The No Apical Meristem Gene of Petunia Is Required for Pattern Formation in Embryos and Flowers and Is Expressed at Meristem and Primordia Boundaries

The war of the whorls: genetic interactions controlling flower development

Coen, E., & Meyerowitz, E. M. (1991) · Nature · doi:10.1038/353031a0 · Cited by 3,045

A member of the KNOTTED class of homeodomain proteins encoded by the STM gene of Arabidopsis

Long, J. A., Moan, E. I., Medford, J. I., & Barton, M. K. (1996) · Nature · doi:10.1038/379066a0 · Cited by 1,537

Genetic interactions among floral homeotic genes of Arabidopsis

Bowman, J. L., Smyth, D. R., & Meyerowitz, E. M. (1991) · Development · doi:10.1242/dev.112.1.1 · Cited by 1,167

The ABCs of floral homeotic genes

Weigel, D., & Meyerowitz, E. M. (1994) · Cell · doi:10.1016/0092-8674(94)90291-7 · Cited by 1,027

Prosite: a dictionary of sites and patterns in proteins

Bairoch, A. (1992) · Nucleic Acids Research · doi:10.1093/nar/20.suppl.2013 · Cited by 930

CLAVATA1, a regulator of meristem and flower development in Arabidopsis

Clark, S. E., Running, M., & Meyerowitz, E. M. (1993) · Development · doi:10.1242/dev.119.2.397 · Cited by 887

Genetic Control of Flower Development by Homeotic Genes in Antirrhinum majus

Schwarz‐Sommer, Z., Huijser, P., Nacken, W. K. F., Saedler, H., & Sommer, H. (1990) · Science · doi:10.1126/science.250.4983.931 · Cited by 879

Formation of the shoot apical meristem in Arabidopsis thaliana: an analysis of development in the wild type and in the shoot meristemless mutant

Barton, M. K., & Poethig, R. S. (1993) · Development · doi:10.1242/dev.119.3.823 · Cited by 626

Genes Galore: A Summary of Methods for Accessing Results from Large-Scale Partial Sequencing of Anonymous Arabidopsis cDNA Clones

Newman, T., de Bruijn, F. J., Green, P., Keegstra, K., Kende, H., McIntosh, L., Ohlrogge, J. B., Raikhel, N. V., Somerville, S. C., Thomashow, M. F., et al. (1994) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.4.1241 · Cited by 623

Plant Embryogenesis: Zygote to Seed

Goldberg, R. B., de Paiva, G. R., & Yadegari, R. (1994) · Science · doi:10.1126/science.266.5185.605 · Cited by 613

The nuclear localization of the Arabidopsis transcription factor TIP is blocked by its interaction with the coat protein of Turnip crinkle virus

Ren, T., Qu, F., & Morris, T. J. (2004) · Virology · doi:10.1016/j.virol.2004.10.039 · Cited by 66

Cell Differentiation and Organ Initiation at the Shoot Apical Meristem

Carraro, N., Peaucelle, A., Laufs, P., & Traas, J. A. (2006) · Plant Molecular Biology · doi:10.1007/s11103-005-2761-6 · Cited by 67

The NAC-type transcription factor GmNAC20 improves cold, salinity tolerance, and lateral root formation in transgenic rice plants

Yarra, R., & Wei, W. (2021) · Functional & Integrative Genomics · doi:10.1007/s10142-021-00790-z · Cited by 65

Tomato Transcriptional Responses to a Foliar and a Vascular Fungal Pathogen Are Distinct

van Esse, H. P., Fradin, E. F., de Groot, P. J., WIT, P. J. G. M. D., & Thomma, B. P. H. J. (2009) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-22-3-0245 · Cited by 65

Molecular Characterization and Expression Analysis of NAC Family Transcription Factors in Tomato

Kou, X., Wang, S., Wu, M., Guo, R., Xue, Z., Meng, N., Tao, X., Chen, M., & Zhang, Y. (2013) · Plant Molecular Biology Reporter · doi:10.1007/s11105-013-0655-3 · Cited by 64

ATAF2, a NAC Transcription Factor, Binds to the Promoter and Regulates NIT2 Gene Expression Involved in Auxin Biosynthesis

