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Items: 1 to 50 of 206

1.

Antibacterial Activity Against Methicillin-Resistant Staphylococcus aureus of Colloidal Polydopamine Prepared by Carbon Dot Stimulated Polymerization of Dopamine.

Maruthapandi M, Natan M, Jacobi G, Banin E, Luong JHT, Gedanken A.

Nanomaterials (Basel). 2019 Dec 4;9(12). pii: E1731. doi: 10.3390/nano9121731.

2.

An Ashkenazi Jewish founder mutation in CACNA1F causes retinal phenotype in both hemizygous males and heterozygous female carriers.

Kimchi A, Meiner V, Silverstein S, Macarov M, Mor-Shaked H, Blumenfeld A, Audo I, Zeitz C, Mechoulam H, Banin E, Sharon D, Yahalom C.

Ophthalmic Genet. 2019 Oct;40(5):443-448. doi: 10.1080/13816810.2019.1681008. Epub 2019 Oct 25.

PMID:
31651202
3.

A nationwide genetic analysis of inherited retinal diseases in Israel as assessed by the Israeli inherited retinal disease consortium (IIRDC).

Sharon D, Ben-Yosef T, Goldenberg-Cohen N, Pras E, Gradstein L, Soudry S, Mezer E, Zur D, Abbasi AH, Zeitz C, Cremers FPM, Khan MI, Levy J, Rotenstreich Y, Birk OS, Ehrenberg M, Leibu R, Newman H, Shomron N, Banin E, Perlman I.

Hum Mutat. 2020 Jan;41(1):140-149. doi: 10.1002/humu.23903. Epub 2019 Sep 15.

PMID:
31456290
4.

TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations.

AlTalbishi A, Zelinger L, Zeitz C, Hendler K, Namburi P, Audo I, Sheffer R, Yahalom C, Khateb S, Banin E, Sharon D.

Sci Rep. 2019 Aug 19;9(1):12047. doi: 10.1038/s41598-019-46811-7.

5.

The Algal Symbiont Modifies the Transcriptome of the Scleractinian Coral Euphyllia paradivisa During Heat Stress.

Meron D, Maor-Landaw K, Weizman E, Waldman Ben-Asher H, Eyal G, Banin E, Loya Y, Levy O.

Microorganisms. 2019 Aug 12;7(8). pii: E256. doi: 10.3390/microorganisms7080256.

6.

Engineering Irrigation Drippers with Rechargeable N-Halamine Nanoparticles for Antifouling Applications.

Natan M, Gutman O, Segev D, Margel S, Banin E.

ACS Appl Mater Interfaces. 2019 Jul 3;11(26):23584-23590. doi: 10.1021/acsami.9b05353. Epub 2019 Jun 18.

PMID:
31252498
7.

Antibacterial properties of polypyrrole-treated fabrics by ultrasound deposition.

Sanchez Ramirez DO, Varesano A, Carletto RA, Vineis C, Perelshtein I, Natan M, Perkas N, Banin E, Gedanken A.

Mater Sci Eng C Mater Biol Appl. 2019 Sep;102:164-170. doi: 10.1016/j.msec.2019.04.016. Epub 2019 Apr 17.

8.

The combination of whole-exome sequencing and clinical analysis allows better diagnosis of rare syndromic retinal dystrophies.

Abu Diab A, AlTalbishi A, Rosin B, Kanaan M, Kamal L, Swaroop A, Chowers I, Banin E, Sharon D, Khateb S.

Acta Ophthalmol. 2019 Sep;97(6):e877-e886. doi: 10.1111/aos.14095. Epub 2019 Mar 29.

PMID:
30925032
9.

Where are the missing gene defects in inherited retinal disorders? Intronic and synonymous variants contribute at least to 4% of CACNA1F-mediated inherited retinal disorders.

