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Auxin-mediated developmental control in the moss Physcomitrella patens
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9781444316070.ch10openalex-snapshot
Hormonal Regulation of Development by Auxin and Cytokinin in Moss
inferredcites →https://doi.org/10.1002/9781444316070.ch7openalex-snapshot
Gametangia Development in the MossPhyscomitrella patens
inferredcites →https://doi.org/10.1007/bf00262639openalex-snapshot
Comparison of mechanisms controlling uptake and accumulation of 2,4-dichlorophenoxy acetic acid, naphthalene-1-acetic acid, and indole-3-acetic acid in suspension-cultured tobacco cells
inferredcites →https://doi.org/10.1007/bf00380118openalex-snapshot
Analysis of gametophytic development in the moss, Physcomitrella patens, using auxin and cytokinin resistant mutants
inferredcites →https://doi.org/10.1007/bf00391040openalex-snapshot
Estimation of indole-3-acetic acid in gametophytes of the moss, Physcomitrella patens
inferredcites →https://doi.org/10.1007/bf00392232openalex-snapshot
Induction of budding on chloronemata and caulonemata of the moss, Physcomitrella patens, using isopentenyladenine
inferredcites →https://doi.org/10.1007/s00299-003-0646-1openalex-snapshot
Use of an inducible reporter gene system for the analysis of auxin distribution in the moss Physcomitrella patens
inferredcites →https://doi.org/10.1007/s004250050391openalex-snapshot
Expression of the bacterial ipt gene in Physcomitrella rescues mutations in budding and in plastid division
inferredcites →https://doi.org/10.1007/s11103-007-9176-5openalex-snapshot
The moss genes PpSKI1 and PpSKI2 encode nuclear SnRK1 interacting proteins with homologues in vascular plants
inferredcites →https://doi.org/10.1016/j.cell.2008.01.047openalex-snapshot
TAA1-Mediated Auxin Biosynthesis Is Essential for Hormone Crosstalk and Plant Development
inferredcites →https://doi.org/10.1016/j.cell.2008.01.049openalex-snapshot
Rapid Synthesis of Auxin via a New Tryptophan-Dependent Pathway Is Required for Shade Avoidance in Plants
inferredcites →https://doi.org/10.1016/j.cub.2009.02.050openalex-snapshot
Local Cues and Asymmetric Cell Divisions Underpin Body Plan Transitions in the Moss Physcomitrella patens
inferredcites →https://doi.org/10.1016/j.cub.2010.08.050openalex-snapshot
Physcomitrella patens Auxin-Resistant Mutants Affect Conserved Elements of an Auxin-Signaling Pathway
inferredcites →https://doi.org/10.1016/j.cub.2013.11.017openalex-snapshot
cis-Regulatory Requirements for Tissue-Specific Programs of the Circadian Clock
inferredcites →https://doi.org/10.1016/j.cub.2014.09.054openalex-snapshot
Plasma Membrane-Targeted PIN Proteins Drive Shoot Development in a Moss
inferredcites →https://doi.org/10.1016/j.cub.2014.09.056openalex-snapshot
Directional Auxin Transport Mechanisms in Early Diverging Land Plants
inferredcites →https://doi.org/10.1016/j.devcel.2013.12.008openalex-snapshot
Auxin-Callose-Mediated Plasmodesmal Gating Is Essential for Tropic Auxin Gradient Formation and Signaling
inferredcites →https://doi.org/10.1016/j.devcel.2016.01.010openalex-snapshot
Ancient trans-Acting siRNAs Confer Robustness and Sensitivity onto the Auxin Response
inferredcites →https://doi.org/10.1016/j.molp.2015.12.002openalex-snapshot
A Transcriptome Atlas of Physcomitrella patens Provides Insights into the Evolution and Development of Land Plants
inferredcites →https://doi.org/10.1016/j.pbi.2012.09.008openalex-snapshot
Physcomitrella patens: a model for tip cell growth and differentiation
inferredcites →https://doi.org/10.1016/j.pbi.2013.10.007openalex-snapshot
Eight types of stem cells in the life cycle of the moss Physcomitrella patens
inferredcites →https://doi.org/10.1016/j.pbi.2014.06.006openalex-snapshot
Diversity and specificity: auxin perception and signaling through the TIR1/AFB pathway
inferredcites →https://doi.org/10.1016/j.plaphy.2015.10.013openalex-snapshot
Knockout of GH3 genes in the moss Physcomitrella patens leads to increased IAA levels at elevated temperature and in darkness
inferredcites →https://doi.org/10.1016/j.tplants.2009.11.003openalex-snapshot
TCP genes: a family snapshot ten years later
inferredcites →https://doi.org/10.1016/j.tplants.2012.08.009openalex-snapshot
Origin and evolution of PIN auxin transporters in the green lineage
inferredcites →https://doi.org/10.1016/j.ydbio.2012.05.039openalex-snapshot
AUXOLOGY: When auxin meets plant evo-devo
inferredcites →https://doi.org/10.1016/s0044-328x(79)80253-6openalex-snapshot
Interaction of Auxin, Antiauxin and Cytokinin in Relation to the Formation of Buds in Moss Protonema
inferredcites →https://doi.org/10.1016/s0044-328x(83)80189-5openalex-snapshot
The Hormonal Regulation of Protonema Development in Mosses I. Auxin-Cytokinin Interaction
inferredcites →https://doi.org/10.1016/s0176-1617(11)80628-0openalex-snapshot
The Physiological Role of Indole Acetic Acid in the Moss Funaria Hygrometrica Hedw.