Huh, S. U., Lee, S.-B., Kim, H. H., & Paek, K.-H. (2012) · Molecules and Cells · doi:10.1007/s10059-012-0122-2 · Cited by 64

May the Fittest Protein Evolve: Favoring the Plant‐Specific Origin and Expansion of NAC Transcription Factors

Mathew, I. E., & Agarwal, P. (2018) · BioEssays · doi:10.1002/bies.201800018 · Cited by 65

Networks for shoot design

van der Schoot, C., & Rinne, P. (1999) · Trends in Plant Science · doi:10.1016/s1360-1385(98)01362-4 · Cited by 64

The C Terminus of the Immunophilin PASTICCINO1 Is Required for Plant Development and for Interaction with a NAC-like Transcription Factor

Smyczynski, C., Roudier, F., Gissot, L., Vaillant, E., Grandjean, O., Morin, H., Masson, T., Bellec, Y., Geelen, D., & Faure, J. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.m601815200 · Cited by 64

Role of petunia pMADS3 in determination of floral organ and meristem identity, as revealed by its loss of function

Kapoor, M., Tsuda, S., Tanaka, Y., Tsuchida‐Mayama, T., Okuyama, Y., Tsuchimoto, S., & Takatsuji, H. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01402.x · Cited by 64

Genome-Wide Identification of SNAC1-Targeted Genes Involved in Drought Response in Rice

Li, X., Chang, Y., Ma, S., Shen, J., Hu, H., & Xiong, L. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00982 · Cited by 64

The osa‐miR164 target OsCUC1 functions redundantly with OsCUC3 in controlling rice meristem/organ boundary specification

Wang, J., Bao, J., Zhou, B., Li, M., Li, X., & Jin, J. (2020) · New Phytologist · doi:10.1111/nph.16939 · Cited by 63

The Role of Plant Transcription Factors in the Fight against Plant Viruses

Kotapati, K. V., Kuo, S., Tu, C., Hsu, Y., Huang, Y., & Hu, C. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24098433 · Cited by 63

Plant NAC transcription factors in the battle against pathogens

Dong, B., Liu, Y., Huang, G., Song, A., Chen, S., Jiang, J., Chen, F., & Fang, W. (2024) · BMC Plant Biology · doi:10.1186/s12870-024-05636-x · Cited by 63

Molecular regulation of somatic embryogenesis in potato: an auxin led perspective

Sharma, S. K., Millam, S., Hedley, P. E., McNicol, J., & Bryan, G. J. (2008) · Plant Molecular Biology · doi:10.1007/s11103-008-9360-2 · Cited by 63

Characterization and identification of the candidate gene of rice thermo-sensitive genic male sterile gene tms5 by mapping

Qingkai, Y., Liang, C., Wen, Z., Li, J., Deng, H., Deng, Q., & Wang, B. (2006) · Planta · doi:10.1007/s00425-006-0353-6 · Cited by 63

A CELD‐fusion method for rapid determination of the DNA‐binding sequence specificity of novel plant DNA‐binding proteins

Xue, G. (2005) · The Plant Journal · doi:10.1111/j.1365-313x.2004.02323.x · Cited by 62

A Comparison of DNA Extraction Methods using Petunia hybrida Tissues

Tamari, F., Hinkley, C. S., & Ramprashad, N. (2013) · Journal of Biomolecular Techniques JBT · doi:10.7171/jbt.13-2403-001 · Cited by 62

Characterization of a ripening-related transcription factor FcNAC1 from Fragaria chiloensis fruit

Carrasco-Orellana, C., Stappung, Y., Méndez-Yáñez, Á., Allan, A. C., Espley, R. V., Plunkett, B. J., Moya‐León, M. A., & Herrera, R. (2018) · Scientific Reports · doi:10.1038/s41598-018-28226-y · Cited by 62

Dual role of MdSND1 in the biosynthesis of lignin and in signal transduction in response to salt and osmotic stress in apple

Chen, K., Guo, Y., Song, M., Liu, L., Xue, H., Dai, H., & Zhang, Z. (2020) · Horticulture Research · doi:10.1038/s41438-020-00433-7 · Cited by 62

