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The Dynamic Shift in Mitochondria from Mature Pollen Grains
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/j.1537-2197.1979.tb06206.xopenalex-extracted
ORGANELLE SIZE AND NUMBER IN FERTILE AND T‐CYTOPLASMIC MALE‐STERILE CORN
inferredcites →https://doi.org/10.1007/978-1-0716-1653-6_2openalex-extracted
Cell Type–Specific Isolation of Mitochondria in Arabidopsis
inferredcites →https://doi.org/10.1007/s00122-023-04398-8openalex-extracted
Molecular genetics of cytoplasmic male sterility and restorer-of-fertility for the fine tuning of pollen production in crops
inferredcites →https://doi.org/10.1007/s004250050606openalex-extracted
The selective increase or decrease of organellar DNA in generative cells just after pollen mitosis one controls cytoplasmic inheritance
inferredcites →https://doi.org/10.1007/s00497-022-00452-5openalex-extracted
Regulatory dynamics of gene expression in the developing male gametophyte of Arabidopsis
inferredcites →https://doi.org/10.1007/s004970000022openalex-extracted
Regulation of LAT52 promoter activity during pollen tube growth through the pistil of Nicotiana alata .
inferredcites →https://doi.org/10.1016/j.bbamcr.2012.10.009openalex-extracted
Calcium - a central regulator of pollen germination and tube growth
inferredcites →https://doi.org/10.1016/j.gene.2018.05.102openalex-extracted
Genome-wide identification and analysis of MICU genes in land plants and their potential role in calcium stress
inferredcites →https://doi.org/10.1016/j.pbi.2021.102118openalex-extracted
From birth to function: Male gametophyte development in flowering plants
inferredcites →https://doi.org/10.1021/pr400304ropenalex-extracted
Degradation Rate of Mitochondrial Proteins in Arabidopsis thaliana Cells
inferredcites →https://doi.org/10.1038/nbt.1511openalex-extracted
MaxQuant enables high peptide identification rates, individualized p.p.b.-range mass accuracies and proteome-wide protein quantification
inferredcites →https://doi.org/10.1038/s41467-017-01323-8openalex-extracted
Structural basis for receptor recognition of pollen tube attraction peptides
inferredcites →https://doi.org/10.1038/s41467-022-35486-wopenalex-extracted
Bioenergetics of pollen tube growth in Arabidopsis thaliana revealed by ratiometric genetically encoded biosensors
inferredcites →https://doi.org/10.1038/s41477-023-01538-2openalex-extracted
Targeted knockout of a conserved plant mitochondrial gene by genome editing
inferredcites →https://doi.org/10.1038/s41588-023-01505-9openalex-extracted
Molecular basis for maternal inheritance of human mitochondrial DNA
inferredcites →https://doi.org/10.1080/14789450.2022.2160324openalex-extracted
Proteomic repository data submission, dissemination, and reuse: key messages
inferredcites →https://doi.org/10.1080/15592324.2023.2271799openalex-extracted
An Arabidopsis mutant line lacking the mitochondrial calcium transport regulator MICU shows an altered metabolite profile
inferredcites →https://doi.org/10.1093/aob/mcs070openalex-extracted
Water status and associated processes mark critical stages in pollen development and functioning
inferredcites →https://doi.org/10.1093/bioinformatics/btp101openalex-extracted
ClueGO: a Cytoscape plug-in to decipher functionally grouped gene ontology and pathway annotation networks
inferredcites →https://doi.org/10.1093/jxb/ern355openalex-extracted
Male gametophyte development: a molecular perspective
inferredcites →https://doi.org/10.1093/nar/gkw1041openalex-extracted
SUBA4: the interactive data analysis centre for Arabidopsis subcellular protein locations
inferredcites →https://doi.org/10.1093/pcp/pcq066openalex-extracted
MALE GAMETOPHYTE DEFECTIVE 1, Encoding the FAd Subunit of Mitochondrial F1F0-ATP Synthase, is Essential for Pollen Formation in Arabidopsis thaliana
inferredcites →https://doi.org/10.1093/plphys/kiac082openalex-extracted
orf137 triggers cytoplasmic male sterility in tomato
inferredcites →https://doi.org/10.1101/gr.1239303openalex-extracted
Cytoscape: A Software Environment for Integrated Models of Biomolecular Interaction Networks