inferredcites →https://doi.org/10.1016/s0176-1617(11)80629-2openalex-snapshot
The Physiological Role of Indole Acetic Acid in the Moss Funaria hygrometrica Hedw.
inferredcites →https://doi.org/10.1021/cb200404copenalex-snapshot
Rational Design of an Auxin Antagonist of the SCF TIR1 Auxin Receptor Complex
inferredcites →https://doi.org/10.1038/nature10791openalex-snapshot
A novel sensor to map auxin response and distribution at high spatio-temporal resolution
inferredcites →https://doi.org/10.1038/newbio245223a0openalex-snapshot
Auxin Regulation of Caulonema Formation in Moss Protonema
inferredcites →https://doi.org/10.1038/s41598-019-51632-9openalex-snapshot
Mutations in Glucan, Water Dikinase Affect Starch Degradation and Gametophore Development in the Moss Physcomitrella patens
inferredcites →https://doi.org/10.1055/s-2002-35440openalex-snapshot
Day Length and Temperature Strongly Influence Sexual Reproduction and Expression of a Novel MADS‐Box Gene in the Moss Physcomitrella patens
inferredcites →https://doi.org/10.1055/s-2006-923952openalex-snapshot
Moss Systems Biology en Route: Phytohormones in Physcomitrella Development
inferredcites →https://doi.org/10.1073/pnas.1108434108openalex-snapshot
The main auxin biosynthesis pathway in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1108436108openalex-snapshot
Conversion of tryptophan to indole-3-acetic acid by TRYPTOPHAN AMINOTRANSFERASES OF ARABIDOPSIS and YUCCAs in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1305457110openalex-snapshot
Recruitment and remodeling of an ancient gene regulatory network during land plant evolution
inferredcites →https://doi.org/10.1073/pnas.1416324112openalex-snapshot
Conserved regulatory mechanism controls the development of cells with rooting functions in land plants
inferredcites →https://doi.org/10.1073/pnas.1604375113openalex-snapshot
Dioxygenase-encoding AtDAO1 gene controls IAA oxidation and homeostasis in Arabidopsis
inferredcites →https://doi.org/10.1073/pnas.1604769113openalex-snapshot
DAO1 catalyzes temporal and tissue-specific oxidative inactivation of auxin in Arabidopsis thaliana
inferredcites →https://doi.org/10.1074/jbc.m006185200openalex-snapshot
Identification and Biochemical Characterization of anArabidopsis Indole-3-acetic Acid Glucosyltransferase
inferredcites →https://doi.org/10.1080/09168451.2015.1086259openalex-snapshot
Current aspects of auxin biosynthesis in plants
inferredcites →https://doi.org/10.1093/emboj/18.8.2066openalex-snapshot
AUX1 regulates root gravitropism in Arabidopsis by facilitating auxin uptake within root apical tissues
inferredcites →https://doi.org/10.1093/jxb/eri040openalex-snapshot
Effect of the energy supply on filamentous growth and development in Physcomitrella patens
inferredcites →https://doi.org/10.1093/jxb/erm047openalex-snapshot
Both chloronemal and caulonemal cells expand by tip growth in the moss Physcomitrella patens
inferredcites →https://doi.org/10.1093/jxb/eru515openalex-snapshot
New insights into root gravitropic signalling
inferredcites →https://doi.org/10.1093/molbev/msu147openalex-snapshot
Paralogous Radiations of PIN Proteins with Multiple Origins of Noncanonical PIN Structure
inferredcites →https://doi.org/10.1093/mp/ssr068openalex-snapshot
Myosin VIII Regulates Protonemal Patterning and Developmental Timing in the Moss Physcomitrella patens
inferredcites →https://doi.org/10.1093/mp/ssr109openalex-snapshot
Cellular Auxin Homeostasis: Gatekeeping Is Housekeeping
inferredcites →https://doi.org/10.1104/pp.109.143867openalex-snapshot
Conservation of Lotus and Arabidopsis Basic Helix-Loop-Helix Proteins Reveals New Players in Root Hair Development
