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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1995 | 1 |
1996 | 3 |
1997 | 1 |
1998 | 1 |
2011 | 1 |
2024 | 0 |
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Page 1
Characterization of bacterial communities in venous insufficiency wounds by use of conventional culture and molecular diagnostic methods.
J Clin Microbiol. 2011 Nov;49(11):3812-9. doi: 10.1128/JCM.00847-11. Epub 2011 Aug 31.
J Clin Microbiol. 2011.
PMID: 21880958
Free PMC article.
Blinded multiplex PCR analyses of middle ear and nasopharyngeal fluids from chinchilla models of single- and mixed-pathogen-induced otitis media.
Bakaletz LO, White GJ, Post JC, Ehrlich GD.
Bakaletz LO, et al.
Clin Diagn Lab Immunol. 1998 Mar;5(2):219-24. doi: 10.1128/CDLI.5.2.219-224.1998.
Clin Diagn Lab Immunol. 1998.
PMID: 9521146
Free PMC article.
Item in Clipboard
Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis.
Gorry MC, Gabbaizedeh D, Furey W, Gates LK Jr, Preston RA, Aston CE, Zhang Y, Ulrich C, Ehrlich GD, Whitcomb DC.
Gorry MC, et al.
Gastroenterology. 1997 Oct;113(4):1063-8. doi: 10.1053/gast.1997.v113.pm9322498.
Gastroenterology. 1997.
PMID: 9322498
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Hereditary pancreatitis is caused by a mutation in the cationic trypsinogen gene.
Whitcomb DC, Gorry MC, Preston RA, Furey W, Sossenheimer MJ, Ulrich CD, Martin SP, Gates LK Jr, Amann ST, Toskes PP, Liddle R, McGrath K, Uomo G, Post JC, Ehrlich GD.
Whitcomb DC, et al.
Nat Genet. 1996 Oct;14(2):141-5. doi: 10.1038/ng1096-141.
Nat Genet. 1996.
PMID: 8841182
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A gene for hereditary pancreatitis maps to chromosome 7q35.
Whitcomb DC, Preston RA, Aston CE, Sossenheimer MJ, Barua PS, Zhang Y, Wong-Chong A, White GJ, Wood PG, Gates LK Jr, Ulrich C, Martin SP, Post JC, Ehrlich GD.
Whitcomb DC, et al.
Gastroenterology. 1996 Jun;110(6):1975-80. doi: 10.1053/gast.1996.v110.pm8964426.
Gastroenterology. 1996.
PMID: 8964426
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PCR-based detection of bacterial DNA after antimicrobial treatment is indicative of persistent, viable bacteria in the chinchilla model of otitis media.
Post JC, Aul JJ, White GJ, Wadowsky RM, Zavoral T, Tabari R, Kerber B, Doyle WJ, Ehrlich GD.
Post JC, et al.
Am J Otolaryngol. 1996 Mar-Apr;17(2):106-11. doi: 10.1016/s0196-0709(96)90005-8.
Am J Otolaryngol. 1996.
PMID: 8820185
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Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome.
Gorry MC, Preston RA, White GJ, Zhang Y, Singhal VK, Losken HW, Parker MG, Nwokoro NA, Post JC, Ehrlich GD.
Gorry MC, et al.
Hum Mol Genet. 1995 Aug;4(8):1387-90. doi: 10.1093/hmg/4.8.1387.
Hum Mol Genet. 1995.
PMID: 7581378
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