Pallavi Goel

Dr. Pallavi Goel

orcid

Research Focus & Metrics

Academic Career Length

6Years (2021-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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3 June 2024 in Veterinary Research Communications
Verified
Journal Article
Closed access
PDF file
DKDeepak Kumar
Deepak Kumar
MTManish Tiwari
Manish Tiwari
PGPallavi Goel
Pallavi Goel
MSManoj Kumar Singh
Manoj Kumar Singh
NSNaresh Lala Selokar
Naresh Lala Selokar
PPPrabhat Palta
Prabhat Palta

1 March 2022 in Genes
Verified
Journal Article
Open access
PDF file
PGPallavi Goel
Pallavi Goel
SMShivani Malpotra
Shivani Malpotra
SSSongyukta Shyam
Songyukta Shyam
DKDeepak Kumar
Deepak Kumar
MSManoj Kumar Singh
Manoj Kumar Singh
PPPrabhat Palta
Prabhat Palta
Despite the success of cloning technology in the production of offspring across several species, its application on a wide scale is severely limited by the very low offspring rate obtained with cloned embryos. The expression profile of microRNAs (miRNAs) in cloned embryos throughout embryonic development is reported to deviate from regular patterns. The present study is aimed at determining the dynamics of the global expression of miRNA profile in cloned and in-vitro fertilization (IVF) pre-implantation embryos at different developmental stages, i.e., the two-cell, eight-cell, and blastocyst stages, using next-generation sequencing. The results of this study suggest that there is a profound difference in global miRNA profile between cloned and IVF embryos. These differences are manifested throughout the course of embryonic development. The cloned embryos differ from their IVF counterparts in enriched Gene Ontology (GO) terms of biological process, molecular function, cellular component, and protein class categories in terms of the targets of differentially expressed miRNAs. The major pathways related to embryonic development, such as the Wnt signaling pathway, the apoptosis signaling pathway, the FGF signaling pathway, the p53 pathway, etc., were found to be affected in cloned relative to IVF embryos. Overall, these data reveal the distinct miRNA profile of cloned relative to IVF embryos, suggesting that the molecules or pathways affected may play an important role in cloned embryo development.

21 May 2021 in Research Square
Verified
Preprint
Open access
PDF file
PGPallavi Goel
Pallavi Goel
SMShivani Malpotra
Shivani Malpotra
SSSongyukta Shyam
Songyukta Shyam
DKDeepak Kumar
Deepak Kumar
MSManoj Kumar Singh
Manoj Kumar Singh
PPPrabhat Palta
Prabhat Palta
Despite the success of cloning technology in production of offspring across several species, its application on a wide scale is severely limited by the very low offspring rate obtained with cloned embryos. MicroRNAs (miRNAs) expression profile in cloned embryos throughout the embryonic development are reported to deviate from regular pattern. In present study, aimed at determining the dynamics of global expression of miRNA profile in cloned and IVF pre-implantation embryos at different developmental stages i.e 2-cell, 8-cell and blastocyst using next-generation sequencing. The results of this study suggested that there is a profound difference in the global miRNA profile between cloned and IVF embryos. These differences are manifested throughout the course of embryonic development. The cloned embryos differ from their IVF counterparts in the enriched GO terms of Biological Process, Molecular Function, Cellular Component and Protein Class categories in terms of the targets of differentially expressed miRNAs. The major pathways related to embryonic development such as Wnt signaling pathway, apoptosis signaling pathway, FGF signaling pathway, p53 pathway etc. were found to be affected in cloned relative to IVF embryos.