Zeitz C, Michiels C, Neuillé M, Friedburg C, Condroyer C, Boyard F, Antonio A, Bouzidi N, Milicevic D, Veaux R, Tourville A, Zoumba A, Seneina I, Foussard M, Andrieu C, N Preising M, Blanchard S, Saraiva JP, Mesrob L, Le Floch E, Jubin C, Meyer V, Blanché H, Boland A, Deleuze JF, Sharon D, Drumare I, Defoort-Dhellemmes S, De Baere E, Leroy BP, Zanlonghi X, Casteels I, de Ravel TJ, Balikova I, Koenekoop RK, Laffargue F, McLean R, Gottlob I, Bonneau D, Schorderet DF, L Munier F, McKibbin M, Prescott K, Pelletier V, Dollfus H, Perdomo-Trujillo Y, Faure C, Reiff C, Wissinger B, Meunier I, Kohl S, Banin E, Zrenner E, Jurklies B, Lorenz B, Sahel JA, Audo I.

Hum Mutat. 2019 Jun;40(6):765-787. doi: 10.1002/humu.23735. Epub 2019 Mar 28.

PMID:
30825406
10.

A novel intronic mutation of PDE6B is a major cause of autosomal recessive retinitis pigmentosa among Caucasus Jews.

Tatour Y, Tamaiev J, Shamaly S, Colombo R, Bril E, Rabinowitz T, Yaakobi A, Mezer E, Leibu R, Tiosano B, Shomron N, Chowers I, Banin E, Sharon D, Ben-Yosef T.

Mol Vis. 2019 Feb 22;25:155-164. eCollection 2019.

11.

[THE ISRAELI INHERITED RETINAL DISEASES CONSORTIUM (IIRDC)- CLINICAL-GENETIC MAPPING AND FUTURE PERSPECTIVES].

Sharon D, Ben-Yosef T, Pras E, Goldenberg-Cohen N, Gradstein L, Shomron N, Birk O, Ehrenberg M, Levy J, Mezer E, Soudry S, Rotenstreich Y, Newman H, Leibu R, Banin E, Perlman I.

Harefuah. 2019 Feb;158(2):91-95. Hebrew.

PMID:
30779484
12.

Consecutive unilateral recording of the two eyes affects dark-adapted ERG responses, when compared to simultaneous bilateral recording.

Ross M, Honig H, Ezra-Elia R, Banin E, Obolensky A, Averbukh E, Rosov A, Gootwine E, Ofri R.

Doc Ophthalmol. 2018 Dec;137(3):183-192. doi: 10.1007/s10633-018-9661-y. Epub 2018 Nov 9.

PMID:
30411184
13.

Photoreceptor Guanylate Cyclase (GUCY2D) Mutations Cause Retinal Dystrophies by Severe Malfunction of Ca2+-Dependent Cyclic GMP Synthesis.

Wimberg H, Lev D, Yosovich K, Namburi P, Banin E, Sharon D, Koch KW.

Front Mol Neurosci. 2018 Sep 25;11:348. doi: 10.3389/fnmol.2018.00348. eCollection 2018.

14.

Can an in vivo imaging system be used to determine localization and biodistribution of AAV5-mediated gene expression following subretinal and intravitreal delivery in mice?

Ezra-Elia R, Obolensky A, Ejzenberg A, Ross M, Mintz D, Banin E, Ofri R.

Exp Eye Res. 2018 Nov;176:227-234. doi: 10.1016/j.exer.2018.08.021. Epub 2018 Aug 29.

PMID:
30171858
15.

Immunological Properties of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells.

Idelson M, Alper R, Obolensky A, Yachimovich-Cohen N, Rachmilewitz J, Ejzenberg A, Beider E, Banin E, Reubinoff B.

Stem Cell Reports. 2018 Sep 11;11(3):681-695. doi: 10.1016/j.stemcr.2018.07.009. Epub 2018 Aug 16.

16.

