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Search: authors:"Priyanka Agarwal"

6 papers found.
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A study of CCD8 genes/proteins in seven monocots and eight dicots

Agarwal, Sandhya Tyagi, Dinesh Kumar Saini, Vikas Kumar, Anuj Kumar, Sanjay Kumar. Formal analysis: Ritu Batra, Priyanka Agarwal, Sandhya Tyagi. Methodology: Ritu Batra, Renu Pandey. Resources: Harindra ... Genetics & Plant Breeding, CCS University, Meerut. Author Contributions Conceptualization: Ritu Batra, Harindra Singh Balyan, Renu Pandey, Pushpendra Kumar Gupta. Data curation: Ritu Batra, Priyanka

A Predictable Aesthetic Rehabilitation of Deciduous Anterior Teeth in Early Childhood Caries

2018; Accepted 18 February 2018; Published 3 April 2018 Academic Editor: Andrea Scribante Copyright © 2018 Priyanka Agarwal et al. This is an open access article distributed under the Creative Commons

Identification of miRNA-mediated drought responsive multi-tiered regulatory network in drought tolerant rice, Nagina 22

Balyan, Mukesh Kumar, Roseeta Devi Mutum, Utkarsh Raghuvanshi, Priyanka Agarwal & Saurabh RaghuvanshiNational Institute of Plant Genome Research, Aruna Asaf Ali Road, New Delhi, 110067, IndiaSaloni Mathur ... Research journals • PubMed • Google Scholar Search for Utkarsh Raghuvanshi in:Nature Research journals • PubMed • Google Scholar Search for Priyanka Agarwal in:Nature Research journals • PubMed • Google

Identification of Novel SNP in Promoter Sequence of TaGW2-6A Associated with Grain Weight and Other Agronomic Traits in Wheat (Triticum aestivum L.)

TaGW2 is an orthologue of rice gene OsGW2, which encodes E3 RING ubiquitin ligase and controls the grain size in rice. In wheat, three copies of TaGW2 have been identified and mapped on wheat homoeologous group 6 viz. TaGW2-6A, TaGW2-6B and TaGW2-6D. In the present study, using as many as 207 Indian wheat genotypes, we identified four SNPs including two novel SNPs (SNP-988 and...

Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations

Background Females with the neurological disorder Rett syndrome are heterozygous for mutations in X-linked MECP2 that encodes methyl-CpG binding protein 2 (MeCP2) thought to act as a transcriptional repressor. To identify target genes for MeCP2 modulation, we studied global gene expression in single cell-derived wild-type and mutant MECP2 expressing fibroblast clones with four...

Gene expression patterns vary in clonal cell cultures from Rett syndrome females with eight different MECP2 mutations

Females with the neurological disorder Rett syndrome are heterozygous for mutations in X-linked MECP2 that encodes methyl-CpG binding protein 2 (MeCP2) thought to act as a transcriptional repressor. To identify target genes for MeCP2 modulation, we studied global gene expression in single cell-derived wild-type and mutant MECP2 expressing fibroblast clones with four common...