N. Balgobin
About
N. Balgobin is a scholar working on Molecular Biology, Organic Chemistry and Spectroscopy.
According to data from OpenAlex, N. Balgobin has authored 30 papers receiving a total of 387 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 11 papers in Organic Chemistry and 2 papers in Spectroscopy. Recurrent topics in N. Balgobin's work include DNA and Nucleic Acid Chemistry (20 papers), RNA and protein synthesis mechanisms (12 papers) and Advanced biosensing and bioanalysis techniques (7 papers). N. Balgobin is often cited by papers focused on DNA and Nucleic Acid Chemistry (20 papers), RNA and protein synthesis mechanisms (12 papers) and Advanced biosensing and bioanalysis techniques (7 papers). N. Balgobin collaborates with scholars based in Sweden, Netherlands and Germany. N. Balgobin's co-authors include Jyoti Chattopadhyaya, Gérald S. Remaud, Staffan Josephson, Stellan Hjertén, Ulf Pettersson, Lars‐Göran Öfverstedt, András Földesi, A. Sandström, Léo H. Koole and Ulrika Örn and has published in prestigious journals such as Tetrahedron, Tetrahedron Letters and JAIDS Journal of Acquired Immune Deficiency Syndromes.
In The Last Decade
N. Balgobin
28 papers receiving 373 citations
Peers
N. Balgobin
George C. Slim New Zealand
V. A. Efimov Russia
Stephen J. Brewer United Kingdom
Oleg Werbitzky Germany
Robert A. Goldman United States
C. Hornung Germany
Seiichi Ohkuma Japan
Wendy J. Dixon United States
David R. Jackson United States
Markus Windwarder Austria
Citations per year, relative to N. Balgobin N. Balgobin (= 1×)
peers
George C. Slim
Countries citing papers authored by N. Balgobin
Since
Specialization
Citations
This map shows the geographic impact of N. Balgobin's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by N. Balgobin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N. Balgobin more than expected).
Fields of papers citing papers by N. Balgobin
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by N. Balgobin. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by N. Balgobin. The network helps show where N. Balgobin may publish in the future.
Co-authorship network of co-authors of N. Balgobin
This figure shows the co-authorship network connecting the top 25 collaborators of N. Balgobin. A scholar is included among the top collaborators of N. Balgobin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with N. Balgobin. N. Balgobin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Schwartz, Jennifer A., J. de Saint Martin, Wenlei Zhang, et al.. (2016). P-C1 Full length single chain, a novel gp120-CD4 fusion HIV Subunit vaccine, does not cause a deleterious autoimmune CD4 response in cynomolgus macaques. JAIDS Journal of Acquired Immune Deficiency Syndromes. 71(Supplement 1). 89–89.
2.
Balgobin, N., et al.. (1989). Synthesis of Branched Oligoribonucleotides (“Lariat”). Nucleosides and Nucleotides. 8(5-6). 793–797.
3.
Remaud, Gérald S., N. Balgobin, A. Sandström, et al.. (1989). Why do all lariat RNA introns have adenosine as the branch-point nucleotide? Conformational study of naturally-occuring branched trinucleotides and its eleven analogues by 1H-, 31P-NMR and CD spectroscopy. Journal of Biochemical and Biophysical Methods. 18(1). 1–35.
4.
Sandström, A., et al.. (1988). Conformation of Lariat Structures Formed in the Splicing of Pre-mRNA by NMR Spectroscopy. Nucleosides and Nucleotides. 7(5-6). 827–830.
5.
Balgobin, N., et al.. (1988). A new regiospecific synthesis of “Branched” tetraribonucleotide and its three analogues to delineate the chemospecific role of the “Branch-point” adenine nucleotide in splicing. Tetrahedron. 44(22). 6929–6939.
6.
Balgobin, N., et al.. (1987). A Convergent Regiospecific Synthesis of the Lariat-Trinucleotides and A2′p 5′Gand A2′p 5′G3′p 5′Cfrom A O4-2-Nitrophenyl) -Uridine Building Block. Nucleosides and Nucleotides. 6(1-2). 209–226.
7.
Remaud, Gérald S., et al.. (1987). A 270 MHz 1H-NMR study of three “branched” ribonucleotides A2'p5'U3'p5'g, A2'p5'C3'p5'G and A2'p5'G3'p5'G the importance of being branched with a 2'→5' phosphodiester bond in the pre-mRNA processing reactions (splicing). Tetrahedron. 43(17). 3997–4006.