inferredcites →https://doi.org/10.1104/pp.109.149708openalex-snapshot
Auxin Metabolism and Function in the Multicellular Brown Alga Ectocarpus siliculosus
inferredcites →https://doi.org/10.1104/pp.113.214023openalex-snapshot
The Moss Physcomitrella patens Reproductive Organ Development Is Highly Organized, Affected by the Two SHI/STY Genes and by the Level of Active Auxin in the SHI/STY Expression Domain
inferredcites →https://doi.org/10.1104/pp.81.3.934openalex-snapshot
The Effect of Salt Concentration on Auxin Stability in Culture Media
inferredcites →https://doi.org/10.1105/tpc.010388openalex-snapshot
Cryptochrome Light Signals Control Development to Suppress Auxin Sensitivity in the Moss Physcomitrella patens
inferredcites →https://doi.org/10.1105/tpc.104.026690openalex-snapshot
Characterization of an Arabidopsis Enzyme Family That Conjugates Amino Acids to Indole-3-Acetic Acid
inferredcites →https://doi.org/10.1105/tpc.107.051706openalex-snapshot
Common Functions for Diverse Small RNAs of Land Plants
inferredcites →https://doi.org/10.1105/tpc.111.089029openalex-snapshot
A Small-Molecule Screen Identifies l -Kynurenine as a Competitive Inhibitor of TAA1/TAR Activity in Ethylene-Directed Auxin Biosynthesis and Root Growth in Arabidopsis
inferredcites →https://doi.org/10.1105/tpc.114.134874openalex-snapshot
PIN-Dependent Auxin Transport: Action, Regulation, and Evolution
inferredcites →https://doi.org/10.1105/tpc.5.10.1483openalex-snapshot
The Moss Physcomitrella patens, a Model System with Potential for the Study of Plant Reproduction
inferredcites →https://doi.org/10.1111/j.1399-3054.1983.tb04142.xopenalex-snapshot
The mechanism of auxin uptake and accumulation in moss protonemata
inferredcites →https://doi.org/10.1111/j.1399-3054.1983.tb04143.xopenalex-snapshot
Uptake and polar transport of indoleacetic acid in moss rhizoids
inferredcites →https://doi.org/10.1111/j.1438-8677.1998.tb00670.xopenalex-snapshot
Development, Genetics and Molecular Biology of Mosses
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02677.xopenalex-snapshot
Moss ( Physcomitrella patens ) GH3 proteins act in auxin homeostasis
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03805.xopenalex-snapshot
Auxin promotes the transition from chloronema to caulonema in moss protonema by positively regulating PpRSL1and PpRSL2 in Physcomitrella patens
inferredcites →https://doi.org/10.1111/j.1525-142x.2008.00225.xopenalex-snapshot
Convergent evolution of shoots in land plants: lack of auxin polar transport in moss shoots
inferredcites →https://doi.org/10.1111/j.1751-1097.1978.tb07596.xopenalex-snapshot
GENETIC AND PHYSIOLOGICAL STUDIES OF THE EFFECT OF LIGHT ON THE DEVELOPMENT OF THE MOSS, PHYSCOMITRELLA PATENS
inferredcites →https://doi.org/10.1111/nph.12437openalex-snapshot
Defining the selectivity of processes along the auxin response chain: a study using auxin analogues
inferredcites →https://doi.org/10.1111/nph.14333openalex-snapshot
Auxin transport in the evolution of branching forms
inferredcites →https://doi.org/10.1111/tpj.13501openalex-snapshot
Sexual reproduction, sporophyte development and molecular variation in the model moss Physcomitrella patens: introducing the ecotype Reute
inferredcites →https://doi.org/10.1126/science.1142618openalex-snapshot
An Ancient Mechanism Controls the Development of Cells with a Rooting Function in Land Plants
inferredcites →https://doi.org/10.1126/science.1150646openalex-snapshot
The Physcomitrella Genome Reveals Evolutionary Insights into the Conquest of Land by Plants
