Cosgrove D - Search Results

1

Modular retro-vectors for transgenic and therapeutic use.

Solaiman F, Zink MA, Xu G, Grunkemeyer J, Cosgrove D, Saenz J, Hodgson CP. Solaiman F, et al. Among authors: cosgrove d. Mol Reprod Dev. 2000 Jun;56(2 Suppl):309-15. doi: 10.1002/(SICI)1098-2795(200006)56:2+<309::AID-MRD22>3.0.CO;2-Y. Mol Reprod Dev. 2000. PMID: 10824992 Review.

2

Collagen COL4A3 knockout: a mouse model for autosomal Alport syndrome.

Cosgrove D, Meehan DT, Grunkemeyer JA, Kornak JM, Sayers R, Hunter WJ, Samuelson GC. Cosgrove D, et al. Genes Dev. 1996 Dec 1;10(23):2981-92. doi: 10.1101/gad.10.23.2981. Genes Dev. 1996. PMID: 8956999 Free article.

3

Determinants of vascular permeability in the kidney glomerulus.

Hamano Y, Grunkemeyer JA, Sudhakar A, Zeisberg M, Cosgrove D, Morello R, Lee B, Sugimoto H, Kalluri R. Hamano Y, et al. Among authors: cosgrove d. J Biol Chem. 2002 Aug 23;277(34):31154-62. doi: 10.1074/jbc.M204806200. Epub 2002 May 30. J Biol Chem. 2002. PMID: 12039968 Free article.

4

Sodium butyrate-mediated induction of the glycoprotein hormone alpha-subunit gene: requirement for continued protein synthesis, identification of a butyrate-responsive element, and inhibition of promoter activation by 2-deoxyglucose.

Haas MJ, Cosgrove DE, Xiong W, Cox GS. Haas MJ, et al. Among authors: cosgrove de. J Cell Biochem. 1999 Aug 1;74(2):242-63. J Cell Biochem. 1999. PMID: 10404394

5

EIAV-based retinal gene therapy in the shaker1 mouse model for usher syndrome type 1B: development of UshStat.

Zallocchi M, Binley K, Lad Y, Ellis S, Widdowson P, Iqball S, Scripps V, Kelleher M, Loader J, Miskin J, Peng YW, Wang WM, Cheung L, Delimont D, Mitrophanous KA, Cosgrove D. Zallocchi M, et al. Among authors: cosgrove d. PLoS One. 2014 Apr 4;9(4):e94272. doi: 10.1371/journal.pone.0094272. eCollection 2014. PLoS One. 2014. PMID: 24705452 Free PMC article.

6

Isolation of an Alu repetitive DNA binding protein and effect of CpG methylation on binding to its recognition sequence.

Cox GS, Gutkin DW, Haas MJ, Cosgrove DE. Cox GS, et al. Among authors: cosgrove de. Biochim Biophys Acta. 1998 Mar 4;1396(1):67-87. doi: 10.1016/s0167-4781(97)00175-9. Biochim Biophys Acta. 1998. PMID: 9524225

7

Choosing a mouse model to study the molecular pathobiology of Alport glomerulonephritis.

Cosgrove D, Kalluri R, Miner JH, Segal Y, Borza DB. Cosgrove D, et al. Kidney Int. 2007 Apr;71(7):615-8. doi: 10.1038/sj.ki.5002115. Epub 2007 Feb 7. Kidney Int. 2007. PMID: 17290292 Free article. Review.

8

Glomerular basement membrane deposition of collagen α1(III) in Alport glomeruli by mesangial filopodia injures podocytes via aberrant signaling through DDR1 and integrin α2β1.

Madison J, Wilhelm K, Meehan DT, Delimont D, Samuelson G, Cosgrove D. Madison J, et al. Among authors: cosgrove d. J Pathol. 2022 Sep;258(1):26-37. doi: 10.1002/path.5969. Epub 2022 Jun 22. J Pathol. 2022. PMID: 35607980 Free PMC article.

9

Expression of basement membrane type IV collagen chains during postnatal development in the murine cochlea.

Cosgrove D, Kornak JM, Samuelson G. Cosgrove D, et al. Hear Res. 1996 Oct;100(1-2):21-32. doi: 10.1016/0378-5955(96)00114-1. Hear Res. 1996. PMID: 8922977

10

Ultrastructural, physiological, and molecular defects in the inner ear of a gene-knockout mouse model for autosomal Alport syndrome.

Cosgrove D, Samuelson G, Meehan DT, Miller C, McGee J, Walsh EJ, Siegel M. Cosgrove D, et al. Hear Res. 1998 Jul;121(1-2):84-98. doi: 10.1016/s0378-5955(98)00069-0. Hear Res. 1998. PMID: 9682811

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