Morphogenic Regulators Baby boom and Wuschel Improve Monocot Transformation

Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT Method

Livak, K. J., & Schmittgen, T. D. (2001) · Methods · doi:10.1006/meth.2001.1262 · Cited by 180,860 · see citing works

Assaying chimeric genes in plants: The GUS gene fusion system

Jefferson, R. (1987) · Plant Molecular Biology Reporter · doi:10.1007/bf02667740 · Cited by 4,512 · see citing works

Mutation of the mouse klotho gene leads to a syndrome resembling ageing

Kuro-o, M., Matsumura, Y., Aizawa, H., Kawaguchi, H., Suga, T., Utsugi, T., Ohyama, Y., Kurabayashi, M., Kaname, T., Kume, E., et al. (1997) · Nature · doi:10.1038/36285 · Cited by 3,837 · see citing works

Fluorescent proteins from nonbioluminescent Anthozoa species

Matz, M. V., Fradkov, A. F., Labas, Y. A., Savitsky, A. P., Zaraisky, A. G., Markelov, M. L., & Lukyanov, S. (1999) · Nature Biotechnology · doi:10.1038/13657 · Cited by 1,839 · see citing works

Preparation of PCR-Quality Mouse Genomic DNA with Hot Sodium Hydroxide and Tris (HotSHOT)

Truett, G. E., Heeger, P. S., Mynatt, R. L., Truett, A. A., Walker, J. A., & Warman, M. L. (2000) · BioTechniques · doi:10.2144/00291bm09 · Cited by 1,748 · see citing works

Role of WUSCHEL in Regulating Stem Cell Fate in the Arabidopsis Shoot Meristem

Mayer, K., Schoof, H., Haecker, A., Lenhard, M., Jürgens, G., & Laux, T. (1998) · Cell · doi:10.1016/s0092-8674(00)81703-1 · Cited by 1,688 · see citing works

The WUSCHEL gene is required for shoot and floral meristem integrity in Arabidopsis

Laux, T., Mayer, K., Berger, J., & Jürgens, G. (1996) · Development · doi:10.1242/dev.122.1.87 · Cited by 1,270 · see citing works

Plant Microtechnique and Microscopy

Ruzin, S. E. (1999) · Medical Entomology and Zoology · Cited by 1,152 · see citing works

Ectopic Expression of BABY BOOM Triggers a Conversion from Vegetative to Embryonic Growth

Boutilier, K., Offringa, R., Sharma, V. K., Kieft, H., Ouellet, T., Zhang, L., Hattori, J., Liu, C., van Lammeren, A. A. M., Miki, B. L. A., et al. (2002) · The Plant Cell · doi:10.1105/tpc.001941 · Cited by 1,081 · see citing works

A DNA Transformation–Competent Arabidopsis Genomic Library in Agrobacterium

Lazo, G. R., Stein, P. A., & Ludwig, R. A. (1991) · Nature Biotechnology · doi:10.1038/nbt1091-963 · Cited by 1,073 · see citing works

Arabidopsis LEAFY COTYLEDON1 Is Sufficient to Induce Embryo Development in Vegetative Cells

Lotan, T., Ohto, M., Yee, K. M., West, M. A. L., Lo, R. S., Kwong, R. W., Yamagishi, K., Fischer, R. L., Goldberg, R. B., & Harada, J. J. (1998) · Cell · doi:10.1016/s0092-8674(00)81463-4 · Cited by 1,063 · see citing works

Maize polyubiquitin genes: structure, thermal perturbation of expression and transcript splicing, and promoter activity following transfer to protoplasts by electroporation

Christensen, A. H., Sharrock, R., & Quail, P. H. (1992) · Plant Molecular Biology · doi:10.1007/bf00020010 · Cited by 1,007 · see citing works

Biochemistry, mutagenesis, and oligomerization of DsRed, a red fluorescent protein from coral

Baird, G. S., Zacharias, D. A., & Tsien, R. Y. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.97.22.11984 · Cited by 924 · see citing works

High efficiency transformation of maize (Zea mays L.) mediated by Agrobacterium tumefaciens

Ishida, Y., Saito, H., Ohta, S., Hiei, Y., Komari, T., & Kumashiro, T. (1996) · Nature Biotechnology · doi:10.1038/nbt0696-745 · Cited by 876 · see citing works

Construction of an intron-containing marker gene: Splicing of the intron in transgenic plants and its use in monitoring early events in Agrobacterium-mediated plant transformation

Vancanneyt, G., Schmidt, R., O’Connor-Sánchez, A., Willmitzer, L., & Rocha‐Sosa, M. (1990) · Molecular and General Genetics MGG · doi:10.1007/bf00260489 · Cited by 869 · see citing works

Early infection of scutellum tissue with Agrobacterium allows high‐speed transformation of rice

Toki, S., Hara, N., Ono, K., Onodera, H., Tagiri, A., Oka, S., & TANAKA, H. L. (2006) · The Plant Journal · doi:10.1111/j.1365-313x.2006.02836.x · Cited by 795 · see citing works

LEAFY COTYLEDON2 encodes a B3 domain transcription factor that induces embryo development

Stone, S. L., Kwong, L. W., Yee, K. M., Pelletier, J., Lepiniec, L., Fischer, R. L., Goldberg, R. B., & Harada, J. J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.201413498 · Cited by 784 · see citing works

Transformation of Maize Cells and Regeneration of Fertile Transgenic Plants.

Gordon-Kamm, W. J., Spencer, T., Mangano, M. L., Adams, T. R., Daines, R. J., Start, W. G., O'Brien, J., Chambers, S. A., Adams, W. R., Willetts, N. G., et al. (1990) · The Plant Cell · doi:10.1105/tpc.2.7.603 · Cited by 765 · see citing works

The WUSCHEL gene promotes vegetative‐to‐embryonic transition in Arabidopsis

Zuo, J., Niu, Q., Frugis, G., & Chua, N. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01289.x · Cited by 688 · see citing works

WUSCHEL protein movement mediates stem cell homeostasis in the Arabidopsis shoot apexPreprint

Yadav, R. K., Perales, M., Gruel, J., Girke, T., Jönsson, H., & Reddy, G. V. (2011) · Genes & Development · doi:10.1101/gad.17258511 · Cited by 622 · see citing works

Vectors carrying two separate T‐DNAs for co‐transformation of higher plants mediated by Agrobacterium tumefaciens and segregation of transformants free from selection markers

Komari, T., Hiei, Y., Saito, Y., Murai, N., & Kumashiro, T. (1996) · The Plant Journal · doi:10.1046/j.1365-313x.1996.10010165.x · Cited by 572 · see citing works

Inheritance and Expression of Chimeric Genes in the Progeny of Transgenic Maize Plants

Fromm, M., Morrish, F. M., Armstrong, C. L., Williams, R., Thomas, J., & Klein, T. M. (1990) · Nature Biotechnology · doi:10.1038/nbt0990-833 · Cited by 528 · see citing works

Transformation of rice mediated by Agrobacterium tumefaciens

Hiei, Y., Komari, T., & Kubo, T. (1997) · Springer eBooks · doi:10.1007/978-94-011-5794-0_20 · Cited by 478 · see citing works

Agrobacterium tumefaciens -Mediated Transformation of Maize Embryos Using a Standard Binary Vector System

Frame, B. R., Shou, H., Chikwamba, R. K., Zhang, Z., Xiang, C., Fonger, T. M., Pegg, S. E., Li, B., Nettleton, D. S., Pei, D., et al. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.000653 · Cited by 477 · see citing works

Establishment and maintenance of friable, embryogenic maize callus and the involvement of L-proline

Armstrong, C. L., & Green, C. E. (1985) · Planta · doi:10.1007/bf00396083 · Cited by 459 · see citing works

Systemic Endopolyploidy in Arabidopsis thaliana

Galbraith, D. W., Harkins, K. R., & Knapp, S. J. (1991) · PLANT PHYSIOLOGY · doi:10.1104/pp.96.3.985 · Cited by 435 · see citing works

Plant cell-size control: growing by ploidy?

