Journal articles: 'Physcomitrella patens'

1

Reski, Ralf, and David J. Cove. "Physcomitrella patens." Current Biology 14, no. 7 (April 2004): R261—R262. http://dx.doi.org/10.1016/j.cub.2004.03.016.

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Cove, David. "The Moss, Physcomitrella patens." Journal of Plant Growth Regulation 19, no. 3 (September 1, 2000): 275–83. http://dx.doi.org/10.1007/s003440000031.

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Zhou, Xun, Guan Nan Guo, Le Qi Wang, Su Lan Bai, Chun Li Li, Rong Yu, and Yan Hong Li. "Paenibacillus physcomitrellae sp. nov., isolated from the moss Physcomitrella patens." International Journal of Systematic and Evolutionary Microbiology 65, Pt_10 (October 1, 2015): 3400–3406. http://dx.doi.org/10.1099/ijsem.0.000428.

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A Gram-stain-positive, facultatively anaerobic and rod-shaped bacterium, designated strain XBT, was isolated from Physcomitrella patens growing in Beijing, China. The isolate was identified as a member of the genus Paenibacillus based on phenotypic characteristics and phylogenetic inferences. The novel strain was spore-forming, motile, catalase-negative and weakly oxidase-positive. Optimal growth of strain XBT occurred at 28°C and pH 7.0–7.5. The major polar lipids contained diphosphatidylglycerol, phosphatidylglycerol, phosphatidylethanolamine and several unidentified components, including one phospholipid, two aminophospholipids, three glycolipids, one aminolipid and one lipid. The predominant isoprenoid quinone was MK-7. The diamino acid found in the cell-wall peptidoglycan was meso-diaminopimelic acid. The major fatty acid components (>5 %) were anteiso-C15 : 0 (51.2 %), anteiso-C17 : 0 (20.6 %), iso-C16 : 0 (8.3 %) and C16 : 0 (6.7 %). The G+C content of the genomic DNA was 53.3 mol%. Phylogenetic analysis, based on the 16S rRNA gene sequence, showed that strain XBT fell within the evolutionary distances encompassed by the genus Paenibacillus; its closest phylogenetic neighbour was Paenibacillus yonginensis DCY84T (96.6 %). Based on phenotypic, chemotaxonomic and phylogenetic properties, strain XBT is considered to represent a novel species of the genus Paenibacillus, for which the name Paenibacillus physcomitrellae sp. nov., is proposed. The type strain is XBT ( = CGMCC 1.15044T = DSM 29851T).

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4

Schaefer, D. "Gene targeting in Physcomitrella patens." Current Opinion in Plant Biology 4, no. 2 (April 1, 2001): 143–50. http://dx.doi.org/10.1016/s1369-5266(00)00150-3.

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Cove, D. J., P. F. Perroud, A. J. Charron, S. F. McDaniel, A. Khandelwal, and R. S. Quatrano. "Culturing the Moss Physcomitrella patens." Cold Spring Harbor Protocols 2009, no. 2 (February 1, 2009): pdb.prot5136. http://dx.doi.org/10.1101/pdb.prot5136.

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Bricker, Terry M., Adam J. Bell, Lan Tran, Laurie K. Frankel, and Steven M. Theg. "Photoheterotrophic growth of Physcomitrella patens." Planta 239, no. 3 (November 27, 2013): 605–13. http://dx.doi.org/10.1007/s00425-013-2000-3.

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Sha, Wei, Li Wu, and Xiao Hong Song. "In Silicon Cloning and Bioinformatics Analysis of an Eukaryotic Initiation Factor 4E Gene from Grimmia pilifera." Applied Mechanics and Materials 138-139 (November 2011): 1132–38. http://dx.doi.org/10.4028/www.scientific.net/amm.138-139.1132.

