The DOI matches its Crossref record; 42 of the 42 references it cites were found in a registry or an index.
Impairment of calcineurin function in Neurospora crassa reveals its essential role in hyphal growth, morphology and maintenance of the apical Ca2+ gradient
Abstract
The function of Neurospora crassa calcineurin was investigated in N. crassa strains transformed with a construct that provides for the inducible expression of antisense RNA for the catalytic subunit of calcineurin (cna-1). Induction of antisense RNA expression was associated with reduced levels of cna-1 mRNA and of immunodetectable CNA1 protein and decreased calcineurin enzyme activity, indicating that a conditional reduction of the target function had been achieved in antisense transformants with multiple construct integrations. Induction conditions caused growth arrest which indicated that the cna-1 gene is essential for growth of N. crassa. Growth arrest was preceded by an increase in hyphal branching, changes in hyphal morphology and concomitant loss of the distinctive tip-high Ca2+ gradient typical for growing wild-type hyphae. This demonstrates a novel and specific role for calcineurin in the precise regulation of apical growth, a common form of cellular proliferation. In vitro inhibition of N. crassa calcineurin by the complex of cyclosporin A (CsA) and cyclophilin20, and increased sensitivity of the induced transformants to the calcineurin-specific drugs CsA and FK506 imply that the drugs act in N. crassa, as in T-cells and Saccharomyces cerevisiae, by inactivating calcineurin. The finding that exposure of growing wild-type mycelium to these drugs leads to a phenotype very similar to that of the cna-1 antisense mutants is consistent with this idea.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In the model filamentous fungi Neurospora crassa, calcineurin was shown to influence the tip high calcium gradient necessary for growing hyphal tip and normal vegetative growth (Kothe and Free, 1998; Prokisch et al., 1997).”
From Calcineurin as a multifunctional regulator: Unraveling novel functions in fungal stress responses, hyphal growth, drug resistance, and pathogenesis (2014) · cites this paper as Prokisch et al., 1997
Citations
Cites
Calcineurin is a common target of cyclophilin-cyclosporin A and FKBP-FK506 complexes
Liu, J., Farmer, J. D., Lane, W. S., Friedman, J., Weissman, I., & Schreiber, S. L. (1991) · Cell · doi:10.1016/0092-8674(91)90124-h · Cited by 4,116
The mechanism of action of cyclosporin A and FK506
Schreiber, S. L., & Crabtree, G. R. (1992) · Immunology Today · doi:10.1016/0167-5699(92)90111-j · Cited by 2,127
[4] Genetic and microbiological research techniques for Neurospora crassa
Davis, R. H., & de Serres, F. J. (1970) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(71)17168-6 · Cited by 1,130
PREMEIOTIC INSTABILITY OF REPEATED SEQUENCES IN NEUROSPORA CRASSA
Selker, E. U. (1990) · Annual Review of Genetics · doi:10.1146/annurev.ge.24.120190.003051 · Cited by 644
SIGNAL TRANSMISSION BETWEEN THE PLASMA MEMBRANE AND NUCLEUS OF T LYMPHOCYTES
Crabtree, G. R., & Clipstone, N. A. (1994) · Annual Review of Biochemistry · doi:10.1146/annurev.bi.63.070194.005145 · Cited by 635
Cunningham, K. W., & Fink, G. R. (1994) · The Journal of Cell Biology · doi:10.1083/jcb.124.3.351 · Cited by 432
Differential Expression and Function of Two Homologous Subunits of Yeast 1,3-β-D-Glucan Synthase
Mazur, P., Morin, N. R., Baginsky, W. F., El-Sherbeini, M., Clemas, J. A., NIELSEN, J. B. K., & Foor, F. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.10.5671 · Cited by 425
Dumont, F. J., Melino, M. R., Staruch, M. J., Koprak, S., Fischer, P. A., & SIGAL, N. H. (1990) · The Journal of Immunology · doi:10.4049/jimmunol.144.4.1418 · Cited by 355
The protein phosphatase calcineurin is essential for NaCl tolerance of Saccharomyces cerevisiae.
