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Copy number alterations in childhood acute lymphoblastic leukemia and their association with minimal residual disease.
Genes Chromosomes Cancer. 2008 Jun;47(6):471-80. doi: 10.1002/gcc.20557.
Genes Chromosomes Cancer. 2008.
PMID: 18311775
Assessment of differentiation and progression of hepatic tumors using array-based comparative genomic hybridization.
Steinemann D, Skawran B, Becker T, Tauscher M, Weigmann A, Wingen L, Tauscher S, Hinrichsen T, Hertz S, Flemming P, Flik J, Wiese B, Kreipe H, Lichter P, Schlegelberger B, Wilkens L.
Steinemann D, et al. Among authors: weigmann a.
Clin Gastroenterol Hepatol. 2006 Oct;4(10):1283-91. doi: 10.1016/j.cgh.2006.07.010. Epub 2006 Sep 18.
Clin Gastroenterol Hepatol. 2006.
PMID: 16979954
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Gene expression profiling in hepatocellular carcinoma: upregulation of genes in amplified chromosome regions.
Skawran B, Steinemann D, Weigmann A, Flemming P, Becker T, Flik J, Kreipe H, Schlegelberger B, Wilkens L.
Skawran B, et al. Among authors: weigmann a.
Mod Pathol. 2008 May;21(5):505-16. doi: 10.1038/modpathol.3800998. Epub 2008 Feb 15.
Mod Pathol. 2008.
PMID: 18277965
Free article.
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Analysis of array-CGH data using the R and Bioconductor software suite.
Hofmann WA, Weigmann A, Tauscher M, Skawran B, Focken T, Buurman R, Wingen LU, Schlegelberger B, Steinemann D.
Hofmann WA, et al. Among authors: weigmann a.
Comp Funct Genomics. 2009;2009:201325. doi: 10.1155/2009/201325. Epub 2009 Aug 19.
Comp Funct Genomics. 2009.
PMID: 19696946
Free PMC article.
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Ephrin B1 is expressed on neuroepithelial cells in correlation with neocortical neurogenesis.
Stuckmann I, Weigmann A, Shevchenko A, Mann M, Huttner WB.
Stuckmann I, et al. Among authors: weigmann a.
J Neurosci. 2001 Apr 15;21(8):2726-37. doi: 10.1523/JNEUROSCI.21-08-02726.2001.
J Neurosci. 2001.
PMID: 11306625
Free PMC article.
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Prominin, a novel microvilli-specific polytopic membrane protein of the apical surface of epithelial cells, is targeted to plasmalemmal protrusions of non-epithelial cells.
Weigmann A, Corbeil D, Hellwig A, Huttner WB.
Weigmann A, et al.
Proc Natl Acad Sci U S A. 1997 Nov 11;94(23):12425-30. doi: 10.1073/pnas.94.23.12425.
Proc Natl Acad Sci U S A. 1997.
PMID: 9356465
Free PMC article.
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AC133 hematopoietic stem cell antigen: human homologue of mouse kidney prominin or distinct member of a novel protein family?
Corbeil D, Röper K, Weigmann A, Huttner WB.
Corbeil D, et al. Among authors: weigmann a.
Blood. 1998 Apr 1;91(7):2625-6.
Blood. 1998.
PMID: 9516170
Free article.
No abstract available.
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A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration.
Maw MA, Corbeil D, Koch J, Hellwig A, Wilson-Wheeler JC, Bridges RJ, Kumaramanickavel G, John S, Nancarrow D, Röper K, Weigmann A, Huttner WB, Denton MJ.
Maw MA, et al. Among authors: weigmann a.
Hum Mol Genet. 2000 Jan 1;9(1):27-34. doi: 10.1093/hmg/9.1.27.
Hum Mol Genet. 2000.
PMID: 10587575
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