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Showing 1 to 12 of 438 entries
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Intravascular large B-cell lymphoma presenting as Richter's syndrome with cerebral involvement in a patient with chronic lymphocytic leukemia.

Clinical case reports

Puckrin R, Pop P, Ghorab Z, Keith J, Chodirker L, Lin Y, Callum J.
PMID: 28878900
Clin Case Rep. 2017 Jul 20;5(9):1444-1449. doi: 10.1002/ccr3.1087. eCollection 2017 Sep.

Intravascular large B-cell lymphoma (IVLBCL) is an aggressive non-Hodgkin's lymphoma which can present with B symptoms, rash, and neurological deterioration. Up to 10% of cases of IVLBCL are associated with other hematological neoplasms, including this extremely rare presentation of...

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Puckrin R, Pop P, Ghorab Z, et al. Intravascular large B-cell lymphoma presenting as Richter's syndrome with cerebral involvement in a patient with chronic lymphocytic leukemia. Clin Case Rep. 2017;5(9):1444-1449doi: 10.1002/ccr3.1087.
Puckrin, R., Pop, P., Ghorab, Z., Keith, J., Chodirker, L., Lin, Y., & Callum, J. (2017). Intravascular large B-cell lymphoma presenting as Richter's syndrome with cerebral involvement in a patient with chronic lymphocytic leukemia. Clinical case reports, 5(9), 1444-1449. https://doi.org/10.1002/ccr3.1087
Puckrin, Robert, et al. "Intravascular large B-cell lymphoma presenting as Richter's syndrome with cerebral involvement in a patient with chronic lymphocytic leukemia." Clinical case reports vol. 5,9 (2017): 1444-1449. doi: https://doi.org/10.1002/ccr3.1087
Puckrin R, Pop P, Ghorab Z, Keith J, Chodirker L, Lin Y, Callum J. Intravascular large B-cell lymphoma presenting as Richter's syndrome with cerebral involvement in a patient with chronic lymphocytic leukemia. Clin Case Rep. 2017 Jul 20;5(9):1444-1449. doi: 10.1002/ccr3.1087. eCollection 2017 Sep. PMID: 28878900; PMCID: PMC5582220.
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Transition-Metal-Free Synthesis of Homo- and Hetero-1,2,4-Triaryl Benzenes by an Unexpected Base-Promoted Dearylative Pathway.

Angewandte Chemie (International ed. in English)

Rehan M, Maity S, Morya LK, Pal K, Ghorai P.
PMID: 27061117
Angew Chem Int Ed Engl. 2016 Jun 27;55(27):7728-32. doi: 10.1002/anie.201511424. Epub 2016 Apr 09.

An unprecedented approach for the synthesis of homo- and hetero-1,2,4-triaryl benzenes has been developed using a simple base-mediated reaction of either α-aryl cinnamyl alcohols or α,γ-di-aryl propanones. The salient feature of this strategy involves the sequential hydride transfer, regiospecific...

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Rehan M, Maity S, Morya LK, et al. Transition-Metal-Free Synthesis of Homo- and Hetero-1,2,4-Triaryl Benzenes by an Unexpected Base-Promoted Dearylative Pathway. Angew Chem Int Ed Engl. 2016;55(27):7728-32doi: 10.1002/anie.201511424.
Rehan, M., Maity, S., Morya, L. K., Pal, K., & Ghorai, P. (2016). Transition-Metal-Free Synthesis of Homo- and Hetero-1,2,4-Triaryl Benzenes by an Unexpected Base-Promoted Dearylative Pathway. Angewandte Chemie (International ed. in English), 55(27), 7728-32. https://doi.org/10.1002/anie.201511424
Rehan, Mohammad, et al. "Transition-Metal-Free Synthesis of Homo- and Hetero-1,2,4-Triaryl Benzenes by an Unexpected Base-Promoted Dearylative Pathway." Angewandte Chemie (International ed. in English) vol. 55,27 (2016): 7728-32. doi: https://doi.org/10.1002/anie.201511424
Rehan M, Maity S, Morya LK, Pal K, Ghorai P. Transition-Metal-Free Synthesis of Homo- and Hetero-1,2,4-Triaryl Benzenes by an Unexpected Base-Promoted Dearylative Pathway. Angew Chem Int Ed Engl. 2016 Jun 27;55(27):7728-32. doi: 10.1002/anie.201511424. Epub 2016 Apr 09. PMID: 27061117.
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SMAR1 binds to T(C/G) repeat and inhibits tumor progression by regulating miR-371-373 cluster.