Psl: a novel Spm‐like transposable element from Petunia hybrida

Snowden, K. C., & Napoli, C. A. (1998) · The Plant Journal · doi:10.1046/j.1365-313x.1998.00098.x · Cited by 62

Formation and Shaping of the Antirrhinum Flower through Modulation of the CUP Boundary Gene

Rebocho, A. B., Kennaway, R., Bangham, J., & Coen, E. (2017) · Current Biology · doi:10.1016/j.cub.2017.07.064 · Cited by 61

Arabidopsis ANAC069 binds to C[A/G]CG[T/G] sequences to negatively regulate salt and osmotic stress tolerance

He, L., Shi, X., Wang, Y., Guo, Y., Wang, Y., & Wang, Y. (2016) · Plant Molecular Biology · doi:10.1007/s11103-016-0567-3 · Cited by 61

Molecular and Hormonal Regulation of Leaf Morphogenesis in Arabidopsis

Ali, S., Khan, N., & Xie, L. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21145132 · Cited by 62

Signals that regulate stem cell activity during plant development

Vernoux, T., & Benfey, P. N. (2005) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2005.06.008 · Cited by 61

Morphogenesis of Flowers—Our Evolving View

Smyth, D. R. (2005) · The Plant Cell · doi:10.1105/tpc.104.030353 · Cited by 61

Plant Growth and Development - Basic Knowledge and Current Views

Brukhin, V. B., & Morozova, N. (2010) · Mathematical Modelling of Natural Phenomena · doi:10.1051/mmnp/20116201 · Cited by 62

Genome-Wide Identification of NAC Transcription Factors and Their Functional Prediction of Abiotic Stress Response in Peanut

Li, P., Peng, Z., Xu, P., Tang, G., Ma, C., Zhu, J., Shan, L., & Wan, S. (2021) · Frontiers in Genetics · doi:10.3389/fgene.2021.630292 · Cited by 60

Extracellular Matrix Proteome of Chickpea (Cicer arietinum L.) Illustrates Pathway Abundance, Novel Protein Functions and Evolutionary Perspect

Bhushan, D., Pandey, A., Chattopadhyay, A., Choudhary, M. K., Chakraborty, S., Datta, A., & Chakraborty, N. (2006) · Journal of Proteome Research · doi:10.1021/pr060116f · Cited by 59

TheNAC-like geneANTHER INDEHISCENCE FACTORacts as a repressor that controls anther dehiscence by regulating genes in the jasmonate biosynthesis pathway inArabidopsis

Shih, C., Hsu, W., Peng, Y., & Yang, C. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert412 · Cited by 59

Three stress‐responsive NAC transcription factors from Populus euphratica differentially regulate salt and drought tolerance in transgenic plants

Lu, X., Zhang, X., Duan, H., Lian, C., Liu, C., Yin, W., & Xia, X. (2017) · Physiologia Plantarum · doi:10.1111/ppl.12613 · Cited by 59

Phenotypic and Genomic Local Adaptation across Latitude and Altitude in Populus trichocarpa

Zhang, M., Suren, H., & Holliday, J. A. (2019) · Genome Biology and Evolution · doi:10.1093/gbe/evz151 · Cited by 59

Isolation and expression profiling of GhNAC transcription factor genes in cotton (Gossypium hirsutum L.) during leaf senescence and in response to stresses

Shah, S. T., Pang, C., Shuli, F., Song, M., Arain, S. M., & Yu, S. (2013) · Gene · doi:10.1016/j.gene.2013.09.007 · Cited by 58

Genome wide identification and predicted functional analyses of NAC transcription factors in Asian pears

Ahmad, M., Yan, X., Li, J., Yang, Q., Jamil, W., Teng, Y., & Bai, S. (2018) · BMC Plant Biology · doi:10.1186/s12870-018-1427-x · Cited by 58

The transcription factor ZmNAC126 accelerates leaf senescence downstream of the ethylene signalling pathway in maize

