of bacteremia by universal amplification of 23S ribosomal DNA followed by hybridization to an oligonucleotide array. J. Clin. Microbiol. 38: 781-788
PUBMED
|
19 |
Ma, J. and C. C. Liew. 2003. Gene profiling identifies secreted protein transcripts from peripheral blood cells in coronary artery disease. J. Mol. Cell. Cardiol. 35: 993-998
DOI
ScienceOn
|
20 |
Stewart, H. S., A. E. Ridgway, M. J. Dixon, R. Bonshek, R. Parveen, and G. Black. 1999. Heterogeneity in granular corneal dystrophy: Identification of three causative mutations in the TGFBI (BIGH3) gene - lessons for corneal amyloidogenesis. Hum. Mutat. 14: 126-132
DOI
ScienceOn
|
21 |
Kotilainen, P., J. Jalava, O. Meurman, O. P. Lehtonen, E. Rintala, O. P. Sepp l , E. Eerola, and S. Nikkari. 1998. Diagnosis of meningococcal meningitis by broad-range bacterial PCR with cerebrospinal fluid. J. Clin. Microbiol. 36: 2205-2209
PUBMED
ScienceOn
|
22 |
Wang, R. F., S. J. Kim, L. H. Robertson, and C. E. Cerniglia. 2002. Development of a membrane-array method for the detection of human intestinal bacteria in fecal samples. Mol. Cell. Probes. 16: 341-350
DOI
ScienceOn
|
23 |
Vanittanakom, N. and T. Sirisanthana. 1997. Penicillium marneffei infection in patients infected with human immunodeficiency virus. Curr. Top. Med. Mycol. 8: 35-42
PUBMED
|
24 |
Fridkin, S. K. and W. R. Jarvis. 1996. Epidemiology of nosocomial fungal infections. Clin. Microbiol. Rev. 9: 499- 511
PUBMED
ScienceOn
|
25 |
Kawaguchi, K., S. Kaneko, M. Honda, F. H. Kawai, S. Yukihiro, and K. Kenichi. 2003. Detection of hepatitis B virus DNA in sera from patients with chronic hepatitis B virus infection by DNA microarray method. J. Clin. Microbiol. 41: 1701-1704
DOI
ScienceOn
|
26 |
Petrukhin, K., S. Lutsenko, I. Chernov, B. M. Ross, J. H. Kaplan, and T. C. Gilliam. 1994. Characterization of the Wilson disease gene encoding a P-type copper transporting ATPase: Genomic organization, alternative splicing, and structure/function predictions. Hum. Mol. Genet. 3: 1647-1656
DOI
ScienceOn
|
27 |
Gladkevich, A., S. A. Nelemans, H. F. Kauffman, and J. Korf. 2005. Microarray profiling of lymphocytes in internal diseases with an altered immune response: Potential and methodology. Mediators Inflamm. 2005: 317-330
DOI
ScienceOn
|
28 |
Hugot, J. P. and G. Thomas. 1998. Genome-wide scanning in inflammatory bowel diseases. Dig. Dis. 16: 364-369
DOI
ScienceOn
|
29 |
Jun, R. M., H. W. Tchah, T. I. Kim, D. R. Stulting, S. E. Jung, K. Y. Seo, D. H. Lee, and E. K. Kim. 2004. Avellino corneal dystrophy after LASIK. Ophthalmology 111: 463-468
DOI
ScienceOn
|
30 |
Kennedy, S. M., M. McNamara, M. Hillery, C. Hurley, L. M. Collum, and S. Giles. 1996. Combined granular lattice dystrophy (Avellino corneal dystrophy). Br J Ophthalmol. 80: 489-490
DOI
ScienceOn
|
31 |
Strikas, R. A., L. Anderson, and R. A. Parker. 1986. Temporal and geographic patterns of isolates of nonpolio enteroviruses in the United States, 1970-1983. J. Infect. Dis. 153: 346-351
DOI
PUBMED
ScienceOn
|
32 |
Delgado, I. J., D. S. Kim, K. N. Thatcher, J. M. LaSalle, and I. B. Van den Veyver. 2006. Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients. BMC Med. Genet. 7: 61
DOI
PUBMED
ScienceOn
|
33 |
Dolmetsch, A. M., F. A. Stockl, R. Folberg, I. Gensini, and M. N. Burnier Jr. 1996. Combined granular lattice dystrophy (Avellino) in a patient with no known Italian ancestry. Can. J. Ophthalmol. 31: 29-31
|
34 |
Rennie, R. P., C. E. Nord, L. Sjoberg, and I. B. R. Duncan. 1978. Comparison of bacteriophage typing, serotyping, and biotyping as aids in epidemiologic surveillance of Klebsiella infections. J. Clin. Microbiol. 8: 638-642
PUBMED
|
35 |
Andersen, P. S., C. Jespersgaard, J. Vuust, M. Christiansen, and L. A. Larsen. 2003. Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening. Hum. Mutat. 21: 455-465
DOI
ScienceOn
|
36 |