Mendoza, I., Rubio, F., Rodriguez-Navarro, A., & Pardo, J. M. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(17)37038-2 · Cited by 350
Dual Calcium Ion Regulation of Calcineurin by Calmodulin and Calcineurin B
Stemmer, P. M., & Klee, C. B. (1994) · Biochemistry · doi:10.1021/bi00188a015 · Cited by 298
Cited by
Sorted by citations
Calcineurin: Form and Function
Rusnak, F. M., & Mertz, P. S. (2000) · Physiological Reviews · doi:10.1152/physrev.2000.80.4.1483 · Cited by 1,375
Borkovich, K. A., Alex, L. A., Yarden, O., Freitag, M., Turner, G., Read, N. D., Seiler, S., Bell‐Pedersen, D., Paietta, J. V., Plesofsky, N. S., et al. (2004) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.68.1.1-108.2004 · Cited by 636
Sanglard, D., Ischer, F., Marchetti, O., Entenza, J., & Bille, J. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03495.x · Cited by 350
Calcineurin: From structure to function
Aramburu, J. F., Rao, A., & Klee, C. B. (2001) · Current topics in cellular regulation · doi:10.1016/s0070-2137(01)80011-x · Cited by 299
Calcineurin Controls Growth, Morphology, and Pathogenicity in Aspergillus fumigatus
Steinbach, W. J., Cramer, R. A., Perfect, B. Z., Asfaw, Y. G., Sauer, T. C., Najvar, L. K., Kirkpatrick, W. R., Patterson, T. F., Benjamin, D. K., Heitman, J., et al. (2006) · Eukaryotic Cell · doi:10.1128/ec.00139-06 · Cited by 264
CRZ1 , a target of the calcineurin pathway in Candida albicans
Karababa, M., Valentino, E., Pardini, G., Coste, A. T., Bille, J., & Sanglard, D. (2006) · Molecular Microbiology · doi:10.1111/j.1365-2958.2005.05037.x · Cited by 231
Synergistic Effect of Calcineurin Inhibitors and Fluconazole against Candida albicans Biofilms
Uppuluri, P., Nett, J., Heitman, J., & Andes, D. (2008) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.01397-07 · Cited by 228
The Genomes of Three Uneven Siblings: Footprints of the Lifestyles of Three Trichoderma Species
Schmoll, M., Dattenböck, C., Carreras-Villaseñor, N., Mendoza‐Mendoza, A., Tisch, D., Alemán-Duarte, M. I., Baker, S., Brown, C. M., Cervantes-Badillo, M. G., Cetz-Chel, J. E., et al. (2016) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00040-15 · Cited by 197
Regulation of Apical Dominance in Aspergillus nidulans Hyphae by Reactive Oxygen Species
Semighini, C. P., & Harris, S. D. (2008) · Genetics · doi:10.1534/genetics.108.089318 · Cited by 183
A Magnaporthe grisea Cyclophilin Acts as a Virulence Determinant during Plant Infection
Viaud, M., Balhadère, P. V., & Talbot, N. J. (2002) · The Plant Cell · doi:10.1105/tpc.010389 · Cited by 177
Fox, D. S., Cruz, M. C., Sia, R. A. L., Ke, H., Cox, G. M., Cardenas, M. E., & Heitman, J. (2001) · Molecular Microbiology · doi:10.1046/j.1365-2958.2001.02295.x · Cited by 175
Lee, S. C., Li, A., Calo, S., & Heitman, J. (2013) · PLoS Pathogens · doi:10.1371/journal.ppat.1003625 · Cited by 175
Görlach, J. M., Fox, D. S., Cutler, N. S., Cox, G. M., Perfect, J. R., & Heitman, J. (2000) · The EMBO Journal · doi:10.1093/emboj/19.14.3618 · Cited by 172
Del Poeta, M., Cruz, M. C., Cardenas, M. E., Perfect, J. R., & Heitman, J. (2000) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.44.3.739-746.2000 · Cited by 169
Functional characterization of the Aspergillus fumigatus CRZ1 homologue, CrzA