Scientific reports

Mathai J, Mittal SP, Alam A, Ranade P, Mogare D, Patel S, Saxena S, Ghorai S, Kulkarni AP, Chattopadhyay S.
PMID: 27671416
Sci Rep. 2016 Sep 27;6:33779. doi: 10.1038/srep33779.

Chromatin architecture and dynamics are regulated by various histone and non-histone proteins. The matrix attachment region binding proteins (MARBPs) play a central role in chromatin organization and function through numerous regulatory proteins. In the present study, we demonstrate that...

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Mathai J, Mittal SP, Alam A, et al. SMAR1 binds to T(C/G) repeat and inhibits tumor progression by regulating miR-371-373 cluster. Sci Rep. 2016;6:33779doi: 10.1038/srep33779.
Mathai, J., Mittal, S. P., Alam, A., Ranade, P., Mogare, D., Patel, S., Saxena, S., Ghorai, S., Kulkarni, A. P., & Chattopadhyay, S. (2016). SMAR1 binds to T(C/G) repeat and inhibits tumor progression by regulating miR-371-373 cluster. Scientific reports, 633779. https://doi.org/10.1038/srep33779
Mathai, Jinumary, et al. "SMAR1 binds to T(C/G) repeat and inhibits tumor progression by regulating miR-371-373 cluster." Scientific reports vol. 6 (2016): 33779. doi: https://doi.org/10.1038/srep33779
Mathai J, Mittal SP, Alam A, Ranade P, Mogare D, Patel S, Saxena S, Ghorai S, Kulkarni AP, Chattopadhyay S. SMAR1 binds to T(C/G) repeat and inhibits tumor progression by regulating miR-371-373 cluster. Sci Rep. 2016 Sep 27;6:33779. doi: 10.1038/srep33779. PMID: 27671416; PMCID: PMC5037395.
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Draft Genome Sequence of a Moderately Halophilic Bacillus megaterium Strain, MSP20.1, Isolated from a Saltern of the Little Rann of Kutch, India.

Genome announcements

Pal KK, Dey R, Sherathia D, Vanpariya S, Patel I, Dalsania T, Savsani K, Sukhadiya B, Mandaliya M, Thomas M, Ghorai S, Rupapara R, Rawal P, Shah A, Bhayani S.
PMID: 24407642
Genome Announc. 2014 Jan 09;2(1). doi: 10.1128/genomeA.01134-13.

The 4.37-Mbp draft genome of a moderately halophilic Bacillus megaterium strain, MSP20.1, isolated from a saltern of the Little Rann of Kutch, India, is reported here. To understand the mechanism(s) of moderate halophilism and to isolate the gene(s) involved...

