Importance of calcium to the regulation of polymorphism in Wangiella (Exophiala) dermatitidis

References

• Kwon-Chung KJ, Bennett JE. Medical Mycology. Lea & Febiger, Philadelphia 1992
   Google Scholar
• Matsumoto T, Padhye AA, Ajello L. Medical significance of the so-called black yeasts. Eur J Epidemiol 1987; 3: 87–95
   PubMed Web of Science ®Google Scholar
• Matsumoto T, Matsuda T, McGinnis MR, Ajello L. Clinical and mycological spectra of Wangiella dermatitidis. Mycoses 1993; 36: 145–155
   PubMed Web of Science ®Google Scholar
• Matsumoto T, Ajello L, Matsuda T, Szaniszlo PJ, Walsh TJ. Developments in hyalohyphomycosis and phaeohyphomycosis. J Vet Med Mycol 1994; 32(Suppl. 1)329–349
   PubMedGoogle Scholar
• De Hoog, GS, Takeo, K, Yoshida, S, et al. Pleoanamorphic life cycle of Exophiala (Wangiella) dermatitidis. Antonie van Leeuwenhoek 1994; 65: 143–153
   PubMed Web of Science ®Google Scholar
• Nachman SA, Alpan O, Malowitz R, Spitzer ED. Catheter-associated fungemia due to Wangiella (Exophiala) dermatitidis. J Clin Microbiol 1996; 34: 1011–1013
   PubMed Web of Science ®Google Scholar
• McGinnis MR. Chromoblastomycosis and phaeohyphomycosis; new concepts, diagnosis, and mycology. J Am Acad Dermatol 1983; 8: 1–16
   PubMed Web of Science ®Google Scholar
• Szaniszlo PJ, Mendoza L, Karuppayil SM. Clues about chromoblastomycotic and other dematiaceous fungal pathogens based on Wangiella as a model. Dimorphic Fungi in Biology and Medicine, H Vanden Bossche, FC Odds, D Kerridge. Plenum Press, New York 1993; 241–255, In
   Google Scholar
• Szaniszlo PJ, Karuppayil SM, Mendoza L, Rennard RJ. Cell cycle regulation of polymorphism in Wangiella dermatitids. Arch Med Res 1993; 24: 251–261
   Google Scholar
• Szaniszlo PJ, Geis PA, Jacobs CW, Cooper CR, Harris JL. Cell wall changes associated with yeast to multicellular form conversion in Wangiella dermatitidis. Microbiology—1983, D Schlessinger. American Society for Microbiology, Washington, DC 1983; 239–244, In
   Google Scholar
• Geis PA, Jacobs CW. Polymorphism of Wangiella dermatitidis. Fungal Dimorphism: With Emphasis on Fungi Pathogenic for Humans, PJ Szaniszlo. Plenum Press, New York 1985; 205–233, In
   Google Scholar
• Szaniszlo PJ, Heish PH, Marlowe JD. Induction and ultrastructure of the multicellular (sclerotic) morphology in Phialophora dermatitidis. Mycologia 1976; 68: 117–130
   PubMed Web of Science ®Google Scholar
• Roberts RL, Szaniszlo PJ. Isolation of multicellular mutants of Wangiella dermatitidis. J. Bacteriol 1978; 135: 622–632
   PubMed Web of Science ®Google Scholar
• Cooper CR, Jr, Szaniszlo PJ. Evidence for two cell division cycle (CDC) genes that govern yeast bud emergence in the pathogenic fungus Wangiella dermatitidis. Infect Immun 1993; 61: 2069–2081
   PubMed Web of Science ®Google Scholar
• Jacobs CW, Szaniszlo PJ. Microtubule function and its relation to cellular development and the yeast cell cycle in Wangiella dermatitidis. Arch Microbiol 1982; 133: 155–161
   PubMed Web of Science ®Google Scholar
• Roberts RL, Lo RJ, Szaniszlo PJ. Nuclear division in temperature-sensitive multicellular mutants of Wangiella dermatitidis. J Bacteriol 1979; 135: 1456–1458
   Google Scholar
• Cooper CR, Jr, Harris JL, Jacobs CW, Szaniszlo PJ. Effects of polyoxin AL on cellular developments in Wangiella dermatitidis. Exp Mycol 1984; 8: 349–363
   Google Scholar
• Kester SA, Garrett DC. Morphometry and stereology of the conversion of thin-walled yeasts to phase I yeast cells of Wangiella dermatitidis. Mycologia 1995; 87: 153–160
   Google Scholar
• Szaniszlo PJ, Jacobs CW, Geis PA. Dimorphism: morphological and biochemical aspects. Fungi Pathogenic for Humans and Animals, part A (Biology), D Howard. Dekker, New York 1983; 322–336, In
   Google Scholar