Soriani, F. M., Malavazi, I., Da Silva Ferreira, M. E., Savoldi, M., Von Zeska Kress, M. R., De Souza Goldman, M. H., Loss, O., Bignell, E., & Goldman, G. H. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06122.x · Cited by 168
Serine/Threonine Protein Kinases and Phosphatases in Filamentious Fungi
Dickman, M. B., & Yarden, O. (1999) · Fungal Genetics and Biology · doi:10.1006/fgbi.1999.1118 · Cited by 164
Cruz, M. C., Fox, D. S., & Heitman, J. (2001) · The EMBO Journal · doi:10.1093/emboj/20.5.1020 · Cited by 150
Good fungi gone bad: The corruption of calcineurin
Fox, D. S., & Heitman, J. (2002) · BioEssays · doi:10.1002/bies.10157 · Cited by 137
In Vitro Interactions between Antifungals and Immunosuppressants against Aspergillus fumigatus
Steinbach, W. J., Schell, W. A., Blankenship, J. R., Onyewu, C., Heitman, J., & Perfect, J. R. (2004) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.48.5.1664-1669.2004 · Cited by 135
The information highways of a biotechnological workhorse – signal transduction in Hypocrea jecorina
Schmoll, M. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-430 · Cited by 134
Viaud, M., Simon, A., Brygoo, Y., Pradier, J., & Levis, C. (2003) · Molecular Microbiology · doi:10.1046/j.1365-2958.2003.03798.x · Cited by 129
Calcineurin Is Essential for Virulence in Candida albicans
Bader, T., Bodendorfer, B., Schröppel, K., & Morschhäuser, J. (2003) · Infection and Immunity · doi:10.1128/iai.71.9.5344-5354.2003 · Cited by 121
Functional characterization of the Aspergillus fumigatus calcineurin
Ferreira, M. E. D. S., Heinekamp, T., Härtl, A., Brakhage, A. A., Semighini, C. P., Harris, S. D., Savoldi, M., de Gouvêa, P. F., Goldman, M. H. D. S., & Goldman, G. H. (2007) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2006.08.004 · Cited by 121
Juvvadi, P. R., Lamoth, F., & Steinbach, W. J. (2014) · Fungal Biology Reviews · doi:10.1016/j.fbr.2014.02.004 · Cited by 116
Majetschak, M. (2010) · Journal of Leukocyte Biology · doi:10.1189/jlb.0510316 · Cited by 114
Harel, A., Bercovich, S., & Yarden, O. (2006) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-19-0682 · Cited by 112
Schumacher, J., Viaud, M., Simon, A., & Tudzynski, B. (2008) · Molecular Microbiology · doi:10.1111/j.1365-2958.2008.06105.x · Cited by 110
Comparison of Morphogenetic Networks of Filamentous Fungi and Yeast
Wendland, J. (2001) · Fungal Genetics and Biology · doi:10.1006/fgbi.2001.1290 · Cited by 104
Bowman, B. J., Drašković, M., Freitag, M., & Bowman, E. J. (2009) · Eukaryotic Cell · doi:10.1128/ec.00174-09 · Cited by 108
Cardenas, M. E., Cruz, M. C., Poeta, M. D., Chung, N., Perfect, J. R., & Heitman, J. (1999) · Clinical Microbiology Reviews · doi:10.1128/cmr.12.4.583 · Cited by 103
The N‐ and C‐terminal fragments of ubiquitin are important for the antimicrobial activities
Kieffer, A., Goumon, Y., Ruh, O., Chasserot‐Golaz, S., Nullans, G., Gasnier, C., Aunis, D., & Metz‐Boutigue, M. (2003) · The FASEB Journal · doi:10.1096/fj.02-0699fje · Cited by 102
Global Analysis of Serine-Threonine Protein Kinase Genes in Neurospora crassa
Park, G., Servin, J. A., Turner, G., Altamirano, L., Colot, H. V., Collopy, P. D., Litvinkova, L., Li, L., Jones, C., Diala, F. G. I., et al. (2011) · Eukaryotic Cell · doi:10.1128/ec.05140-11 · Cited by 102