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Pal KK, Dey R, Sherathia D, et al. Draft Genome Sequence of a Moderately Halophilic Bacillus megaterium Strain, MSP20.1, Isolated from a Saltern of the Little Rann of Kutch, India. Genome Announc. 2014;2(1)doi: 10.1128/genomeA.01134-13.
Pal, K. K., Dey, R., Sherathia, D., Vanpariya, S., Patel, I., Dalsania, T., Savsani, K., Sukhadiya, B., Mandaliya, M., Thomas, M., Ghorai, S., Rupapara, R., Rawal, P., Shah, A., & Bhayani, S. (2014). Draft Genome Sequence of a Moderately Halophilic Bacillus megaterium Strain, MSP20.1, Isolated from a Saltern of the Little Rann of Kutch, India. Genome announcements, 2(1), . https://doi.org/10.1128/genomeA.01134-13
Pal, Kamal Krishna, et al. "Draft Genome Sequence of a Moderately Halophilic Bacillus megaterium Strain, MSP20.1, Isolated from a Saltern of the Little Rann of Kutch, India." Genome announcements vol. 2,1 (2014). doi: https://doi.org/10.1128/genomeA.01134-13
Pal KK, Dey R, Sherathia D, Vanpariya S, Patel I, Dalsania T, Savsani K, Sukhadiya B, Mandaliya M, Thomas M, Ghorai S, Rupapara R, Rawal P, Shah A, Bhayani S. Draft Genome Sequence of a Moderately Halophilic Bacillus megaterium Strain, MSP20.1, Isolated from a Saltern of the Little Rann of Kutch, India. Genome Announc. 2014 Jan 09;2(1). doi: 10.1128/genomeA.01134-13. PMID: 24407642; PMCID: PMC3886955.
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Mechanical Properties of a Series of Macro- and Nanodimensional Organic Cocrystals Correlate with Atomic Polarizability.

Journal of the American Chemical Society

Rupasinghe TP, Hutchins KM, Bandaranayake BS, Ghorai S, Karunatilake C, Bučar DK, Swenson DC, Arnold MA, MacGillivray LR, Tivanski AV.
PMID: 26407029
J Am Chem Soc. 2015 Oct 14;137(40):12768-71. doi: 10.1021/jacs.5b07873. Epub 2015 Oct 02.

A correlation between Young's modulus, as determined by using nanoindentation atomic force microscopy (AFM), and atomic polarizability is observed for members of a series of cocrystals based on systematic changes to one cocrystal component. Time domain spectroscopy over terahertz...

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Rupasinghe TP, Hutchins KM, Bandaranayake BS, et al. Mechanical Properties of a Series of Macro- and Nanodimensional Organic Cocrystals Correlate with Atomic Polarizability. J Am Chem Soc. 2015;137(40):12768-71doi: 10.1021/jacs.5b07873.
Rupasinghe, T. P., Hutchins, K. M., Bandaranayake, B. S., Ghorai, S., Karunatilake, C., Bučar, D. K., Swenson, D. C., Arnold, M. A., MacGillivray, L. R., & Tivanski, A. V. (2015). Mechanical Properties of a Series of Macro- and Nanodimensional Organic Cocrystals Correlate with Atomic Polarizability. Journal of the American Chemical Society, 137(40), 12768-71. https://doi.org/10.1021/jacs.5b07873
Rupasinghe, Thilini P, et al. "Mechanical Properties of a Series of Macro- and Nanodimensional Organic Cocrystals Correlate with Atomic Polarizability." Journal of the American Chemical Society vol. 137,40 (2015): 12768-71. doi: https://doi.org/10.1021/jacs.5b07873
Rupasinghe TP, Hutchins KM, Bandaranayake BS, Ghorai S, Karunatilake C, Bučar DK, Swenson DC, Arnold MA, MacGillivray LR, Tivanski AV. Mechanical Properties of a Series of Macro- and Nanodimensional Organic Cocrystals Correlate with Atomic Polarizability. J Am Chem Soc. 2015 Oct 14;137(40):12768-71. doi: 10.1021/jacs.5b07873. Epub 2015 Oct 02. PMID: 26407029.
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Catalytic Asymmetric Conjugate Addition of Carboxylic Acids via Oxa-Michael Reaction of Peroxy Hemiacetals followed by Kornblum DeLaMare Fragmentation.

Organic letters

Parhi B, Maity S, Ghorai P.
PMID: 27690466
Org Lett. 2016 Oct 21;18(20):5220-5223. doi: 10.1021/acs.orglett.6b02463. Epub 2016 Oct 03.

