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Helmut Zarbl

Researcher at Rutgers University

Publications -  83
Citations -  4078

Helmut Zarbl is an academic researcher from Rutgers University. The author has contributed to research in topics: Gene & Gene expression. The author has an hindex of 31, co-authored 83 publications receiving 3947 citations. Previous affiliations of Helmut Zarbl include Massachusetts Institute of Technology & McGill University.

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Direct mutagenesis of Ha- ras -1 oncogenes by N -nitroso- N -methylurea during initiation of mammary carcinogenesis in rats

TL;DR: Each of the Ha-ras-1 oncogenes present in tumours induced by N-nitroso-N-methylurea, but not in those induced by 7,12-dimethylbenz(a)anthracene, became activated by the same G → A transition, the type of mutation induced by W → N → G → M transition.
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Standardizing global gene expression analysis between laboratories and across platforms

TL;DR: In this paper, the authors proposed a method for standardizing global gene expression analysis between laboratories and across platforms, which can be found in Section 5.2.1.1].
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Mismatch amplification mutation assay (MAMA): application to the c-H-ras gene.

TL;DR: It is found that under appropriate conditions, an allele-specific polymerase chain reaction (PCR) can achieve a sensitivity suitable for measuring specific, infrequent mutations in single cell systems or in animal tissues.
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N-nitroso-N-methylurea-induced rat mammary tumors arise from cells with preexisting oncogenic Hras1 gene mutations.

TL;DR: It is concluded that the NMU-induced mammary tumors carrying the G to A transition at the 12th codon of the Hras gene arose from preexisting ras mutants and that an independent effect of NMU was directly or indirectly responsible for tumor formation.
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Gene expression profiling and differentiation assessment in primary human hepatocyte cultures, established hepatoma cell lines, and human liver tissues

TL;DR: The robustness of the primary hepatocyte cultures was reflected by the extent of unchanged expression character when compared directly to liver, with more than 77% of the probe sets unchanged in each of the over-represented categories, representing such genes as C/EBPalpha, HNF4alpha, CYP2D6, and ABCB1.