Yang, Z., Wang, C., Qiu, K., Chen, H., Li, Z., Li, X., Song, J., Wang, X., Gao, J., Kuai, B., et al. (2020) · Plant Cell & Environment · doi:10.1111/pce.13803 · Cited by 57

WOX2 and STIMPY‐LIKE/WOX8 promote cotyledon boundary formation in Arabidopsis

Lie, C., Kelsom, C., & Wu, X. (2012) · The Plant Journal · doi:10.1111/j.1365-313x.2012.05113.x · Cited by 57

Genome-Wide Identification and Expression Analysis of the CaNAC Family Members in Chickpea during Development, Dehydration and ABA Treatments

Ha, C. V., Esfahani, M. N., Watanabe, Y., Tran, U. T., Sulieman, S., Mochida, K., Nguyen, D. V., & Tran, L. P. (2014) · PLoS ONE · doi:10.1371/journal.pone.0114107 · Cited by 57

Expression of PaNAC01, a Picea abies CUP-SHAPED COTYLEDON orthologue, is regulated by polar auxin transport and associated with differentiation of the shoot apical meristem and formation of separated cotyledons

Larsson, E., Sundström, J. F., Sitbon, F., & von Arnold, S. (2012) · Annals of Botany · doi:10.1093/aob/mcs151 · Cited by 57

Two Brassica napus genes encoding NAC transcription factors are involved in response to high-salinity stress

Zhong, H., Guo, Q., Chen, L., Ren, F., Wang, Q., Zheng, Y., & Li, X. (2012) · Plant Cell Reports · doi:10.1007/s00299-012-1311-3 · Cited by 57

The barley HvNAC6 transcription factor affects ABA accumulation and promotes basal resistance against powdery mildew

Chen, Y., Perera, V., Christiansen, M. W., Holme, I. B., Gregersen, P. L., Grant, M., Collinge, D. B., & Lyngkjær, M. F. (2013) · Plant Molecular Biology · doi:10.1007/s11103-013-0109-1 · Cited by 57

kNACking on heaven’s door: how important are NAC transcription factors for leaf senescence and Fe/Zn remobilization to seeds?

Ricachenevsky, F. K., Menguer, P. K., & Sperotto, R. A. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00226 · Cited by 58

Leaving the meristem behind: The genetic and molecular control of leaf patterning and morphogenesis

Hasson, A., Blein, T., & Laufs, P. (2010) · Comptes Rendus Biologies · doi:10.1016/j.crvi.2010.01.013 · Cited by 57

Identification and expression pattern of one stress-responsive NAC gene from Solanum lycopersicum

Han, Q., Zhang, J., Li, J., Luo, Z., Ziaf, K., Ouyang, B., Wang, T., & Ye, Z. (2011) · Molecular Biology Reports · doi:10.1007/s11033-011-0911-2 · Cited by 56

The pleiotropic effects of the bar gene and glufosinate on the Arabidopsis transcriptome

Abdeen, A., & Miki, B. L. A. (2009) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2008.00398.x · Cited by 56

The NAC Transcription Factor Gene OsY37 (ONAC011) Promotes Leaf Senescence and Accelerates Heading Time in Rice

Mannai, Y. E., Akabane, K., Hiratsu, K., Satoh‐Nagasawa, N., & Wabiko, H. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18102165 · Cited by 56

Genome-wide identification and comprehensive analysis of the NAC transcription factor family in Sesamum indicum

Zhang, Y., Li, D., Wang, Y., Zhou, R., Wang, L., Zhang, Y., Yu, J., Gong, H., You, J., & Zhang, X. (2018) · PLoS ONE · doi:10.1371/journal.pone.0199262 · Cited by 56

SlNAC2 overexpression in Arabidopsis results in enhanced abiotic stress tolerance with alteration in glutathione metabolism

Borgohain, P., Saha, B., Agrahari, R. K., Chowardhara, B., Sahoo, S., van der Vyver, C., & Panda, S. K. (2019) · PROTOPLASMA · doi:10.1007/s00709-019-01368-0 · Cited by 57

Transcriptomic adaptations in rice suspension cells under sucrose starvation

Wang, H., Wan, A.-R., Hsu, C., Lee, K., Yu, S., & Jauh, G. (2006) · Plant Molecular Biology · doi:10.1007/s11103-006-9100-4 · Cited by 56