• Karuppayil SM, Mendoza L, Szaniszlo PJ. Reversal of cell cycle arrest in Wangiella dermatitidis. 92nd General Meeting of the American Society of Microbiology, New Orleans, LA, 1992, 509–509, (abstract)
   Google Scholar
• Mendoza L, Karuppayil SM, Szaniszlo PJ. Calcium regulates in vitro dimorphism in chromoblastomycotic fungi. Mycoses 1993; 36: 157–164
   Google Scholar
• Cooper BH. Phialophora verrucosa and other chromoblastomycotic fungi. Fungal Dimorphism: With Emphasis on Fungi Pathogenic to Humans, PJ Szaniszlo. Plenum Press, New York 1985; 263–280, In
   Google Scholar
• Slater M. Rapid nuclear staining method for Saccharomyces cerevisiae. J. Bacteriol 1976; 126: 1339–1341
   PubMed Web of Science ®Google Scholar
• Jacobs CW, Roberts RL, Szaniszlo PJ. Reversal of multicellular form development in a conditional morphological mutant of the fungus Wangiella dermatitidis. J Gen Microbiol 1985; 131: 1719–1728
   Google Scholar
• Pringle JR, Hartwell LH. Saccharomyces cerevisiae cell cycle. The Molecular Biology of the Yeast Saccharomyces, JM Strathern, EW Jones, JR Broach, New York, Cold Spring Harbor 1981; 97–142, In
   Google Scholar
• Sloat BF, Adams A, Pringle JR. Roles of CDC24 gene product in cellular morphogenesis during Saccharomyces cerevisiae cell cycle. J Cell Biol 1981; 89: 395–405
   PubMedGoogle Scholar
• Miyomoto S, Ohyo Y, Oshumi Y, Anraku Y. Nucleotide sequence of CLS4 (CDC24) gene of Saccharomyces cerevisiae. Gene 1987; 54: 125–128
   Google Scholar
• Ohya Y, Miyamoto S, Ohsumi Y, Anraku Y. Calcium sensitive cls4 mutant of Saccharomyces cerevisae with a defect in bud formation. J Bacteriol 1986; 165: 28–33
   PubMedGoogle Scholar
• Ohya Y, Ohsumi Y, Anraku Y. Genetic study of the role of calcium ions in the cell division cycle of Saccharomyces cerevisiae: a calcium dependent mutant and its trifluoperazine-dependent pseudorevertant. Mol Gen Genet 1984; 193: 389–394
   PubMedGoogle Scholar
• Lida HS, Sakaguchi S, Yagawa Y, Anraku Y. Cell cycle control by Ca2+ in Saccharomyces cerevisiae. J Biol Chem 1990; 265: 21216–21222
   Google Scholar
• Roberts RL, Szaniszlo PJ. Yeast-phase cell cycle of the polymorphic fungus Wangiella dermatitidis. J Bacteriol 1980; 144: 721–731
   PubMed Web of Science ®Google Scholar
• Anraky Y, Ohya Y, Lida H. Cell cycle control by calcium and calmodulin in Saccharomyces cerevisiae. Biochem Biophys Acta 1991; 1093: 169–177
   Google Scholar
• Whitaker M, Patel R. Calcium and cell cycle control. Development 1990; 108: 525–542
   PubMed Web of Science ®Google Scholar
• Ohya Y, Anraku Y. A galactose-dependent cmd1 mutant of Saccharomyces cerevisiae: involvement of calmodulin in nuclear division. Curr Genet 1989; 15: 113–120
   Google Scholar
• Rasmussen CD, Means RL, Lu KP, May GS, Means AR. Characterization of and expression of the unique calmodulin gene of Aspergillus nidulans. J Biol Chem 1990; 265: 13767–13775
   PubMedGoogle Scholar
• Baum P, Furlong C, Byers B. Yeast gene required for spindle pole body duplication: homology of its product with Ca2+ binding proteins. Proc Natl Acad Sci USA 1986; 83: 5512–5516
   PubMed Web of Science ®Google Scholar
• Spang A, Courtney I, Fackler U, Matzner M, Schiebel E. The calcium-binding protein cell division cycle 31 of Saccharomyces cerevisiae is a component of the half bridge of the spindle pole body. J Cell Biol 1993; 123: 405–416
   PubMed Web of Science ®Google Scholar
• Sun G-H, Ohya Y, Anraku Y. Yeast calmodulin localizes to sites of cell growth. Protoplasma 1992; 166: 110–113
   Google Scholar
• Brockerhoff SE, Davis TN. Calmodulin concentrates at regions of cell growth in Saccharomyces cerevisiae. J Cell Biol 1992; 118: 619–629
   PubMedGoogle Scholar
• Davis TN. A temperature sensitive calmodulin mutant loses viability during mitosis. J Cell Biol 1992; 118: 607–617
   PubMedGoogle Scholar