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Showing 1 to 12 of 17 entries
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Ectopic Expression of Snail and Twist in Ph+ Leukemia Cells Upregulates CD44 Expression and Alters Their Differentiation Potential.

Journal of Cancer

Kidan N, Khamaisie H, Ruimi N, Roitman S, Eshel E, Dally N, Ruthardt M, Mahajna J.
PMID: 29187870
J Cancer. 2017 Oct 23;8(19):3952-3968. doi: 10.7150/jca.19633. eCollection 2017.

Philadelphia chromosome-positive (Ph+) leukemia is characterized by reciprocal translocation between chromosomes 9 and 22. The resultant BCR/ABL fusion protein displays constitutive tyrosine kinase activity, leading to the induction of aberrant proliferation and neoplastic transformation. The bone marrow (BM) microenvironment...

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Kidan N, Khamaisie H, Ruimi N, et al. Ectopic Expression of Snail and Twist in Ph+ Leukemia Cells Upregulates CD44 Expression and Alters Their Differentiation Potential. J Cancer. 2017;8(19):3952-3968doi: 10.7150/jca.19633.
Kidan, N., Khamaisie, H., Ruimi, N., Roitman, S., Eshel, E., Dally, N., Ruthardt, M., & Mahajna, J. (2017). Ectopic Expression of Snail and Twist in Ph+ Leukemia Cells Upregulates CD44 Expression and Alters Their Differentiation Potential. Journal of Cancer, 8(19), 3952-3968. https://doi.org/10.7150/jca.19633
Kidan, Noa, et al. "Ectopic Expression of Snail and Twist in Ph+ Leukemia Cells Upregulates CD44 Expression and Alters Their Differentiation Potential." Journal of Cancer vol. 8,19 (2017): 3952-3968. doi: https://doi.org/10.7150/jca.19633
Kidan N, Khamaisie H, Ruimi N, Roitman S, Eshel E, Dally N, Ruthardt M, Mahajna J. Ectopic Expression of Snail and Twist in Ph+ Leukemia Cells Upregulates CD44 Expression and Alters Their Differentiation Potential. J Cancer. 2017 Oct 23;8(19):3952-3968. doi: 10.7150/jca.19633. eCollection 2017. PMID: 29187870; PMCID: PMC5705997.
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Correction to: High‑Mobility Group Box‑1‑Induced Angiogenesis After Indirect Bypass Surgery in a Chronic Cerebral Hypoperfusion Model.

Neuromolecular medicine

Nishihiro S, Hishikawa T, Hiramatsu M, Kidani N, Takahashi Y, Murai S, Sugiu K, Higaki Y, Yasuhara T, Borlongan CV, Date I.
PMID: 32103453
Neuromolecular Med. 2020 Jun;22(2):332-333. doi: 10.1007/s12017-020-08594-3.

The original version of this article unfortunately contained a mistake. Figure 5a, b were incorrect. The correct figures are given below.

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Nishihiro S, Hishikawa T, Hiramatsu M, et al. Correction to: High‑Mobility Group Box‑1‑Induced Angiogenesis After Indirect Bypass Surgery in a Chronic Cerebral Hypoperfusion Model. Neuromolecular Med. 2020;22(2):332-333doi: 10.1007/s12017-020-08594-3.
Nishihiro, S., Hishikawa, T., Hiramatsu, M., Kidani, N., Takahashi, Y., Murai, S., Sugiu, K., Higaki, Y., Yasuhara, T., Borlongan, C. V., & Date, I. (2020). Correction to: High‑Mobility Group Box‑1‑Induced Angiogenesis After Indirect Bypass Surgery in a Chronic Cerebral Hypoperfusion Model. Neuromolecular medicine, 22(2), 332-333. https://doi.org/10.1007/s12017-020-08594-3
Nishihiro, Shingo, et al. "Correction to: High‑Mobility Group Box‑1‑Induced Angiogenesis After Indirect Bypass Surgery in a Chronic Cerebral Hypoperfusion Model." Neuromolecular medicine vol. 22,2 (2020): 332-333. doi: https://doi.org/10.1007/s12017-020-08594-3
Nishihiro S, Hishikawa T, Hiramatsu M, Kidani N, Takahashi Y, Murai S, Sugiu K, Higaki Y, Yasuhara T, Borlongan CV, Date I. Correction to: High‑Mobility Group Box‑1‑Induced Angiogenesis After Indirect Bypass Surgery in a Chronic Cerebral Hypoperfusion Model. Neuromolecular Med. 2020 Jun;22(2):332-333. doi: 10.1007/s12017-020-08594-3. PMID: 32103453; PMCID: PMC7645495.
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[Breast milk proteins as a focus for the improvement of recipes for infant adapted milk formulae].