Botany and Physiology: Storage Root Formation and Development

Firon, N., LaBonte, D., Villordon, A., McGregor, C., Kfir, Y., & Pressman, E. (2009) · The Sweetpotato · doi:10.1007/978-1-4020-9475-0_3 · Cited by 55

Genome-Wide Analysis of NAC Gene Family in Betula pendula

Chen, S., Lin, X., Zhang, D., Li, Q., Zhao, X., & Chen, S. (2019) · Forests · doi:10.3390/f10090741 · Cited by 55

Genome-Wide Identification and Characterization of the NAC Transcription Factor Family in Musa Acuminata and Expression Analysis during Fruit Ripening

Li, B., Fan, R., Yang, Q., Hu, C. T., Sheng, O., Deng, G., Dong, T., Li, C., Peng, X., Bi, F., et al. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21020634 · Cited by 55

ZmNAC074, a maize stress-responsive NAC transcription factor, confers heat stress tolerance in transgenic Arabidopsis

Xi, Y., Ling, Q., Zhou, Y., Liu, X., & Qian, Y. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.986628 · Cited by 55

Genetic and physical characterisation of the locus controlling columnar habit in apple (Malus × domestica Borkh.)

Baldi, P., Wolters, P. J., Komjanc, M., Viola, R., Velasco, R., & Salvi, S. (2012) · Molecular Breeding · doi:10.1007/s11032-012-9800-1 · Cited by 55

Comparative Genomics of NAC Transcriptional Factors in Angiosperms: Implications for the Adaptation and Diversification of Flowering Plants

Pereira‐Santana, A., Alcaraz, L. D., Castaño, E., Sánchez-Calderón, L., Sánchez‐Teyer, L. F., & Rodríguez‐Zapata, L. C. (2015) · PLoS ONE · doi:10.1371/journal.pone.0141866 · Cited by 55

Comprehensive gene expression analysis of the NAC gene family under normal growth conditions, hormone treatment, and drought stress conditions in rice using near-isogenic lines (NILs) generated from crossing Aday Selection (drought tolerant) and IR64

Nuruzzaman, M., Sharoni, A. M., Satoh, K., Moumeni, A., Venuprasad, R., Serraj, R., Kumar, A., Leung, H., Attia, K. A., & Kikuchi, S. (2012) · Molecular Genetics and Genomics · doi:10.1007/s00438-012-0686-8 · Cited by 54

NAC transcription factor family genes are differentially expressed in rice during infections with Rice dwarf virus, Rice black-streaked dwarf virus, Rice grassy stunt virus, Rice ragged stunt virus, and Rice transitory yellowing virus

Nuruzzaman, M., Sharoni, A. M., Satoh, K., Karim, M. R., Harikrishna, J. A., Shimizu, T., Sasaya, T., Omura, T., Haque, M. A., Hasan, S. M. Z., et al. (2015) · Frontiers in Plant Science · doi:10.3389/fpls.2015.00676 · Cited by 54

OoNAC72, a NAC-Type Oxytropis ochrocephala Transcription Factor, Conferring Enhanced Drought and Salt Stress Tolerance in Arabidopsis

Guan, H., Liu, X., Niu, F., Zhao, Q., Fan, N., Cao, D., Meng, D., He, W., Guo, B., Wei, Y., et al. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00890 · Cited by 54

Two recently duplicated maize NAC transcription factor paralogs are induced in response to Colletotrichum graminicola infection

Voitsik, A. M., Muench, S., Deising, H. B., & Voll, L. M. (2013) · BMC Plant Biology · doi:10.1186/1471-2229-13-85 · Cited by 54

Genome-wide identification and comprehensive analysis of the NAC transcription factor family in sunflower during salt and drought stress

Li, W., Zeng, Y., Yin, F., Wei, R., & Mao, X. (2021) · Scientific Reports · doi:10.1038/s41598-021-98107-4 · Cited by 53

Identification and characterization of plant-specific NAC gene family in canola (Brassica napus L.) reveal novel members involved in cell death