inferredcites →https://doi.org/10.1126/science.1248417openalex-snapshot
Contribution of NAC Transcription Factors to Plant Adaptation to Land
inferredcites →https://doi.org/10.1126/science.282.5397.2226openalex-snapshot
Regulation of Polar Auxin Transport by AtPIN1 in Arabidopsis Vascular Tissue
inferredcites →https://doi.org/10.1146/annurev-arplant-043015-112122openalex-snapshot
Transcriptional Responses to the Auxin Hormone
inferredcites →https://doi.org/10.1146/annurev.arplant.49.1.501openalex-snapshot
HORMONE-INDUCED SIGNALING DURING MOSS DEVELOPMENT
inferredcites →https://doi.org/10.1146/annurev.arplant.57.032905.105338openalex-snapshot
MOSSES AS MODEL SYSTEMS FOR THE STUDY OF METABOLISM AND DEVELOPMENT
inferredcites →https://doi.org/10.1146/annurev.genet.39.073003.110214openalex-snapshot
The MossPhyscomitrella patens
inferredcites →https://doi.org/10.1186/1471-2148-9-126openalex-snapshot
The evolution of nuclear auxin signalling
inferredcites →https://doi.org/10.1242/dev.00644openalex-snapshot
Involvement of auxin and a homeodomain-leucine zipper I gene in rhizoid development of the moss Physcomitrella patens
inferredcites →https://doi.org/10.1242/dev.039594openalex-snapshot
Homologues of the Arabidopsis thaliana SHI/STY/LRP1 genes control auxin biosynthesis and affect growth and development in the moss Physcomitrella patens
inferredcites →https://doi.org/10.1242/dev.049023openalex-snapshot
Evolutionary crossroads in developmental biology: Physcomitrella patens
inferredcites →https://doi.org/10.1242/dev.051987openalex-snapshot
Strigolactones enhance competition between shoot branches by dampening auxin transport
inferredcites →https://doi.org/10.1242/dev.060582openalex-snapshot
RSL genes are sufficient for rhizoid system development in early diverging land plants
inferredcites →https://doi.org/10.1242/dev.074831openalex-snapshot
The cyclophilin DIAGEOTROPICA has a conserved role in auxin signaling
inferredcites →https://doi.org/10.1242/dev.076091openalex-snapshot
AP2-type transcription factors determine stem cell identity in the moss Physcomitrella patens
inferredcites →https://doi.org/10.1242/dev.086363openalex-snapshot
Auxin metabolism and homeostasis during plant development
inferredcites →https://doi.org/10.1242/jcs.159418openalex-snapshot
Auxin transporters and binding proteins at a glance
inferredcites →https://doi.org/10.1371/journal.pone.0125411openalex-snapshot
Phytohormone Profiling across the Bryophytes
inferredcites →https://doi.org/10.1639/0007-2745(1968)71[11:tdosoa]2.0.co;2openalex-snapshot
The Development of Sex Organs and Sporophyte in Physcomitrium cyathicarpum Mitt.
inferredcites →https://doi.org/10.2307/2656792openalex-snapshot
Auxin metabolism in mosses and liverworts
inferredcites →https://doi.org/10.3389/fpls.2012.00017openalex-snapshot
Diversification and Expression of the PIN, AUX/LAX, and ABCB Families of Putative Auxin Transporters in Populus
inferredcites →https://doi.org/10.3389/fpls.2012.00227openalex-snapshot
Evolution and structural diversification of PILS putative auxin carriers in plants
inferredcites →https://doi.org/10.3389/fpls.2018.01410openalex-snapshot
Getting to the Roots: A Developmental Genetic View of Root Anatomy and Function From Arabidopsis to Lycophytes
inferredcites →https://doi.org/10.3390/ijms20246343openalex-snapshot
The Roles of Auxin Biosynthesis YUCCA Gene Family in Plants
inferredcites →https://doi.org/10.4161/psb.19283openalex-snapshot
TOPLESS co-repressor interactions and their evolutionary conservation in plants
inferredcites →https://doi.org/10.4161/psb.4.2.7536openalex-snapshot
Dead end for auxin conjugates in Physcomitrella?