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GH425 gene comes from the Grimmia pilifera drought stress of cDNA library.In this experiment,we have got the full sequence of GH425NO.1 by E-cloning which using GH425 as gene probe,in Physcomitrella patens DNA Datebase.Through using ORFfinder to find out the longest ORF and design primer for it,then, validated the Physcomitrella patens by PT-PCR,and we have obtained corresponding band and proved that the result of silicon cloning is correct and the fragment is contained in Grimmia pilifera P.Beauv.Now,we know the sequence encodes Eukaryotic initiation factor 4E by Blastx,and analysis it with Bioinformatics.

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8

Sarnighausen, Eric, Virginie Wurtz, Dimitri Heintz, Alain Van Dorsselaer, and Ralf Reski. "Mapping of the Physcomitrella patens proteome." Phytochemistry 65, no. 11 (June 2004): 1589–607. http://dx.doi.org/10.1016/j.phytochem.2004.04.028.

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9

Arazi, Tzahi. "MicroRNAs in the moss Physcomitrella patens." Plant Molecular Biology 80, no. 1 (March 4, 2011): 55–65. http://dx.doi.org/10.1007/s11103-011-9761-5.

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Scholz, Julia, Florian Brodhun, Ellen Hornung, Cornelia Herrfurth, Michael Stumpe, Anna K. Beike, Bernd Faltin, Wolfgang Frank, Ralf Reski, and Ivo Feussner. "Biosynthesis of allene oxides in Physcomitrella patens." BMC Plant Biology 12, no. 1 (2012): 228. http://dx.doi.org/10.1186/1471-2229-12-228.

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Schaefer, Didier G., and Jean-Pierre Zrÿd. "The Moss Physcomitrella patens, Now and Then." Plant Physiology 127, no. 4 (December 1, 2001): 1430–38. http://dx.doi.org/10.1104/pp.010786.

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12

Bezanilla, Magdalena, Aihong Pan, and Ralph S. Quatrano. "RNA Interference in the Moss Physcomitrella patens." Plant Physiology 133, no. 2 (October 2003): 470–74. http://dx.doi.org/10.1104/pp.103.024901.

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QUATRANO, R., S. MCDANIEL, A. KHANDELWAL, P. PERROUD, and D. COVE. "Physcomitrella patens: mosses enter the genomic age." Current Opinion in Plant Biology 10, no. 2 (April 2007): 182–89. http://dx.doi.org/10.1016/j.pbi.2007.01.005.

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14

Peramuna, Anantha, Hansol Bae, Erling Koch Rasmussen, Bjørn Dueholm, Thomas Waibel, Joanna H. Critchley, Kerstin Brzezek, Michael Roberts, and Henrik Toft Simonsen. "Evaluation of synthetic promoters in Physcomitrella patens." Biochemical and Biophysical Research Communications 500, no. 2 (June 2018): 418–22. http://dx.doi.org/10.1016/j.bbrc.2018.04.092.

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15

Schaefer, D., J. P. Zryd, C. D. Knight, and D. J. Cove. "Stable transformation of the moss Physcomitrella patens." Molecular and General Genetics MGG 226, no. 3 (May 1991): 418–24. http://dx.doi.org/10.1007/bf00260654.

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Prigge, M. J., and M. Bezanilla. "Evolutionary crossroads in developmental biology: Physcomitrella patens." Development 137, no. 21 (October 12, 2010): 3535–43. http://dx.doi.org/10.1242/dev.049023.

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17

Boyd, Philip J., Nigel H. Grimsley, and David J. Cove. "Somatic mutagenesis of the moss, Physcomitrella patens." Molecular and General Genetics MGG 211, no. 3 (March 1988): 545–46. http://dx.doi.org/10.1007/bf00425715.

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18

Krumm, Andrea. "Entwicklung eines Produktionsorganismus — das Moos Physcomitrella patens." BIOspektrum 26, no. 2 (March 2020): 187–88. http://dx.doi.org/10.1007/s12268-020-1350-1.

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19

Reski, Ralf, Hansol Bae, and Henrik Toft Simonsen. "Physcomitrella patens, a versatile synthetic biology chassis." Plant Cell Reports 37, no. 10 (May 24, 2018): 1409–17. http://dx.doi.org/10.1007/s00299-018-2293-6.