Wang, B., Guo, X., Wang, C., Ma, J., Niu, F., Zhang, H., Yang, B., Liang, W., Han, F., & Jiang, Y. (2015) · Plant Molecular Biology · doi:10.1007/s11103-015-0286-1 · Cited by 53

Identification of an NAP‐like transcription factor BeNAC1 regulating leaf senescence in bamboo (Bambusa emeiensis‘Viridiflavus’)

Chen, Y., Qiu, K., Kuai, B., & Ding, Y. (2011) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2011.01472.x · Cited by 53

Transcriptome analysis of rosette and folding leaves in Chinese cabbage using high-throughput RNA sequencing

Wang, F., Li, L., Li, H., Liu, L., Zhang, Y., Gao, J., & Wang, X. (2012) · Genomics · doi:10.1016/j.ygeno.2012.02.005 · Cited by 53

Biological roles of NAC transcription factors in the regulation of biotic and abiotic stress responses in solanaceous crops

Tweneboah, S., & Oh, S. (2017) · Journal of Plant Biotechnology · doi:10.5010/jpb.2017.44.1.001 · Cited by 53

Systematic analysis of NAC transcription factors’ gene family and identification of post-flowering drought stress responsive members in sorghum

Sanjari, S., Shirzadian-Khorramabad, R., Shobbar, Z., & Shahbazi, M. (2019) · Plant Cell Reports · doi:10.1007/s00299-019-02371-8 · Cited by 53

Dissecting the pathways coordinating patterning and growth by plant boundary domains

Maugarny-Calès, A., Cortizo, M., Adroher, B., Borrega, N., Gonçalves, B., Brunoud, G., Vernoux, T., Arnaud, N., & Laufs, P. (2019) · PLoS Genetics · doi:10.1371/journal.pgen.1007913 · Cited by 55

Genome-wide analysis of the NAC transcription factor family in broomcorn millet (Panicum miliaceum L.) and expression analysis under drought stress

Shan, Z., Jiang, Y., Li, H., Guo, J., Dong, M., Zhang, J., & Liu, G. (2020) · BMC Genomics · doi:10.1186/s12864-020-6479-2 · Cited by 53

The shoot apical meristem: the dynamics of a stable structure

Traas, J. A., & Vernoux, T. (2002) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2002.1091 · Cited by 53

Developmental and Wound-, Cold-, Desiccation-, Ultraviolet-B-Stress-Induced Modulations in the Expression of the Petunia Zinc Finger Transcription Factor Gene ZPT2-2

van der Krol, A. R., Poecke, R. M. P. V., Vorst, O., Voogd, C., van Leeuwen, W., Borst-Vrensen, T. W. M., Takatsuji, H., & van der Plas, L. H. W. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.121.4.1153 · Cited by 53

Recent Discoveries in Cancer Genetics of Exocrine Pancreatic Neoplasia

Hahn, S. A., & Schmiegel, W. (1998) · Digestion · doi:10.1159/000007526 · Cited by 53

Meristem maintenance and compound-leaf patterning utilize common genetic mechanisms in tomato

Brand, A., Shirding, N., Shleizer, S., & Ori, N. (2007) · Planta · doi:10.1007/s00425-007-0540-0 · Cited by 52

Transcription Factor ZmNAC20 Improves Drought Resistance by Promoting Stomatal Closure and Activating Expression of Stress-Responsive Genes in Maize

Liu, H., Song, S., Liu, M., Mu, Y., Li, Y., Xuan, Y., Niu, L., Zhang, H., & Wang, W. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24054712 · Cited by 52

Premature arrest of the male flower meristem precedes sexual dimorphism in the dioecious plant Silene latifolia

Žlůvová, J., Nicolas, M., Berger, A., Negrutiu, I., & Monéger, F. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0606622103 · Cited by 52

Analysis of transcripts differentially expressed between fruited and deflowered ‘Gala’ adult trees: a contribution to biennial bearing understanding in apple

Guitton, B., Kelner, J., Celton, J., Sabau, X., Renou, J., Chagné, D., & Costes, E. (2016) · BMC Plant Biology · doi:10.1186/s12870-016-0739-y · Cited by 51