Kondorosi, É., Roudier, F., & Gendreau, E. (2000) · Current Opinion in Plant Biology · doi:10.1016/s1369-5266(00)00118-7 · Cited by 348 · see citing works

Comparative analysis of transgenic rice plants obtained by Agrobacterium-mediated transformation and particle bombardment

Dai, S., Zheng, P., Marmey, P., Zhang, S., Tian, W., Chen, S., Beachy, R. N., & Fauquet, C. (2001) · Molecular Breeding · doi:10.1023/a:1009687511633 · Cited by 320 · see citing works

Plant regeneration from cultured immature embryos and inflorescences ofTriticum aestivum L. (wheat): Evidence for somatic embryogenesis

Ozias‐Akins, P., & Vasil, I. K. (1982) · PROTOPLASMA · doi:10.1007/bf01281535 · Cited by 307 · see citing works

Development of Plant Promoter Expression Vectors and Their Use for Analysis of Differential Activity of Nopaline Synthase Promoter in Transformed Tobacco Cells

An, G. (1986) · PLANT PHYSIOLOGY · doi:10.1104/pp.81.1.86 · Cited by 302 · see citing works

Selection of marker-free transgenic plants using the isopentenyl transferase gene

Ebinuma, H., Sugita, K., Matsunaga, E., & Yamakado, M. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.6.2117 · Cited by 289 · see citing works

Factors influencing Agrobacterium-mediated transformation of monocotyledonous species

Cheng, M. J., Lowe, B., Spencer, T., Ye, X., & Armstrong, C. L. (2004) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1079/ivp2003501 · Cited by 282 · see citing works

Combined SHOOT MERISTEMLESS and WUSCHEL trigger ectopic organogenesis in Arabidopsis

Gallois, J., Woodward, C. J. D. A., Reddy, G. V., & Sablowski, R. W. M. (2002) · Development · doi:10.1242/dev.129.13.3207 · Cited by 277 · see citing works

The use of phosphomannose-isomerase as a selectable marker to recover transgenic maize plants ( Zea mays L.) via Agrobacterium transformation

Negrotto, D. V., Jolley, M., Beer, S., Wenck, A., & Hansen, G. (2000) · Plant Cell Reports · doi:10.1007/s002999900187 · Cited by 260 · see citing works

Plant Regeneration from Cultured Immature Embryos and Inflorescences of 25 Cultivars of Wheat (Triticum aestivum)

Maddock, S., Lancaster, V., Risiott, R., & Franklin, J. F. (1983) · Journal of Experimental Botany · doi:10.1093/jxb/34.7.915 · Cited by 221 · see citing works

Agrobacterium‐mediated transformation of cereals: a promising approach crossing barriers

Shrawat, A. K., & Lörz, H. (2006) · Plant Biotechnology Journal · doi:10.1111/j.1467-7652.2006.00209.x · Cited by 215 · see citing works

The Shoot Stem Cell Niche in Angiosperms: Expression Patterns of WUS Orthologues in Rice and Maize Imply Major Modifications in the Course of Mono- and Dicot Evolution

Nardmann, J., & Werr, W. (2006) · Molecular Biology and Evolution · doi:10.1093/molbev/msl125 · Cited by 198 · see citing works

Heterologous expression of the BABY BOOM AP2/ERF transcription factor enhances the regeneration capacity of tobacco (Nicotiana tabacum L.)

Srinivasan, C., Liu, Z., Heidmann, I., Supena, E. D. J., Fukuoka, H., Joosen, R. V. L., Lambalk, J., Angenent, G. C., Scorza, R., Custers, J. B. M., et al. (2006) · Planta · doi:10.1007/s00425-006-0358-1 · Cited by 195 · see citing works

Gene sequence, developmental expression, and protein phosphorylation of RAB-17 in maize

Vilardell, J., Goday, A., Freire, M. A., Torrent, M., Martı́nez, M. C., Torné, J. M., & Pag�s, M. (1990) · Plant Molecular Biology · doi:10.1007/bf00028778 · Cited by 192 · see citing works

Cytokinin gene fused with a strong promoter enhances shoot organogenesis and zeatin levels in transformed plant cells

Smigocki, A. C., & Owens, L. D. (1988) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.85.14.5131 · Cited by 190 · see citing works

Plant Regeneration from Protoplasts Isolated from Embryogenic Maize Cell Cultures

Rhodes, C. A., Lowe, K. S., & Ruby, K. (1988) · Nature Biotechnology · doi:10.1038/nbt0188-56 · Cited by 187 · see citing works

Regeneration of Fertile Plants from Protoplasts of Elite Inbread Maize.

Shillito, R. D., Carswell, G. K., Johnson, C. M., DiMaio, J. J., & Harms, C. T. (1989) · Nature Biotechnology · doi:10.1038/nbt0689-581 · Cited by 181 · see citing works

Transformation and inheritance of a hygromycin phosphotransferase gene in maize plants

Walters, D. A., Vetsch, C. S., Potts, D. E., & Lundquist, R. C. (1992) · Plant Molecular Biology · doi:10.1007/bf00034948 · Cited by 163 · see citing works

Direct Embryogenesis from Mesophyll Cells of Orchardgrass

Conger, B. V., Hanning, G. E., Gray, D. J., & McDaniel, J. K. (1983) · Science · doi:10.1126/science.221.4613.850 · Cited by 161 · see citing works

Production of fertile transgenic maize plants by silicon carbide whisker‐mediated transformation

Frame, B. R., Drayton, P. R., Bagnall, S. V., Lewnau, C. J., Bullock, W. P., Wilson, H. M., Dunwell, J. M., Thompson, J. A., & Wang, K. (1994) · The Plant Journal · doi:10.1046/j.1365-313x.1994.6060941.x · Cited by 161 · see citing works

A transformation vector for the production of marker‐free transgenic plants containing a single copy transgene at high frequency

Sugita, K., Kasahara, T., Matsunaga, E., & Ebinuma, H. (2000) · The Plant Journal · doi:10.1046/j.1365-313x.2000.00745.x · Cited by 158 · see citing works

Plant stem cell maintenance involves direct transcriptional repression of differentiation program

Yadav, R. K., Perales, M., Gruel, J., Ohno, C. K., Heisler, M. G., Girke, T., Jönsson, H., & Reddy, G. V. (2013) · Molecular Systems Biology · doi:10.1038/msb.2013.8 · Cited by 150 · see citing works

Embryogenesis from cultured immature inflorescences ofSorghum bicolor

Brettell, R. I. S., Wernicke, W., & Thomas, E. (1980) · PROTOPLASMA · doi:10.1007/bf01279376 · Cited by 135 · see citing works

