Showing 38,481 - 38,500 results of 128,656 for search '(( i d decrease ) OR ( 5 ((wt decrease) OR (((nn decrease) OR (a decrease)))) ))', query time: 2.25s Refine Results
  1. 38481
  2. 38482
  3. 38483

    Table5_Dynamic Epicardial Contribution to Cardiac Interstitial c-Kit and Sca1 Cellular Fractions.DOCX by C. Pogontke (12677213)

    Published 2022
    “…</p><p>Results: Our data show that approximately 50% of cardiac c-Kit<sup>POS</sup> cells are derived from the Wt1-lineage at E15.5. This subpopulation decreased along with embryonic development, disappearing from P7 onwards. …”
  4. 38484
  5. 38485

    Dopaminergic neuron differentiation is disrupted in <i>Dkk1</i> mutants. by Diogo Ribeiro (230483)

    Published 2011
    “…Quantification in (B) revealed a 40% decrease in the numbers of dopaminergic neurons in <i>Dkk1<sup>+/−</sup></i> embryos when compared to <i>Wt</i> littermate controls (mean ± s.e.m- <b><i>Wt</i></b><b>:</b> 568.3±31.7, N = 3; <b><i>Dkk1<sup><b>+/−</b></sup></i></b><b>:</b> 346.5±27.2, N = 8 p = 0.0015 ** unpaired t-test). …”
  6. 38486

    Table_5_Transcriptome characteristics during cell wall formation of endosperm cellularization and embryo differentiation in Arabidopsis.xls by Chengcheng Li (2591632)

    Published 2022
    “…Here, we characterized the early embryo and endosperm development of the naa15 mutant that had abnormal embryo differentiation and incomplete endosperm cellularization compared to WT of Arabidopsis, and comparatively investigated the changes of gene expressions in WT seeds at 3, 4, and 5 days after pollination (3W, 4W, and 5W) and the white homozygous aborted naa15 seeds at 5, 6, and 7 DAP (5M, 6M, and 7M) from naa15-1/+ siliques using RNA sequencing and qPCR assays. …”
  7. 38487

    Image_5_Transcriptome characteristics during cell wall formation of endosperm cellularization and embryo differentiation in Arabidopsis.jpeg by Chengcheng Li (2591632)

    Published 2022
    “…Here, we characterized the early embryo and endosperm development of the naa15 mutant that had abnormal embryo differentiation and incomplete endosperm cellularization compared to WT of Arabidopsis, and comparatively investigated the changes of gene expressions in WT seeds at 3, 4, and 5 days after pollination (3W, 4W, and 5W) and the white homozygous aborted naa15 seeds at 5, 6, and 7 DAP (5M, 6M, and 7M) from naa15-1/+ siliques using RNA sequencing and qPCR assays. …”
  8. 38488

    Image 1_Polymorphous corneal dystrophy subtype 3 and keratoconus aggravation after corneal refractive surgery in a three-generation family carrying both ZEB1 and ZNF469 pathogenic... by Qinghong Lin (14162640)

    Published 2025
    “…We detected both Zinc finger E-box-binding homeobox 1 (ZEB1) gene and zinc finger protein 469 (ZNF469) gene pathogenic variant in the proband and another two patients in this family, including a heterozygous missense variation c.13C>G (p.P5A, rs753301298) in the ZEB1 gene, and a heterozygous non-frameshift variant c. 3093_3104del (p.D1035_K1038del) in the ZNF469 gene. …”
  9. 38489

    Image 3_Polymorphous corneal dystrophy subtype 3 and keratoconus aggravation after corneal refractive surgery in a three-generation family carrying both ZEB1 and ZNF469 pathogenic... by Qinghong Lin (14162640)

    Published 2025
    “…We detected both Zinc finger E-box-binding homeobox 1 (ZEB1) gene and zinc finger protein 469 (ZNF469) gene pathogenic variant in the proband and another two patients in this family, including a heterozygous missense variation c.13C>G (p.P5A, rs753301298) in the ZEB1 gene, and a heterozygous non-frameshift variant c. 3093_3104del (p.D1035_K1038del) in the ZNF469 gene. …”
  10. 38490

    Image 2_Polymorphous corneal dystrophy subtype 3 and keratoconus aggravation after corneal refractive surgery in a three-generation family carrying both ZEB1 and ZNF469 pathogenic... by Qinghong Lin (14162640)

    Published 2025
    “…We detected both Zinc finger E-box-binding homeobox 1 (ZEB1) gene and zinc finger protein 469 (ZNF469) gene pathogenic variant in the proband and another two patients in this family, including a heterozygous missense variation c.13C>G (p.P5A, rs753301298) in the ZEB1 gene, and a heterozygous non-frameshift variant c. 3093_3104del (p.D1035_K1038del) in the ZNF469 gene. …”
  11. 38491

