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Items: 1 to 50 of 202

1.

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. 2019 Aug 27. doi: 10.1002/humu.23903. [Epub ahead of print]

PMID:
31456290
2.

Application of CRISPR-Cas9 Screening Technologies to Study Mitochondrial Biology in Healthy and Disease States.

Sharon D, Chan SM.

Adv Exp Med Biol. 2019;1158:269-277. doi: 10.1007/978-981-13-8367-0_15.

PMID:
31452146
3.

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.

4.

Comment on 'AIRE-deficient patients harbor unique high-affinity disease-ameliorating autoantibodies'.

Landegren N, Rosen LB, Freyhult E, Eriksson D, Fall T, Smith G, Ferre EMN, Brodin P, Sharon D, Snyder M, Lionakis M, Anderson M, Kämpe O.

Elife. 2019 Jun 27;8. pii: e43578. doi: 10.7554/eLife.43578.

5.

The Mitochondrial Transacylase, Tafazzin, Regulates AML Stemness by Modulating Intracellular Levels of Phospholipids.

Seneviratne AK, Xu M, Aristizabal Henao JJ, Fajardo VA, Hao Z, Voisin V, Xu GW, Hurren R, Kim S, MacLean N, Wang X, Gronda M, Jeyaraju D, Jitkova Y, Ketela T, Mullokandov M, Sharon D, Thomas G, Chouinard-Watkins R, Hawley JR, Schafer C, Yau HL, Khuchua Z, Aman A, Al-Awar R, Gross A, Claypool SM, Bazinet RP, Lupien M, Chan S, De Carvalho DD, Minden MD, Bader GD, Stark KD, LeBlanc P, Schimmer AD.

Cell Stem Cell. 2019 Jun 6;24(6):1007. doi: 10.1016/j.stem.2019.04.020. No abstract available.

PMID:
31173706
6.

The Mitochondrial Transacylase, Tafazzin, Regulates for AML Stemness by Modulating Intracellular Levels of Phospholipids.

Seneviratne AK, Xu M, Henao JJA, Fajardo VA, Hao Z, Voisin V, Xu GW, Hurren R, Kim S, MacLean N, Wang X, Gronda M, Jeyaraju D, Jitkova Y, Ketela T, Mullokandov M, Sharon D, Thomas G, Chouinard-Watkins R, Hawley JR, Schafer C, Yau HL, Khuchua Z, Aman A, Al-Awar R, Gross A, Claypool SM, Bazinet RP, Lupien M, Chan S, De Carvalho DD, Minden MD, Bader GD, Stark KD, LeBlanc P, Schimmer AD.

Cell Stem Cell. 2019 Apr 4;24(4):621-636.e16. doi: 10.1016/j.stem.2019.02.020. Epub 2019 Mar 28. Erratum in: Cell Stem Cell. 2019 Jun 6;24(6):1007.

PMID:
30930145
7.

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
8.
9.

Chromatic pupilloperimetry for objective diagnosis of Best vitelliform macular dystrophy.

Ben Ner D, Sher I, Hamburg A, Mhajna MO, Chibel R, Derazne E, Sharvit-Ginon I, Pras E, Newman H, Levy J, Khateb S, Sharon D, Rotenstreich Y.

Clin Ophthalmol. 2019 Mar 5;13:465-475. doi: 10.2147/OPTH.S191486. eCollection 2019.

10.

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
11.

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.

12.

[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
13.

Validation of the self-administered version of the international Restless Legs Syndrome study group severity rating scale - The sIRLS.

Sharon D, Allen RP, Martinez-Martin P, Walters AS, Ferini Strambi L, Högl B, Trotti LM, Buchfuhrer M, Swieca J, Bogan RK, Zak R, Hensley JG, Schaefer LA, Marelli S, Zucconi M, Stefani A, Holzknecht E, Olvera V, Meaklim H, Laska I, Becker PM; International RLS Study Group.

Sleep Med. 2019 Feb;54:94-100. doi: 10.1016/j.sleep.2018.10.014. Epub 2018 Oct 29.

PMID:
30529783
14.

Transcriptomic study of Herpes simplex virus type-1 using full-length sequencing techniques.

Boldogkői Z, Szűcs A, Balázs Z, Sharon D, Snyder M, Tombácz D.

Sci Data. 2018 Nov 27;5:180266. doi: 10.1038/sdata.2018.266.

15.

Modified Battlefield Acupuncture Does Not Reduce Pain or Improve Quality of Life in Patients with Lower Extremity Surgery.

Crawford P, Moss DA, Crawford AJ, Sharon DJ.