Disclosed herein an overall methodology constitutes an equivalent to the long sought after enantioselective intramolecular oxa-Michael (IOM) reaction of carboxylic acids. An organocatalyzed IOM reaction of in situ formed peroxy hemiacetals followed by a Kornblum DeLaMare type rearrangement cascade...

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Parhi B, Maity S, Ghorai P. Catalytic Asymmetric Conjugate Addition of Carboxylic Acids via Oxa-Michael Reaction of Peroxy Hemiacetals followed by Kornblum DeLaMare Fragmentation. Org Lett. 2016;18(20):5220-5223doi: 10.1021/acs.orglett.6b02463.
Parhi, B., Maity, S., & Ghorai, P. (2016). Catalytic Asymmetric Conjugate Addition of Carboxylic Acids via Oxa-Michael Reaction of Peroxy Hemiacetals followed by Kornblum DeLaMare Fragmentation. Organic letters, 18(20), 5220-5223. https://doi.org/10.1021/acs.orglett.6b02463
Parhi, Biswajit, et al. "Catalytic Asymmetric Conjugate Addition of Carboxylic Acids via Oxa-Michael Reaction of Peroxy Hemiacetals followed by Kornblum DeLaMare Fragmentation." Organic letters vol. 18,20 (2016): 5220-5223. doi: https://doi.org/10.1021/acs.orglett.6b02463
Parhi B, Maity S, Ghorai P. Catalytic Asymmetric Conjugate Addition of Carboxylic Acids via Oxa-Michael Reaction of Peroxy Hemiacetals followed by Kornblum DeLaMare Fragmentation. Org Lett. 2016 Oct 21;18(20):5220-5223. doi: 10.1021/acs.orglett.6b02463. Epub 2016 Oct 03. PMID: 27690466.
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Diastereoselective synthesis of functionalized tetrahydrocarbazoles via a domino-ring opening-cyclization of donor-acceptor cyclopropanes with substituted 2-vinylindoles.

Organic letters

Talukdar R, Tiwari DP, Saha A, Ghorai MK.
PMID: 25008386
Org Lett. 2014 Aug 01;16(15):3954-7. doi: 10.1021/ol501763n. Epub 2014 Jul 10.

A new domino synthetic approach for the synthesis of highly functionalized tetrahydrocarbazoles via DROC of various functionalized DA-cyclopropanes with 2-indolylnitroethylene and indole-substituted alkylidene malonate is described. The tetrahydrocarbazoles were obtained with excellent diastereoselectivity having cis alignment of the 1,4-appendages...

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Talukdar R, Tiwari DP, Saha A, et al. Diastereoselective synthesis of functionalized tetrahydrocarbazoles via a domino-ring opening-cyclization of donor-acceptor cyclopropanes with substituted 2-vinylindoles. Org Lett. 2014;16(15):3954-7doi: 10.1021/ol501763n.
Talukdar, R., Tiwari, D. P., Saha, A., & Ghorai, M. K. (2014). Diastereoselective synthesis of functionalized tetrahydrocarbazoles via a domino-ring opening-cyclization of donor-acceptor cyclopropanes with substituted 2-vinylindoles. Organic letters, 16(15), 3954-7. https://doi.org/10.1021/ol501763n
Talukdar, Ranadeep, et al. "Diastereoselective synthesis of functionalized tetrahydrocarbazoles via a domino-ring opening-cyclization of donor-acceptor cyclopropanes with substituted 2-vinylindoles." Organic letters vol. 16,15 (2014): 3954-7. doi: https://doi.org/10.1021/ol501763n
Talukdar R, Tiwari DP, Saha A, Ghorai MK. Diastereoselective synthesis of functionalized tetrahydrocarbazoles via a domino-ring opening-cyclization of donor-acceptor cyclopropanes with substituted 2-vinylindoles. Org Lett. 2014 Aug 01;16(15):3954-7. doi: 10.1021/ol501763n. Epub 2014 Jul 10. PMID: 25008386.
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Synthesis of air- and moisture-stable, storable chiral oxorhenium complexes and their application as catalysts for the enantioselective imine reduction.