Optimized Agrobacterium-mediated sorghum transformation protocol and molecular data of transgenic sorghum plants

Wu, E., Lenderts, B., Glassman, K., Berezowska-Kaniewska, M., Christensen, H., Asmus, T., Zhen, S., Chu, U. C., Cho, M., & Zhao, Z. (2013) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-013-9583-z · Cited by 129 · see citing works

A novel method for induction of plant regeneration via somatic embryogenesis

Deng, W., Luo, K., Li, Z., & Yang, Y. (2009) · Plant Science · doi:10.1016/j.plantsci.2009.03.009 · Cited by 126 · see citing works

A protocol for consistent, large-scale production of fertile transgenic rice plants

Chen, L., Zhang, S., Beachy, R. N., & Fauquet, C. (1998) · Plant Cell Reports · doi:10.1007/s002990050526 · Cited by 121 · see citing works

Single‐step transformation for generating marker‐free transgenic rice using the ipt‐type MAT vector system

Endo, S., Sugita, K., Sakai, M., TANAKA, H. L., & Ebinuma, H. (2002) · The Plant Journal · doi:10.1046/j.1365-313x.2002.01272.x · Cited by 116 · see citing works

Transformation of cultured cells of Chenopodium quinoa by binary vectors that carry a fragment of DNA from the virulence region of pTiBo542

Komari, T. (1990) · Plant Cell Reports · doi:10.1007/bf00232856 · Cited by 116 · see citing works

Developmental and hormonal regulation of direct shoot organogenesis and somatic embryogenesis in sugarcane (Saccharum spp. interspecific hybrids) leaf culture

Lakshmanan, P., Geijskes, R. J., Wang, L., Elliott, A. R., Grof, C. P. L., Berding, N., & Smith, G. R. (2006) · Plant Cell Reports · doi:10.1007/s00299-006-0154-1 · Cited by 114 · see citing works

Stimulation of the cell cycle and maize transformation by disruption of the plant retinoblastoma pathway

Gordon-Kamm, W. J., Dilkes, B. P., Lowe, K. S., Hoerster, G., Sun, X., Ross, M., Church, L., Bunde, C., Farrell, J., Hill, P., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.142409899 · Cited by 109 · see citing works

Cytogenetics of tetraploid maize

Randolph, L. F. (1935) · Cited by 104 · see citing works

Optimization of a mature embryo-based in vitro culture system for high-frequency somatic embryogenic callus induction and plant regeneration from japonica rice cultivars

Lee, K., Jeon, H., & Kim, M. (2002) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1023/a:1020305432315 · Cited by 102 · see citing works

Production of transgenic tall fescue and red fescue plants by particle bombardment of mature seed-derived highly regenerative tissues

Cho, M.-J., Ha, C. D., & Lemaux, P. G. (2000) · Plant Cell Reports · doi:10.1007/s002990000238 · Cited by 101 · see citing works

Transgenic cereal (tritordeum) plants obtained at high efficiency by microprojectile bombardment of inflorescence tissue

Barcelo, P., Hagel, C., Becker, D., Martín, A., & Lörz, H. (1994) · The Plant Journal · doi:10.1046/j.1365-313x.1994.5040583.x · Cited by 95 · see citing works

Production of transgenic maize plants and progeny by bombardment of hi-II immature embryos

Songstad, D. D., Armstrong, C. L., Petersen, W. L., Hairston, B., & Hinchee, M. A. W. (1996) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/bf02822763 · Cited by 93 · see citing works

The Competence of Maize Shoot Meristems for Integrative Transformation and Inherited Expression of Transgenes

Zhong, H., Sun, B., Warkentin, D., Zhang, S., Wu, R., Wu, T., & Sticklen, M. B. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.4.1097 · Cited by 92 · see citing works

A leaf-based regeneration and transformation system for maize (Zea mays L.)

Ahmadabadi, M., Ruf, S., & Bock, R. (2006) · Transgenic Research · doi:10.1007/s11248-006-9046-y · Cited by 91 · see citing works

Production of transgenic maize plants by direct DNA uptake into embryogenic protoplasts

Golovkin, M., Ábrahám, M., Mórocz, S., Bottka, S., Fehér, A., & Dudits, D. (1993) · Plant Science · doi:10.1016/0168-9452(93)90154-r · Cited by 90 · see citing works

A cassette containing thebargene ofStreptomyces hygroscopicus: a selectable marker for plant transformation

White, J., Chang, S.-Y. P., Bibb, M. J., & Bibb, M. J. (1990) · Nucleic Acids Research · doi:10.1093/nar/18.4.1062 · Cited by 89 · see citing works

In-vitro morphogenesis of corn (Zea mays L.)

Zhong, H., Srinivasan, C., & Sticklen, M. B. (1992) · Planta · doi:10.1007/bf00199966 · Cited by 87 · see citing works

Artificial chromosome formation in maize (Zea mays L.)

Ananiev, E. V., Wu, C. C., Chamberlin, M. A., Svitashev, S. K., Schwartz, C. S., Gordon-Kamm, W. J., & Tingey, S. V. (2008) · Chromosoma · doi:10.1007/s00412-008-0191-3 · Cited by 85 · see citing works

Type I callus as a bombardment target for generating fertile transgenic maize (Zea mays L.)

Wan, Y., Widholm, J., & Lemaux, P. G. (1995) · Planta · doi:10.1007/bf00193211 · Cited by 80 · see citing works

Agrobacterium-mediated transformation of seedling-derived maize callus

Sidorov, V. A., Gilbertson, L. A., Addae, P., & Duncan, D. (2005) · Plant Cell Reports · doi:10.1007/s00299-005-0058-5 · Cited by 76 · see citing works

Somatic embryogenesis and plant regeneration from cultured young inflorescences of Oryza sativa L. (rice)

Chen, T., Lam, L., & Chen, S.-C. (1985) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/bf00041655 · Cited by 71 · see citing works

EgAP2-1, an AINTEGUMENTA-like (AIL) gene expressed in meristematic and proliferating tissues of embryos in oil palm

Morcillo, F., Gallard, A., Pillot, M., Jouannic, S., Aberlenc‐Bertossi, F., Collin, M., Verdeil, J., & Tregear, J. W. (2007) · Planta · doi:10.1007/s00425-007-0574-3 · Cited by 61 · see citing works

Stable transformation of rice ( Oryza sativa L.) via microprojectile bombardment of highly regenerative, green tissues derived from mature seed

Cho, M.-J., Yano, H., Okamoto, D., Kim, H.-K., Jung, H., Newcomb, K., Le, V. K., Yoo, H. S., Langham, R. J., Buchanan, B. B., et al. (2004) · Plant Cell Reports · doi:10.1007/s00299-003-0713-7 · Cited by 61 · see citing works

Regulation of the maizerab17 gene promoter in transgenic heterologous systems

Vilardell, J., Mundy, J., Stilling, B., Leroux, B., Pla, M., Freyssinet, G., & Pag�s, M. (1991) · Plant Molecular Biology · doi:10.1007/bf00037138 · Cited by 55 · see citing works

High-frequency transformation of oat via microprojectile bombardment of seed-derived highly regenerative cultures

Cho, M., Jiang, W. G., & Lemaux, P. G. (1999) · Plant Science · doi:10.1016/s0168-9452(99)00082-5 · Cited by 54 · see citing works