Functional characterization of NAC55 transcription factor from oilseed rape (Brassica napus L.) as a novel transcriptional activator modulating reactive oxygen species accumulation and cell death

Niu, F., Wang, C., Yan, J., Guo, X., Wu, F., Yang, B., Deyholos, M. K., & Jiang, Y. (2016) · Plant Molecular Biology · doi:10.1007/s11103-016-0502-7 · Cited by 51

Genomic targeting and mapping of tiller inhibition gene (tin3) of wheat using ESTs and synteny with rice

Kuraparthy, V., Sood, S., & Gill, B. S. (2007) · Functional & Integrative Genomics · doi:10.1007/s10142-007-0057-4 · Cited by 51

Generation of a 3D indexed Petunia insertion database for reverse genetics

Vandenbussche, M., Janssen, A., Zethof, J., van Orsouw, N. J., Peters, J. L., van Eijk, M. J. T., Rijpkema, A. S., Schneiders, H., Santhanam, P., de Been, M., et al. (2008) · The Plant Journal · doi:10.1111/j.1365-313x.2008.03482.x · Cited by 51

Initiation of shoot apical meristem in rice: characterization of four SHOOTLESS genes

Satoh, N., Hong, S., Nishimura, A., Matsuoka, M., Kitano, H., & Nagato, Y. (1999) · Development · doi:10.1242/dev.126.16.3629 · Cited by 51

Microsatellite instability

Atkin, N. B. (2001) · Cytogenetic and Genome Research · doi:10.1159/000056898 · Cited by 51

Comparative transcriptomic analysis of male and female flowers of monoecious Quercus suber

Rocheta, M., Sobral, R. S., Magalhães, J., Amorim, I., Ribeiro, T., Pinheiro, M. M., Egas, C., Morais–Cecílio, L., & Costa, M. M. R. (2014) · Frontiers in Plant Science · doi:10.3389/fpls.2014.00599 · Cited by 50

Evolution and genetic control of the floral ground plan

Smyth, D. R. (2018) · New Phytologist · doi:10.1111/nph.15282 · Cited by 50

TaNAC48 positively regulates drought tolerance and ABA responses in wheat (Triticum aestivum L.)

Chen, J., Gong, Y., Gao, Y., Zhou, Y., Chen, M., Xu, Z., Guo, C., & Ma, Y.-Z. (2020) · The Crop Journal · doi:10.1016/j.cj.2020.09.010 · Cited by 49

A transcriptomic analysis of bermudagrass (Cynodon dactylon) provides novel insights into the basis of low temperature tolerance

Liang, C., Fan, J., Hu, L., Hu, Z., Xie, Y., Zhang, Y., Lou, Y., Nevo, E., & Fu, J. (2015) · BMC Plant Biology · doi:10.1186/s12870-015-0598-y · Cited by 49

Ontogeny of the sheathing leaf base in maize ( Zea mays )

Johnston, R., Leiboff, S., & Scanlon, M. J. (2014) · New Phytologist · doi:10.1111/nph.13010 · Cited by 50

The many roles of small RNAs in leaf development

Kidner, C. A. (2010) · Journal of genetics and genomics/Journal of Genetics and Genomics · doi:10.1016/s1673-8527(09)60021-7 · Cited by 51

Genome-wide identification, classification and expression analysis of NAC family of genes in sorghum [Sorghum bicolor (L.) Moench]

Kadier, Y., Zu, Y.-Y., Dai, Q.-M., Song, G., Lin, S.-W., Sun, Q., Pan, J., & Lu, M. (2017) · Plant Growth Regulation · doi:10.1007/s10725-017-0295-y · Cited by 49

Phyllotaxis — a new chapter in an old tale about beauty and magic numbers

Reinhardt, D. (2005) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2005.07.012 · Cited by 49

High local protein concentrations at promoters: Strategies in prokaryotic and eukaryotic cells

Dröge, P., & Müller‐Hill, B. (2001) · BioEssays · doi:10.1002/1521-1878(200102)23:2 · Cited by 60

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Kurowska, M. M., & Daszkowska‐Golec, A. (2023) · Plant Science · doi:10.1016/j.plantsci.2023.111894 · Cited by 49