Engineering of a New Bisphosphonate Monomer and Nanoparticles of Narrow Size Distribution for Antibacterial Applications.

Tal N, Rudnick-Glick S, Grinberg I, Natan M, Banin E, Margel S.

ACS Omega. 2018 Feb 28;3(2):1458-1469. doi: 10.1021/acsomega.7b01686. Epub 2018 Feb 2.

17.

Six Years and Counting: Restoration of Photopic Retinal Function and Visual Behavior Following Gene Augmentation Therapy in a Sheep Model of CNGA3 Achromatopsia.

Ofri R, Averbukh E, Ezra-Elia R, Ross M, Honig H, Obolensky A, Rosov A, Hauswirth WW, Gootwine E, Banin E.

Hum Gene Ther. 2018 Dec;29(12):1376-1386. doi: 10.1089/hum.2018.076. Epub 2018 Jul 30.

PMID:
29926749
18.

Contrary to popular belief, chinchillas do not have a pure rod retina.

Sandalon S, Boykova A, Ross M, Obolensky A, Banin E, Ofri R.

Vet Ophthalmol. 2019 Jan;22(1):93-97. doi: 10.1111/vop.12581. Epub 2018 Jun 10.

PMID:
29888430
19.

Structural and functional characterization of PL28 family ulvan lyase NLR48 from Nonlabens ulvanivorans.

Ulaganathan T, Banin E, Helbert W, Cygler M.

J Biol Chem. 2018 Jul 20;293(29):11564-11573. doi: 10.1074/jbc.RA118.003659. Epub 2018 Jun 6.

20.

Carrier frequency analysis of mutations causing autosomal-recessive-inherited retinal diseases in the Israeli population.

Hanany M, Allon G, Kimchi A, Blumenfeld A, Newman H, Pras E, Wormser O, S Birk O, Gradstein L, Banin E, Ben-Yosef T, Sharon D.

Eur J Hum Genet. 2018 Aug;26(8):1159-1166. doi: 10.1038/s41431-018-0152-0. Epub 2018 Apr 30.

21.

Imparting superhydrophobic and biocidal functionalities to a polymeric substrate by the sonochemical method.

Svirinovsky A, Perelshtein I, Natan M, Banin E, Gedanken A.

Ultrason Sonochem. 2018 Jun;44:398-403. doi: 10.1016/j.ultsonch.2018.02.009. Epub 2018 Feb 7.

PMID:
29680626
22.

The Genetics of Usher Syndrome in the Israeli and Palestinian Populations.

Khalaileh A, Abu-Diab A, Ben-Yosef T, Raas-Rothschild A, Lerer I, Alswaiti Y, Chowers I, Banin E, Sharon D, Khateb S.

Invest Ophthalmol Vis Sci. 2018 Feb 1;59(2):1095-1104. doi: 10.1167/iovs.17-22817.

PMID:
29490346
23.

Structure-function analyses of a PL24 family ulvan lyase reveal key features and suggest its catalytic mechanism.

Ulaganathan T, Helbert W, Kopel M, Banin E, Cygler M.

J Biol Chem. 2018 Mar 16;293(11):4026-4036. doi: 10.1074/jbc.RA117.001642. Epub 2018 Jan 30.

24.

A homozygous founder missense variant in arylsulfatase G abolishes its enzymatic activity causing atypical Usher syndrome in humans.

Khateb S, Kowalewski B, Bedoni N, Damme M, Pollack N, Saada A, Obolensky A, Ben-Yosef T, Gross M, Dierks T, Banin E, Rivolta C, Sharon D.

Genet Med. 2018 Sep;20(9):1004-1012. doi: 10.1038/gim.2017.227. Epub 2018 Jan 4.

PMID:
29300381
25.

Nonsyndromic Retinitis Pigmentosa in the Ashkenazi Jewish Population: Genetic and Clinical Aspects.