Voprosy pitaniia

Skidan IN, Pyrieva EA, Kon' IY.
PMID: 30695610
Vopr Pitan. 2017;86(4):37-49. doi: 10.24411/0042-8833-2017-00058. Epub 2017 Jun 30.

After a long evolutionary development starting at the appearance of the first mammals about 200 million years ago, breast milk (BM) was formed into a unique functional nutrition system with an individual composition that promotes normal growth and development...

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Skidan IN, Pyrieva EA, Kon' IY. [Breast milk proteins as a focus for the improvement of recipes for infant adapted milk formulae]. Vopr Pitan. 2017;86(4):37-49doi: 10.24411/0042-8833-2017-00058.
Skidan, I. N., Pyrieva, E. A., & Kon', I. Y. (2017). [Breast milk proteins as a focus for the improvement of recipes for infant adapted milk formulae]. Voprosy pitaniia, 86(4), 37-49. https://doi.org/10.24411/0042-8833-2017-00058
Skidan, I N, et al. "[Breast milk proteins as a focus for the improvement of recipes for infant adapted milk formulae]." Voprosy pitaniia vol. 86,4 (2017): 37-49. doi: https://doi.org/10.24411/0042-8833-2017-00058
Skidan IN, Pyrieva EA, Kon' IY. [Breast milk proteins as a focus for the improvement of recipes for infant adapted milk formulae]. Vopr Pitan. 2017;86(4):37-49. doi: 10.24411/0042-8833-2017-00058. Epub 2017 Jun 30. Russian. PMID: 30695610.
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Mesenchymal soluble factors confer imatinib drug resistance in chronic myelogenous leukemia cells.

Archives of medical science : AMS

Regev O, Kidan N, Nicola M, Khamisie H, Ruthardt M, Mahajna J.
PMID: 33488882
Arch Med Sci. 2020 Nov 20;17(1):266-274. doi: 10.5114/aoms.2020.101042. eCollection 2021.

No abstract available.

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Regev O, Kidan N, Nicola M, et al. Mesenchymal soluble factors confer imatinib drug resistance in chronic myelogenous leukemia cells. Arch Med Sci. 2020;17(1):266-274doi: 10.5114/aoms.2020.101042.
Regev, O., Kidan, N., Nicola, M., Khamisie, H., Ruthardt, M., & Mahajna, J. (2021). Mesenchymal soluble factors confer imatinib drug resistance in chronic myelogenous leukemia cells. Archives of medical science : AMS, 17(1), 266-274. https://doi.org/10.5114/aoms.2020.101042
Regev, Ofer, et al. "Mesenchymal soluble factors confer imatinib drug resistance in chronic myelogenous leukemia cells." Archives of medical science : AMS vol. 17,1 (2021): 266-274. doi: https://doi.org/10.5114/aoms.2020.101042
Regev O, Kidan N, Nicola M, Khamisie H, Ruthardt M, Mahajna J. Mesenchymal soluble factors confer imatinib drug resistance in chronic myelogenous leukemia cells. Arch Med Sci. 2020 Nov 20;17(1):266-274. doi: 10.5114/aoms.2020.101042. eCollection 2021. PMID: 33488882; PMCID: PMC7811319.
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Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions.