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20

Wu, Guochun, Sha Li, Xiaochuan Li, Yunhong Liu, Shuangshuang Zhao, Baohui Liu, Huapeng Zhou, and Honghui Lin. "A Functional Alternative Oxidase Modulates Plant Salt Tolerance in Physcomitrella patens." Plant and Cell Physiology 60, no. 8 (May 23, 2019): 1829–41. http://dx.doi.org/10.1093/pcp/pcz099.

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Abstract Alternative oxidase (AOX) has been reported to be involved in mitochondrial function and redox homeostasis, thus playing an essential role in plant growth as well as stress responses. However, its biological functions in nonseed plants have not been well characterized. Here, we report that AOX participates in plant salt tolerance regulation in moss Physcomitrella patens (P. patens). AOX is highly conserved and localizes to mitochondria in P. patens. We observed that PpAOX rescued the impaired cyanide (CN)-resistant alternative (Alt) respiratory pathway in Arabidopsis thaliana (Arabidopsis) aox1a mutant. PpAOX transcription and Alt respiration were induced upon salt stress in P. patens. Using homologous recombination, we generated PpAOX-overexpressing lines (PpAOX OX). PpAOX OX plants exhibited higher Alt respiration and lower total reactive oxygen species accumulation under salt stress condition. Strikingly, we observed that PpAOX OX plants displayed decreased salt tolerance. Overexpression of PpAOX disturbed redox homeostasis in chloroplasts. Meanwhile, chloroplast structure was adversely affected in PpAOX OX plants in contrast to wild-type (WT) P. patens. We found that photosynthetic activity in PpAOX OX plants was also lower compared with that in WT. Together, our work revealed that AOX participates in plant salt tolerance in P. patens and there is a functional link between mitochondria and chloroplast under challenging conditions.

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21

Ikram, Kashkooli, Peramuna, Krol, Bouwmeester, and Simonsen. "Insights into Heterologous Biosynthesis of Arteannuin B and Artemisinin in Physcomitrella patens." Molecules 24, no. 21 (October 23, 2019): 3822. http://dx.doi.org/10.3390/molecules24213822.

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: Metabolic engineering is an integrated bioengineering approach, which has made considerable progress in producing terpenoids in plants and fermentable hosts. Here, the full biosynthetic pathway of artemisinin, originating from Artemisia annua, was integrated into the moss Physcomitrella patens. Different combinations of the five artemisinin biosynthesis genes were ectopically expressed in P. patens to study biosynthesis pathway activity, but also to ensure survival of successful transformants. Transformation of the first pathway gene, ADS, into P. patens resulted in the accumulation of the expected metabolite, amorpha-4,11-diene, and also accumulation of a second product, arteannuin B. This demonstrates the presence of endogenous promiscuous enzyme activity, possibly cytochrome P450s, in P. patens. Introduction of three pathway genes, ADS-CYP71AV1-ADH1 or ADS-DBR2-ALDH1 both led to the accumulation of artemisinin, hinting at the presence of one or more endogenous enzymes in P. patens that can complement the partial pathways to full pathway activity. Transgenic P. patens lines containing the different gene combinations produce artemisinin in varying amounts. The pathway gene expression in the transgenic moss lines correlates well with the chemical profile of pathway products. Moreover, expression of the pathway genes resulted in lipid body formation in all transgenic moss lines, suggesting that these may have a function in sequestration of heterologous metabolites. This work thus provides novel insights into the metabolic response of P. patens and its complementation potential for A. annua artemisinin pathway genes. Identification of the related endogenous P. patens genes could contribute to a further successful metabolic engineering of artemisinin biosynthesis, as well as bioengineering of other high-value terpenoids in P. patens.

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22

Luo, Weifeng, Setsuko Komatsu, Tatsuya Abe, Hideyuki Matsuura, and Kosaku Takahashi. "Comparative Proteomic Analysis of Wild-Type Physcomitrella Patens and an OPDA-Deficient Physcomitrella Patens Mutant with Disrupted PpAOS1 and PpAOS2 Genes after Wounding." International Journal of Molecular Sciences 21, no. 4 (February 19, 2020): 1417. http://dx.doi.org/10.3390/ijms21041417.