Mil Med. 2019 Mar 1;184(Suppl 1):545-549. doi: 10.1093/milmed/usy277.

PMID:
30371882
16.

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.

17.

Possible Predictive Factors for In-hospital Cardiac Arrest in Patients with Cancer: A Retrospective Single Center Study.

Sardar M, Shaikh N, Malik SU, Anwer F, Lee P, Sharon D, Eng MH.

Cureus. 2018 Jun 18;10(6):e2828. doi: 10.7759/cureus.2828.

18.

Transcriptome-wide survey of pseudorabies virus using next- and third-generation sequencing platforms.

Tombácz D, Sharon D, Szűcs A, Moldován N, Snyder M, Boldogkői Z.

Sci Data. 2018 Jun 19;5:180119. doi: 10.1038/sdata.2018.119.

19.

Nursing students' stress and satisfaction in clinical practice along different stages: A cross-sectional study.

Admi H, Moshe-Eilon Y, Sharon D, Mann M.

Nurse Educ Today. 2018 Sep;68:86-92. doi: 10.1016/j.nedt.2018.05.027. Epub 2018 Jun 5.

PMID:
29894915
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.

Shedding Light on the Oxygen Reduction Reaction Mechanism in Ether-Based Electrolyte Solutions: A Study Using Operando UV-Vis Spectroscopy.

Hirshberg D, Sharon D, Afri M, Lavi R, Frimer AA, Metoki N, Eliaz N, Kwak WJ, Sun YK, Aurbach D.

ACS Appl Mater Interfaces. 2018 Apr 4;10(13):10860-10869. doi: 10.1021/acsami.7b18376. Epub 2018 Mar 20.

PMID:
29513511
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.

Does the level of emotional intelligence affect the degree of success in nursing studies?

Sharon D, Grinberg K.

Nurse Educ Today. 2018 May;64:21-26. doi: 10.1016/j.nedt.2018.01.030. Epub 2018 Feb 7.

PMID:
29454875
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.

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.

Cardiovascular effects of Hodgkin's lymphoma: a review of literature.

Jacob A, Thyagarajan B, Kumar MP, Shaikh N, Sharon D.

J Cancer Res Clin Oncol. 2018 Jan;144(1):99-107. doi: 10.1007/s00432-017-2560-x. Epub 2017 Dec 18. Review.

PMID:
29255934
28.

Genotype-functional-phenotype correlations in photoreceptor guanylate cyclase (GC-E) encoded by GUCY2D.

Sharon D, Wimberg H, Kinarty Y, Koch KW.

Prog Retin Eye Res. 2018 Mar;63:69-91. doi: 10.1016/j.preteyeres.2017.10.003. Epub 2017 Oct 20. Review.

PMID:
29061346
29.

Advancements in the design and scalable production of viral gene transfer vectors.

Sharon D, Kamen A.

Biotechnol Bioeng. 2018 Jan;115(1):25-40. doi: 10.1002/bit.26461. Epub 2017 Oct 30. Review.

PMID:
28941274
30.

2,4-Dimethoxy-2,4-dimethylpentan-3-one: An Aprotic Solvent Designed for Stability in Li-O2 Cells.

Sharon D, Sharon P, Hirshberg D, Salama M, Afri M, Shimon LJW, Kwak WJ, Sun YK, Frimer AA, Aurbach D.

J Am Chem Soc. 2017 Aug 30;139(34):11690-11693. doi: 10.1021/jacs.7b06414. Epub 2017 Aug 18.

PMID:
28789521
31.

Long-Read Isoform Sequencing Reveals a Hidden Complexity of the Transcriptional Landscape of Herpes Simplex Virus Type 1.

Tombácz D, Csabai Z, Szűcs A, Balázs Z, Moldován N, Sharon D, Snyder M, Boldogkői Z.

Front Microbiol. 2017 Jun 20;8:1079. doi: 10.3389/fmicb.2017.01079. eCollection 2017.

32.

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.

33.

The importance of solvent selection in Li-O2 cells.

Sharon D, Hirshberg D, Afri M, Frimer AA, Aurbach D.

Chem Commun (Camb). 2017 Mar 14;53(22):3269-3272. doi: 10.1039/c6cc09086a.

PMID:
28261729
34.

Characterization of the Dynamic Transcriptome of a Herpesvirus with Long-read Single Molecule Real-Time Sequencing.

Tombácz D, Balázs Z, Csabai Z, Moldován N, Szűcs A, Sharon D, Snyder M, Boldogkői Z.

Sci Rep. 2017 Mar 3;7:43751. doi: 10.1038/srep43751.

35.

