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

The developmental gene Knotted-1 is a member of a maize homeobox gene family

Vollbrecht, E., Veit, B. E., Sinha, N. R., & Hake, S. (1991) · Nature · doi:10.1038/350241a0 · Cited by 760

Expression of maize KNOTTED1 related homeobox genes in the shoot apical meristem predicts patterns of morphogenesis in the vegetative shoot

Jackson, D., Veit, B. E., & Hake, S. (1994) · Development · doi:10.1242/dev.120.2.405 · Cited by 754

A knotted1-Like Homeobox Gene in Arabidopsis Is Expressed in the Vegetative Meristem and Dramatically Alters Leaf Morphology When Overexpressed in Transgenic Plants

Lincoln, C., Long, J. C., Yamaguchi, J., Serikawa, K. A., & Hake, S. (1994) · The Plant Cell · doi:10.1105/tpc.6.12.1859 · Cited by 684

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

Overexpression of the maize homeo box gene, KNOTTED-1, causes a switch from determinate to indeterminate cell fates.Preprint

Sinha, N. R., Williams, R., & Hake, S. (1993) · Genes & Development · doi:10.1101/gad.7.5.787 · Cited by 457

A dominant mutation in the maize homeobox gene, Knotted-1, causes its ectopic expression in leaf cells with altered fates

Smith, L. G., Greene, B. A., Veit, B. E., & Hake, S. (1992) · Development · doi:10.1242/dev.116.1.21 · Cited by 441

Sequence analysis and expression patterns divide the maize knotted1-like homeobox genes into two classes.

Kerstetter, R. A., Vollbrecht, E., Lowe, B., Veit, B. E., Yamaguchi, J., & Hake, S. (1994) · The Plant Cell · doi:10.1105/tpc.6.12.1877 · Cited by 332

The barley Hooded mutation caused by a duplication in a homeobox gene intron

Müller, K. J., Romano, N., Gerstner, O., García‐Maroto, F., Pozzi, C. M., Salamini, F., & Rohde, W. (1995) · Nature · doi:10.1038/374727a0 · Cited by 217

Early embryogenesis in Arabidopsis thaliana. I. The mature embryo sac

Mansfield, S. G., BRIARTY, L. G., & Erni, S. (1991) · Canadian Journal of Botany · doi:10.1139/b91-062 · Cited by 171

Effect of mutations in the PINHEAD gene of Arabidopsis on the formation of shoot apical meristems

McConnell, J. R., & Barton, M. K. (1995) · Developmental Genetics · doi:10.1002/dvg.1020160409 · Cited by 129

From the laboratory to the field: assaying histone methylation at FLOWERING LOCUS C in naturally growing Arabidopsis halleri

Nishio, H., Buzas, D. M., Nagano, A. J., Suzuki, Y., Sugano, S., Itô, M., Morinaga, S., & Kudoh, H. (2016) · Genes & Genetic Systems · doi:10.1266/ggs.15-00071 · Cited by 22

Increased STM expression is associated with drought tolerance in Arabidopsis

Lee, H. G., Choi, Y.-R., & Seo, P. J. (2016) · Journal of Plant Physiology · doi:10.1016/j.jplph.2016.07.002 · Cited by 22

Two tonoplast proton pumps function in Arabidopsis embryo development

Jiang, Y., Tang, R., Zhang, Y., Xue, H., Ferjani, A., Luan, S., & Lin, W. (2019) · New Phytologist · doi:10.1111/nph.16231 · Cited by 22

Genome-wide identification and phylogenetic analysis of rice FTIP gene family

Zhu, M., Yan, B., Hu, Y., Cui, Z., & Wang, X. (2020) · Genomics · doi:10.1016/j.ygeno.2020.03.003 · Cited by 22

Characterization of the KNOTTED1-LIKE HOMEOBOX (KNOX) gene family in Pinus pinaster Ait.