Somatic embryogenesis from cultured leaf segments of Zea mays

Conger, B. V., Novak, F. J., Afza, R., & Erdelský, K. (1987) · Plant Cell Reports · doi:10.1007/bf00269556 · Cited by 53 · see citing works

Transformation of recalcitrant maize elite inbreds using in vitro shoot meristematic cultures induced from germinated seedlings

Zhang, S., Williams-Carrier, R. E., & Lemaux, P. G. (2002) · Plant Cell Reports · doi:10.1007/s00299-002-0513-5 · Cited by 52 · see citing works

Transgenic orchardgrass (Dactylis glomerata) plants by direct embryogenesis from microprojecticle bombarded leaf cells

Denchev, P. D., Songstad, D. D., McDaniel, J. K., & Conger, B. V. (1997) · Plant Cell Reports · doi:10.1007/s002990050326 · Cited by 49 · see citing works

Split-seed: a new tool for maize researchers

Alabed, D., Rudrabhatla, S. V., Talla, R., & Goldman, S. L. (2006) · Planta · doi:10.1007/s00425-006-0237-9 · Cited by 49 · see citing works

Efficient in vitro plant regeneration via leaf base segments of indica rice (Oryza sativa L.).

Ramesh, M., Murugiah, V., & Gupta, A. K. (2009) · PubMed · Cited by 43 · see citing works

Transgenic maize plants of tropical and subtropical genotypes obtained from calluses containing organogenic and embryogenic-like structures derived from shoot tips

O'Connor-S�nchez, A., Cabrera‐Ponce, J. L., Valdez-Melara, M., T�llez-Rodr�guez, P., Pons-Hern�ndez, J., & Herrera‐Estrella, L. (2002) · Plant Cell Reports · doi:10.1007/s00299-002-0502-8 · Cited by 42 · see citing works

Cloning of a cDNA Encoding Cytosolic Acetoacetyl-Coenzyme A Thiolase from Radish by Functional Expression in Saccharomyces cerevisiae

Vollack, K., & Bach, T. J. (1996) · PLANT PHYSIOLOGY · doi:10.1104/pp.111.4.1097 · Cited by 40 · see citing works

Stable transformation of a recalcitrant kentucky bluegrass (Poa pratensis L.) cultivar using mature seed-derived highly regenerative tissues

Ha, C. D., Lemaux, P. G., & Cho, M. (2001) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-001-0002-5 · Cited by 35 · see citing works

Transformed T0 orchardgrass (Dactylis glomerata L.) plants produced from highly regenerative tissues derived from mature seeds

Cho, M.-J., Choi, H. W., & Lemaux, P. G. (2001) · Plant Cell Reports · doi:10.1007/s002990100330 · Cited by 32 · see citing works

Elimination of Marker Genes From Transgenic Plants Using MAT Vector Systems

Ebinuma, H., Sugita, K., Endo, S., Matsunaga, E., & Yamada, K. (2004) · Humana Press eBooks · doi:10.1385/1-59259-827-7:237 · Cited by 26 · see citing works

Callus induction and plant regeneration from anther and inflorescence culture of Sorghum

Wen, F., Sorensen, E. L., Barnett, F. L., & Liang, G. H. (1991) · Euphytica · doi:10.1007/bf00029394 · Cited by 26 · see citing works

Characterization and manipulation of embryogenic response from in-vitro-cultured immature inflorescences of rice (Oryza sativa L.)

Rout, J., & Lucas, W. (1996) · Planta · doi:10.1007/bf00197595 · Cited by 25 · see citing works

High frequency wheat regeneration from leaf tissue explants of regenerated plantlets

Yu, H., Wang, W., Wang, Y., & Hou, B. (2012) · Advances in Bioscience and Biotechnology · doi:10.4236/abb.2012.31008 · Cited by 25 · see citing works

Comparison of Shoot Apex and Leaf Development and Structure in Diploid and Tetraploid Maize

Randolph, L. F., Abbe, E. C., & Einset, J. (1944) · Cited by 25 · see citing works

Mapping regions of the maize leaf capable of proliferation in culture

Wenzler, H., & Meins, F. (1986) · PROTOPLASMA · doi:10.1007/bf01281691 · Cited by 21 · see citing works

Establishment of regeneration and transformation system of sugarcane cultivar GT54-9 (C9)

Dessoky, E. S., Ismail, R. M., Abdelhadi, A. A., & Abdallah, N. A. (2011) · GM Crops · doi:10.4161/gmcr.2.2.17288 · Cited by 19 · see citing works

The Nuclear Endoreduplication Cycle in Metaxylem Cells of Primary Roots of Zea mays L.

Barlow, P. W. (1985) · Annals of Botany · doi:10.1093/oxfordjournals.aob.a086923 · Cited by 19 · see citing works

Overexpression of coconut AINTEGUMENTA-like gene, CnANT, promotes in vitro regeneration in transgenic Arabidopsis

Bandupriya, H. D. D., Gibbings, J. G., & Dunwell, J. M. (2013) · Plant Cell Tissue and Organ Culture (PCTOC) · doi:10.1007/s11240-013-0383-2 · Cited by 17 · see citing works

Isolation of transgenic progeny of maize by embryo rescue under selective conditions

Weymann, K. B., Urban, K., Ellis, D. M., Novitzky, R., Dunder, E., Jayne, S. M., & Pace, G. M. (1993) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/bf02632236 · Cited by 16 · see citing works

Endoreduplication is not involved in bundle-sheath formation in the C4 species Cleome gynandra

Aubry, S., Kneřová, J., & Hibberd, J. M. (2013) · Journal of Experimental Botany · doi:10.1093/jxb/ert350 · Cited by 10 · see citing works

CRISPR/Cas Genome Editing and Precision Plant Breeding in Agriculture

Chen, K., Wang, Y., Zhang, R., Zhang, H., & Gao, C. (2019) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050718-100049 · Cited by 1,643 · see citing works

Engineering Quantitative Trait Variation for Crop Improvement by Genome Editing

Rodríguez-Leal, D., Lemmon, Z. H., Man, J., Bartlett, M. E., & Lippman, Z. B. (2017) · Cell · doi:10.1016/j.cell.2017.08.030 · Cited by 1,165 · see citing works

Breeding crops to feed 10 billion

Hickey, L. T., Hafeez, A. N., Robinson, H. M., Jackson, S. A., Leal‐Bertioli, S. C. M., Tester, M. A., Gao, C., Godwin, I. D., Hayes, B. J., & Wulff, B. B. H. (2019) · Nature Biotechnology · doi:10.1038/s41587-019-0152-9 · Cited by 1,075 · see citing works

Genome engineering for crop improvement and future agriculture

Gao, C. (2021) · Cell · doi:10.1016/j.cell.2021.01.005 · Cited by 1,037 · see citing works

Applications of CRISPR–Cas in agriculture and plant biotechnology

Zhu, H., Li, C., & Gao, C. (2020) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-020-00288-9 · Cited by 870 · see citing works

Genome editing in maize directed by CRISPR–Cas9 ribonucleoprotein complexes

Svitashev, S. K., Schwartz, C., Lenderts, B., Young, J. K., & Cigan, A. M. (2016) · Nature Communications · doi:10.1038/ncomms13274 · Cited by 826 · see citing works

Genetic Regulation of Shoot Architecture

Wang, B., Smith, S. M., & Li, J. (2018) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042817-040422 · Cited by 771 · see citing works