inferredcites →https://doi.org/10.7554/elife.06808openalex-snapshot
Three ancient hormonal cues co-ordinate shoot branching in a moss
inferredcites →https://doi.org/10.7554/elife.13325openalex-snapshot
Constitutive auxin response in Physcomitrella reveals complex interactions between Aux/IAA and ARF proteins
inferredcites →https://doi.org/10.82465/5747openalex-snapshot
An Examination of Leaf Morphogenesis In The Moss, Physcomitrella Patens
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/oneeco.9.e117655zenodo-depositor-declared
What we really know about the dormancy, reproduction, germination and cultivation of charophytes (Characeae)
inferred← citeshttps://doi.org/10.1002/ajb2.1200openalex-snapshot
Chiral events in developing gametophores of Physcomitrella patens and other moss species are driven by an unknown, universal direction‐sensing mechanism
inferred← citeshttps://doi.org/10.1002/nzb2.70180openalex-snapshot
Beyond the Model Species: Comparative Salt‐Stress Responses in Phylogenetically Related Mosses Physcomitrium patens and P. eurystomum (Funariaceae)
inferred← citeshttps://doi.org/10.1007/s00425-020-03354-wopenalex-snapshot
Evolutionary insights into FYVE and PHOX effector proteins from the moss Physcomitrella patens
inferred← citeshttps://doi.org/10.1007/s00425-020-03501-3openalex-snapshot
Light- and hormone-mediated development in non-flowering plants: An overview
inferred← citeshttps://doi.org/10.1007/s11103-021-01126-yopenalex-snapshot
Fundamental mechanisms of the stem cell regulation in land plants: lesson from shoot apical cells in bryophytes
inferred← citeshttps://doi.org/10.1007/s11103-021-01152-wopenalex-snapshot
The nuclear GUCT domain-containing DEAD-box RNA helicases govern gametophytic and sporophytic development in Physcomitrium patens
inferred← citeshttps://doi.org/10.1007/s11103-021-01172-6openalex-snapshot
Phytohormone biosynthesis and signaling pathways of mosses
inferred← citeshttps://doi.org/10.1007/s11240-026-03579-9openalex-snapshot
Optimized surface decontamination of gametophores for axenic in vitro culture of the moss Warnstorfia sarmentosa (Wahlenb.) Hedenäs, with application to other polar mosses
inferred← citeshttps://doi.org/10.1007/s40502-024-00809-0openalex-snapshot
Enhancement of salt stress tolerance of Sorghum bicolor grown in soil remediated by Thidium gratum fern via upregulation of Na+/ K + transporter genes
inferred← citeshttps://doi.org/10.1016/j.celrep.2024.114524openalex-snapshot
Single-cell RNA sequencing reveals dynamics of gene expression for 2D elongation and 3D growth in Physcomitrium patens
inferred← citeshttps://doi.org/10.1016/j.celrep.2026.117089openalex-snapshot
Lipocalins regulate development and various stress responses in Physcomitrium patens
inferred← citeshttps://doi.org/10.1016/j.crmicr.2024.100284openalex-snapshot
Unraveling growth-promoting potential of plant beneficial actinobacteria on tropical bryophytes
inferred← citeshttps://doi.org/10.1016/j.cub.2019.09.021openalex-snapshot
Design Principles of Branching Morphogenesis in Filamentous Organisms
inferred← citeshttps://doi.org/10.1016/j.cub.2022.06.064openalex-snapshot
Apical dominance control by TAR-YUC-mediated auxin biosynthesis is a deep homology of land plants
inferred← citeshttps://doi.org/10.1016/j.devcel.2025.02.006openalex-snapshot
snRNA-seq analysis of the moss Physcomitrium patens identifies a conserved cytokinin-ESR module promoting pluripotent stem cell identity
inferred← citeshttps://doi.org/10.1016/j.gene.2021.146168openalex-snapshot
Building an embryo: An auxin gene toolkit for zygotic and somatic embryogenesis in Brazilian pine
inferred← citeshttps://doi.org/10.1016/j.hazl.2025.100167openalex-snapshot
Copper and cadmium toxicity affecting in vitro growth and Scopelophila cataractae development
inferred← citeshttps://doi.org/10.1016/j.molp.2018.12.012openalex-snapshot
Auxin EvoDevo: Conservation and Diversification of Genes Regulating Auxin Biosynthesis, Transport, and Signaling
inferred← citeshttps://doi.org/10.1016/j.pbi.2023.102486openalex-snapshot
Hormonal and genetic control of pluripotency in bryophyte model systems
inferred← citeshttps://doi.org/10.1016/j.plantsci.2021.111070openalex-snapshot
Regulation of the Development in Physcomitrium (Physcomitrella) patens implicates the functional differentiation of plant RNase H1s
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111661openalex-snapshot
Autophagy contributes to auxin-driven developmental plasticity in response to changes in carbon and nitrogen availability in Physcomitrium patens
inferred← citeshttps://doi.org/10.1016/j.rhisph.2022.100592openalex-snapshot