Bueno, N., Álvarez, J. M., & Ordás, R. J. (2020) · Plant Science · doi:10.1016/j.plantsci.2020.110691 · Cited by 22

Review of forests, wood products and wood biotechnology of Iran and Germany - Part II

Kharazipour, A., Schöpper, C., & Müller, C. (2008) · doi:10.17875/gup2008-263 · Cited by 22

Formation, Maintenance and Function of the Shoot Apical Meristem in Rice

Itoh, J.-I., Sato, Y., Nagato, Y., & Matsuoka, M. (2006) · Plant Molecular Biology · doi:10.1007/s11103-005-5579-3 · Cited by 23

Embryology-Seeds

Yam, T. W., Yeung, E. C.-T., Ye, X., Zee, S., & Arditti, J. (2002) · Springer eBooks · doi:10.1007/978-94-017-2500-2_6 · Cited by 22

Overexpression of a Novel LcKNOX Transcription Factor from Liriodendron chinense Induces Lobed Leaves in Arabidopsis thaliana

Ma, J., Mei, G., Liu, H., & Li, H. (2019) · Forests · doi:10.3390/f11010033 · Cited by 21

Tomato transcriptional repressor SlBES1 .8 influences shoot apical meristem development by inhibiting the DNA binding ability of SlWUS

Su, D., Wen, L., Xiang, W., Shi, Y., Wang, L., Liu, Y., Xian, Z., & Li, Z. (2022) · The Plant Journal · doi:10.1111/tpj.15683 · Cited by 21

Transcription factors KNAT3 and KNAT4 are essential for integument and ovule formation in Arabidopsis

Chen, J.-J., Wang, W., Qin, W., Men, S., Li, H.-L., Mitsuda, N., Ohme‐Takagi, M., & Wu, A. (2022) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiac513 · Cited by 21

ERF5 enhances protocorm‐like body regeneration via enhancement of STM expression in Dendrobium orchid

Zeng, D., Si, C., Zhang, M., Duan, J., & He, C. (2023) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13534 · Cited by 21

Traveling with purpose: cell-to-cell transport of plant mRNAs

Kitagawa, M., Tran, T. M., & Jackson, D. P. (2023) · Trends in Cell Biology · doi:10.1016/j.tcb.2023.05.010 · Cited by 21

Altered HBK3 expression affects glutathione and ascorbate metabolism during the early phases of Norway spruce (Picea abies) somatic embryogenesis

Belmonte, M. F., & Stasolla, C. (2009) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2009.05.011 · Cited by 21

Expression of KxhKN4 and KxhKN5 genes in Kalanchoë blossfeldiana ‘Molly’ results in novel compact plant phenotypes: towards a cisgenesis alternative to growth retardants

Lütken, H., Laura, M., Borghi, C., Ørgaard, M., Allavena, A., & Rasmussen, S. K. (2011) · Plant Cell Reports · doi:10.1007/s00299-011-1132-9 · Cited by 21

ZRF1 Chromatin Regulators Have Polycomb Silencing and Independent Roles in Development

Feng, J., Chen, D.-H., Berr, A., & Shen, W. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.00193 · Cited by 21

Ectopic expression of the transcription factor CUC2 restricts growth by cell cycle inhibition inArabidopsisleaves

Li, X., Zheng, Y., Xing, Q., Ardiansyah, R., Zhou, H., Ali, S., Jing, T., Tian, J., Song, X., Li, Y., et al. (2020) · Plant Signaling & Behavior · doi:10.1080/15592324.2019.1706024 · Cited by 21

Network analyses identify a transcriptomic proximodistal prepattern in the maize leaf primordium

Leiboff, S., Strable, J., Johnston, R., Federici, S., Sylvester, A. W., & Scanlon, M. J. (2020) · New Phytologist · doi:10.1111/nph.17132 · Cited by 21

Evolutionary Relationships and Divergence of KNOTTED1-Like Family Genes Involved in Salt Tolerance and Development in Cotton (Gossypium hirsutum L.)