Lugardon, K., Chasserot‐Golaz, S., Kieffer, A., Maget‐Dana, R., Nullans, G., Kieffer, B., Aunis, D., & Metz‐Boutigue, M. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m104670200 · Cited by 98
Cyclosporin A-resistance based gene placement system for Neurospora crassa
Bardiya, N., & Shiu, P. (2007) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2006.12.011 · Cited by 96
Lee, S. C., Li, A., Calo, S., Inoue, M., Tonthat, N. K., Bain, J. M., Louw, J., Shinohara, M. L., Erwig, L. P., Schumacher, M. A., et al. (2015) · Molecular Microbiology · doi:10.1111/mmi.13071 · Cited by 90
Delgado‐Jarana, J., Martínez-Rocha, A. L., Roldán-Rodríguez, R., Roncero, M. I. G., & Pietro, A. D. (2004) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2004.10.001 · Cited by 85
Calcium gradient dependence of Neurospora crassa hyphal growth
Silverman‐Gavrila, L. B., & Lew, R. R. (2003) · Microbiology · doi:10.1099/mic.0.26302-0 · Cited by 84
Juvvadi, P. R., Fortwendel, J. R., Rogg, L. E., Burns, K. A., Randell, S. H., & Steinbach, W. J. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07886.x · Cited by 80
Calcium signaling is involved in diverse cellular processes in fungi
Roy, A., Kumar, A., Baruah, D., & Tamuli, R. (2020) · Mycology: An International Journal on Fungal Biology · doi:10.1080/21501203.2020.1785962 · Cited by 76
Cruz, M. C., Sia, R. A. L., Olson, M. E., Cox, G. M., & Heitman, J. (2000) · Infection and Immunity · doi:10.1128/iai.68.2.982-985.2000 · Cited by 75
Kim, S., Hu, J., Oh, Y., Park, J., Choi, J., Lee, Y., Dean, R. A., & Mitchell, T. K. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000909 · Cited by 72
Innate immunity: involvement of new neuropeptides
Metz‐Boutigue, M., Kieffer, A., Goumon, Y., & Aunis, D. (2003) · Trends in Microbiology · doi:10.1016/j.tim.2003.10.001 · Cited by 70
Hagiwara, D., Kondo, A., Fujioka, T., & Abe, K. (2008) · Current Genetics · doi:10.1007/s00294-008-0220-z · Cited by 69
Regulation of the tip-high [Ca2+] gradient in growing hyphae of the fungus Neurospora crassa
Silverman‐Gavrila, L. B., & Lew, R. R. (2001) · European Journal of Cell Biology · doi:10.1078/0171-9335-00175 · Cited by 66
de Castro, P. A., Chen, C., Almeida, R. S., Freitas, F. Z., Bertolini, M. C., Morais, E. R., Brown, N. A., Ramalho, L. N. Z., Hagiwara, D., Mitchell, T. K., et al. (2014) · Molecular Microbiology · doi:10.1111/mmi.12785 · Cited by 54
Bowman, E. J., Kendle, R. F., & Bowman, B. J. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.1.167 · Cited by 56
Hyphal tip growth and nuclear migration
Xiang, X., & Morris, N. R. (1999) · Current Opinion in Microbiology · doi:10.1016/s1369-5274(99)00034-x · Cited by 54
Molecular cloning of the calcium and sodium ATPases in Neurospora crassa
Benito, B., Garcíadeblas, B., & Rodríguez‐Navarro, A. (2000) · Molecular Microbiology · doi:10.1046/j.1365-2958.2000.01776.x · Cited by 54
Cytoskeletal and Ca2+ regulation of hyphal tip growth and initiation
Torralba, S., & Heath, I. B. (2001) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(01)51005-4 · Cited by 54
Li, F., Wang, Z., Zhang, L.-B., Ying, S., & Feng, M. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-6124-6 · Cited by 53
Ghosh, A., Servin, J. A., Park, G., & Borkovich, K. A. (2013) · G3 Genes Genomes Genetics · doi:10.1534/g3.113.008813 · Cited by 48