Isolation and characterization of endophytic bacteria associated with gametophytes of bryophytes in Mount Abu (Rajasthan)
inferred← citeshttps://doi.org/10.1016/j.tplants.2019.05.006openalex-snapshot
Auxin Metabolism Controls Developmental Decisions in Land Plants
inferred← citeshttps://doi.org/10.1016/j.xplc.2023.100669openalex-snapshot
Divergence of trafficking and polarization mechanisms for PIN auxin transporters during land plant evolution
inferred← citeshttps://doi.org/10.1016/j.xplc.2026.101892openalex-snapshot
Evolutionary shifts in plant adaptation mediated by phytohormones
inferred← citeshttps://doi.org/10.1038/s41477-025-01973-3openalex-snapshot
Comparative mutant analyses reveal a novel mechanism of ARF regulation in land plants
inferred← citeshttps://doi.org/10.1038/s41598-019-51632-9openalex-snapshot
Mutations in Glucan, Water Dikinase Affect Starch Degradation and Gametophore Development in the Moss Physcomitrella patens
inferred← citeshttps://doi.org/10.1038/s41598-023-31417-xopenalex-snapshot
Overexpression of Physcomitrium patens cell cycle regulators leads to larger gametophytes
inferred← citeshttps://doi.org/10.1073/pnas.2603045123openalex-snapshot
WIP transcriptional regulators modulate developmental progression in both life cycle phases of a moss
inferred← citeshttps://doi.org/10.1093/aob/mcae081openalex-snapshot
Cell death in bryophytes: emerging models to study core regulatory modules and conserved pathways
inferred← citeshttps://doi.org/10.1093/jxb/eraa169openalex-snapshot
The evolutionary origins of auxin transport: what we know and what we need to know
inferred← citeshttps://doi.org/10.1093/jxb/erab009openalex-snapshot
The production of auxin by dying cells
inferred← citeshttps://doi.org/10.1093/jxb/erad299openalex-snapshot
The ratio of auxin to cytokinin controls leaf development and meristem initiation in Physcomitrium patens
inferred← citeshttps://doi.org/10.1093/jxb/erae162openalex-snapshot
Crosstalk between Rho of Plants GTPase signalling and plant hormones
inferred← citeshttps://doi.org/10.1093/jxb/eraf183openalex-snapshot
The role of auxin-mediated gene activation in the bryophyte, Physcomitrium patens
inferred← citeshttps://doi.org/10.1093/pcp/pcaa098openalex-snapshot
An Evolutionarily Primitive and Distinct Auxin Metabolism in the Lycophyte Selaginella moellendorffii
inferred← citeshttps://doi.org/10.1093/plcell/koac069openalex-snapshot
Division site determination during asymmetric cell division in plants
inferred← citeshttps://doi.org/10.1093/plcell/koae009openalex-snapshot
SUPPRESSOR OF MAX2 1-LIKE (SMXL) homologs are MAX2-dependent repressors of Physcomitrium patens growth
inferred← citeshttps://doi.org/10.1093/plphys/kiab261openalex-snapshot
The unique bryophyte-specific repeat-containing protein SHORT-LEAF regulates gametophore development in moss
inferred← citeshttps://doi.org/10.1101/2021.06.24.449551openalex-snapshot
PpRPK2 modulates auxin homeostasis and transport to specify stem cell identity and plant shape in the moss Physcomitrella
inferred← citeshttps://doi.org/10.1101/2021.11.24.469821openalex-snapshot
FAMOSS, a conserved 41-aa peptide involved in plant tip growth regulation
inferred← citeshttps://doi.org/10.1101/2022.10.25.513742openalex-snapshot
A Clade-D Auxin Response Factor is a Major Regulator of Auxin Signaling in Physcomitrium patens
inferred← citeshttps://doi.org/10.1101/2023.02.03.526932openalex-snapshot
Identification and characterization of DICER-LIKE genes and their roles in Marchantia polymorpha development and stress adaptation
inferred← citeshttps://doi.org/10.1101/2023.04.06.534998openalex-snapshot
Phytohormone profiling in an evolutionary framework
inferred← citeshttps://doi.org/10.1101/2023.04.11.536386openalex-snapshot
Physcomitrium patens SMXL homologs are PpMAX2-dependent negative regulators of growth
inferred← citeshttps://doi.org/10.1101/2024.05.03.592339openalex-snapshot
Analysis of auxin responses in the fern Ceratopteris richardii identifies tissue ontogeny as a major determinant for response properties
inferred← citeshttps://doi.org/10.1101/2024.07.22.604381openalex-snapshot
Early morphogenetic patterns of protonemata and gametophores of Physcomitrium patens (Hedw.) Mitt
inferred← citeshttps://doi.org/10.1101/2024.07.31.606100openalex-snapshot
snRNA-seq analysis of the moss Physcomitrium patens reveals a conserved cytokinin-ESR module promoting pluripotent stem cell identity
inferred← citeshttps://doi.org/10.1101/2025.03.13.638958openalex-snapshot
Lipocalins are versatile regulators of development and stress response in mosses
inferred← citeshttps://doi.org/10.1101/2025.06.11.659030openalex-snapshot