Yoo, S. Y., T.-I. Kim, S. Y. Lee, E. K. Kim, K. C. Keum, N. C. Yoo, and W. M. Yoo. 2007. Development of DNA chip for the diagnosis of most common corneal dystrophies caused by mutations in the betaigh3 gene. Br. J. Opththalmol. 91: 722-727
DOI
ScienceOn
|
37 |
Broeks, A., J. H. Urbanus, A. N. Floore, E. C. Dahler, J. G. Klijn, E. J. Rutgers, et al. 2000. ATM-heterozygous germline mutations contribute to breast cancer-susceptibility. Am. J. Hum. Genet. 66: 494-500
DOI
ScienceOn
|
38 |
Waldenstrom, E., A. Lagerkvist, T. Dahlman, K. Westermark, and U. Landegren. 1996. Efficient detection of mutations in Wilson disease by manifold sequencing. Genomics 37: 303-309
DOI
ScienceOn
|
39 |
Warnock, D. W. 1995. Fungal complications of transplantation: Diagnosis, treatment, and prevention. J. Antimicrob. Chemother. 36(Suppl B): 73-90
PUBMED
|
40 |
Wright, J., S. Teraoka, A. Onengut, S. A. Tolun, R. A. Gatti, H. D. Ochs, and P. Concannon. 1996. A high frequency of distinct ATM gene mutations in ataxia-telangiectasia. Am. J. Hum. Genet. 59: 839-846
PUBMED
|
41 |
Hampe, J., S. Schreiber, S. H. Shaw, K. F. Lau, S. Bridger, A. J. Macpherson, et al. 1999. A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort. Am. J. Hum. Genet. 64: 808-816
DOI
ScienceOn
|
42 |
Becker, K. G., R. M. Simon, J. E. Bailey-Wilson, B. Freidlin, W. E. Biddison, H. F. McFarland, and J. M. Trent. 1998. Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases. Proc. Natl. Acad. Sci. USA 95: 9979-9984
DOI
ScienceOn
|
43 |
Thomas, G. R., O. Jensson, G. Gudmundsson, L. Thorsteinsson, and D. W. Cox. 1995. Wilson disease in Iceland: A clinical and genetic study. Am. J. Hum. Genet. 56: 1140-1146
PUBMED
|
44 |
Baelde, H. J., M. Eikmans, P. P. Doran, D. W. Lappin, E. de Heer, and J. A. Bruijn. 2004. Gene expression profiling in glomeruli from human kidneys with diabetic nephropathy. Am. J. Kidney Dis. 43: 636-650
DOI
ScienceOn
|
45 |
Swift, M., D. Morrell, E. Cromartie, A. R. Chamberlin, M. H. Skolnick, and D. T. Bishop. 1986. The incidence and gene frequency of ataxia-telangiectasia in the United States. Am. J. Hum. Genet. 39: 573-583
PUBMED
|
46 |
White, P. C., M. I. New, and B. Dupont. 1987. Congenital adrenal hyperplasia. N. Engl. J. Med. 316: 1519-1524
DOI
PUBMED
ScienceOn
|
47 |
Ampel, N. M., D. G. Mosley, B. England, P. D. Vertz, K. Komatsu, and R. A. Hajjeh. 1998. Coccidioidomycosis in Arizona: Increase in incidence from 1990 to 1995. Clin. Infect. Dis. 27: 1528-1530
DOI
ScienceOn
|
48 |
Acquila, M., F. Bottini, A. Valetto, D. Caprino, P. G. Mori, and M. P. Bicocchi. 2001. A new strategy for prenatal diagnosis in a sporadic haemophilia B family. Haemophilia 7: 416-418
DOI
ScienceOn
|
49 |
Cleven, B. E., M. Palka-Santini, J. Gielen, S. Meembor, M. Krönke, and O. Krut. 2006. Identification and characterization of bacterial pathogens causing bloodstream infections by DNA microarray. J. Clin. Microbiol. 44: 2389-2397
DOI
ScienceOn
|
50 |
Denning, D. W. 1996. Diagnosis and management of invasive aspergillosis. Curr. Clin. Top. Infect. Dis. 16: 277-299
PUBMED
ScienceOn
|
51 |
Afshari, N., J. Mullaly, M. Afshari, R. F. Steinert, A. P. Adamis, D. Azar, and J. Talamo. 2001. Survey of patients with granular, lattice, Avellino, and Reis-Bucklers corneal dystrophies for mutations in the BIGH3 and gelsolin genes. Arch. Ophthalmol. 119: 16-22
ScienceOn
|
52 |
Iida, K. and I. Nishimura. 2002. Gene expression profiling by DNA microarray technology. Crit. Rev. Oral Biol. Med. 13: 35-50
DOI
ScienceOn
|
53 |
Korkko, J., I. Kaitila, L. Lonnqvist, L. Peltonen, and L. Ala-Kokko. 2002. Sensitivity of conformation sensitive gel electrophoresis in detecting mutations in Marfan syndrome and related conditions. J. Med. Genet. 30: 34-41
|
54 |
Morens, D. M., G. K. Folkers, and A. S. Fauci. 2004. The challenge of emerging and re-emerging infectious diseases. Nature 430: 242-249
DOI
ScienceOn
|
55 |
Speiser, P. W., B. Dupont, P. Rubinstein, A. Piazza, A. Kastelan, and M. I. New. 1985. High frequency of nonclassical steroid 21-hydroxylase deficiency. Am. J. Hum. Genet. 37: 650-667
|