American journal of perinatology

Zitouni S, Bouatrous E, Laabidi O, Boudrigua I, Chaouachi D, Saidani N, Kraiem I, Ayachi A, Abbes S, Mourali M, Menif S, Ouragini H.
PMID: 33374024
Am J Perinatol. 2020 Dec 29; doi: 10.1055/s-0040-1722199. Epub 2020 Dec 29.

OBJECTIVE:  This study was aimed to establish local reference values for hematological indices and hemoglobin (Hb) fractions in umbilical cord blood (UCB) for the northern population of Tunisia.STUDY DESIGN:  Our study included full-term newborns by vaginal deliveries. Hematological parameters...

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Zitouni S, Bouatrous E, Laabidi O, et al. Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions. Am J Perinatol. 2020;doi: 10.1055/s-0040-1722199.
Zitouni, S., Bouatrous, E., Laabidi, O., Boudrigua, I., Chaouachi, D., Saidani, N., Kraiem, I., Ayachi, A., Abbes, S., Mourali, M., Menif, S., & Ouragini, H. (2020). Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions. American journal of perinatology, . https://doi.org/10.1055/s-0040-1722199
Zitouni, Sana, et al. "Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions." American journal of perinatology vol. (2020). doi: https://doi.org/10.1055/s-0040-1722199
Zitouni S, Bouatrous E, Laabidi O, Boudrigua I, Chaouachi D, Saidani N, Kraiem I, Ayachi A, Abbes S, Mourali M, Menif S, Ouragini H. Tunisian Newborn's Cord Blood: Reference Values of Complete Blood Count and Hemoglobin Fractions. Am J Perinatol. 2020 Dec 29; doi: 10.1055/s-0040-1722199. Epub 2020 Dec 29. PMID: 33374024.
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Synthesis of Dihydrophenanthridines and Oxoimidazolidines from Anilines and Ethylglyoxylate via Aza Diels-Alder Reaction of Arynes and KF-Induced Annulation.

Organic letters

Reddy RS, Lagishetti C, Chen S, Kiran IN, He Y.
PMID: 27571345
Org Lett. 2016 Sep 16;18(18):4546-9. doi: 10.1021/acs.orglett.6b02186. Epub 2016 Aug 29.

The transition-metal-free multicomponent coupling of arynes, anilines, and ethylglyoxylate, proceeding via an inverse electron-demand aza Diels-Alder cycloaddition and N-arylation, has been demonstrated. This protocol allows rapid access to N-aryl dihydrophenanthridine derivatives in moderate to high yields at room temperature...

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Reddy RS, Lagishetti C, Chen S, et al. Synthesis of Dihydrophenanthridines and Oxoimidazolidines from Anilines and Ethylglyoxylate via Aza Diels-Alder Reaction of Arynes and KF-Induced Annulation. Org Lett. 2016;18(18):4546-9doi: 10.1021/acs.orglett.6b02186.
Reddy, R. S., Lagishetti, C., Chen, S., Kiran, I. N., & He, Y. (2016). Synthesis of Dihydrophenanthridines and Oxoimidazolidines from Anilines and Ethylglyoxylate via Aza Diels-Alder Reaction of Arynes and KF-Induced Annulation. Organic letters, 18(18), 4546-9. https://doi.org/10.1021/acs.orglett.6b02186
Reddy, R Santhosh, et al. "Synthesis of Dihydrophenanthridines and Oxoimidazolidines from Anilines and Ethylglyoxylate via Aza Diels-Alder Reaction of Arynes and KF-Induced Annulation." Organic letters vol. 18,18 (2016): 4546-9. doi: https://doi.org/10.1021/acs.orglett.6b02186
Reddy RS, Lagishetti C, Chen S, Kiran IN, He Y. Synthesis of Dihydrophenanthridines and Oxoimidazolidines from Anilines and Ethylglyoxylate via Aza Diels-Alder Reaction of Arynes and KF-Induced Annulation. Org Lett. 2016 Sep 16;18(18):4546-9. doi: 10.1021/acs.orglett.6b02186. Epub 2016 Aug 29. PMID: 27571345.
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One-dimensional Wolter optics with a sub-50 nm spatial resolution.