Zhang, X., Zhao, J., Wu, X., Hu, G., Shuli, F., & Ma, Q. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.774161 · Cited by 21

Isolation and characterization of cgchi3, a nodule‐specific gene from Casuarina glauca encoding a class III chitinase

Fortunato, A. S., Santos, P., Graça, I., Gouveia, M. M., Martins, S. M., Ricardo, C. P., Pawlowski, K., & Ribeiro-Barros, A. I. (2007) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2006.00864.x · Cited by 21

Homologs of animal eyes absent (eya) genes are found in higher plants

Takeda, Y., Hatano, S., Sentoku, N., & Matsuoka, M. (1999) · Molecular and General Genetics MGG · doi:10.1007/s004380051067 · Cited by 21

Os ARID 3, an AT ‐rich Interaction Domain‐containing protein, is required for shoot meristem development in rice

Xu, Y., Zong, W., Hou, X., Yao, J., Liu, H., Li, X., Zhao, Y., & Xiong, L. (2015) · The Plant Journal · doi:10.1111/tpj.12927 · Cited by 21

An integrated strategy to identify key genes in almond adventitious shoot regeneration

Santos, A. M., Oliver, M. J., Sánchez, A. M., Payton, P., Gomes, J. P., Miguel, C. M. G., & Oliveira, M. M. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp250 · Cited by 21

Cytokinin biosynthesis genes expressed during nodule organogenesis are directly regulated by the KNOX3 protein in Medicago truncatula

Azarakhsh, M., Rumyantsev, A. M., Lebedeva, M. A., & Lutova, L. A. (2020) · PLoS ONE · doi:10.1371/journal.pone.0232352 · Cited by 21

Site-directed mutagenesis and footprinting analysis of the interaction of the sunflower KNOX protein HAKN1 with DNA

Tioni, M. F., Viola, I. L., Chan, R. L., & González, D. H. (2004) · FEBS Journal · doi:10.1111/j.1742-4658.2005.04402.x · Cited by 21

The formation and patterning of leaves: recent advances

Canales, C., Grigg, S. P., & Tsiantis, M. (2005) · Planta · doi:10.1007/s00425-005-1549-x · Cited by 21

Plasmodesmata distribution and sugar partitioning in nitrogen-fixing root nodules of Datisca glomerata

Schubert, M., Koteyeva, N. K., Wabnitz, P. W., Santos, P., Büttner, M., Sauer, N., Demchenko, K. N., & Pawlowski, K. (2010) · Planta · doi:10.1007/s00425-010-1285-8 · Cited by 21

The expression of Brostm, a KNOTTED1-like gene, marks the cell type and timing of in vitro shoot induction in Brassica oleracea

Teo, W. L.-L., Kumar, P. P., Goh, C., & Swarup, S. (2001) · Plant Molecular Biology · doi:10.1023/a:1010686931889 · Cited by 21

Of Blades and Branches: Understanding and Expanding the Arabidopsis Ad/Abaxial Regulatory Network through Target Gene IdentificationPreprint

Liu, T., Reinhart, B. J., Magnani, E., Huang, T., Kerstetter, R. A., & Barton, M. K. (2012) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2013.77.014480 · Cited by 21

Knowing When to Silence: Roles of Polycomb-Group Proteins in SAM Maintenance, Root Development, and Developmental Phase Transition

Yan, B., Lv, Y., Zhao, C., & Wang, X. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21165871 · Cited by 21

Single-cell transcriptomic analysis of flowering regulation and vernalization in Chinese cabbage shoot apex

Dai, Y., Zhang, S.-F., Guan, J., Wang, S., Zhang, H., Li, G., Sun, R., Li, F., & Zhang, S. (2024) · Horticulture Research · doi:10.1093/hr/uhae214 · Cited by 20