Fox, D. S., & Heitman, J. (2005) · Eukaryotic Cell · doi:10.1128/ec.4.9.1526-1538.2005 · Cited by 47
Cabrera, I. E., Pacentine, I. V., Lim, A., Guerrero, N., Kryštofová, S., Li, L., Michkov, A. V., Servin, J. A., Ahrendt, S. R., Carrillo, A. J., et al. (2015) · G3 Genes Genomes Genetics · doi:10.1534/g3.115.020974 · Cited by 47
Juvvadi, P. R., Kuroki, Y., Arioka, M., Nakajima, H., & Kitamoto, K. (2003) · Archives of Microbiology · doi:10.1007/s00203-003-0546-3 · Cited by 44
Bowman, B. J., Abreu, S., Margolles‐Clark, E., Drašković, M., & Bowman, E. J. (2011) · Eukaryotic Cell · doi:10.1128/ec.00239-10 · Cited by 44
Protein phosphatase 2A is involved in hyphal growth of Neurospora crassa
Yatzkan, E., Szöőr, B., Fehér, Z., Dombrádi, V., & Yarden, O. (1998) · Molecular and General Genetics MGG · doi:10.1007/s004380050844 · Cited by 44
Cao, Y., Du, M., Luo, S., & Xia, Y. (2014) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-014-5876-3 · Cited by 43
de Campos, C. B. L., Benedette, J. P. T. D., Morais, F. V., Ovalle, R., & Nóbrega, M. P. (2008) · Eukaryotic Cell · doi:10.1128/ec.00110-08 · Cited by 42
Calcium and tip growth inNeurospora crassa
Silverman‐Gavrila, L. B., & Lew, R. R. (2000) · PROTOPLASMA · doi:10.1007/bf01282158 · Cited by 42
CYP1, a hypovirus‐regulated cyclophilin, is required for virulence in the chestnut blight fungus
CHEN, M., Jiang, M., Shang, J., Lan, X., Yang, F., HUANG, J., Nuss, D. L., & Chen, B. (2010) · Molecular Plant Pathology · doi:10.1111/j.1364-3703.2010.00665.x · Cited by 39
Yatzkan, E., & Yarden, O. (1999) · Molecular Microbiology · doi:10.1046/j.1365-2958.1999.01161.x · Cited by 38
Perkins, D. D., & Davis, R. H. (2000) · Fungal Genetics and Biology · doi:10.1006/fgbi.2000.1248 · Cited by 38
Calcineurin-Mediated Regulation of Hyphal Growth, Septation, and Virulence in Aspergillus fumigatus
Juvvadi, P. R., Lamoth, F., & Steinbach, W. J. (2014) · Mycopathologia · doi:10.1007/s11046-014-9794-9 · Cited by 35
Bormann, J., & Tudzynski, P. (2009) · Microbiology · doi:10.1099/mic.0.030825-0 · Cited by 35
Juvvadi, P. R., & Steinbach, W. J. (2015) · Pathogens · doi:10.3390/pathogens4040883 · Cited by 33
Tsai, H.-C., & Chung, K.-R. (2014) · Microbiology · doi:10.1099/mic.0.077818-0 · Cited by 31
Cinnamic acid inhibits the growth of the fungus Neurospora crassa, but is eliminated as acetophenone
Said, S., Neves, F. M., & Griffiths, A. J. F. (2004) · International Biodeterioration & Biodegradation · doi:10.1016/j.ibiod.2003.11.002 · Cited by 31
Gorovits, R., Propheta, O., Kolot, M. N., Dombrádi, V., & Yarden, O. (1999) · Fungal Genetics and Biology · doi:10.1006/fgbi.1999.1152 · Cited by 31
Sone, T., & Griffiths, A. J. F. (1999) · Fungal Genetics and Biology · doi:10.1006/fgbi.1999.1169 · Cited by 29
Warwar, V., Oved, S., & Dickman, M. B. (2000) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2000.tb09342.x · Cited by 27
Structure and Function Analysis of the Calcium-Related Gene spray in Neurospora crassa
Bok, J.-W., Sone, T., Silverman‐Gavrila, L. B., Lew, R. R., Bowring, F. J., Catcheside, D., & Griffiths, A. J. F. (2001) · Fungal Genetics and Biology · doi:10.1006/fgbi.2000.1259 · Cited by 25
Glutamate decarboxylase activity in Trichoderma viride conidia and developing mycelia