A GRF–GIF chimeric protein improves the regeneration efficiency of transgenic plants

Debernardi, J. M., Tricoli, D. M., Ercoli, M. F., Hayta, Ş., Ronald, P. C., Palatnik, J. F., & Dubcovsky, J. (2020) · Nature Biotechnology · doi:10.1038/s41587-020-0703-0 · Cited by 621 · see citing works

Plant gene editing through de novo induction of meristems

Maher, M. F., Nasti, R. A., Vollbrecht, M., Starker, C. G., Clark, M. D., & Voytas, D. F. (2020) · Nature Biotechnology · doi:10.1038/s41587-019-0337-2 · Cited by 541 · see citing works

Molecular Mechanisms of Plant Regeneration

Ikeuchi, M., Favero, D. S., Sakamoto, Y., Iwase, A., Coleman, D., Rymen, B., & Sugimoto, K. (2019) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-050718-100434 · Cited by 528 · see citing works

Rapid improvement of domestication traits in an orphan crop by genome editing

Lemmon, Z. H., Reem, N. T., Dalrymple, J., Soyk, S., Swartwood, K., Rodríguez-Leal, D., Eck, J. M. V., & Lippman, Z. B. (2018) · Nature Plants · doi:10.1038/s41477-018-0259-x · Cited by 520 · see citing works

The Enhancement of Plant Disease Resistance Using CRISPR/Cas9 Technology

Borrelli, V. M. G., Brambilla, V., Rogowsky, P., Marocco, A., & Lanubile, A. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.01245 · Cited by 518 · see citing works

Nanoparticle-Mediated Delivery towards Advancing Plant Genetic Engineering

Cunningham, F. J., Goh, N. S., Demirer, G. S., Matos, J. L., & Landry, M. P. (2018) · Trends in biotechnology · doi:10.1016/j.tibtech.2018.03.009 · Cited by 501 · see citing works

A male-expressed rice embryogenic trigger redirected for asexual propagation through seeds

Khanday, I., Skinner, D. J., Yang, B., Mercier, R., & Sundaresan, V. (2018) · Nature · doi:10.1038/s41586-018-0785-8 · Cited by 470 · see citing works

Progress and prospects in plant genome editing

Yin, K., Gao, C., & Qiu, J. (2017) · Nature Plants · doi:10.1038/nplants.2017.107 · Cited by 436 · see citing works

De Novo Domestication: An Alternative Route toward New Crops for the Future

Fernie, A. R., & Yan, J. (2019) · Molecular Plant · doi:10.1016/j.molp.2019.03.016 · Cited by 401 · see citing works

The emerging and uncultivated potential of CRISPR technology in plant science

Zhang, Y., Malzahn, A. A., Sretenovic, S., & Qi, Y. (2019) · Nature Plants · doi:10.1038/s41477-019-0461-5 · Cited by 404 · see citing works

Callus, Dedifferentiation, Totipotency, Somatic Embryogenesis: What These Terms Mean in the Era of Molecular Plant Biology?

Fehér, A. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00536 · Cited by 379 · see citing works

Smart breeding driven by big data, artificial intelligence, and integrated genomic-enviromic prediction

Xu, Y., Zhang, X., Li, H., Zheng, H., Zhang, J., Olsen, M. S., Varshney, R. K., Prasanna, B. M., & Qian, Q. (2022) · Molecular Plant · doi:10.1016/j.molp.2022.09.001 · Cited by 391 · see citing works

The BABY BOOM Transcription Factor Activates the LEC1-ABI3-FUS3-LEC2 Network to Induce Somatic Embryogenesis

Horstman, A., Li, M., Heidmann, I., Weemen, M., Chen, B., Muiño, J. M., Angenent, G. C., & Boutilier, K. (2017) · PLANT PHYSIOLOGY · doi:10.1104/pp.17.00232 · Cited by 361 · see citing works

One-step genome editing of elite crop germplasm during haploid induction

Kelliher, T., Starr, D., Su, X., Tang, G., Chen, Z., Carter, J., Wittich, P. E., Dong, S., Green, J., Burch, E., et al. (2019) · Nature Biotechnology · doi:10.1038/s41587-019-0038-x · Cited by 349 · see citing works

A wheat resistosome defines common principles of immune receptor channels

Förderer, A., Li, E., Lawson, A. W., Deng, Y.-N., Sun, Y., Logemann, E., Zhang, X., Wen, J., Han, Z., Chang, J., et al. (2022) · Nature · doi:10.1038/s41586-022-05231-w · Cited by 296 · see citing works

Rapid genotype “independent” Zea mays L. (maize) transformation via direct somatic embryogenesis

Lowe, K. S., Rota, M. L., Hoerster, G., Hastings, C., Wang, N., Chamberlin, M. A., Wu, E., Jones, T. J., & Gordon-Kamm, W. J. (2018) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-018-9905-2 · Cited by 319 · see citing works

Towards CRISPR /Cas crops – bringing together genomics and genome editing

Scheben, A., Wolter, F., Batley, J., Puchta, H., & Edwards, D. (2017) · New Phytologist · doi:10.1111/nph.14702 · Cited by 319 · see citing works

Nanotechnology to advance CRISPR–Cas genetic engineering of plants

Demirer, G. S., Silva, T. N., Jackson, C. T., Thomas, J. B., Ehrhardt, D. W., Rhee, S. Y., Mortimer, J. C., & Landry, M. P. (2021) · Nature Nanotechnology · doi:10.1038/s41565-021-00854-y · Cited by 305 · see citing works

The gene TaWOX5 overcomes genotype dependency in wheat genetic transformation

Wang, K., Shi, L., Liang, X., Zhao, P., Wang, W., Liu, J., Chang, Y., Hiei, Y., Yanagihara, C., Du, L., et al. (2022) · Nature Plants · doi:10.1038/s41477-021-01085-8 · Cited by 303 · see citing works

Developing naturally stress-resistant crops for a sustainable agriculture

Zhang, H., Li, Y., & Zhu, J. (2018) · Nature Plants · doi:10.1038/s41477-018-0309-4 · Cited by 285 · see citing works

Plant genome editing with TALEN and CRISPR

Malzahn, A. A., Lowder, L. G., & Qi, Y. (2017) · Cell & Bioscience · doi:10.1186/s13578-017-0148-4 · Cited by 280 · see citing works

Designing future crops: challenges and strategies for sustainable agriculture

Tian, Z., Wang, J., Li, J., & Han, B. (2020) · The Plant Journal · doi:10.1111/tpj.15107 · Cited by 272 · see citing works

Engineering Non-transgenic Gynoecious Cucumber Using an Improved Transformation Protocol and Optimized CRISPR/Cas9 System

Hu, B., Li, D., Liu, X., Qi, J., Gao, D., Zhao, S., Huang, S., Sun, J., & Yang, L. (2017) · Molecular Plant · doi:10.1016/j.molp.2017.09.005 · Cited by 248 · see citing works

Targeted genome-modification tools and their advanced applications in crop breeding

Li, B., Sun, C., Li, J., & Gao, C. (2024) · Nature Reviews Genetics · doi:10.1038/s41576-024-00720-2 · Cited by 259 · see citing works

Application of CRISPR/Cas9 Genome Editing Technology for the Improvement of Crops Cultivated in Tropical Climates: Recent Progress, Prospects, and Challenges