Dysfunction of mitotic cell division at shoot apices triggered severe growth abortion in interspecific hybrids between tetraploid wheat and Aegilops tauschii

Hatano, H., Mizuno, N., Matsuda, R., Shitsukawa, N., Park, P., & Takumi, S. (2012) · New Phytologist · doi:10.1111/j.1469-8137.2012.04125.x · Cited by 21

Rice Homeobox Transcription Factor HOX1a Positively Regulates Gibberellin Responses by Directly Suppressing EL1F

Wen, B.-Q., Xing, M., Zhang, H., Dai, C., & Xue, H. (2011) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2011.01075.x · Cited by 20

Novel Insights from Live‐imaging in Shoot Meristem Development

Sijacic, P., & Liu, Z. (2010) · Journal of Integrative Plant Biology · doi:10.1111/j.1744-7909.2010.00941.x · Cited by 21

The AG Dinucleotide Terminating Introns Is Important but Not Always Required for Pre-mRNA Splicing in the Maize Endosperm1

Lal, S. K., Choi, J., & Hannah, L. C. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.120.1.65 · Cited by 20

Ectopic Gene Expression and Organogenesis inArabidopsisMutants Missing BRU1 Required for Genome Maintenance

Ohno, Y., Narangajavana, J., Yamamoto, A., Hattori, T., Kagaya, Y., Paszkowski, J., Gruissem, W., Hennig, L., & Takeda, S. (2011) · Genetics · doi:10.1534/genetics.111.130062 · Cited by 22

Transcription factors in developmental genetics and the evolution of higher plants

Lutova, L. A., Dodueva, I. E., Lebedeva, M. A., & Tvorogova, V. E. (2015) · Russian Journal of Genetics · doi:10.1134/s1022795415030084 · Cited by 20

Maintaining the shoot meristem — the role of CLAVATA1

Laux, T., & Schoof, H. (1997) · Trends in Plant Science · doi:10.1016/s1360-1385(97)84613-4 · Cited by 20

Oncogene 6b from Agrobacterium tumefaciens Induces Abaxial Cell Division at Late Stages of Leaf Development and Modifies Vascular Development in Petioles

Terakura, S., Kitakura, S., Ishikawa, M., Ueno, Y., Fujita, T., Machida, C., Wabiko, H., & Machida, Y. (2006) · Plant and Cell Physiology · doi:10.1093/pcp/pcj036 · Cited by 20

Control of Shoot Cell Fate: Beyond Homeoboxes

Tsiantis, M. (2001) · The Plant Cell · doi:10.1105/tpc.13.4.733 · Cited by 20

Cells and domains: Two views of the shoot meristem in Arabidopsis

Laufs, P., Jonak, C., & Traas, J. A. (1998) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(98)80089-2 · Cited by 20

Proteolysis in plants: mechanisms and functions

Vierstra, R. D. (1996) · Springer eBooks · doi:10.1007/978-94-009-0353-1_12 · Cited by 23

Overexpression of miR390b promotes stem elongation and height growth in Populus

Shi, Q.-F., Tian, D., Wang, J., Chen, A., Miao, Y., Chen, Y., Li, J., Wu, X., Zheng, B., Guo, W., et al. (2022) · Horticulture Research · doi:10.1093/hr/uhac258 · Cited by 19

Influence of 5′-azacitidine on promoting recovery of cell competence for shoot organogenesis in Arabidopsis

Tokuji, Y., Takano, S., Tonomura, M., Tanaka, S., Igari, K., & Watanabe, T. (2011) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-011-9920-z · Cited by 19

Toward Molecular Understanding of In Vitro and In Planta Shoot Organogenesis

Meng, L., Zhang, S., & Lemaux, P. G. (2010) · Critical Reviews in Plant Sciences · doi:10.1080/07352681003617327 · Cited by 19

A Recently Formed Triploid Cardamine insueta Inherits Leaf Vivipary and Submergence Tolerance Traits of Parents

