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  • [[File:BC12_5.jpg|right|thumb|320px|'''Figure 3.''' ''Phylogenetic tree of '''BC12''' and representative homologs from Arab ...from various kinesin subfamilies are divided into separated clades(Figure 3). Kinesin-4 proteins from several representative species were clustered tog
    8 KB (1,217 words) - 09:37, 12 June 2015
  • early heading date3. Plant Physiol. 2014 Mar;164(3):1326-37. doi: ...ategory:Genes]][[Category:Oryza Sativa Japonica Group]][[Category:Japonica Chromosome 9]]
    2 KB (352 words) - 07:52, 12 October 2016
  • 3 The Howard Hughes Medical Institute and the Department of Cellular and Mole [[Category:Japonica Chromosome 9]]
    4 KB (541 words) - 09:38, 12 June 2015
  • OsABC1-12 encodes a protein with 716 amino acids, and this gene locates in chromosome 9 with 18 extrons. ...ABC1genes distributed on all rice chromosomes randomly except chromosomes 3, 8, 10, and 12 in rice, and were named from OsABC1-1 to OsABC1-15 according
    4 KB (602 words) - 09:38, 12 June 2015
  • ...PR-11 families work as chitinases, whereas the PR-2 family represent β-1,3-glucanases. By contrast, the microbial targets of many PR-families are stil [3]Shandong academy of agricultural sciences high-tech research center, jinan,
    3 KB (468 words) - 09:38, 12 June 2015
  • ...pression01.jpg|left|thumb|200px|'''Figure 2.''''' Expression of OsNHX1, 2, 3, and 5 in rice tissues.(from reference <ref name="ref1"/>).'']] [[File: OsNHX5 promoter–GUS.jpg|right|thumb|200px|'''Figure 3.''''' OsNHX5 promoter–GUS expression pattern in transgenic rice plants.(f
    14 KB (2,126 words) - 08:27, 1 July 2016
  • [[File:Os09g0298200.png|right|thumb|427px|'''Figure 3.''' ''Expression of rice AGPases in leaves, stems and roots during light/da ...ategory:Genes]][[Category:Oryza Sativa Japonica Group]][[Category:Japonica Chromosome 9]]
    2 KB (282 words) - 04:11, 9 November 2016
  • *two inducible expression lines (IE-3 and IE-4) [[Category:Japonica Chromosome 9]]
    13 KB (1,918 words) - 08:59, 1 July 2016
  • ...genetic regulation of flowering in rice, in which SDG724 mediates H3K36me2/3 deposition at the MADS50 and RFT1loci and promotes flowering through MADS50 ...3K36me2/3 levels at the RFT1, but not the Hd3alocus. In addition, H3K36me2/3 levels at the Ehd1locus were also found to be unchanged in lvp1 plants, eve
    20 KB (1,496 words) - 00:56, 6 June 2014
  • eukaryotes and expansion in plants. BMC Evol Biol. 2005 Jan 3;5:1. PubMed PMID: ...ategory:Genes]][[Category:Oryza Sativa Japonica Group]][[Category:Japonica Chromosome 9]]
    3 KB (374 words) - 07:08, 23 March 2017
  • ...a consensus sequence for these was defined as C-X 4–15 -C-X 4–6 -C-X 3 -H (X represents any amino acid) based on the whole-genome analysis of rice ...ategory:Genes]][[Category:Oryza Sativa Japonica Group]][[Category:Japonica Chromosome 9]]
    2 KB (351 words) - 04:05, 28 March 2017
  • ...ial side <ref name="ref1" />.]] [[File: ZhangF3.jpg|right|thumb|100px|Fig 3. Map-based cloning of ''SLL1'', which encodes an MYB transcription factor < ...late the relevant mutant gene, ''SLL1'' was mapped to the long arm of rice chromosome 9 between markers RM1896 and RM3700. A large F2 mapping population was then
    6 KB (953 words) - 06:31, 8 March 2017
  • rice, moss, and algae. Plant Physiol. 2010 Jul;153(3):1398-412. doi: ...ategory:Genes]][[Category:Oryza Sativa Japonica Group]][[Category:Japonica Chromosome 9]]
    3 KB (452 words) - 01:14, 22 March 2017
  • rice, moss, and algae. Plant Physiol. 2010 Jul;153(3):1398-412. doi: ...ategory:Genes]][[Category:Oryza Sativa Japonica Group]][[Category:Japonica Chromosome 9]]
    3 KB (452 words) - 13:08, 22 March 2017
  • ...KY IIa transcription factors modulate rice innate immunity[J]. Rice, 2010, 3(1): 36-42. [[Category:Japonica Chromosome 9]]
    7 KB (918 words) - 16:37, 7 May 2017
  • eukaryotes and expansion in plants. BMC Evol Biol. 2005 Jan 3;5:1. PubMed PMID: ...ategory:Genes]][[Category:Oryza Sativa Japonica Group]][[Category:Japonica Chromosome 9]]
    3 KB (374 words) - 07:09, 23 March 2017
  • ...-GCAGTTCCCGCAGAGGTTCGACGGC-3′) and PM-R1 (5′-ATCGACGTCCACGACCGATACGCC-3′). These constructs were introduced into the wild-type plant, T65, by an ...c plants were stained with a solution containing 0.5 mM 5-bromo-4-chloro-3-indolyl-β-D-glucuronide, 0.5 mM potassium ferrocyanide, 0.5 mM potassi
    13 KB (1,976 words) - 09:42, 12 June 2015
  • ...s in rice after treatment with 100mM JA for 24 h, EightJAZ genes (OsJAZ 1, 3, 4, 7, 8, 9, 10and 12) were significantly up-regulated by JA, with OsJAZ8 e ...contains all the JAZ gene cluster (OsTIFY11e, OsTIFY11f, and OsTIFY11d)on chromosome 10. Among the 20 OsTIFY genes, 16 members are located either in tandem dupl
    5 KB (783 words) - 09:42, 12 June 2015
  • ...ber per panicle and a QTL for panicle density are located in the region of chromosome 9 defined by the molecular markers RM3700 and RM7424, respectively, which c ...ep1-32'' alleles exhibit insensitive growth to nitrogen input level(Figure 3)<ref name="ref2" />. dep1 is the mutant DEP1 allele.The variant involves th
    21 KB (3,207 words) - 10:07, 29 June 2016
  • ...with TDR in regulating programmed anther development and pollen formation[3]. ...al cross analysis. All of the F1 progeny were fertile, with an approximate 3:1 ratio for phenotypic segregation in F2 plants. Compared with wild-type pl
    11 KB (1,614 words) - 09:44, 12 June 2015

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