Haque, E., Taniguchi, H., Hassan, M. M., Bhowmik, P., Karim, M. R., Śmiech, M., Zhao, K., Rahman, M., & Islam, T. (2018) · Frontiers in Plant Science · doi:10.3389/fpls.2018.00617 · Cited by 236 · see citing works

High-Throughput CRISPR/Cas9 Mutagenesis Streamlines Trait Gene Identification in Maize

Liu, H., Jian, L., Xu, J., Zhang, Q., Zhang, M., Jin, M., Peng, Y., Yan, J., Han, B., Liu, J., et al. (2020) · The Plant Cell · doi:10.1105/tpc.19.00934 · Cited by 232 · see citing works

Plant Genome Engineering for Targeted Improvement of Crop Traits

Sedeek, K. E. M., Mahas, A., & Mahfouz, M. M. (2019) · Frontiers in Plant Science · doi:10.3389/fpls.2019.00114 · Cited by 232 · see citing works

Overexpression of the Transcription Factor GROWTH-REGULATING FACTOR5 Improves Transformation of Dicot and Monocot Species

Kong, J., Martin‐Ortigosa, S., Finer, J. J., Orchard, N., Gunadi, A., Batts, L. A., Thakare, D., Rush, B., Schmitz, O., Stuiver, M. H., et al. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.572319 · Cited by 209 · see citing works

WUSCHEL: a master regulator in plant growth signaling

Jha, P., Ochatt, S., & Kumar, V. (2020) · Plant Cell Reports · doi:10.1007/s00299-020-02511-5 · Cited by 208 · see citing works

CRISPR–Act3.0 for highly efficient multiplexed gene activation in plants

Pan, C., Wu, X., Markel, K., Malzahn, A. A., Kundagrami, N., Sretenovic, S., Zhang, Y., Cheng, Y., Shih, P. M., & Qi, Y. (2021) · Nature Plants · doi:10.1038/s41477-021-00953-7 · Cited by 206 · see citing works

Technological advances in maize breeding: past, present and future

Andorf, C. M., Beavis, W. D., Hufford, M. B., Smith, S. J., Suza, W. P., Wang, K., Woodhouse, M. R., Yu, J., & Lübberstedt, T. (2019) · Theoretical and Applied Genetics · doi:10.1007/s00122-019-03306-3 · Cited by 198 · see citing works

Maize smart-canopy architecture enhances yield at high densities

Tian, J., Wang, C., Chen, F., Qin, W., Yang, H. Y., Zhao, S., Xia, J., Du, X., Zhu, Y., Wu, L., et al. (2024) · Nature · doi:10.1038/s41586-024-07669-6 · Cited by 199 · see citing works

Highly efficient heritable genome editing in wheat using an RNA virus and bypassing tissue culture

Li, T., Hu, J., Sun, Y., Li, B., Zhang, D., Li, W., Liu, J., Li, D., Gao, C., Zhang, Y., et al. (2021) · Molecular Plant · doi:10.1016/j.molp.2021.07.010 · Cited by 196 · see citing works

Nanoparticle‐mediated gene transformation strategies for plant genetic engineering

Lv, Z., Jiang, R. J., Chen, J., & Chen, W. (2020) · The Plant Journal · doi:10.1111/tpj.14973 · Cited by 193 · see citing works

CRISPR /Cas9 and TALEN s generate heritable mutations for genes involved in small RNA processing of Glycine max and Medicago truncatula

Curtin, S. J., Xiong, Y., Michno, J., Campbell, B. W., Stec, A. O., Čermák, T., Starker, C. G., Voytas, D. F., Eamens, A. L., & Stupar, R. M. (2017) · Plant Biotechnology Journal · doi:10.1111/pbi.12857 · Cited by 192 · see citing works

Chromatin Accessibility Dynamics and a Hierarchical Transcriptional Regulatory Network Structure for Plant Somatic Embryogenesis

Wang, F., Shang, G.-D., Wu, L., Xu, Z.-G., Zhao, X., & Wang, J. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.07.003 · Cited by 191 · see citing works

Genome Editing in Plants: Exploration of Technological Advancements and Challenges

Vats, S., Kumawat, S., Kumar, V., Patil, G., Joshi, T., Sonah, H., Sharma, T. R., & Deshmukh, R. K. (2019) · Cells · doi:10.3390/cells8111386 · Cited by 191 · see citing works

A CRISPR way for accelerating improvement of food crops

Zhang, Y., Pribil, M., Palmgren, M. B., & Gao, C. (2020) · Nature Food · doi:10.1038/s43016-020-0051-8 · Cited by 189 · see citing works

CRISPR-Cas12a (Cpf1): A Versatile Tool in the Plant Genome Editing Tool Box for Agricultural Advancement

Bandyopadhyay, A., Kancharla, N., Javalkote, V. S., Dasgupta, S., & Brutnell, T. P. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2020.584151 · Cited by 179 · see citing works

Zygotic Genome Activation Occurs Shortly after Fertilization in Maize

Chen, J., Strieder, N., Krohn, N. G., Cyprys, P., Sprunck, S., Engelmann, J. C., & Dresselhaus, T. (2017) · The Plant Cell · doi:10.1105/tpc.17.00099 · Cited by 174 · see citing works

Drought Resistance by Engineering Plant Tissue-Specific Responses

Martignago, D., Rico‐Medina, A., Blasco‐Escámez, D., Fontanet‐Manzaneque, J. B., & Caño‐Delgado, A. I. (2020) · Frontiers in Plant Science · doi:10.3389/fpls.2019.01676 · Cited by 173 · see citing works

A five-transgene cassette confers broad-spectrum resistance to a fungal rust pathogen in wheat

Luo, M., Xie, L., Chakraborty, S., Wang, A., Matny, O., Jugovich, M., KOLMER, J. A., Richardson, T. M., Bhatt, D., Hoque, M. S., et al. (2021) · Nature Biotechnology · doi:10.1038/s41587-020-00770-x · Cited by 172 · see citing works

Selectable marker independent transformation of recalcitrant maize inbred B73 and sorghum P898012 mediated by morphogenic regulators BABY BOOM and WUSCHEL2

Mookkan, M., Nelson-Vasilchik, K., Hague, J., Zhang, Z. J., & Kausch, A. P. (2017) · Plant Cell Reports · doi:10.1007/s00299-017-2169-1 · Cited by 162 · see citing works

Using Morphogenic Genes to Improve Recovery and Regeneration of Transgenic Plants

Gordon-Kamm, W. J., Sardesai, N., Arling, M., Lowe, K. S., Hoerster, G., Betts, S. D., & Jones, T. J. (2019) · Plants · doi:10.3390/plants8020038 · Cited by 169 · see citing works

Perspectives on the Application of Genome-Editing Technologies in Crop Breeding

Hua, K., Zhang, J., Botella, J. R., Ma, C., Kong, F., Liu, B., & Zhu, J. (2019) · Molecular Plant · doi:10.1016/j.molp.2019.06.009 · Cited by 170 · see citing works

Boosting plant genome editing with a versatile CRISPR-Combo system

Pan, C., Li, G., Malzahn, A. A., Cheng, Y., Leyson, B., Sretenovic, S., Gürel, F., Coleman, G. D., & Qi, Y. (2022) · Nature Plants · doi:10.1038/s41477-022-01151-9 · Cited by 167 · see citing works