Left Ventricular Compressions Improve Hemodynamics in a Swine Model of Out-of-Hospital Cardiac Arrest.

Anderson KL, Castaneda MG, Boudreau SM, Sharon DJ, Bebarta VS.

Prehosp Emerg Care. 2017 Mar-Apr;21(2):272-280. doi: 10.1080/10903127.2016.1241328. Epub 2016 Dec 5.

PMID:
27918847
36.

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.

37.

OR2W3 sequence variants are unlikely to cause inherited retinal diseases.

Sharon D, Kimchi A, Rivolta C.

Ophthalmic Genet. 2016 Dec;37(4):366-368. Epub 2016 Feb 18. Review.

PMID:
26891008
38.

Feasibility of Full (Li-Ion)-O2 Cells Comprised of Hard Carbon Anodes.

Hirshberg D, Sharon D, De La Llave E, Afri M, Frimer AA, Kwak WJ, Sun YK, Aurbach D.

ACS Appl Mater Interfaces. 2017 Feb 8;9(5):4352-4361. doi: 10.1021/acsami.6b10974. Epub 2016 Oct 27.

PMID:
27786463
39.

Full-Length Isoform Sequencing Reveals Novel Transcripts and Substantial Transcriptional Overlaps in a Herpesvirus.

Tombácz D, Csabai Z, Oláh P, Balázs Z, Likó I, Zsigmond L, Sharon D, Snyder M, Boldogkői Z.

PLoS One. 2016 Sep 29;11(9):e0162868. doi: 10.1371/journal.pone.0162868. eCollection 2016.

40.

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.

41.

Activation of the Chicken Anemia Virus Apoptin Protein by Chk1/2 Phosphorylation Is Required for Apoptotic Activity and Efficient Viral Replication.

Kucharski TJ, Ng TF, Sharon DM, Navid-Azarbaijani P, Tavassoli M, Teodoro JG.

J Virol. 2016 Sep 29;90(20):9433-45. doi: 10.1128/JVI.00936-16. Print 2016 Oct 15.

42.

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.

43.

Computation Sheds Insight into Iron Porphyrin Carbenes' Electronic Structure, Formation, and N-H Insertion Reactivity.

Sharon DA, Mallick D, Wang B, Shaik S.

J Am Chem Soc. 2016 Aug 3;138(30):9597-610. doi: 10.1021/jacs.6b04636. Epub 2016 Jul 20.

PMID:
27347808
44.

The Impact of Nursing Students' Cultural Diversity on the Intention and Attitudes Towards the Use of Information Technology (IT).

Gonen A, Sharon D, Lev-Ari L, Straus E, Segev R.

Stud Health Technol Inform. 2016;225:881-2.

PMID:
27332390
45.

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
46.

Breast cancer gene therapy using an adenovirus encoding human IL-2 under control of mammaglobin promoter/enhancer sequences.

Chaurasiya S, Hew P, Crosley P, Sharon D, Potts K, Agopsowicz K, Long M, Shi C, Hitt MM.

Cancer Gene Ther. 2016 Jun;23(6):178-87. doi: 10.1038/cgt.2016.18. Epub 2016 May 6.

PMID:
27151235
47.

A missense mutation in ASRGL1 is involved in causing autosomal recessive retinal degeneration.

Biswas P, Chavali VR, Agnello G, Stone E, Chakarova C, Duncan JL, Kannabiran C, Homsher M, Bhattacharya SS, Naeem MA, Kimchi A, Sharon D, Iwata T, Riazuddin S, Reddy GB, Hejtmancik JF, Georgiou G, Riazuddin SA, Ayyagari R.

Hum Mol Genet. 2016 Jun 15;25(12):2483-2497. Epub 2016 Apr 22.

48.

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.

49.

Imaging the Neocortex Functional Architecture Using Multiple Intrinsic Signals: Implications for Hemodynamic-Based Functional Imaging.

Grinvald A, Sharon D, Omer D, Vanzetta I.

Cold Spring Harb Protoc. 2016 Mar 1;2016(3):pdb.top089375. doi: 10.1101/pdb.top089375.

PMID:
26933255
50.

Mutations in POMGNT1 cause non-syndromic retinitis pigmentosa.

Xu M, Yamada T, Sun Z, Eblimit A, Lopez I, Wang F, Manya H, Xu S, Zhao L, Li Y, Kimchi A, Sharon D, Sui R, Endo T, Koenekoop RK, Chen R.

Hum Mol Genet. 2016 Apr 15;25(8):1479-88. doi: 10.1093/hmg/ddw022. Epub 2016 Jan 28.

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