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Wounding is a serious environmental stress in plants. Oxylipins such as jasmonic acid play an important role in defense against wounding. Mechanisms to adapt to wounding have been investigated in vascular plants; however, those mechanisms in nonvascular plants remain elusive. To examine the response to wounding in Physcomitrella patens, a model moss, a proteomic analysis of wounded P. patens was conducted. Proteomic analysis showed that wounding increased the abundance of proteins related to protein synthesis, amino acid metabolism, protein folding, photosystem, glycolysis, and energy synthesis. 12-Oxo-phytodienoic acid (OPDA) was induced by wounding and inhibited growth. Therefore, OPDA is considered a signaling molecule in this plant. Proteomic analysis of a P. patens mutant in which the PpAOS1 and PpAOS2 genes, which are involved in OPDA biosynthesis, are disrupted showed accumulation of proteins involved in protein synthesis in response to wounding in a similar way to the wild-type plant. In contrast, the fold-changes of the proteins in the wild-type plant were significantly different from those in the aos mutant. This study suggests that PpAOS gene expression enhances photosynthesis and effective energy utilization in response to wounding in P. patens.

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23

Odahara, Masaki. "Factors Affecting Organelle Genome Stability in Physcomitrella patens." Plants 9, no. 2 (January 23, 2020): 145. http://dx.doi.org/10.3390/plants9020145.

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Organelle genomes are essential for plants; however, the mechanisms underlying the maintenance of organelle genomes are incompletely understood. Using the basal land plant Physcomitrella patens as a model, nuclear-encoded homologs of bacterial-type homologous recombination repair (HRR) factors have been shown to play an important role in the maintenance of organelle genome stability by suppressing recombination between short dispersed repeats. In this review, I summarize the factors and pathways involved in the maintenance of genome stability, as well as the repeats that cause genomic instability in organelles in P. patens, and compare them with findings in other plant species. I also discuss the relationship between HRR factors and organelle genome structure from the evolutionary standpoint.

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24

Schaefer, Didier G., and Jean-Pierre Zryd. "Efficient gene targeting in the moss Physcomitrella patens." Plant Journal 11, no. 6 (June 1997): 1195–206. http://dx.doi.org/10.1046/j.1365-313x.1997.11061195.x.

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25

Miyazaki, Sho, Mariho Hara, Shinsaku Ito, Keisuke Tanaka, Tadao Asami, Ken-ichiro Hayashi, Hiroshi Kawaide, and Masatoshi Nakajima. "An Ancestral Gibberellin in a Moss Physcomitrella patens." Molecular Plant 11, no. 8 (August 2018): 1097–100. http://dx.doi.org/10.1016/j.molp.2018.03.010.

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26

Mueller, Stefanie J., Sebastian N. W. Hoernstein, and Ralf Reski. "The mitochondrial proteome of the moss Physcomitrella patens." Mitochondrion 33 (March 2017): 38–44. http://dx.doi.org/10.1016/j.mito.2016.07.007.

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27

Martínez-Cortés, Teresa, Federico Pomar, Fuencisla Merino, and Esther Novo-Uzal. "A proteomic approach to Physcomitrella patens rhizoid exudates." Journal of Plant Physiology 171, no. 17 (November 2014): 1671–78. http://dx.doi.org/10.1016/j.jplph.2014.08.004.

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Liu, Yunhong, Qianyuan Gong, Jiaxian He, Xia Sun, Xiaochuan Li, Shuangshuang Zhao, Qingwei Meng, Honghui Lin, and Huapeng Zhou. "PpAOX regulates ER stress tolerance in Physcomitrella patens." Journal of Plant Physiology 251 (August 2020): 153218. http://dx.doi.org/10.1016/j.jplph.2020.153218.