Current and future editing reagent delivery systems for plant genome editing

Ran, Y., Liang, Z., & Gao, C. (2017) · Science China Life Sciences · doi:10.1007/s11427-017-9022-1 · Cited by 161 · see citing works

CRISPR ribonucleoprotein-mediated genetic engineering in plants

Zhang, Y., Iaffaldano, B. J., & Qi, Y. (2021) · Plant Communications · doi:10.1016/j.xplc.2021.100168 · Cited by 169 · see citing works

A barley stripe mosaic virus‐based guide RNA delivery system for targeted mutagenesis in wheat and maize

Hu, J., Li, S., Li, Z., Li, H., Song, W., Zhao, H., Lai, J., Xia, L., Li, D., & Zhang, Y. (2019) · Molecular Plant Pathology · doi:10.1111/mpp.12849 · Cited by 160 · see citing works

Genome-edited crops for improved food security of smallholder farmers

Pixley, K. V., Falck‐Zepeda, J. B., Paarlberg, R., Phillips, P. W. B., Slamet‐Loedin, I. H., Dhugga, K. S., Campos, H., & Gutterson, N. I. (2022) · Nature Genetics · doi:10.1038/s41588-022-01046-7 · Cited by 160 · see citing works

Uncovering the transcriptional regulatory network involved in boosting wheat regeneration and transformation

Liu, X., Bie, X. M., Lin, X., Li, M., Wang, H., Zhang, X., Yang, Y., Zhang, X. S., Zhang, X. S., & Xiao, J. Y. (2023) · Nature Plants · doi:10.1038/s41477-023-01406-z · Cited by 160 · see citing works

Peptide REF1 is a local wound signal promoting plant regeneration

Yang, W., Zhai, H., Wu, F., Deng, L., Chao, Y., Meng, X., Chen, Q., Liu, C., Bie, X., Sun, C., et al. (2024) · Cell · doi:10.1016/j.cell.2024.04.040 · Cited by 160 · see citing works

Plant cell totipotency: Insights into cellular reprogramming

Su, Y. H., Tang, L. P., Zhao, X., & Zhang, X. S. (2020) · Journal of Integrative Plant Biology · doi:10.1111/jipb.12972 · Cited by 158 · see citing works

Nanotechnology Strategies for Plant Genetic Engineering

Yan, Y., Zhu, X., Yu, Y., Li, C., Zhang, Z., & Wang, F. (2021) · Advanced Materials · doi:10.1002/adma.202106945 · Cited by 158 · see citing works

Auxin EvoDevo: Conservation and Diversification of Genes Regulating Auxin Biosynthesis, Transport, and Signaling

Matthes, M. S., Best, N. B., Robil, J. M., Malcomber, S. T., Gallavotti, A., & McSteen, P. (2018) · Molecular Plant · doi:10.1016/j.molp.2018.12.012 · Cited by 154 · see citing works

Cacao biotechnology: current status and future prospects

Wickramasuriya, A. M., & Dunwell, J. M. (2017) · Plant Biotechnology Journal · doi:10.1111/pbi.12848 · Cited by 146 · see citing works

A serine/threonine protein kinase encoding gene KERNEL NUMBER PER ROW6 regulates maize grain yield

Jia, H., Li, M., Li, W., Liu, L., Jian, Y., Yang, Z., Shen, X., Ning, Q., Du, Y., Zhao, R., et al. (2020) · Nature Communications · doi:10.1038/s41467-020-14746-7 · Cited by 147 · see citing works

Efficient genotype‐independent cotton genetic transformation and genome editing

Ge, X., Xu, J., Yang, Z., Yang, X., Wang, Y., Chen, Y., Wang, P., & Li, F. (2022) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13427 · Cited by 145 · see citing works

Current progress and challenges in crop genetic transformation

Anjanappa, R. B., & Gruissem, W. (2021) · Journal of Plant Physiology · doi:10.1016/j.jplph.2021.153411 · Cited by 142 · see citing works

Crop biotechnology and the future of food

Steinwand, M. A., & Ronald, P. C. (2020) · Nature Food · doi:10.1038/s43016-020-0072-3 · Cited by 146 · see citing works

Construct design for CRISPR/Cas-based genome editing in plants

Hassan, M. M., Zhang, Y., Yuan, G., De, K., Chen, J., Muchero, W., Tuskan, G. A., Qi, Y., & Yang, X. (2021) · Trends in Plant Science · doi:10.1016/j.tplants.2021.06.015 · Cited by 136 · see citing works

Brachypodium: A Monocot Grass Model Genus for Plant Biology

Scholthof, K. G., Irigoyen, S. C., Catalán, P., & Mandadi, K. K. (2018) · The Plant Cell · doi:10.1105/tpc.18.00083 · Cited by 137 · see citing works

Engineered biocontainable RNA virus vectors for non-transgenic genome editing across crop species and genotypes

Liu, Q., Zhao, C., Sun, K., Deng, Y., & Li, Z. (2023) · Molecular Plant · doi:10.1016/j.molp.2023.02.003 · Cited by 136 · see citing works

Where are the drought tolerant crops? An assessment of more than two decades of plant biotechnology effort in crop improvement

Nuccio, M. L., Paul, M. J., Bate, N. J., Cohn, J., & Cutler, S. R. (2018) · Plant Science · doi:10.1016/j.plantsci.2018.01.020 · Cited by 136 · see citing works

The Past, Present, and Future of Maize Improvement: Domestication, Genomics, and Functional Genomic Routes toward Crop Enhancement

Liu, J., Fernie, A. R., & Yan, J. (2019) · Plant Communications · doi:10.1016/j.xplc.2019.100010 · Cited by 134 · see citing works

Control of Meristem Size

Kitagawa, M., & Jackson, D. P. (2019) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042817-040549 · Cited by 132 · see citing works

CRISPR–Cas applications in agriculture and plant research

Tuncel, A., Pan, C., Clem, J. S., Liu, D., & Qi, Y. (2025) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-025-00834-3 · Cited by 139 · see citing works

Creation and judicious application of a wheat resistance gene atlas

Hafeez, A. N., Arora, S., Ghosh, S., Gilbert, D. J., Bowden, R. L., & Wulff, B. B. H. (2021) · Molecular Plant · doi:10.1016/j.molp.2021.05.014 · Cited by 127 · see citing works

CRISPR–Cas9-mediated 75.5-Mb inversion in maize

Schwartz, C. S., Lenderts, B., Feigenbutz, L., Barone, P., Llaca, V., Fengler, K. A., & Svitashev, S. K. (2020) · Nature Plants · doi:10.1038/s41477-020-00817-6 · Cited by 129 · see citing works

Genome Engineering and Agriculture: Opportunities and Challenges

Baltes, N. J., Gil‐Humanes, J., & Voytas, D. F. (2017) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2017.03.011 · Cited by 127 · see citing works

An improved ternary vector system for Agrobacterium-mediated rapid maize transformation

Anand, A., Bass, S., Wu, E., Wang, N., McBride, K. E., Annaluru, N., Miller, M., Mo, H., & Jones, T. J. (2018) · Plant Molecular Biology · doi:10.1007/s11103-018-0732-y · Cited by 124 · see citing works

Advances in Maize Transformation Technologies and Development of Transgenic Maize