Molecular and Phenotypic Characterization of Telomere Repeat Binding (TRBs) Proteins in Moss: Evolutionary and Functional Perspectives
inferred← citeshttps://doi.org/10.1101/603175openalex-snapshot
Evolution of Auxin Response Factors in plants characterized by phylogenomic synteny network analyses
inferred← citeshttps://doi.org/10.1101/cshperspect.a039875openalex-snapshot
Auxin Transporters—A Biochemical View
inferred← citeshttps://doi.org/10.1101/cshperspect.a040055openalex-snapshot
Auxin Biology in Bryophyta: A Simple Platform with Versatile Functions
inferred← citeshttps://doi.org/10.1111/nph.16068openalex-snapshot
Minimal auxin sensing levels in vegetative moss stem cells revealed by a ratiometric reporter
inferred← citeshttps://doi.org/10.1111/nph.16914openalex-snapshot
Studies of moss reproductive development indicate that auxin biosynthesis in apical stem cells may constitute an ancestral function for focal growth control
inferred← citeshttps://doi.org/10.1111/nph.17955openalex-snapshot
Developmental regulation of leaf venation patterns: monocot versus eudicots and the role of auxin
inferred← citeshttps://doi.org/10.1111/nph.17969openalex-snapshot
CLAVATA modulates auxin homeostasis and transport to regulate stem cell identity and plant shape in a moss
inferred← citeshttps://doi.org/10.1111/nph.18691openalex-snapshot
A Physcomitrella PIN protein acts in spermatogenesis and sporophyte retention
inferred← citeshttps://doi.org/10.1111/nph.19728openalex-snapshot
Ethylene controls three‐dimensional growth involving reduced auxin levels in the moss Physcomitrium patens
inferred← citeshttps://doi.org/10.1111/ppl.13140openalex-snapshot
PHYTOCHROME INTERACTING FACTORs in the moss Physcomitrella patens regulate light‐controlled gene expression
inferred← citeshttps://doi.org/10.1111/tpj.16322openalex-snapshot
The TOPLESS corepressor regulates developmental switches in the bryophyte Physcomitrium patens that were critical for plant terrestrialisation
inferred← citeshttps://doi.org/10.1111/tpj.17236openalex-snapshot
Identification and characterization of DICER‐LIKE genes and their roles in Marchantia polymorpha development and salt stress response
inferred← citeshttps://doi.org/10.1111/tpj.70574openalex-snapshot
TRB proteins in moss reveal their evolutionarily conserved roles in plant development and telomere maintenance
inferred← citeshttps://doi.org/10.1126/sciadv.aee6959openalex-snapshot
Morphogenesis of moss leaf-like organs through variations in deeply shared developmental principles
inferred← citeshttps://doi.org/10.1139/cjb-2025-0154openalex-snapshot
Establishment capacity of rhizoidal tubers of the moss Bryum billarderii Schwagr. (Bryaceae, Bryophyta) under copper-induced stress
inferred← citeshttps://doi.org/10.1186/s12870-025-07172-8openalex-snapshot
The potential role of short internodes/stylish (SHI/STY) and SHI related sequence (SRS) in potato tuberization
inferred← citeshttps://doi.org/10.1186/s12870-026-08611-wopenalex-snapshot
Tubulin post-translational modifications are conserved during land plant evolution
inferred← citeshttps://doi.org/10.1186/s13007-020-00609-1openalex-snapshot
Phylogenomic synteny network analyses reveal ancestral transpositions of auxin response factor genes in plants
inferred← citeshttps://doi.org/10.1186/s13007-023-01077-zopenalex-snapshot
Protocol: an improved method for inducing sporophyte generation in the model moss Physcomitrium patens under nitrogen starvation
inferred← citeshttps://doi.org/10.1242/dev.184762openalex-snapshot
VAPYRIN-like is required for development of the moss Physcomitrella patens
inferred← citeshttps://doi.org/10.1242/dev.201635openalex-snapshot
A cornichon protein controls polar localization of the PINA auxin transporter in Physcomitrium patens
inferred← citeshttps://doi.org/10.1242/dev.203026openalex-snapshot
Analysis of auxin responses in the fern Ceratopteris richardii identifies the developmental phase as a major determinant for response properties
inferred← citeshttps://doi.org/10.1371/journal.pbio.3002163openalex-snapshot
Clade-D auxin response factors regulate auxin signaling and development in the moss Physcomitrium patens
inferred← citeshttps://doi.org/10.15407/knit2025.06.063openalex-snapshot
MORPHOLOGICAL PLASTICITY OF MOSSES AS AN ADAPTIVE RESPONSE TO GRAVITY
inferred← citeshttps://doi.org/10.1639/0007-2745-121.3.426openalex-snapshot
Recent literature on bryophytes — 121(3)
inferred← citeshttps://doi.org/10.18174/511017openalex-snapshot
Proteomics perspective on auxin biology
inferred← citeshttps://doi.org/10.18297/etd/3830openalex-snapshot
Functional role of PPAL and potential for moss in industrial applications.