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29

Smidkova, M., M. Hola, and K. J. Angelis. "Efficient biolistic transformation of the moss Physcomitrella patens." Biologia plantarum 54, no. 4 (December 1, 2010): 777–80. http://dx.doi.org/10.1007/s10535-010-0141-9.

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30

Fojtová, Miloslava, Eva Sýkorová, Lucie Najdekrová, Pavla Polanská, Dagmar Zachová, Radka Vagnerová, Karel J. Angelis, and Jiří Fajkus. "Telomere dynamics in the lower plant Physcomitrella patens." Plant Molecular Biology 87, no. 6 (February 21, 2015): 591–601. http://dx.doi.org/10.1007/s11103-015-0299-9.

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31

ASHTON, NEIL W., CONNIE E. M. CHAMPAGNE, TRACEY WEILER, and LAURENT K. VERKOCZY. "The bryophyte Physcomitrella patens replicates extrachromosomal transgenic elements." New Phytologist 146, no. 3 (June 2000): 391–402. http://dx.doi.org/10.1046/j.1469-8137.2000.00671.x.

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32

Tran, M. L., and A. W. Roberts. "Cellulose synthase gene expression profiling of Physcomitrella patens." Plant Biology 18, no. 3 (December 7, 2015): 362–68. http://dx.doi.org/10.1111/plb.12416.

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33

Agarwal, Tanushree, Gouranga Upadhyaya, Tanmoy Halder, Abhishek Mukherjee, Arun Lahiri Majumder, and Sudipta Ray. "Different dehydrins perform separate functions in Physcomitrella patens." Planta 245, no. 1 (September 16, 2016): 101–18. http://dx.doi.org/10.1007/s00425-016-2596-1.

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Banerjee, Aparajita, Jonathan A. Arnesen, Daniel Moser, Balindile B. Motsa, Sean R. Johnson, and Bjoern Hamberger. "Engineering modular diterpene biosynthetic pathways in Physcomitrella patens." Planta 249, no. 1 (November 23, 2018): 221–33. http://dx.doi.org/10.1007/s00425-018-3053-0.

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35

Schlink, Katja, and Ralf Reski. "Preparing high-quality DNA from moss (Physcomitrella patens)." Plant Molecular Biology Reporter 20, no. 4 (December 2002): 423. http://dx.doi.org/10.1007/bf02772133.

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36

von Schwartzenberg, K., W. Schultze, and H. Kassner. "The moss Physcomitrella patens releases a tetracyclic diterpene." Plant Cell Reports 22, no. 10 (February 12, 2004): 780–86. http://dx.doi.org/10.1007/s00299-004-0754-6.

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37

Zhao, Mengkai, Qilong Li, Zhenhua Chen, Qiang Lv, Fang Bao, Xiaoqin Wang, and Yikun He. "Regulatory Mechanism of ABA and ABI3 on Vegetative Development in the Moss Physcomitrella patens." International Journal of Molecular Sciences 19, no. 9 (September 12, 2018): 2728. http://dx.doi.org/10.3390/ijms19092728.

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The moss Physcomitrella patens is a model system for studying plant developmental processes. ABSCISIC ACID INSENSITIVE3 (ABI3), a transcription factor of the ABA signaling pathway, plays an important role in plant growth and development in vascular plant. To understand the regulatory mechanism of ABA and PpABI3 on vegetative development in Physcomitrella patens, we applied physiological, cellular, and RNA-seq analyses in wild type (WT) plants and ∆abi3 mutants. During ABA treatment, the growth of gametophytes was inhibited to a lesser extent ∆abi3 plants compared with WT plants. Microscopic observation indicated that the differentiation of caulonemata from chloronemata was accelerated in ∆abi3 plants when compared with WT plants, with or without 10 μM of ABA treatment. Under normal conditions, auxin concentration in ∆abi3 plants was markedly higher than that in WT plants. The auxin induced later differentiation of caulonemata from chloronemata, and the phenotype of ∆abi3 plants was similar to that of WT plants treated with exogenous indole-3-acetic acid (IAA). RNA-seq analysis showed that the PpABI3-regulated genes overlapped with genes regulated by the ABA treatment, and about 78% of auxin-related genes regulated by the ABA treatment overlapped with those regulated by PpABI3. These results suggested that ABA affected vegetative development partly through PpABI3 regulation in P. patens; PpABI3 is a negative regulator of vegetative development in P. patens, and the vegetative development regulation by ABA and PpABI3 might occur by regulating the expression of auxin-related genes. PpABI3 might be associated with cross-talk between ABA and auxin in P. patens.