Sun, J., Shimizu‐Inatsugi, R., Hofhuis, H. F., Shimizu, K. K., Hay, A., Shimizu, K. K., & Sese, J. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.567262 · Cited by 19

Thin Cell Layers and Floral Morphogenesis, Floral Genetics and in Vitro Flowering

da Silva, J. A. T., & Nhựt, D. T. (2003) · Springer eBooks · doi:10.1007/978-94-017-3522-3_8 · Cited by 19

Core pathways controlling shoot meristem maintenance

Lee, C.-H., & Clark, S. E. (2013) · Wiley Interdisciplinary Reviews Developmental Biology · doi:10.1002/wdev.110 · Cited by 19

WUS and STM-based reporter genes for studying meristem development in poplar

Bao, Y., Dharmawardhana, P. D., Arias, R. S., Allen, M. B., Ma, C., & Strauss, S. H. (2009) · Plant Cell Reports · doi:10.1007/s00299-009-0685-3 · Cited by 19

Transcriptome reprogramming in the shoot apical meristem of CymRSV‐infected Nicotiana benthamiana plants associates with viral exclusion and the lack of recovery

Medzihradszky, A., Gyula, P., Sós‐Hegedűs, A., Szittya, G., & Burgyán, J. (2019) · Molecular Plant Pathology · doi:10.1111/mpp.12875 · Cited by 19

5 Digging out Roots: Pattern Formation, Cell Division, and Morphogenesis in Plants

Scheres, B., & Heidstra, R. (1999) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/s0070-2153(08)60317-8 · Cited by 19

Switching on Gene Expression: Analysis of the Factors that Spatially and Temporally Regulate Plant Gene Expression

Meisel, L. A., & Lam, E. (1997) · Springer eBooks · doi:10.1007/978-1-4615-5925-2_10 · Cited by 19

Alternative splicing of two leading exons partitions promoter activity between the coding regions of the maize homeobox gene Zmhox1a and Trap (transposon-associated protein)

Comelli, P., König, J., & Werr, W. (1999) · Plant Molecular Biology · doi:10.1023/a:1006382725952 · Cited by 19

Diversity of tomato leaf form provides novel insights into breeding

Nakayama, H., Ichihashi, Y., & Kimura, S. (2023) · Ikushugaku zasshi · doi:10.1270/jsbbs.22061 · Cited by 18

Re-examining meristems through the lens of evo-devo

Arnoux-Courseaux, M., & Coudert, Y. (2023) · Trends in Plant Science · doi:10.1016/j.tplants.2023.11.003 · Cited by 18

Shaping leaves through TALE homeodomain transcription factors

Byrne, M. E., Imlay, E. E., & Ridza, N. N. B. (2024) · Journal of Experimental Botany · doi:10.1093/jxb/erae118 · Cited by 18

afila , the origin and nature of a major innovation in the history of pea breeding

Tayeh, N., Hofer, J. M. I., Aubert, G., Jacquin, F., Turner, L., Kreplak, J., Paajanen, P., Signor, C. L., Dalmais, M., Pflieger, S., et al. (2024) · New Phytologist · doi:10.1111/nph.19800 · Cited by 21

A dynamic regulome of shoot-apical-meristem-related homeobox transcription factors modulates plant architecture in maize

Luo, Z. W., Wu, L., Miao, X., Zhang, S., Wei, N., Zhao, S., Shang, X., Hu, H., Xue, J., Zhang, T., et al. (2024) · Genome biology · doi:10.1186/s13059-024-03391-8 · Cited by 18

Gynoecium Patterning in Arabidopsis: A Basic Plan behind a Complex Structure

Sundberg, E., & Ferrándiz, C. (2009) · Wiley-Blackwell eBooks · doi:10.1002/9781444314557.ch2 · Cited by 19