8.
Lemmen, Peter, et al.. (1987). Bausteine für Oligonucleotid-Synthesen mit einheitlich fragmentierbaren β-halogenierten Schutzgruppen /Building Blocks for Oligonucleotide Syntheses with Uniformly Fragmentable β-Halogenated Protecting Groups. Zeitschrift für Naturforschung C. 42(4). 442–445.
9.
Balgobin, N. & Jyoti Chattopadhyaya. (1987). Solid Phase Synthesis of DNA Under a Non-Depurinating Condition with a Base Labile 5′-Protecting Group (Fmoc) Using Phosphiteamidite Approach. Nucleosides and Nucleotides. 6(1-2). 461–463.
10.
UGI, I., J. Bauer, Eric Fontain, et al.. (1986). ChemInform Abstract: New Phosphorylating Reagents and Protective Group Techniques for Oligonucleotide Synthesis, as Well as Computer Assistance in the Design of Reagents. Chemischer Informationsdienst. 17(38).
11.
Balgobin, N., Jyoti Chattopadhyaya, Martin Nilsson, et al.. (1985). Use of 2-Phenylsulfonylethyl as a Phosphate Protecting Group in DNA Synthesis Using the Phosphite-Triester Approach.. Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry. 39b. 883–888.
12.
Öfverstedt, Lars‐Göran, et al.. (1984). Rapid and quantitative recovery of DNA fragments from gels by displacement electrophoresis (isotachophoresis). Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression. 782(2). 120–126.
13.
Balgobin, N., Marek Kwiatkowski, & Jyoti Chattopadhyaya. (1983). ChemInform Abstract: A NOVEL STRATEGY FOR THE CHEMICAL SYNTHESIS OF DNA AND RNA FRAGMENTS USING 2‐OXYMETHYLENEANTHRAQUINONE (MAQ) AS A 3′‐TERMINAL PHOSPHATE PROTECTING GROUP. Chemischer Informationsdienst. 14(4).
14.
Balgobin, N., et al.. (1983). The 2-Nitrophenylsulfenyl (Nps) Group for the Protection of Amino Functions of Cytidine, Adenosine, Guanosine and Their 2'-Deoxysugar Derivatives.. Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry. 37b(9). 857–862.
15.
Balgobin, N. & Jyoti Chattopadhyaya. (1982). りん酸保護基としての2‐(4‐ニトロフェニル)チオエチル基およびりん酸トリエステル法によるドデカチミジル酸合成へのその応用. 20(3). 144–146.
16.
Balgobin, N. & Jyoti Chattopadhyaya. (1982). ChemInform Abstract: AN EFFICIENT CHEMICAL SYNTHESIS OF A BIOLOGICALLY FUNCTIONAL DNA MOLECULE, 5′D(A‐T‐G‐G‐G‐T‐T‐T‐C‐T‐T‐C‐G‐C‐)3′, THROUGH THE PHOSPHOTRIESTER APPROACH. Chemischer Informationsdienst. 13(52).
17.
Josephson, Staffan, N. Balgobin, & Jyoti Chattopadhyaya. (1981). The application of 2-(4-chlorophenyl)-sulfonylethoxycarbonyl (CPSEC) group in the synthesis of a DNA segment using the phosphotriester approach. Tetrahedron Letters. 22(45). 4537–4540.
18.
Balgobin, N., Staffan Josephson, & Jyoti Chattopadhyaya. (1981). 2-Phenylsulfonylethyl, a new phosphate protecting group: Its application in the synthesis of dodecathymidylic acid.. Tetrahedron Letters. 22(20). 1915–1918.
19.
Balgobin, N., Staffan Josephson, Jyoti Chattopadhyaya, Povl Krogsgaard‐Larsen, & Ulrika Örn. (1981). A General Approach to the Chemical Synthesis of Oligodeoxyribonucleotides.. Acta chemica Scandinavica/Acta chemica Scandinavica. B, Organic chemistry and biochemistry/Acta chemica Scandinavica. A, Physical and inorganic chemistry/Acta chemica Scandinavica. Series B. Organic chemistry and biochemistry/Acta chemica Scandinavica. Series A, Physical and inorganic chemistry. 35b. 201–212.
20.
Balgobin, N., Staffan Josephson, & Jyoti Chattopadhyaya. (1981). The 2-phenylsulfonylethylcarbonyl (PSEC) group for the protection of the hydroxyl function. Tetrahedron Letters. 22(37). 3667–3670.
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