Kimchi A, Khateb S, Wen R, Guan Z, Obolensky A, Beryozkin A, Kurtzman S, Blumenfeld A, Pras E, Jacobson SG, Ben-Yosef T, Newman H, Sharon D, Banin E.

Ophthalmology. 2018 May;125(5):725-734. doi: 10.1016/j.ophtha.2017.11.014. Epub 2017 Dec 22. Erratum in: Ophthalmology. 2020 Jan;127(1):139.

PMID:
29276052
26.

Whole-exome sequencing reveals POC5 as a novel gene associated with autosomal recessive retinitis pigmentosa.

Weisz Hubshman M, Broekman S, van Wijk E, Cremers F, Abu-Diab A, Khateb S, Tzur S, Lagovsky I, Smirin-Yosef P, Sharon D, Haer-Wigman L, Banin E, Basel-Vanagaite L, de Vrieze E.

Hum Mol Genet. 2018 Feb 15;27(4):614-624. doi: 10.1093/hmg/ddx428.

PMID:
29272404
27.

SawR a new regulator controlling pyomelanin synthesis in Pseudomonas aeruginosa.

Ben-David Y, Zlotnik E, Zander I, Yerushalmi G, Shoshani S, Banin E.

Microbiol Res. 2018 Jan;206:91-98. doi: 10.1016/j.micres.2017.10.004. Epub 2017 Oct 13.

28.

Measuring Cyclic Diguanylate (c-di-GMP)-Specific Phosphodiesterase Activity Using the MANT-c-di-GMP Assay.

Eli D, Randall TE, Almblad H, Harrison JJ, Banin E.

Methods Mol Biol. 2017;1657:263-278. doi: 10.1007/978-1-4939-7240-1_20.

PMID:
28889300
29.

Ferric Uptake Regulator Fur Is Conditionally Essential in Pseudomonas aeruginosa.

Pasqua M, Visaggio D, Lo Sciuto A, Genah S, Banin E, Visca P, Imperi F.

J Bacteriol. 2017 Oct 17;199(22). pii: e00472-17. doi: 10.1128/JB.00472-17. Print 2017 Nov 15.

30.

A symbiotic-like biologically-driven regenerating fabric.

Raab N, Davis J, Spokoini-Stern R, Kopel M, Banin E, Bachelet I.

Sci Rep. 2017 Aug 17;7(1):8528. doi: 10.1038/s41598-017-09105-4.

31.

NANOCI-Nanotechnology Based Cochlear Implant With Gapless Interface to Auditory Neurons.

Senn P, Roccio M, Hahnewald S, Frick C, Kwiatkowska M, Ishikawa M, Bako P, Li H, Edin F, Liu W, Rask-Andersen H, Pyykkö I, Zou J, Mannerström M, Keppner H, Homsy A, Laux E, Llera M, Lellouche JP, Ostrovsky S, Banin E, Gedanken A, Perkas N, Wank U, Wiesmüller KH, Mistrík P, Benav H, Garnham C, Jolly C, Gander F, Ulrich P, Müller M, Löwenheim H.

Otol Neurotol. 2017 Sep;38(8):e224-e231. doi: 10.1097/MAO.0000000000001439. Review.

32.

Long-Term Efficacy of GMP Grade Xeno-Free hESC-Derived RPE Cells Following Transplantation.

McGill TJ, Bohana-Kashtan O, Stoddard JW, Andrews MD, Pandit N, Rosenberg-Belmaker LR, Wiser O, Matzrafi L, Banin E, Reubinoff B, Netzer N, Irving C.

Transl Vis Sci Technol. 2017 Jun 14;6(3):17. doi: 10.1167/tvst.6.3.17. eCollection 2017 Jun.

33.

Editorial: Bacterial pathogens, antibiotics and antibiotic resistance.

Banin E, Hughes D, Kuipers OP.

FEMS Microbiol Rev. 2017 May 1;41(3):450-452. doi: 10.1093/femsre/fux016. No abstract available.

