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  1. 601

    Copy Number Variation of UGT 2B Genes in Indian Families Using Whole Genome Scans by Avinash M. Veerappa, Prakash Padakannaya, Nallur B. Ramachandra

    Published 2016-01-01
    “…These UGT2B genes are highly polymorphic in nature and have distinct polymorphisms associated with specific regions around the globe. Copy number variations (CNVs) status of UGT2B17 in Indian population is not known and their disease associations have been inconclusive. …”
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  2. 602
  3. 603

    Influence of Regional Pollution Outflow on Particle Number Concentration and Particle Size in Airshed of Guangzhou, South China by Hing Cho Cheung, Chengyu Nie, Mintao Huang, Tingting Yang, Hao Wang, Celine Siu Lan Lee, Chenglei Pei, Jun Zhao, Baoling Liang

    Published 2022-06-01
    “…Abstract A measurement campaign of particle number concentration and size distribution was conducted at urban (SYSU) and suburban (Panyu) areas of Guangzhou, South China, during 16 January to 3 February 2020 before and during the Chinese New Year (CNY) holiday. …”
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  4. 604

    Stem cutting, rooting, and shoot growth potentials of some hedge plant species as influenced by number of nodes by Christina Olusola Owolabi, Olukemi Ifetola Adediran, Chimezie Udeh, Deborah Oyinlola Fasasi, Jacob Goke Bodunde

    Published 2024-11-01
    “…Days to shoot initiation was not significantly different (p≤0.05) across the number of nodes for all species, ranging between 8 and 10 days after planting (DAP). …”
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  5. 605

    Copy number variations at the Rhg1 locus and their relationship with resistance to soybean cyst nematode (Heterodera glycines) by Dinesh Poudel, Guiping Yan, Carrie Miranda, Gustavo Fernando Kreutz, Intiaz Amin Chowdhury

    Published 2024-12-01
    “…To determine CNVs at the Rhg1, a SYBR Green-based quantitative PCR (qPCR) assay was optimized and validated using 12 soybean accessions with known copy numbers. The qPCR assay demonstrated 94.36% efficiency for the target gene at Rhg1 locus, Glyma18g02590, with copy number detected by the assay correlating strongly (r=0.994) with whole genome sequencing data in previous study. …”
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