Strigáčová, J., Chovanec, P., Liptaj, T., Hudecová, D., Turský, T., Šimkovič, M., & Varečka, Ĺ. (2001) · Archives of Microbiology · doi:10.1007/s002030000235 · Cited by 24
Stephenson, K. S., Gow, N. A. R., Davidson, F. A., & Gadd, G. M. (2014) · Fungal Biology · doi:10.1016/j.funbio.2013.12.007 · Cited by 23
Bowman, B. J., Abreu, S., Johl, J., & Bowman, E. J. (2012) · Eukaryotic Cell · doi:10.1128/ec.00105-12 · Cited by 23
Tamuli, R., Deka, R., & Borkovich, K. A. (2016) · PLoS ONE · doi:10.1371/journal.pone.0151867 · Cited by 23
Expressed sequence tags from the phytopathogenic fungus Botrytis cinerea
Viaud, M., Legeai, F., Pradier, J., Brygoo, Y., Bitton, F., Weissenbach, J., Simon, A., Duclert, A., Fillinger, S., Fortini, D., et al. (2005) · European Journal of Plant Pathology · doi:10.1007/s10658-004-1429-4 · Cited by 22
Malavazi, I., Ferreira, M. E. D. S., Soriani, F. M., Dinamarco, T. M., Savoldi, M., Uyemura, S. A., Goldman, M. H. S., & Goldman, G. H. (2009) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2009.06.009 · Cited by 21
Virgílio, S., Cupertino, F. B., Ambrósio, D. L., & Bertolini, M. C. (2017) · BMC Genomics · doi:10.1186/s12864-017-3832-1 · Cited by 21
Kameshita, I., Yamada, Y., Nishida, T., Sugiyama, Y., Sueyoshi, N., Watanabe, A., & Asada, Y. (2007) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2007.05.008 · Cited by 20
Kim, M., Park, S.-M., Kim, Y.-H., Cha, B., Yang, M., & Kim, D. (2004) · Fungal Genetics and Biology · doi:10.1016/j.fgb.2003.12.006 · Cited by 19
Hoffmann, B., LaPaglia, S. K., Kübler, E., Andermann, M., Eckert, S. E., & Braus, G. H. (2000) · Molecular and General Genetics MGG · doi:10.1007/pl00008643 · Cited by 19
Hatano, E., Hashidoko, Y., Deora, A., Fukushi, Y., & Tahara, S. (2007) · Bioscience Biotechnology and Biochemistry · doi:10.1271/bbb.70119 · Cited by 17
Characterization of three FK506-binding proteins in the entomopathogenic fungus Beauveria bassiana
Li, Y., Ren, H., Zhao, Y., Sun, J., Fan, Y., Jin, D., & Pei, Y. (2020) · Journal of Invertebrate Pathology · doi:10.1016/j.jip.2020.107334 · Cited by 16
Immunosuppressive Compounds Affect the Fungal Growth and Viability of Defined Aspergillus Species
Schmidt, S., Hogardt, M., Demir, A., Roeger, F., & Lehrnbecher, T. (2019) · Pathogens · doi:10.3390/pathogens8040273 · Cited by 16
Scavello, F., Kharouf, N., Lavall�e, P., Haïkel, Y., Schneider, F., & Metz‐Boutigue, M. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.977175 · Cited by 16
Environmental sensing and the filamentous fungal lifestyle
Read, N. D. (2007) · Cambridge University Press eBooks · doi:10.1017/cbo9780511541797.004 · Cited by 16
Effect of benzene compounds from plants on the growth and hyphal morphology in Neurospora crassa
Neves, F. M., Kawano, C. Y., & Said, S. (2005) · Brazilian Journal of Microbiology · doi:10.1590/s1517-83822005000200016 · Cited by 15
A cDNA Clone for Cyclophilin from Griffithsia japonica and Phylogenetic Analysis of Cyclophilins
Lee, Y. K., Hong, C. B., Suh, Y., & Lee, I. K. (2002) · Molecules and Cells · doi:10.1016/s1016-8478(23)14998-3 · Cited by 15
Kumar, A., Roy, A., Deshmukh, M. V., & Tamuli, R. (2019) · Archives of Microbiology · doi:10.1007/s00203-019-01768-z · Cited by 15
