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9 Records found.
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1.
Wang, X. et al.: Genome-wide analysis of PDX1 target genes in human pancreatic progenitors. Mol. Metab. 9, 57-68 (2018)
2.
Wang, X. et al.: Generation of a human induced pluripotent stem cell (iPSC) line from a patient with family history of diabetes carrying a C18R mutation in the PDX1 gene. Stem Cell Res. 17, 292-295 (2016)
3.
Wang, X. et al.: Generation of a human induced pluripotent stem cell (iPSC) line from a patient carrying a P33T mutation in the PDX1 gene. Stem Cell Res. 17, 273-276 (2016)
4.
Hempel, M. et al.: Microdeletion syndrome 16p11.2-p12.2: Clinical and molecular characterization. Am. J. Med. Genet. A 149A, 2106-2112 (2009)
5.
Langer, S. et al.: Delineation of a 2q deletion in a girl with dysmorphic features and epilepsy. Am. J. Med. Genet. A 140A, 764-768 (2006)
6.
Fauth, C. ; O'Hare, M.J.* ; Lederer, G.* ; Jat, P.S.* & Speicher, M.R.: Order of genetic events is critical determinant of aberrations in chromosome count and structure. Genes Chromosomes Cancer 40, 298-306 (2004)
7.
Geigl, J.B.* et al.: Analysis of gene expression patterns and chromosomal associated with aging. Cancer Res. 64, 8550-8557 (2004)
8.
Kraus, J. et al.: A familiy unbalanced subtelomeric translocation resulting in monosomy 6q27-qter. J. Med. Genet. 40, 1-5 (2003)
9.
Maierhofer, C. ; Jentsch, I. ; Lederer, G. ; Fauth, C. & Speicher, M.R.: Multicolor FISH in two and three dimensions for clastogenic analyses. Mutagen. 17, 523-527 (2002)