Arabidopsis flower development—of protein complexes, targets, and transport

Becker, A., & Ehlers, K. (2015) · PROTOPLASMA · doi:10.1007/s00709-015-0812-7 · Cited by 18

Combinations of Mutations Sufficient to Alter Arabidopsis Leaf Dissection

Blein, T., Pautot, V., & Laufs, P. (2013) · Plants · doi:10.3390/plants2020230 · Cited by 18

Molecular dissection of the pea shoot apical meristem*

Liang, D., Wong, C. E., Singh, M. B., Beveridge, C. A., Phipson, B., Smyth, G. K., & Bhalla, P. L. (2009) · Journal of Experimental Botany · doi:10.1093/jxb/erp254 · Cited by 18

Simple and Divided Leaves in Ferns: Exploring the Genetic Basis for Leaf Morphology Differences in the Genus Elaphoglossum (Dryopteridaceae)

Vasco, A., & Ambrose, B. A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21155180 · Cited by 18

Overexpression of the AtWUSCHEL gene promotes somatic embryogenesis and lateral branch formation in birch (Betula platyphylla Suk.)

Lou, H., Huang, Y., Wang, W., Cai, Z., Cai, H., Liu, Z., Sun, L., & Xu, Q. (2022) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-022-02290-9 · Cited by 18

Asymmetric Cell Division in Plant Development

Heidstra, R. (2007) · Progress in molecular and subcellular biology · doi:10.1007/978-3-540-69161-7_1 · Cited by 18

Leaf Initiation: The Integration of Growth and Cell Division

Fleming, A. J. (2006) · Plant Molecular Biology · doi:10.1007/s11103-005-7703-9 · Cited by 18

Glutathione modulation of in vitro development

Yeung, E. C.-T., Belmonte, M. F., Tu, L. T. T., & Stasolla, C. (2005) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1079/ivp2005683 · Cited by 18

Molecular Mechanisms of Floral Boundary Formation in Arabidopsis

Yu, H., & Huang, T. (2016) · International Journal of Molecular Sciences · doi:10.3390/ijms17030317 · Cited by 19

The Tomato Leaf as a Model System for Organogenesis

Burko, Y., & Ori, N. (2012) · Methods in molecular biology · doi:10.1007/978-1-62703-221-6_1 · Cited by 18

Binding properties of the complex formed by the Arabidopsis TALE homeodomain proteins STM and BLH3 to DNA containing single and double target sites

Viola, I. L., & González, D. H. (2009) · Biochimie · doi:10.1016/j.biochi.2009.04.021 · Cited by 18

Genetic control of shoot and flower meristem behavior

Liljegren, S. J., & Yanofsky, M. F. (1996) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(96)80089-5 · Cited by 18

Molecular mechanism of leaf development

Song, Y. A. N. (2009) · Hereditas (Beijing) · doi:10.3724/sp.j.1005.2008.01127 · Cited by 18

Coagulation, Fibrinolysis and Angiogenesis: New Insights from Knockout Mice

Brodsky, S. V. (2002) · Nephron Experimental Nephrology · doi:10.1159/000065305 · Cited by 18

Experimental approaches to Arabidopsis embryogenesis

Berleth, T. (1998) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(98)80092-2 · Cited by 18

Molecular Architects of Plant Body Plans

Theißen, G., & Saedler, H. (1998) · Progress in botany · doi:10.1007/978-3-642-80446-5_8 · Cited by 18

Berberine enhances defects in the establishment of leaf polarity in asymmetric leaves1 and asymmetric leaves2 of Arabidopsis thaliana

Nakagawa, A., Takahashi, H., Kojima, S., Sato, N., Ohga, K., Yoon, B. H., Woo, J., Nagai, K., Horiguchi, G., Tsukaya, H., et al. (2012) · Plant Molecular Biology · doi:10.1007/s11103-012-9929-7 · Cited by 17

Up-regulation of LsKN1 promotes cytokinin and suppresses gibberellin biosynthesis to generate wavy leaves in lettuce