    <b>Dataset to the article: The toxicological assessment of a novel spiro derivative, 4-amino-1-azaspiro[4.5]dec-3-en-2-one for the Greater wax moth, </b><b><i>Galleria mellonella</... by Jamin Ali (18297142)

    Published 2024
    “…Additionally, a significant decrease in protein content and an increase in phenol-oxidase activity were observed with alterations in α and β-esterase activities. …”
  12. 38492

    Data_Sheet_1_Plant-based default nudges effectively increase the sustainability of catered meals on college campuses: Three randomized controlled trials.docx by Renate D. Boronowsky (14079303)

    Published 2022
    “…</p>Conclusion<p>Results demonstrated plant-based default menu options are effective, providing a low-effort, high-impact way to decrease consumption of animal products in catered events. …”
  13. 38493

    Characteristics of the core genetic components of <i>S</i>. <i>meliloti</i>. by George C. diCenzo (650171)

    Published 2018
    “…Legend abbreviations: AA–amino acid; Attach–attachment; Carb–carbohydrate; Cofact–cofactor; e-–electron; Met–metabolism; Misc–miscellaneous; Mot–motility; Nucl–nucleotide; Oxidoreduct–oxidoreductase activity; Prot–protein; Trans–transduction. (<b>D</b>-<b>F</b>) Scatter plots comparing the fitness phenotypes, shown as the log<sub>10</sub> of the GEI scores (Gene Essentiality Index scores; i.e., number of insertions within the gene divided by gene length in nucleotides) of (<b>D</b>) wild-type grown in rich medium versus wild-type grown in defined medium, (<b>E</b>) wild-type grown in rich medium versus ΔpSymAB grown in rich medium, and (<b>F</b>) wild-type grown in defined medium versus ΔpSymAB grown in defined medium.…”
  14. 38494

    The <i>topbp1</i> gene is disrupted in mutant<sup><i>cas003</i></sup>. by Lei Gao (6566)

    Published 2015
    “…The <i>topbp1</i> MO, as validated in <a href="http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1005346#pgen.1005346.s003" target="_blank">S3 Fig</a>, was injected into one-cell stage wild-type embryos to produce <i>topbp1</i> morphants. …”
  15. 38495

    Expression analysis of <i>FGFR1–4</i> and <i>Sema3A</i>. by Rosa-Eva Huettl (113537)

    Published 2013
    “…(<b>K</b>’, <b>L</b>’) Immunohistochemistry against Isl-1/2 to illustrate sensory neurons in the DRG. (<b>M</b>) Quantification of expression levels reveals a significant decrease of <i>FGFR2 in situ</i> hybridization signal in the LMC of <i>FGFR2<sup>flox/flox</sup>;Olig2-Cre<sup>+</sup></i> mutant embryos, while expression levels of <i>FGFR1, FGFR3</i> and <i>FGFR4</i> in the LMC remain unchanged (p<i><sup>FGFR1</sup></i> = 0,52; p<i><sup>FGFR3</sup></i> = 0,45, p<i><sup>FGFR4</sup></i> = 0,78). …”
  16. 38496

    Eicosapentaenoic acid prevents arterial calcification in <i>klotho</i> mutant mice by Kazufumi Nakamura (336712)

    Published 2017
    “…</p><p>Methods and results</p><p>Four-week-old <i>klotho</i> mutant mice and wild-type (WT) mice were given a diet containing 5% EPA (EPA food, <i>klotho</i> and WT: n = 12, each) or not containing EPA (control food, <i>klotho</i> and WT: n = 12, each) for 4 weeks. …”
  17. 38497
  18. 38498

    Excessive Osteocytic Fgf23 Secretion Contributes to Pyrophosphate Accumulation and Mineralization Defect in Hyp Mice by Sathish K. Murali (2585914)

    Published 2016
    “…<div><p>X-linked hypophosphatemia (XLH) is the most frequent form of inherited rickets in humans caused by mutations in the phosphate-regulating gene with homologies to endopeptidases on the X-chromosome (<i>PHEX</i>). <i>Hyp</i> mice, a murine homologue of XLH, are characterized by hypophosphatemia, inappropriately low serum vitamin D levels, increased serum fibroblast growth factor-23 (Fgf23), and osteomalacia. …”
  19. 38499
  20. 38500

    <i>cul3</i> and <i>kel</i> interact genetically, mutations in <i>kel</i> rescue the <i>cul3</i>-mutant phenotype. by Inna Djagaeva (369627)

    Published 2013
    “…Note: small protrusions were not counted in <i>cul3</i>-mutant ddaE and ddaD neurons. Decreasing levels of Kelch in <i>cul3<sup>gft2</sup> kel<sup>DE1</sup></i> double-mutant single-cell clones partially or completely rescued the <i>cul3</i>-mutant phenotype. ***: p<0.001, **: p<0.01.…”