inferredcites →https://doi.org/10.1104/pp.003970openalex-extracted
NPSN11 Is a Cell Plate-Associated SNARE Protein That Interacts with the Syntaxin KNOLLE
inferredcites →https://doi.org/10.1104/pp.15.00437openalex-extracted
Elevation of Pollen Mitochondrial DNA Copy Number by WHIRLY2: Altered Respiration and Pollen Tube Growth in Arabidopsis
inferredcites →https://doi.org/10.1104/pp.18.00754openalex-extracted
The Mitochondrial Endonuclease M20 Participates in the Down-Regulation of Mitochondrial DNA in Pollen Cells
inferredcites →https://doi.org/10.1104/pp.20.00136openalex-extracted
Mitochondrial CLPP2 Assists Coordination and Homeostasis of Respiratory Complexes
inferredcites →https://doi.org/10.1105/tpc.107.055756openalex-extracted
EMB2473/MIRO1, anArabidopsisMiro GTPase, Is Required for Embryogenesis and Influences Mitochondrial Morphology in Pollen
inferredcites →https://doi.org/10.1105/tpc.15.00509openalex-extracted
The EF-Hand Ca2+ Binding Protein MICU Choreographs Mitochondrial Ca2+ Dynamics in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-2818.2012.03628.xopenalex-extracted
On the fast lane: mitochondria structure, dynamics and function in growing pollen tubes
inferredcites →https://doi.org/10.1111/j.1365-313x.2004.02016.xopenalex-extracted
mapman : a user‐driven tool to display genomics data sets onto diagrams of metabolic pathways and other biological processes
inferredcites →https://doi.org/10.1111/j.1365-313x.2010.04389.xopenalex-extracted
Fewer genes than organelles: extremely low and variable gene copy numbers in mitochondria of somatic plant cells
inferredcites →https://doi.org/10.1111/j.1399-3054.2005.00521.xopenalex-extracted
Preparation of leaf mitochondria from Arabidopsis thaliana
inferredcites →https://doi.org/10.1111/jipb.12642openalex-extracted
Calcium imaging in Arabidopsis pollen cells using G‐CaMP5
inferredcites →https://doi.org/10.1111/nph.15189openalex-extracted
Arabidopsis pollen tube germination and growth depend on the mitochondrial calcium uniporter complex
inferredcites →https://doi.org/10.1111/nph.17822openalex-extracted
The Angiosperm Terrestrial Revolution and the origins of modern biodiversity
inferredcites →https://doi.org/10.1111/tpj.13312openalex-extracted
A high resolution map of the Arabidopsis thaliana developmental transcriptome based on RNA ‐seq profiling
inferredcites →https://doi.org/10.1111/tpj.14723openalex-extracted
Tissue‐specific isolation of Arabidopsis/plant mitochondria – IMTACT (isolation of mitochondria tagged in specific cell types)
inferredcites →https://doi.org/10.1111/tpj.15715openalex-extracted
TALEN ‐mediated depletion of the mitochondrial gene orf312 proves that it is a Tadukan‐type cytoplasmic male sterility‐causative gene in rice
inferredcites →https://doi.org/10.1146/annurev-arplant-080620-021907openalex-extracted
Reproduction Multitasking: The Male Gametophyte
inferredcites →https://doi.org/10.1186/gb-2004-5-11-r85openalex-extracted
Transcriptome analysis of haploid male gametophyte development in Arabidopsis
inferredcites →https://doi.org/10.1242/dev.109.3.705openalex-extracted
Pollen-specific gene expression in transgenic plants: coordinate regulation of two different tomato gene promoters during microsporogenesis
inferredcites →https://doi.org/10.3390/ijms20020420openalex-extracted
Calcium: A Critical Factor in Pollen Germination and Tube Elongation
inferredcites →https://doi.org/10.3732/ajb.1700201openalex-extracted
Pollen wall degradation in the Brassicaceae permits cell emergence after pollination
inferredcites →https://doi.org/10.4161/15592324.2014.977200openalex-extracted
Pollen tube growth: where does the energy come from?
inferredcites →https://doi.org/10.7554/elife.60513openalex-extracted
Structural insights into the Ca2+-dependent gating of the human mitochondrial calcium uniporter
inferredcites →https://doi.org/10.1101/gr.089060.108openalex-snapshot
Deterministic protein inference for shotgun proteomics data provides new insights into Arabidopsis pollen development and function
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