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38

Mahmood, Niaz, and Nahid Tamanna. "Analyses of Physcomitrella patens Ankyrin Repeat Proteins by Computational Approach." Molecular Biology International 2016 (June 27, 2016): 1–8. http://dx.doi.org/10.1155/2016/9156735.

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Ankyrin (ANK) repeat containing proteins are evolutionary conserved and have functions in crucial cellular processes like cell cycle regulation and signal transduction. In this study, through an entirely in silico approach using the first release of the moss genome annotation, we found that at least 54 ANK proteins are present in P. patens. Based on their differential domain composition, the identified ANK proteins were classified into nine subfamilies. Comparative analysis of the different subfamilies of ANK proteins revealed that P. patens contains almost all the known subgroups of ANK proteins found in the other angiosperm species except for the ones having the TPR domain. Phylogenetic analysis using full length protein sequences supported the subfamily classification where the members of the same subfamily almost always clustered together. Synonymous divergence (dS) and nonsynonymous divergence (dN) ratios showed positive selection for the ANK genes of P. patens which probably helped them to attain significant functional diversity during the course of evolution. Taken together, the data provided here can provide useful insights for future functional studies of the proteins from this superfamily as well as comparative studies of ANK proteins.

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39

Greenwood, Joshua L., and Lloyd R. Stark. "The rate of drying determines the extent of desiccation tolerance in Physcomitrella patens." Functional Plant Biology 41, no. 5 (2014): 460. http://dx.doi.org/10.1071/fp13257.

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The effect of differential drying rates on desiccation tolerance in Physcomitrella patens (Hedw.) Bruch & Schimp. is examined. In order to provide more evidence as to the status of desiccation tolerance in P. patens, a system was designed that allowed alteration of the rate of water loss within a specific relative humidity. An artificial substrate consisting of layers of wetted filter paper was used to slow the drying process to as long as 284 h, a significant increase over the commonly used method of exposure (saturated salt solution). By slowing the rate of drying, survival rates and chlorophyll fluorescence parameters improved, and tissue regeneration time was faster. These results indicate a trend where the capacity for desiccation tolerance increases with slower drying, and reveal a much stronger capacity for desiccation tolerance in P. patens than was previously known.

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40

Galotto, Giulia, Isidro Abreu, Catherine Sherman, Boyuan Liu, Manuel Gonzalez-Guerrero, and Luis Vidali. "Chitin Triggers Calcium-Mediated Immune Response in the Plant Model Physcomitrella patens." Molecular Plant-Microbe Interactions® 33, no. 7 (July 2020): 911–20. http://dx.doi.org/10.1094/mpmi-03-20-0064-r.

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A characteristic feature of a plant immune response is the increase of the cytosolic calcium (Ca2+) concentration following infection, which results in the downstream activation of immune response regulators. The bryophyte Physcomitrella patens has been shown to mount an immune response when exposed to bacteria, fungi, or chitin elicitation, in a manner similar to the one observed in Arabidopsis thaliana. Nevertheless, whether the response of P. patens to microorganism exposure is Ca2+ mediated is currently unknown. Here, we show that P. patens plants treated with chitin oligosaccharides exhibit Ca2+ oscillations, and that a calcium ionophore can stimulate the expression of defense-related genes. Treatment with chitin oligosaccharides also results in an inhibition of growth, which can be explained by the depolymerization of the apical actin cytoskeleton of tip growing cells. These results suggest that chitin-triggered calcium oscillations are conserved and were likely present in the common ancestor of bryophytes and vascular plants.