PMID:
28486583
34.

Safety and Efficacy Evaluation of rAAV2tYF-PR1.7-hCNGA3 Vector Delivered by Subretinal Injection in CNGA3 Mutant Achromatopsia Sheep.

Gootwine E, Ofri R, Banin E, Obolensky A, Averbukh E, Ezra-Elia R, Ross M, Honig H, Rosov A, Yamin E, Ye GJ, Knop DR, Robinson PM, Chulay JD, Shearman MS.

Hum Gene Ther Clin Dev. 2017 Jun;28(2):96-107. doi: 10.1089/humc.2017.028. Epub 2017 May 5.

PMID:
28478700
35.

Characterization of physiological defects in adult SIRT6-/- mice.

Peshti V, Obolensky A, Nahum L, Kanfi Y, Rathaus M, Avraham M, Tinman S, Alt FW, Banin E, Cohen HY.

PLoS One. 2017 Apr 27;12(4):e0176371. doi: 10.1371/journal.pone.0176371. eCollection 2017.

36.

From Nano to Micro: using nanotechnology to combat microorganisms and their multidrug resistance.

Natan M, Banin E.

FEMS Microbiol Rev. 2017 May 1;41(3):302-322. doi: 10.1093/femsre/fux003. Review.

PMID:
28419240
37.

Course of Sodium Iodate-Induced Retinal Degeneration in Albino and Pigmented Mice.

Chowers G, Cohen M, Marks-Ohana D, Stika S, Eijzenberg A, Banin E, Obolensky A.

Invest Ophthalmol Vis Sci. 2017 Apr 1;58(4):2239-2249. doi: 10.1167/iovs.16-21255.

PMID:
28418497
38.

Whole-Exome Sequencing Identifies Biallelic IDH3A Variants as a Cause of Retinitis Pigmentosa Accompanied by Pseudocoloboma.

Pierrache LHM, Kimchi A, Ratnapriya R, Roberts L, Astuti GDN, Obolensky A, Beryozkin A, Tjon-Fo-Sang MJH, Schuil J, Klaver CCW, Bongers EMHF, Haer-Wigman L, Schalij N, Breuning MH, Fischer GM, Banin E, Ramesar RS, Swaroop A, van den Born LI, Sharon D, Cremers FPM.

Ophthalmology. 2017 Jul;124(7):992-1003. doi: 10.1016/j.ophtha.2017.03.010. Epub 2017 Apr 13.

39.

New Ulvan-Degrading Polysaccharide Lyase Family: Structure and Catalytic Mechanism Suggests Convergent Evolution of Active Site Architecture.

Ulaganathan T, Boniecki MT, Foran E, Buravenkov V, Mizrachi N, Banin E, Helbert W, Cygler M.

ACS Chem Biol. 2017 May 19;12(5):1269-1280. doi: 10.1021/acschembio.7b00126. Epub 2017 Mar 23.

PMID:
28290654
40.

Gene Augmentation Therapy for a Missense Substitution in the cGMP-Binding Domain of Ovine CNGA3 Gene Restores Vision in Day-Blind Sheep.

Gootwine E, Abu-Siam M, Obolensky A, Rosov A, Honig H, Nitzan T, Shirak A, Ezra-Elia R, Yamin E, Banin E, Averbukh E, Hauswirth WW, Ofri R, Seroussi E.

Invest Ophthalmol Vis Sci. 2017 Mar 1;58(3):1577-1584. doi: 10.1167/iovs.16-20986.

41.

Ga@C-dots as an antibacterial agent for the eradication of Pseudomonas aeruginosa.

Kumar VB, Natan M, Jacobi G, Porat Z, Banin E, Gedanken A.

Int J Nanomedicine. 2017 Jan 23;12:725-730. doi: 10.2147/IJN.S116150. eCollection 2017.

42.

Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.