Martı́n, J. F. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1225774 · Cited by 14
Branch initiation in Neurospora is influenced by events at the previous branch
Watters, M. K., Virag, A., Haynes, J., & Griffiths, A. J. F. (2000) · Mycological Research · doi:10.1017/s0953756299002348 · Cited by 14
Juvvadi, P. R., Arioka, M., Nakajima, H., & Kitamoto, K. (2001) · FEMS Microbiology Letters · doi:10.1111/j.1574-6968.2001.tb10881.x · Cited by 14
Hemenway, C. S., & Heitman, J. (1999) · Molecular and General Genetics MGG · doi:10.1007/s004380050980 · Cited by 14
In silico binding affinity study of calcineurin inhibitors to calcineurin and its close associates
Harish, B., Devaraju, K. S., Gopi, A., Saraswathi, R., Jatrana, A., Babu, R. L., & Sharma, S. (2013) · ePrints@Bangalore University (Bangalore University) · Cited by 13
Gohain, D., & Tamuli, R. (2019) · Molecular Microbiology · doi:10.1111/mmi.14234 · Cited by 13
A Phenylpropanoid Glycoside as a Calcineurin Inhibitor Isolated from Magnolia obovata Thunb.
Lee, W. J., Moon, J. S., Kim, S. I., Bahn, Y., Lee, H., Kang, T. H., Shin, H. M., & Kim, S. U. (2015) · Journal of Microbiology and Biotechnology · doi:10.4014/jmb.1506.06031 · Cited by 13
Martı́n, J. F. (2014) · Microbial Cell Factories · doi:10.1186/preaccept-1552442661133072 · Cited by 12
Mitić, M., Berry, D., Brasell, E. J., Green, K., Young, C. A., Saikia, S., Rakonjac, J., & Scott, B. (2017) · Molecular Plant Pathology · doi:10.1111/mpp.12624 · Cited by 12
Tsolakis, G., Parashi, E., Galland, P., & Kotzabasis, K. (1999) · Fungal Genetics and Biology · doi:10.1006/fgbi.1999.1175 · Cited by 12
Thewes, S., Krohn, S., Schmith, A., Herzog, S., Stach, T., Weissenmayer, B., & Mutzel, R. (2012) · European Journal of Cell Biology · doi:10.1016/j.ejcb.2012.07.006 · Cited by 10
Metadata
- Authors
- Prokisch, H., Yarden, O., Dieminger, M., Tropschug, M., & Barthelmess, I. B.
- Affiliations
- Leibniz University Hannover (DE)
- Hebrew University of Jerusalem (IL)
- University of Freiburg (DE)
- Venue
- Molecular and General Genetics MGG
- Published
- 1997-09
- Volume
- 256
- Issue
- 2
- Pages
- 104-114
- ISSN
- 0026-8925 (ISSN-L)
- 1432-1874
- OpenAlex
- W2049238469
- Cited by
- 125
- References
- 42
- Citations by year
- 2023: 2 · 2022: 1 · 2020: 3 · 2019: 3 · 2017: 3 · 2016: 3 · 2015: 4 · 2014: 9 · 2013: 4 · 2012: 5
- FWCI
- 2.73
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Molecular and General Genetics MGG (publishedVersion)
- PubMed (publishedVersion)
- FreiDok plus (Universitätsbibliothek Freiburg) (submittedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Signaling Pathways in Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
- Keywords
- calcineurin, Neurospora crassa, antisense RNA, hyphal growth, hyphal branching, hyphal morphology, cyclosporine, cyclophilin, FK506, calcineurin inhibitors, essential genes, mycelium
- MeSH terms
- Calcium, Cloning, Molecular, Immunosuppressive Agents, Neurospora crassa, Plasmids, Recombination, Genetic, RNA, Messenger, Transcription, Genetic, Transformation, Genetic, Gene Expression Regulation, Fungal, Gene Expression Regulation, Enzymologic, RNA, Antisense, Tacrolimus, Cyclosporine, Peptidylprolyl Isomerase, Calcineurin
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review