Jia, Y., Yu, P., Shao, W., An, G., Chen, J., Yu, C., & Kuang, H. (2022) · Journal of Experimental Botany · doi:10.1093/jxb/erac311 · Cited by 17

Evolution of a SHOOTMERISTEMLESS transcription factor binding site promotes fruit shape determination

Hu, Z.-C., Majda, M., Sun, H.-R., Zhang, Y., Ding, Y., Yuan, Q., Su, T., Lü, T., Gao, F., Xu, G., et al. (2024) · Nature Plants · doi:10.1038/s41477-024-01854-1 · Cited by 17

The role of floral meristems in patterning

Running, M., & Hake, S. (2001) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(00)00138-2 · Cited by 17

The Mobile bypass Signal Arrests Shoot Growth by Disrupting Shoot Apical Meristem Maintenance, Cytokinin Signaling, and WUS Transcription Factor Expression

Lee, D.-K., Parrott, D. L., Adhikari, E., Fraser, N., & Sieburth, L. (2016) · PLANT PHYSIOLOGY · doi:10.1104/pp.16.00474 · Cited by 17

Flower development: from morphodynamics to morphomechanics

Abad, U., Sassi, M., & Traas, J. A. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2015.0545 · Cited by 18

Seedling‐derived leaf and root tip as alternative explants for callus induction and plant regeneration in maize

Wang, C., Ma, H., Zhu, W., Zhang, J., Zhao, X., & Li, X. (2021) · Physiologia Plantarum · doi:10.1111/ppl.13347 · Cited by 17

Overexpression of LtKNOX1 from Lilium tsingtauense in Nicotiana benthamiana affects the development of leaf morphology

Zhou, R., Fan, M., Zhao, M., Jiang, X., & Liu, Q. (2022) · Plant Signaling & Behavior · doi:10.1080/15592324.2022.2031783 · Cited by 17

Defects in meristem maintenance, cell division, and cytokinin signaling are early responses in the boron deficient maize mutant tassel‐less1

Matthes, M. S., Darnell, Z., Best, N. B., Guthrie, K., Robil, J. M., Amstutz, J., Durbak, A. R., & McSteen, P. (2022) · Physiologia Plantarum · doi:10.1111/ppl.13670 · Cited by 17

HAM proteins promote organ indeterminacy

Engstrom, E. M. (2012) · Plant Signaling & Behavior · doi:10.4161/psb.18958 · Cited by 17

Low Temperature Affects Stem Cell Maintenance in Brassica oleracea Seedlings

de Jonge, J., Kodde, J., Severing, E. I., Bonnema, G., Angenent, G. C., Immink, R. G. H., & Groot, S. P. C. (2016) · Frontiers in Plant Science · doi:10.3389/fpls.2016.00800 · Cited by 17

From shoot to leaf: step-wise shifts in meristem and KNOX1 activity correlate with the evolution of a unifoliate body plan in Gesneriaceae

Nishii, K., Huang, B.-H., Wang, C., & Möller, M. (2016) · Development Genes and Evolution · doi:10.1007/s00427-016-0568-x · Cited by 17

Identification of novel markers for stem-cell niche of Arabidopsis shoot apex

Aggarwal, P., Yadav, R. K., & Reddy, G. V. (2010) · Gene Expression Patterns · doi:10.1016/j.gep.2010.05.004 · Cited by 17

Genetic control of plant development

McSteen, P., & Hake, S. (1998) · Current Opinion in Biotechnology · doi:10.1016/s0958-1669(98)80114-6 · Cited by 17

Scarecrow: Specifying asymmetric cell divisions throughout development

Dolan, L. (1997) · Trends in Plant Science · doi:10.1016/s1360-1385(97)82723-9 · Cited by 17

Expanding insights into the role of cell proliferation in plant development

Clark, S. E., & Schiefelbein, J. (1997) · Trends in Cell Biology · doi:10.1016/s0962-8924(97)01152-5 · Cited by 17

Leaving the meristem behind: regulation of KNOX genes.

