Microarray analysis of gene expression in human donor corneas

Archives of Ophthalmology

Volumn 119, Issue 11, 2001, Pages 1629-1634

  Jun, A S ^a   Liu, S H ^a   Koo, E H ^a   Do, D V ^a   Stark, W J ^a   Gottsch, J D ^a  

^a JOHNS HOPKINS UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; RNA;

ARTICLE; CHROMOSOMAL LOCALIZATION; CORNEA DONOR; DATA BASE; DNA LIBRARY; DNA MICROARRAY; DONOR; GENE EXPRESSION; HUMAN; HUMAN TISSUE; INTERNET; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

EID: 0034767603     PISSN: 00039950     EISSN: None     Source Type: Journal    
DOI: 10.1001/archopht.119.11.1629     Document Type: Article

References (50)

1. Gene expression data analysis
2. The application of DNA microarrays in gene expression analysis
3. Genome-wide expression profiling of midgestation placenta and embryo using a 15000 mouse developmental cDNA microarray
4. Molecular portraits of human breast tumors
5. Altered patterns of gene expression in response to myocardial infarction
6. Isolation of novel mouse genes differentially expressed in brain using cDNA microarray
7. Positional cloning utilizing genomic DNA microarrays: The Niemann-Pick type C gene as a model system
8. Cloning and sequence analysis of human and bovine corneal antigen (CD-Ag) cDNA: Identification of host-parasite protein calgranulin C
9. cDNA clones coding for the pro-α1 (IV) chain of human type IV procollagen reveal and unusual homology of amino acid sequences in two halves of the carboxyl-terminal domain
10. Caspase-7 is activated during lovastatin-induced apoptosis of the prostate cancer cell line LnCaP
11. Isolation and molecular characterization of the 5′-upstream region of the human TRAIL gene
12. Organization and expression of basement membrane collagen N genes and their roles in human disorders
13. Stickler syndrome: Further mutations in COL11A1 and evidence for additional locus heterogeneity
14. Molecular cloning and partial characterization of a novel collagen chain, alpha 1 (XVI), consisting of repetitive collagenous domains and cysteine-containing non-collagenous segments
15. A single base mutation in COL5A2 causes Ehlers-Danlos syndrome type II
16. Autosomal recessive Alport syndrome: Linkage analysis and clinical features in two families
17. Type VI collagen mutations in Bethlem myopathy, and autosomal dominant myopathy with contractures
18. CLARP, a death effector domain-containing protein interacts with caspase-8 and regulates apoptosis
19. Identification and characterization of a new member of the TNF family that induces apoptosis
20. Isolation and molecular characterization of the 5′-upstream region of the human TRAIL gene
21. bcl-x, A bcl-2-related gene that functions as a dominant regulator of apoptotic cell death
22. A novel bispecific antisense oligonucleotide inhibiting both bcl-2 and bcl-xL expression efficiently induces apoptosis in tumor cells
23. The p53-binding protein 53BP2 also interacts with bcl2 and impedes cell cycle progression at G2/M
24. NF-kappaB subunit p65 binds to 53BP2 and inhibits cell death induced by 53BP2
25. Aberrant overexpression of 53BP2 mRNA in lung cancer cell lines
26. Proapoptotic p53-interacting protein 53BP2 is induced by UV irradiation but suppressed by p53
27. Induction of apoptosis in BPH stromal cells by adenoviral-mediated overexpression of caspase-7
28. Potent and selective nonpeptide inhibitors of caspases 3 and 7 inhibit apoptosis and maintain cell functionality
29. The Fas-Fas ligand system and other modulators of apoptosis in the cornea
30. On the role of kerato-epithelin in the pathogenesis of 5q31-linked corneal dystrophies
31. Genetics of the corneal dystrophies: What we have learned in the past twenty-five years
32. Mutations in cornea-specific keratin K3 o r K12 genes cause Meesmann corneal dystrophy
33. Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy
34. Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene
35. Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly
36. Mutation of the PAX6 gene in patients with autosomal dominant keratitis
37. A gene expression profile of corneal epithelium and the isolation of human keratin 12 cDNA
38. Characterization of gene expression in human trabecular meshwork using single-pass sequencing of 1060 clones
39. Microarray analysis of the transcriptional network controlled by the photoreceptor homeobox gene Crx
40. Genes up-regulated in the human trabecular meshwork in response to elevated intraocular pressure
41. The gene for Schnyder's crystalline corneal dystrophy maps to human chromosome 1p34-p36
42. Linkage of posterior polymorphous dystrophy to 20q11
43. Linkage of congenital hereditary endothelial dystrophy to chromosome 20
44. Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping
45. Keratoconus: Further gene linkage studies on chromosome 21
46. Description of X-linked megalocornea with identification of the gene locus