Chemistry (Weinheim an der Bergstrasse, Germany)

Das BG, Nallagonda R, Dey D, Ghorai P.
PMID: 26227426
Chemistry. 2015 Sep 01;21(36):12601-5. doi: 10.1002/chem.201501914. Epub 2015 Jul 21.

Air-/moisture-stable, crystalline, and storable chiral salicyloxazoline based oxorhenium(V) complexes have been synthesized and their catalytic application for the asymmetric reduction of ketimines using hydrosilane as hydride source is disclosed. A broad substrate scope, high yields, and excellent enantioselectivities (up...

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Das BG, Nallagonda R, Dey D, et al. Synthesis of air- and moisture-stable, storable chiral oxorhenium complexes and their application as catalysts for the enantioselective imine reduction. Chemistry. 2015;21(36):12601-5doi: 10.1002/chem.201501914.
Das, B. G., Nallagonda, R., Dey, D., & Ghorai, P. (2015). Synthesis of air- and moisture-stable, storable chiral oxorhenium complexes and their application as catalysts for the enantioselective imine reduction. Chemistry (Weinheim an der Bergstrasse, Germany), 21(36), 12601-5. https://doi.org/10.1002/chem.201501914
Das, Braja Gopal, et al. "Synthesis of air- and moisture-stable, storable chiral oxorhenium complexes and their application as catalysts for the enantioselective imine reduction." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,36 (2015): 12601-5. doi: https://doi.org/10.1002/chem.201501914
Das BG, Nallagonda R, Dey D, Ghorai P. Synthesis of air- and moisture-stable, storable chiral oxorhenium complexes and their application as catalysts for the enantioselective imine reduction. Chemistry. 2015 Sep 01;21(36):12601-5. doi: 10.1002/chem.201501914. Epub 2015 Jul 21. PMID: 26227426.
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Sudden Death Following Exercise; a Case Series.

Emergency (Tehran, Iran)

Najari F, Alimohammadi A, Ghodrati P.
PMID: 27274521
Emerg (Tehran). 2016;4(2):97-100.

INTRODUCTION: Natural and unexpected death that happens within less than one hour of first symptom occurrence is called sudden death. Cardiovascular diseases are the main known reason of sudden death and more than 75% of sudden deaths in athletes...

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Najari F, Alimohammadi A, Ghodrati P. Sudden Death Following Exercise; a Case Series. Emerg (Tehran). 2016;4(2):97-100
Najari, F., Alimohammadi, A., & Ghodrati, P. (2016). Sudden Death Following Exercise; a Case Series. Emergency (Tehran, Iran), 4(2), 97-100.
Najari, Fares, et al. "Sudden Death Following Exercise; a Case Series." Emergency (Tehran, Iran) vol. 4,2 (2016): 97-100.
Najari F, Alimohammadi A, Ghodrati P. Sudden Death Following Exercise; a Case Series. Emerg (Tehran). 2016;4(2):97-100. PMID: 27274521; PMCID: PMC4893759.
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Evidence in support of levitation effect as the reason for size dependence of ionic conductivity in water: a molecular dynamics simulation.

The journal of physical chemistry. B

Ghorai PK, Yashonath S.
PMID: 16800534
J Phys Chem B. 2006 Jun 22;110(24):12179-90. doi: 10.1021/jp061511w.

We report extensive molecular dynamics simulations of (i) model ions in water at high concentrations as a function of the size and charge of the ion as well as (ii) realistic simulation of Cl- and Br- ions at low...