Optics letters

Matsuyama S, Wakioka T, Kidani N, Kimura T, Mimura H, Sano Y, Nishino Y, Yabashi M, Tamasaku K, Ishikawa T, Yamauchi K.
PMID: 21042357
Opt Lett. 2010 Nov 01;35(21):3583-5. doi: 10.1364/OL.35.003583.

We studied an imaging system consisting of an elliptical mirror and a hyperbolic mirror [i.e., one-dimensional (1D) Wolter optics] to realize an achromatic full-field hard x-ray microscopy with a resolution better than 50 nm. We report the performance of...

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Matsuyama S, Wakioka T, Kidani N, et al. One-dimensional Wolter optics with a sub-50 nm spatial resolution. Opt Lett. 2010;35(21):3583-5doi: 10.1364/OL.35.003583.
Matsuyama, S., Wakioka, T., Kidani, N., Kimura, T., Mimura, H., Sano, Y., Nishino, Y., Yabashi, M., Tamasaku, K., Ishikawa, T., & Yamauchi, K. (2010). One-dimensional Wolter optics with a sub-50 nm spatial resolution. Optics letters, 35(21), 3583-5. https://doi.org/10.1364/OL.35.003583
Matsuyama, S, et al. "One-dimensional Wolter optics with a sub-50 nm spatial resolution." Optics letters vol. 35,21 (2010): 3583-5. doi: https://doi.org/10.1364/OL.35.003583
Matsuyama S, Wakioka T, Kidani N, Kimura T, Mimura H, Sano Y, Nishino Y, Yabashi M, Tamasaku K, Ishikawa T, Yamauchi K. One-dimensional Wolter optics with a sub-50 nm spatial resolution. Opt Lett. 2010 Nov 01;35(21):3583-5. doi: 10.1364/OL.35.003583. PMID: 21042357.
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Selective Aza Diels-Alder and Domino [4+2]/[2+2] Cycloaddition Reactions of Arynes with N-Sulfonyl Ketimines.

The Journal of organic chemistry

Kiran IN, Reddy RS, Lagishetti C, Xu H, Wang Z, He Y.
PMID: 28097867
J Org Chem. 2017 Feb 03;82(3):1823-1832. doi: 10.1021/acs.joc.6b02667. Epub 2017 Jan 26.

Transition-metal-free inverse electron-demand aza Diels-Alder and domino [4+2]/[2+2] cycloaddition reaction of arynes and N-sulfonyl ketimines has been demonstrated. This novel, mild, and efficient protocol allows rapid access to isothiazole dioxide-fused dihydroquinoline or dihydrocyclobutaquinoline derivatives selectively by simply varying the...

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Kiran IN, Reddy RS, Lagishetti C, et al. Selective Aza Diels-Alder and Domino [4+2]/[2+2] Cycloaddition Reactions of Arynes with N-Sulfonyl Ketimines. J Org Chem. 2017;82(3):1823-1832doi: 10.1021/acs.joc.6b02667.
Kiran, I. N., Reddy, R. S., Lagishetti, C., Xu, H., Wang, Z., & He, Y. (2017). Selective Aza Diels-Alder and Domino [4+2]/[2+2] Cycloaddition Reactions of Arynes with N-Sulfonyl Ketimines. The Journal of organic chemistry, 82(3), 1823-1832. https://doi.org/10.1021/acs.joc.6b02667
Kiran, I N Chaithanya, et al. "Selective Aza Diels-Alder and Domino [4+2]/[2+2] Cycloaddition Reactions of Arynes with N-Sulfonyl Ketimines." The Journal of organic chemistry vol. 82,3 (2017): 1823-1832. doi: https://doi.org/10.1021/acs.joc.6b02667
Kiran IN, Reddy RS, Lagishetti C, Xu H, Wang Z, He Y. Selective Aza Diels-Alder and Domino [4+2]/[2+2] Cycloaddition Reactions of Arynes with N-Sulfonyl Ketimines. J Org Chem. 2017 Feb 03;82(3):1823-1832. doi: 10.1021/acs.joc.6b02667. Epub 2017 Jan 26. PMID: 28097867.
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[Development of the infant formula industry].

