G. Santangelo

发表

Rap1p requires Gcr1p and Gcr2p homodimers to activate ribosomal protein and glycolytic genes, respectively.

S. J. Deminoff, G. Santangelo, 2001, Genetics.

Coiled coil structures and transcription: an analysis of the S. cerevisiae coilome

S. J. Deminoff, G. Santangelo, Kellie E. Barbara, 2007, Molecular Genetics and Genomics.

Analysis in Cos-1 cells of processing and polyadenylation signals by using derivatives of the herpes simplex virus type 1 thymidine kinase gene

G. Santangelo, C. Cole, 1983, Molecular and cellular biology.

Preparation of a "functional library" of African green monkey DNA fragments which substitute for the processing/polyadenylation signal in the herpes simplex virus type 1 thymidine kinase gene

G. Santangelo, C. Cole, 1983, Molecular and cellular biology.

Saccharomyces cerevisiae ribosomal protein L37 is encoded by duplicate genes that are differentially expressed

G. Santangelo, J. Tornow, 1994, Current Genetics.

Two separable functional domains of simian virus 40 large T antigen: carboxyl-terminal region of simian virus 40 large T antigen is required for efficient capsid protein synthesis

G. Santangelo, C. Cole, J. Tornow, 1985, Journal of virology.

The GCR1 gene of Saccharomyces cerevisiae is a split gene with an unusually long intron.

G. Santangelo, J. Tornow, 1994, Genetics.

Global Climate Change and the ecology of the next decade

G. Santangelo, L. Fronzoni, 2008 .

A Saccharomyces cerevisiae mitochondrial DNA fragment activates Reg1p-dependent glucose-repressible transcription in the nucleus

G. Santangelo, J. Tornow, 1997, Current Genetics.

GCR1, a transcriptional activator in Saccharomyces cerevisiae, complexes with RAP1 and can function without its DNA binding domain.

G. Santangelo, X. Zeng, W. Gao, 1993, The EMBO journal.

The transcription factor Gcr1 stimulates cell growth by participating in nutrient-responsive gene expression on a global level

G. Santangelo, Kellie E. Barbara, Kristine A. Willis, 2007, Molecular Genetics and Genomics.

Glucose Signaling in Saccharomyces cerevisiae

G. Santangelo, George M. Santangelo, 2006, Microbiology and Molecular Biology Reviews.

TwoSeparable Functional DomainsofSimian Virus40LargeT Antigen: Carboxyl-Terminal Region ofSimian Virus40LargeT Antigen IsRequired forEfficient Capsid Protein Synthesis

G. Santangelo, J. Tornow, 1985 .

Properties of promoters cloned randomly from the Saccharomyces cerevisiae genome

G. Santangelo, C. McLaughlin, K. Moldave, 1988, Molecular and cellular biology.

Cloning of open reading frames and promoters from the Saccharomyces cerevisiae genome: construction of genomic libraries of random small fragments.

G. Santangelo, K. Moldave, J. Tornow, 1986, Gene.

The Nuclear Pore Complex Mediates Binding of the Mig1 Repressor to Target Promoters

G. Santangelo, K. Barbara-Haley, Thomas D Buford, 2011, PloS one.

Dependence of Escherichia coli hyperbaric oxygen toxicity on the lipid acyl chain composition

G. Santangelo, H. Rasmussen, J. Harley, 1978, Journal of bacteriology.

Efficient expression of the Saccharomyces cerevisiae glycolytic gene ADH1 is dependent upon a cis-acting regulatory element (UASRPG) found initially in genes encoding ribosomal proteins.

G. Santangelo, J. Tornow, 1990, Gene.

Glucose-Responsive Regulators of Gene Expression in Saccharomyces cerevisiae Function at the Nuclear Periphery via a Reverse Recruitment Mechanism

G. Santangelo, Thomas D Buford, Nayan J. Sarma, 2007, Genetics.

Reverse recruitment: the Nup84 nuclear pore subcomplex mediates Rap1/Gcr1/Gcr2 transcriptional activation.

B. Andrews, S. J. Deminoff, G. Santangelo, 2005, Proceedings of the National Academy of Sciences of the United States of America.

Reverse recruitment : The Nup 84 nuclear pore subcomplex mediates Rap 1 Gcr 1 Gcr 2 transcriptional activation

B. Andrews, S. J. Deminoff, G. Santangelo, 2005 .

Efficient transcription of the glycolytic gene ADH1 and three translational component genes requires the GCR1 product, which can act through TUF/GRF/RAP binding sites

G. Santangelo, J. Tornow, 1990, Molecular and cellular biology.

The global transcriptional activator of Saccharomyces cerevisiae, Gcr1p, mediates the response to glucose by stimulating protein synthesis and CLN-dependent cell cycle progression.

J. Moffat, B. Andrews, G. Santangelo, 2003, Genetics.

Chemical inhibition of CaaX protease activity disrupts yeast Ras localization

G. Santangelo, W. Jacobsen, W. K. Schmidt, 2010, Yeast.

Unigenic evolution: a novel genetic method localizes a putative leucine zipper that mediates dimerization of the Saccharomyces cerevisiae regulator Gcr1p.

S. J. Deminoff, G. Santangelo, J. Tornow, 1995, Genetics.

Heterologous Expression Studies of Saccharomyces cerevisiae Reveal Two Distinct Trypanosomatid CaaX Protease Activities and Identify Their Potential Targets

G. Santangelo, W. K. Schmidt, David Z. Mokry, 2009, Eukaryotic Cell.

Specialized Rap1p/Gcr1p transcriptional activation through Gcr1p DNA contacts requires Gcr2p, as does hyperphosphorylation of Gcr1p.

S. J. Deminoff, G. Santangelo, X. Zeng, 1997, Genetics.