Namburi P, Ratnapriya R, Khateb S, Lazar CH, Kinarty Y, Obolensky A, Erdinest I, Marks-Ohana D, Pras E, Ben-Yosef T, Newman H, Gross M, Swaroop A, Banin E, Sharon D.

Am J Hum Genet. 2016 Nov 3;99(5):1222-1223. doi: 10.1016/j.ajhg.2016.09.012. No abstract available.

43.

Bi-allelic Truncating Mutations in CEP78, Encoding Centrosomal Protein 78, Cause Cone-Rod Degeneration with Sensorineural Hearing Loss.

Namburi P, Ratnapriya R, Khateb S, Lazar CH, Kinarty Y, Obolensky A, Erdinest I, Marks-Ohana D, Pras E, Ben-Yosef T, Newman H, Gross M, Swaroop A, Banin E, Sharon D.

Am J Hum Genet. 2016 Sep 1;99(3):777-784. doi: 10.1016/j.ajhg.2016.07.010. Erratum in: Am J Hum Genet. 2016 Nov 3;99(5):1222-1223.

44.

Graft polymerization of styryl bisphosphonate monomer onto polypropylene films for inhibition of biofilm formation.

Steinmetz HP, Rudnick-Glick S, Natan M, Banin E, Margel S.

Colloids Surf B Biointerfaces. 2016 Nov 1;147:300-306. doi: 10.1016/j.colsurfb.2016.08.007. Epub 2016 Aug 6.

PMID:
27543691
45.

Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome.

Lindstrand A, Frangakis S, Carvalho CM, Richardson EB, McFadden KA, Willer JR, Pehlivan D, Liu P, Pediaditakis IL, Sabo A, Lewis RA, Banin E, Lupski JR, Davis EE, Katsanis N.

Am J Hum Genet. 2016 Aug 4;99(2):318-36. doi: 10.1016/j.ajhg.2015.04.023.

46.

Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred.

Gradstein L, Zolotushko J, Sergeev YV, Lavy I, Narkis G, Perez Y, Guigui S, Sharon D, Banin E, Walter E, Lifshitz T, Birk OS.

BMC Med Genet. 2016 Jul 30;17(1):52. doi: 10.1186/s12881-016-0314-2.

47.

Synthesis and characterization of crosslinked polyisothiouronium methylstyrene nanoparticles of narrow size distribution for antibacterial and antibiofilm applications.

Cohen S, Gelber C, Natan M, Banin E, Corem-Salkmon E, Margel S.

J Nanobiotechnology. 2016 Jul 7;14(1):56. doi: 10.1186/s12951-016-0208-7.

48.

Engineering of Superparamagnetic Core-Shell Iron Oxide/N-Chloramine Nanoparticles for Water Purification.

Haham H, Natan M, Gutman O, Kolitz-Domb M, Banin E, Margel S.

ACS Appl Mater Interfaces. 2016 Jul 20;8(28):18488-95. doi: 10.1021/acsami.6b05806. Epub 2016 Jul 6.

PMID:
27348740
49.

Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing data.

Khateb S, Hanany M, Khalaileh A, Beryozkin A, Meyer S, Abu-Diab A, Abu Turky F, Mizrahi-Meissonnier L, Lieberman S, Ben-Yosef T, Banin E, Sharon D.

J Med Genet. 2016 Sep;53(9):600-7. doi: 10.1136/jmedgenet-2016-103825. Epub 2016 Apr 22.

PMID:
27208209
50.

Genetic Analysis of the Rhodopsin Gene Identifies a Mosaic Dominant Retinitis Pigmentosa Mutation in a Healthy Individual.

Beryozkin A, Levy G, Blumenfeld A, Meyer S, Namburi P, Morad Y, Gradstein L, Swaroop A, Banin E, Sharon D.

Invest Ophthalmol Vis Sci. 2016 Mar;57(3):940-7. doi: 10.1167/iovs.15-18702.

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