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Ghorai PK, Yashonath S. Evidence in support of levitation effect as the reason for size dependence of ionic conductivity in water: a molecular dynamics simulation. J Phys Chem B. 2006;110(24):12179-90doi: 10.1021/jp061511w.
Ghorai, P. K., & Yashonath, S. (2006). Evidence in support of levitation effect as the reason for size dependence of ionic conductivity in water: a molecular dynamics simulation. The journal of physical chemistry. B, 110(24), 12179-90. https://doi.org/10.1021/jp061511w
Ghorai, Pradip Kr, and Yashonath, S. "Evidence in support of levitation effect as the reason for size dependence of ionic conductivity in water: a molecular dynamics simulation." The journal of physical chemistry. B vol. 110,24 (2006): 12179-90. doi: https://doi.org/10.1021/jp061511w
Ghorai PK, Yashonath S. Evidence in support of levitation effect as the reason for size dependence of ionic conductivity in water: a molecular dynamics simulation. J Phys Chem B. 2006 Jun 22;110(24):12179-90. doi: 10.1021/jp061511w. PMID: 16800534.
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Olefin cross-metathesis reactions at room temperature using the nonionic amphiphile "PTS": just add water.

Organic letters

Lipshutz BH, Aguinaldo GT, Ghorai S, Voigtritter K.
PMID: 18335947
Org Lett. 2008 Apr 03;10(7):1325-8. doi: 10.1021/ol800028x. Epub 2008 Mar 12.

The first examples of unsymmetrical olefin cross-metathesis reactions in water, involving water-insoluble substrates, at room temperature and using commercially available catalysts are reported. The key to success is to include small percentages of the nonionic, vitamin E-based amphiphile "PTS"....

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Lipshutz BH, Aguinaldo GT, Ghorai S, et al. Olefin cross-metathesis reactions at room temperature using the nonionic amphiphile "PTS": just add water. Org Lett. 2008;10(7):1325-8doi: 10.1021/ol800028x.
Lipshutz, B. H., Aguinaldo, G. T., Ghorai, S., & Voigtritter, K. (2008). Olefin cross-metathesis reactions at room temperature using the nonionic amphiphile "PTS": just add water. Organic letters, 10(7), 1325-8. https://doi.org/10.1021/ol800028x
Lipshutz, Bruce H, et al. "Olefin cross-metathesis reactions at room temperature using the nonionic amphiphile "PTS": just add water." Organic letters vol. 10,7 (2008): 1325-8. doi: https://doi.org/10.1021/ol800028x
Lipshutz BH, Aguinaldo GT, Ghorai S, Voigtritter K. Olefin cross-metathesis reactions at room temperature using the nonionic amphiphile "PTS": just add water. Org Lett. 2008 Apr 03;10(7):1325-8. doi: 10.1021/ol800028x. Epub 2008 Mar 12. PMID: 18335947.
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Multicomponent reactions of convertible isonitriles.

The Journal of organic chemistry

Pirrung MC, Ghorai S, Ibarra-Rivera TR.
PMID: 19408909
J Org Chem. 2009 Jun 05;74(11):4110-7. doi: 10.1021/jo900414n.

A new family of unsaturated isonitriles has been prepared by the base-promoted ring-opening of oxazoles, offering an alternative to the conventional formamide dehydration route. These compounds undergo the full complement of multicomponent reactions for which isonitriles are known and...

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Pirrung MC, Ghorai S, Ibarra-Rivera TR. Multicomponent reactions of convertible isonitriles. J Org Chem. 2009;74(11):4110-7doi: 10.1021/jo900414n.
Pirrung, M. C., Ghorai, S., & Ibarra-Rivera, T. R. (2009). Multicomponent reactions of convertible isonitriles. The Journal of organic chemistry, 74(11), 4110-7. https://doi.org/10.1021/jo900414n
Pirrung, Michael C, et al. "Multicomponent reactions of convertible isonitriles." The Journal of organic chemistry vol. 74,11 (2009): 4110-7. doi: https://doi.org/10.1021/jo900414n
Pirrung MC, Ghorai S, Ibarra-Rivera TR. Multicomponent reactions of convertible isonitriles. J Org Chem. 2009 Jun 05;74(11):4110-7. doi: 10.1021/jo900414n. PMID: 19408909.
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Showing 1 to 12 of 438 entries