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Svetlana Krystofova

Researcher at University of California, Riverside

Publications -  12
Citations -  2269

Svetlana Krystofova is an academic researcher from University of California, Riverside. The author has contributed to research in topics: Neurospora crassa & Heterotrimeric G protein. The author has an hindex of 9, co-authored 9 publications receiving 2140 citations.

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Journal ArticleDOI

The genome sequence of the filamentous fungus Neurospora crassa

James E. Galagan, +77 more
- 24 Apr 2003 - 
TL;DR: A high-quality draft sequence of the N. crassa genome is reported, suggesting that RIP has had a profound impact on genome evolution, greatly slowing the creation of new genes through genomic duplication and resulting in a genome with an unusually low proportion of closely related genes.
Journal ArticleDOI

Heterotrimeric G protein signaling in filamentous fungi.

TL;DR: A comparative analysis of G protein pathways in several filamentous species is provided, with discussion of both unifying themes and important unique signaling paradigms.
Journal ArticleDOI

The Heterotrimeric G-Protein Subunits GNG-1 and GNB-1 Form a Gβγ Dimer Required for Normal Female Fertility, Asexual Development, and Gα Protein Levels in Neurospora crassa

TL;DR: It is shown that GNB-1 is essential for maintenance of normal steady-state levels of GNG-1, suggesting a functional interaction between GNB -1 and Gng-1.
Journal ArticleDOI

Roles for receptors, pheromones, G proteins, and mating type genes during sexual reproduction in Neurospora crassa.

TL;DR: The results demonstrate that although receptors and pheromones control sexual identity, the mating-type genes must be in two different nuclei to allow meiosis and sexual sporulation to occur.
Book ChapterDOI

High-throughput production of gene replacement mutants in Neurospora crassa.

TL;DR: A 96-well format was used for many steps of the procedure, including fungal transformation, isolation of homokaryons, and verification of mutants, and development of software programs for primer design and restriction enzyme selection facilitated the high-throughput aspects of the overall protocol.