Yadava, P., Abhishek, A., Singh, R., Singh, I., Kaul, T., Pattanayak, A., & Agrawal, P. K. (2017) · Frontiers in Plant Science · doi:10.3389/fpls.2016.01949 · Cited by 123 · see citing works

Genome editing for plant research and crop improvement

Zhan, X., Lu, Y., Zhu, J., & Botella, J. R. (2020) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13063 · Cited by 121 · see citing works

Leaf transformation for efficient random integration and targeted genome modification in maize and sorghum

Wang, N., Ryan, L., Sardesai, N., Wu, E., Lenderts, B., Lowe, K. S., Che, P., Anand, A., Worden, A., van Dyk, D., et al. (2023) · Nature Plants · doi:10.1038/s41477-022-01338-0 · Cited by 123 · see citing works

Use of CRISPR/Cas9 for Crop Improvement in Maize and Soybean

Chilcoat, N. D., Liu, Z.-B., & Sander, J. D. (2017) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2017.04.005 · Cited by 121 · see citing works

Recent advances in crop transformation technologies

Chen, Z., Debernardi, J. M., Dubcovsky, J., & Gallavotti, A. (2022) · Nature Plants · doi:10.1038/s41477-022-01295-8 · Cited by 121 · see citing works

The Zygotic Transition Is Initiated in Unicellular Plant Zygotes with Asymmetric Activation of Parental Genomes

Anderson, S. N., Johnson, C. S., Chesnut, J., Jones, D. S., Khanday, I., Woodhouse, M. R., Li, C., Conrad, L. J., Russell, S. D., & Sundaresan, V. (2017) · Developmental Cell · doi:10.1016/j.devcel.2017.10.005 · Cited by 120 · see citing works

Improving plant-resistance to insect-pests and pathogens: The new opportunities through targeted genome editing

Bisht, D. S., Bhatia, V., & Bhattacharya, R. (2019) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2019.04.008 · Cited by 119 · see citing works

Overcoming bottlenecks in plant gene editing

Atkins, P., & Voytas, D. F. (2020) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2020.01.002 · Cited by 118 · see citing works

What is the molecular basis of nonhost resistance?

Panstruga, R., & Moscou, M. (2020) · Molecular Plant-Microbe Interactions · doi:10.1094/mpmi-06-20-0161-cr · Cited by 62 · see citing works

Wuschel2 enables highly efficient CRISPR/Cas-targeted genome editing during rapid de novo shoot regeneration in sorghum

Che, P., Wu, E., Simon, M. K., Anand, A., Lowe, K. S., Gao, H., Sigmund, A. L., Yang, M., Albertsen, M. C., Gordon-Kamm, W. J., et al. (2022) · Communications Biology · doi:10.1038/s42003-022-03308-w · Cited by 113 · see citing works

A roadmap for gene functional characterisation in crops with large genomes: Lessons from polyploid wheat

Adamski, N. M., Borrill, P., Brinton, J., Harrington, S. A., Marchal, C., Bentley, A. R., Bovill, W. D., Cattivelli, L., Cockram, J., Contreras‐Moreira, B., et al. (2020) · eLife · doi:10.7554/elife.55646 · Cited by 111 · see citing works

Grass inflorescence architecture and meristem determinacy

Bommert, P., & Whipple, C. (2017) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2017.10.004 · Cited by 110 · see citing works

The emerging role of nanotechnology in plant genetic engineering

Squire, H. J., Tomatz, S., Voke, E., Grandío, E. G., & Landry, M. P. (2023) · Nature Reviews Bioengineering · doi:10.1038/s44222-023-00037-5 · Cited by 110 · see citing works

Efficient and genotype independent maize transformation using pollen transfected by DNA‐coated magnetic nanoparticles

Wang, Z., Zhang, Z., Zheng, D., Zhang, T., Li, X., Zhang, C., Yu, R., Wei, J., & Wu, Z. (2022) · Journal of Integrative Plant Biology · doi:10.1111/jipb.13263 · Cited by 109 · see citing works

Applying the latest advances in genomics and phenomics for trait discovery in polyploid wheat

Borrill, P., Harrington, S. A., & Uauy, C. (2018) · The Plant Journal · doi:10.1111/tpj.14150 · Cited by 107 · see citing works

Targeted DNA insertion in plants

Dong, O. X., & Ronald, P. C. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2004834117 · Cited by 106 · see citing works

Challenges Facing CRISPR/Cas9-Based Genome Editing in Plants

Son, S., & Park, S. R. (2022) · Frontiers in Plant Science · doi:10.3389/fpls.2022.902413 · Cited by 111 · see citing works

Use of non-integrating Zm-Wus2 vectors to enhance maize transformation

Hoerster, G., Wang, N., Ryan, L., Wu, E., Anand, A., McBride, K. E., Lowe, K. S., Jones, T. J., & Gordon-Kamm, W. J. (2020) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-019-10042-2 · Cited by 106 · see citing works

Agrobacterium expressing a type III secretion system delivers Pseudomonas effectors into plant cells to enhance transformation

Raman, V., Rojas, C. M., Vasudevan, B., Dunning, K., Kolape, J., Oh, S., Yun, J., Yang, L., Li, G., Pant, B. D., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-30180-3 · Cited by 106 · see citing works

Plant stem cells and de novo organogenesis

Sang, Y. L., Cheng, Z. J., & Zhang, X. S. (2018) · New Phytologist · doi:10.1111/nph.15106 · Cited by 105 · see citing works

BABY BOOM (BBM): a candidate transcription factor gene in plant biotechnology

Jha, P., & Kumar, V. (2018) · Biotechnology Letters · doi:10.1007/s10529-018-2613-5 · Cited by 105 · see citing works

Plant genetic transformation: achievements, current status and future prospects

Wang, P., Si, H., Li, C., Xu, Z., Guo, H., Jin, S., & Cheng, H. (2025) · Plant Biotechnology Journal · doi:10.1111/pbi.70028 · Cited by 103 · see citing works

Maize Transformation Using the Morphogenic Genes Baby Boom and Wuschel2

Jones, T. J., Lowe, K. S., Hoerster, G., Anand, A., Wu, E., Wang, N., Arling, M., Lenderts, B., & Gordon-Kamm, W. J. (2018) · Methods in molecular biology · doi:10.1007/978-1-4939-8778-8_6 · Cited by 60 · see citing works

Rapid genotype “independent” Zea mays L. (maize) transformation via direct somatic embryogenesis

Lowe, K. S., Rota, M. L., Hoerster, G., Hastings, C., Wang, N., Chamberlin, M. A., Wu, E., Jones, T. J., & Gordon-Kamm, W. J. (2018) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-018-9905-2 · Cited by 319 · see citing works

Rapid and highly efficient morphogenic gene-mediated hexaploid wheat transformation

Johnson, K., Chu, U. C., Anthony, G., Wu, E., Che, P., & Jones, T. J. (2023) · Frontiers in Plant Science · doi:10.3389/fpls.2023.1151762 · Cited by 34 · see citing works

Agrobacterium-mediated Immature Embryo Transformation of Recalcitrant Maize Inbred Lines Using Morphogenic Genes

Masters, A. (2020) · doi:10.31274/cc-20240624-137 · Cited by 20 · see citing works

A Breakthrough in Monocot Transformation Methods

Hofmann, N. R. (2016) · The Plant Cell · doi:10.1105/tpc.16.00696 · Cited by 20 · see citing works