Voprosy pitaniia

Skidan IN, Pyrieva EA, Kon' IY.
PMID: 30695633
Vopr Pitan. 2017;86(5):91-98. doi: 10.24411/0042-8833-2017-00081. Epub 2017 Sep 08.

The creation of the first prototypes of modern breastmilk substitutes at the end of the nineteen century brought in a new era in feeding infants in the first year of life. Currently, artificial feeding of newborns consists of adapted...

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Skidan IN, Pyrieva EA, Kon' IY. [Development of the infant formula industry]. Vopr Pitan. 2017;86(5):91-98doi: 10.24411/0042-8833-2017-00081.
Skidan, I. N., Pyrieva, E. A., & Kon', I. Y. (2017). [Development of the infant formula industry]. Voprosy pitaniia, 86(5), 91-98. https://doi.org/10.24411/0042-8833-2017-00081
Skidan, I N, et al. "[Development of the infant formula industry]." Voprosy pitaniia vol. 86,5 (2017): 91-98. doi: https://doi.org/10.24411/0042-8833-2017-00081
Skidan IN, Pyrieva EA, Kon' IY. [Development of the infant formula industry]. Vopr Pitan. 2017;86(5):91-98. doi: 10.24411/0042-8833-2017-00081. Epub 2017 Sep 08. Russian. PMID: 30695633.
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Transition-Metal-Free Cascade Synthesis of 4-Quinolones: Umpolung of Michael Acceptors via Ene Reaction with Arynes.

Organic letters

Santhosh Reddy R, Lagishetti C, Kiran IN, You H, He Y.
PMID: 27434217
Org Lett. 2016 Aug 05;18(15):3818-21. doi: 10.1021/acs.orglett.6b01830. Epub 2016 Jul 19.

A novel "one-pot" aryne transformation is described that affords various 4-quinolone derivatives without recourse to transition-metal catalysis. Arynes react with aza-Morita-Baylis-Hillman (AMBH) adducts through a cascade sequence involving an insertion/cyclization/ene reaction process to afford 4-quinolones in high yields with...

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Santhosh Reddy R, Lagishetti C, Kiran IN, et al. Transition-Metal-Free Cascade Synthesis of 4-Quinolones: Umpolung of Michael Acceptors via Ene Reaction with Arynes. Org Lett. 2016;18(15):3818-21doi: 10.1021/acs.orglett.6b01830.
Santhosh Reddy, R., Lagishetti, C., Kiran, I. N., You, H., & He, Y. (2016). Transition-Metal-Free Cascade Synthesis of 4-Quinolones: Umpolung of Michael Acceptors via Ene Reaction with Arynes. Organic letters, 18(15), 3818-21. https://doi.org/10.1021/acs.orglett.6b01830
Santhosh Reddy, R, et al. "Transition-Metal-Free Cascade Synthesis of 4-Quinolones: Umpolung of Michael Acceptors via Ene Reaction with Arynes." Organic letters vol. 18,15 (2016): 3818-21. doi: https://doi.org/10.1021/acs.orglett.6b01830
Santhosh Reddy R, Lagishetti C, Kiran IN, You H, He Y. Transition-Metal-Free Cascade Synthesis of 4-Quinolones: Umpolung of Michael Acceptors via Ene Reaction with Arynes. Org Lett. 2016 Aug 05;18(15):3818-21. doi: 10.1021/acs.orglett.6b01830. Epub 2016 Jul 19. PMID: 27434217.
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Synthesis of Carbazolequinones by Formal [3 + 2] Cycloaddition of Arynes and 2-Aminoquinones.

