S
Sohini Sanyal
Researcher at Cornell University
Publications - 5
Citations - 530
Sohini Sanyal is an academic researcher from Cornell University. The author has contributed to research in topics: Antigenic variation & Plasmodium falciparum. The author has an hindex of 4, co-authored 5 publications receiving 495 citations.
Papers
More filters
Journal ArticleDOI
Expression switching in the stevor and Pfmc-2TM superfamilies in Plasmodium falciparum
TL;DR: Evidence is provided that the stevor and Pfmc‐2TM gene families play a role in P. falciparum antigenic variation, and chromosomal telomeric deletions are common in clonal lines and result in a spectrum of deletion genotypes.
Journal ArticleDOI
Hypervariability within the Rifin, Stevor and Pfmc-2TM superfamilies in Plasmodium falciparum
TL;DR: Evidence is presented that the Stevor and Pfmc-2TM families are exported to the erythrocyte membrane, thus supporting the hypothesis that host immune pressure drives antigenic diversity within the loop, and an examination of multiple P.falciparum isolates demonstrates that the hypervariable loop within Stevor et al. possesses sequence diversity across isolate boundaries.
Journal ArticleDOI
Plasmodium falciparum STEVOR proteins impact erythrocyte mechanical properties
Sohini Sanyal,Stéphane Egée,Guillaume Bouyer,Sylvie Perrot,Innocent Safeukui,Emmanuel Bischoff,Pierre Buffet,Kirk W. Deitsch,Odile Mercereau-Puijalon,Peter H. David,Thomas J. Templeton,Catherine Lavazec,Catherine Lavazec +12 more
TL;DR: It is shown that stevor expression impacts deformability of the erythrocyte membrane, which may facilitate parasite sequestration in deep tissue vasculature.
Journal ArticleDOI
Frequent recombination events generate diversity within the multi-copy variant antigen gene families of Plasmodium falciparum.
Matthias Frank,Laura A. Kirkman,Daniel Costantini,Sohini Sanyal,Catherine Lavazec,Thomas J. Templeton,Kirk W. Deitsch +6 more
TL;DR: In the course of producing transgenic lines from the original NF54 parasite isolate, cloned and characterised a parasite line, termed E5, which is closely related to but distinct from 3D7, the parasite used for the P. falciparum genome nucleotide sequencing project, and identified examples of frequent recombination events within these gene families, including an example of a duplicative transposition.
Book ChapterDOI
Analysis of variant gene family expression by quantitative PCR.
TL;DR: The materials and methods required to performreal-time RT-PCR, including RNA purification, cDNA synthesis, and real-time PCR analysis of cDNA samples are described.