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Li, S.-W., Shi, R., Leng, Y., & Zhou, Y. (2016) · BMC Genomics · doi:10.1186/s12864-016-2372-4 · Cited by 48

Expression analysis of MusaNAC68 transcription factor and its functional analysis by overexpression in transgenic banana plants

Negi, S., Tak, H., & Ganapathi, T. R. (2015) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-015-0929-6 · Cited by 48

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Robertson, M. (2004) · PLANT PHYSIOLOGY · doi:10.1104/pp.104.041665 · Cited by 48

Connections: The Hard Wiring of the Plant Cell for Perception, Signaling, and Response

Miller, D. L., Hable, W. E., Gottwald, J., Ellard-Ivey, M., Demura, T., Lomax, T. L., & Carpita, N. (1997) · The Plant Cell · doi:10.1105/tpc.9.12.2105 · Cited by 48

Suppression of a NAC-Like Transcription Factor Gene Improves Boron-Toxicity Tolerance in Rice

Ochiai, K., Shimizu, A., Okumoto, Y., Fujiwara, T., & Matoh, T. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.171470 · Cited by 47

Combined small RNA and degradome sequencing reveals microRNA regulation during immature maize embryo dedifferentiation

Shen, Y., Zhou, J., Lu, S., Lin, H., Gao, S., Peng, H., Yuan, G., Liu, L., Zhang, Z., Zhao, M., et al. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2013.10.113 · Cited by 47

Divergent Expression Patterns of miR164 and CUP-SHAPED COTYLEDON Genes in Palms and Other Monocots: Implication for the Evolution of Meristem Function in Angiosperms

Adam, H., Marguerettaz, M., Qadri, R., Adroher, B., Richaud, F., Collin, M., Thuillet, A., Vigouroux, Y., Laufs, P., Tregear, J. W., et al. (2010) · Molecular Biology and Evolution · doi:10.1093/molbev/msq328 · Cited by 47

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Zhu, G., Chen, G., Zhu, J., Zhu, Y. Y., Lu, X., Li, X., Hu, Y., & Yan, Y. (2015) · PLoS ONE · doi:10.1371/journal.pone.0139794 · Cited by 47

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Zhao, H., Lou, Y., Sun, H., Li, L., Wang, L., Dong, L., & Gao, Z. (2016) · BMC Plant Biology · doi:10.1186/s12870-016-0720-9 · Cited by 47

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Zhang, H., Cui, X., Guo, Y., Luo, C., & Zhang, L. (2018) · Plant Molecular Biology · doi:10.1007/s11103-018-0792-z · Cited by 47

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Ding, L., Zhao, K., Zhang, X., Song, A., Su, J., Hu, Y., Zhao, W., Jiang, J., & Chen, F. (2019) · Plant Biotechnology Journal · doi:10.1111/pbi.13143 · Cited by 47

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Peng, H., Yu, X., Cheng, H., Shi, Q., Zhang, H., Li, J., & Ma, H. (2009) · Molecular Biotechnology · doi:10.1007/s12033-009-9202-8 · Cited by 47

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Cheng, X., Peng, J., Ma, J., Tang, Y., Chen, R., Mysore, K. S., & Wen, J. (2012) · New Phytologist · doi:10.1111/j.1469-8137.2012.04147.x · Cited by 93

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Genes involved in organ separation in Arabidopsis: an analysis of the cup-shaped cotyledon mutant.

Aida, M., Ishida, T., Fukaki, H., Fujisawa, H., & Tasaka, M. (1997) · The Plant Cell · doi:10.1105/tpc.9.6.841 · Cited by 1,486

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Sablowski, R. W. M., & Meyerowitz, E. M. (1998) · Cell · doi:10.1016/s0092-8674(00)80902-2 · Cited by 574

Genes Specifying Floral Meristem Identity in Arabidopsis

Yanofsky, M. F., Araki, T., Gustafson‐Brown, C., Kempin, S. A., Mandel, M. A., & Savidge, B. (1994) · Springer eBooks · doi:10.1007/978-3-642-78852-9_6 · Cited by 1