inferred← citeshttps://doi.org/10.30525/978-9934-26-086-5-7openalex-snapshot
Endogenous auxin and abscisic acid in the organs of the Equisetum hyemale L. sporophyte in ontogenesis
inferred← citeshttps://doi.org/10.3389/fmicb.2020.563047openalex-snapshot
Bryophytes Harbor Cultivable Actinobacteria With Plant Growth Promoting Potential
inferred← citeshttps://doi.org/10.3389/fpls.2018.01410openalex-snapshot
Getting to the Roots: A Developmental Genetic View of Root Anatomy and Function From Arabidopsis to Lycophytes
inferred← citeshttps://doi.org/10.3389/fpls.2020.00845openalex-snapshot
A Chloroplast COR413 Protein From Physcomitrella patens Is Required for Growth Regulation Under High Light and ABA Responses
inferred← citeshttps://doi.org/10.3389/fpls.2021.736212openalex-snapshot
Leaf Morphogenesis: Insights From the Moss Physcomitrium patens
inferred← citeshttps://doi.org/10.3389/fpls.2022.1052358openalex-snapshot
Autophagy modulates growth and development in the moss Physcomitrium patens
inferred← citeshttps://doi.org/10.3390/cells11172652openalex-snapshot
Auxin Regulates Apical Stem Cell Regeneration and Tip Growth in the Marine Red Alga Neopyropia yezoensis
inferred← citeshttps://doi.org/10.3390/ijms19092609openalex-snapshot
PpSARK Regulates Moss Senescence and Salt Tolerance through ABA Related Pathway
inferred← citeshttps://doi.org/10.3390/ijms20246343openalex-snapshot
The Roles of Auxin Biosynthesis YUCCA Gene Family in Plants
inferred← citeshttps://doi.org/10.3390/ijms22052626openalex-snapshot
Physcomitrium patens: A Single Model to Study Oriented Cell Divisions in 1D to 3D Patterning
inferred← citeshttps://doi.org/10.3390/ijms23041933openalex-snapshot
Auxin/Cytokinin Antagonistic Control of the Shoot/Root Growth Ratio and Its Relevance for Adaptation to Drought and Nutrient Deficiency Stresses
inferred← citeshttps://doi.org/10.3390/ijms27010478openalex-snapshot
Desiccation Tolerance in Moss and Liverwort: Insights into the Evolutionary Mechanisms of Terrestrialization
inferred← citeshttps://doi.org/10.3390/plants10071398openalex-snapshot
Physcomitrium patens Mutants in Auxin Conjugating GH3 Proteins Show Salt Stress Tolerance but Auxin Homeostasis Is Not Involved in Regulation of Oxidative Stress Factors
inferred← citeshttps://doi.org/10.3390/plants11050707openalex-snapshot
Red Light and Glucose Enhance Cytokinin-Mediated Bud Initial Formation in Physcomitrium patens
inferred← citeshttps://doi.org/10.3390/plants14071027openalex-snapshot
The Extended Synaptotagmins of Physcomitrium patens
inferred← citeshttps://doi.org/10.3390/plants9101380openalex-snapshot
Exogenous Nitric Oxide Delays Plant Regeneration from Protoplast and Protonema Development in Physcomitrella patens
inferred← citeshttps://doi.org/10.6084/m9.figshare.26619886openalex-snapshot
Additional file 1 of Protocol: an improved method for inducing sporophyte generation in the model moss Physcomitrium patens under nitrogen starvation
inferred← citeshttps://doi.org/10.64898/2025.12.28.696759openalex-snapshot
Autophagy as a regulatory node integrating the carbon/nitrogen ratio with the auxin-driven chloronema-to-caulonema transition in Physcomitrium patens
inferred← citeshttps://doi.org/10.64898/2026.01.13.699213openalex-snapshot
Insight into GABA shunt-associated aldehyde dehydrogenases (ALDH) and stress responses of ALDH superfamily in moss and barley
inferred← citeshttps://doi.org/10.70675/bfab313ez7d9az411czbb63z16057ed985adopenalex-snapshot
Strigolactones perception and signal transduction in the moss Physcomitrium patens
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