Barton, M. K. (2001) · Genome biology · doi:10.1186/gb-2001-2-1-reviews1002 · Cited by 17

Expression of novel homeobox genes in early embryogenesis in rice

Ito, Y., Eiguchi, M., & Kurata, N. (1999) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/s0167-4781(99)00023-8 · Cited by 17

TM20, a Gene Coding for a New Class of Transmembrane Proteins Expressed in the Meristematic Tissues of Maize

Stiefel, V., Becerra, E. L., Roca, R., Bastida, M., Jahrmann, T., Graziano, E., & Puigdomènech, P. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.39.27734 · Cited by 17

ARF3-mediated auxin signaling is essential for sex determination in cucumber

Han, L., Li, M., Li, C., Zhao, B., Wang, Z., Liu, Y., Liu, Z., Huang, Y., Liu, L., Geng, H., et al. (2025) · Science · doi:10.1126/science.adv2006 · Cited by 16

SKI-INTERACTING PROTEIN interacts with SHOOT MERISTEMLESS to regulate shoot apical meristem formation

Li, R., Wei, Z., Li, Y., Shang, X., Cao, Y., Duan, L., & Ma, L. (2022) · PLANT PHYSIOLOGY · doi:10.1093/plphys/kiac241 · Cited by 16

Rewiring of a KNOXI regulatory network mediated by UFO underlies the compound leaf development in Medicago truncatula

Lu, Z., Zhang, J., Wang, H., Zhang, K., Gu, Z., Xu, Y., Zhang, J., Wang, M., Han, L., Xiang, F., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-47362-w · Cited by 16

Leaflet initiation is temporally and spatially separated in simple and complex tomato (Solanum lycopersicum) leaf mutants: a developmental analysis

Kang, J., & Sinha, N. R. (2010) · Botany · doi:10.1139/b10-051 · Cited by 16

LFR is functionally associated with AS 2 to mediate leaf development in Arabidopsis

Lin, X., Gu, D., Zhao, H., Peng, Y. P., Zhang, G., Yuan, T., Li, M., Wang, Z., Wang, X., & Cui, S. (2018) · The Plant Journal · doi:10.1111/tpj.13973 · Cited by 16

Alternative repair pathways for UV-induced DNA damage

Yasui, A., & McCready, S. J. (1998) · BioEssays · doi:10.1002/(sici)1521-1878(199804)20:4

Short CommuniCation www.landesbioscience.com Plant Signaling & Behavior e28934-1 Plant Signaling & Behavior 9, e28934; april; © 2014 Landes Bioscience

Communication, S. (2016)

A model for Arabidopsis class-1 KNOX gene function

Scofield, S., Dewitte, W., & Murray, J. A. H. (2008) · Plant Signaling & Behavior · doi:10.4161/psb.3.4.5194 · Cited by 46

Regulation of meristem and hormone function revealed through analysis of directly-regulated SHOOT MERISTEMLESS target genes

Lechón, T., Kent, N. A., Murray, J. A. H., & Scofield, S. (2025) · Scientific Reports · doi:10.1038/s41598-024-83985-1 · Cited by 14

The A rabidopsis homeobox gene SHOOT MERISTEMLESS has cellular and meristem‐organisational roles with differential requirements for cytokinin and CYCD3 activity

Scofield, S., Dewitte, W., Nieuwland, J., & Murray, J. A. H. (2013) · The Plant Journal · doi:10.1111/tpj.12198 · Cited by 104

STM sustains stem cell function in theArabidopsisshoot apical meristem and controlsKNOXgene expression independently of the transcriptional repressor AS1

Scofield, S., Dewitte, W., & Murray, J. A. H. (2014) · Plant Signaling & Behavior · doi:10.4161/psb.28934 · Cited by 57