Organic letters

Guo J, Kiran IN, Reddy RS, Gao J, Tang M, Liu Y, He Y.
PMID: 27149368
Org Lett. 2016 May 20;18(10):2499-502. doi: 10.1021/acs.orglett.6b01090. Epub 2016 May 05.

A formal cycloaddition reaction for the synthesis of biologically and pharmaceutically important carbazolequinones via the annulation of aminoquinones with arynes has been developed. This practical and metal-free cascade reaction proceeds through successive C-C/C-N bond formations. Moreover, this novel method...

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Guo J, Kiran IN, Reddy RS, et al. Synthesis of Carbazolequinones by Formal [3 + 2] Cycloaddition of Arynes and 2-Aminoquinones. Org Lett. 2016;18(10):2499-502doi: 10.1021/acs.orglett.6b01090.
Guo, J., Kiran, I. N., Reddy, R. S., Gao, J., Tang, M., Liu, Y., & He, Y. (2016). Synthesis of Carbazolequinones by Formal [3 + 2] Cycloaddition of Arynes and 2-Aminoquinones. Organic letters, 18(10), 2499-502. https://doi.org/10.1021/acs.orglett.6b01090
Guo, Jian, et al. "Synthesis of Carbazolequinones by Formal [3 + 2] Cycloaddition of Arynes and 2-Aminoquinones." Organic letters vol. 18,10 (2016): 2499-502. doi: https://doi.org/10.1021/acs.orglett.6b01090
Guo J, Kiran IN, Reddy RS, Gao J, Tang M, Liu Y, He Y. Synthesis of Carbazolequinones by Formal [3 + 2] Cycloaddition of Arynes and 2-Aminoquinones. Org Lett. 2016 May 20;18(10):2499-502. doi: 10.1021/acs.orglett.6b01090. Epub 2016 May 05. PMID: 27149368.
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International nosocomial infection control consortium findings of device-associated infections rate in an intensive care unit of a lebanese university hospital.

Journal of global infectious diseases

Kanj S, Kanafani Z, Sidani N, Alamuddin L, Zahreddine N, Rosenthal V.
PMID: 22529622
J Glob Infect Dis. 2012 Jan;4(1):15-21. doi: 10.4103/0974-777X.93755.

OBJECTIVES: To determine the rates of device-associated healthcare-associated infections (DA-HAI), microbiological profile, bacterial resistance, length of stay (LOS), excess mortality and hand hygiene compliance in one intensive care unit (ICU) of a hospital member of the International Infection Control...

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Kanj S, Kanafani Z, Sidani N, et al. International nosocomial infection control consortium findings of device-associated infections rate in an intensive care unit of a lebanese university hospital. J Glob Infect Dis. 2012;4(1):15-21doi: 10.4103/0974-777X.93755.
Kanj, S., Kanafani, Z., Sidani, N., Alamuddin, L., Zahreddine, N., & Rosenthal, V. (2012). International nosocomial infection control consortium findings of device-associated infections rate in an intensive care unit of a lebanese university hospital. Journal of global infectious diseases, 4(1), 15-21. https://doi.org/10.4103/0974-777X.93755
Kanj, Ss, et al. "International nosocomial infection control consortium findings of device-associated infections rate in an intensive care unit of a lebanese university hospital." Journal of global infectious diseases vol. 4,1 (2012): 15-21. doi: https://doi.org/10.4103/0974-777X.93755
Kanj S, Kanafani Z, Sidani N, Alamuddin L, Zahreddine N, Rosenthal V. International nosocomial infection control consortium findings of device-associated infections rate in an intensive care unit of a lebanese university hospital. J Glob Infect Dis. 2012 Jan;4(1):15-21. doi: 10.4103/0974-777X.93755. PMID: 22529622; PMCID: PMC3326952.
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