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41

Richter, Hanna, Reinhard Lieberei, Miroslav Strnad, Ondrej Novák, Jiri Gruz, Stefan A. Rensing, and Klaus von Schwartzenberg. "Polyphenol oxidases in Physcomitrella: functional PPO1 knockout modulates cytokinin-dependent developmentin the moss Physcomitrella patens." Journal of Experimental Botany 63, no. 14 (August 29, 2012): 5121–35. http://dx.doi.org/10.1093/jxb/ers169.

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42

Sun, Ming-Ming, Lin-Hui Li, Hua Xie, Rong-Cai Ma, and Yi-Kun He. "Differentially Expressed Genes under Cold Acclimation in Physcomitrella patens." BMB Reports 40, no. 6 (November 30, 2007): 986–1001. http://dx.doi.org/10.5483/bmbrep.2007.40.6.986.

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43

Leech, Mark J., Wolfgang Kammerer, David J. Cove, Cathie Martin, and Trevor L. Wang. "Expression ofmyb-related genes in the moss,Physcomitrella patens." Plant Journal 3, no. 1 (January 1993): 51–61. http://dx.doi.org/10.1046/j.1365-313x.1993.t01-3-00999.x.

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44

Ludwig-Müller, Jutta, Sabine Jülke, Nicole M. Bierfreund, Eva L. Decker, and Ralf Reski. "Moss (Physcomitrella patens ) GH3 proteins act in auxin homeostasis." New Phytologist 181, no. 2 (November 21, 2008): 323–38. http://dx.doi.org/10.1111/j.1469-8137.2008.02677.x.

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45

Oda, Yoshihisa, Aiko Hirata, Toshio Sano, Tomomichi Fujita, Yuji Hiwatashi, Yoshikatsu Sato, Akeo Kadota, Mitsuyasu Hasebe, and Seiichiro Hasezawa. "Microtubules Regulate Dynamic Organization of Vacuoles in Physcomitrella patens." Plant and Cell Physiology 50, no. 4 (February 27, 2009): 855–68. http://dx.doi.org/10.1093/pcp/pcp031.

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46

Zobell, O., G. Coupland, and B. Reiss. "The Family of CONSTANS‐Like Genes in Physcomitrella patens." Plant Biology 7, no. 3 (May 2005): 266–75. http://dx.doi.org/10.1055/s-2005-865621.

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47

Skripnikov, A. Yu, N. B. Polyakov, E. V. Tolcheva, V. V. Velikodvorskaya, S. V. Dolgov, I. A. Demina, M. A. Rogova, and V. M. Govorun. "Proteome analysis of the moss Physcomitrella patens (Hedw.) B.S.G." Biochemistry (Moscow) 74, no. 5 (May 2009): 480–90. http://dx.doi.org/10.1134/s0006297909050022.

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48

Bressendorff, Simon, Raquel Azevedo, Chandra Shekar Kenchappa, Inés Ponce de León, Jakob V. Olsen, Magnus Wohlfahrt Rasmussen, Gitte Erbs, Mari-Anne Newman, Morten Petersen, and John Mundy. "An Innate Immunity Pathway in the Moss Physcomitrella patens." Plant Cell 28, no. 6 (June 2016): 1328–42. http://dx.doi.org/10.1105/tpc.15.00774.

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49

Itoh, Ryuuichi D., Katsuaki Takechi, Akihiro Hayashida, Shin-ichiro Katsura, and Hiroyoshi Takano. "Two minD Genes in Physcomitrella patens Are Functionally Redundant." CYTOLOGIA 70, no. 1 (2005): 87–92. http://dx.doi.org/10.1508/cytologia.70.87.

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Reski, Ralf, Merle Faust, Xiao-Hui Wang, Michael Wehe, and Wolfgang O. Abel. "Genome analysis of the moss Physcomitrella patens (Hedw.) B.S.G." Molecular and General Genetics MGG 244, no. 4 (July 1994): 352–59. http://dx.doi.org/10.1007/bf00286686.

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Journal articles on the topic 'Physcomitrella patens'

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