E. Levy-Nissenbaum

发表

Megalencephalic leukoencephalopathy with subcortical cysts; a founder effect in Israeli patients and a higher than expected carrier rate among Libyan Jews

Y. Anikster, M. Frydman, E. Pras, 2002, Human Genetics.

Targeted nanoparticles for cancer therapy

Robert Langer, Seungpyo Hong, Rohit Karnik, 2007 .

Formulation of functionalized PLGA-PEG nanoparticles for in vivo targeted drug delivery.

Robert Langer, Jianjun Cheng, Omid C Farokhzad, 2007, Biomaterials.

Pharmacokinetic and efficacy study of cisplatin and paclitaxel formulated in a new injectable poly(sebacic-co-ricinoleic acid) polymer.

A. Domb, Wahid Khan, R. Pawar, 2012, European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.

A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family.

M. Frydman, E. Pras, E. Pras, 2000, Investigative ophthalmology & visual science.

Engineering of targeted nanoparticles for cancer therapy using internalizing aptamers isolated by cell-uptake selection.

Robert Langer, Omid C Farokhzad, Jinjun Shi, 2012, ACS nano.

Nanotechnology and Aptamers: Applications in Drug Delivery

Robert Langer, Omid C Farokhzad, Andrew Z. Wang, 2022 .

Ameliorating Active Ulcerative Colitis via an Orally Available Toll-Like Receptor-9 Modifier: A Prospective Open-Label, Multicenter Phase II Trial

H. Soreq, I. Dotan, E. Israeli, 2016, Digestive Diseases and Sciences.

Genetic analysis of Brugada syndrome in Israel: two novel mutations and possible genetic heterogeneity.

E. Friedman, M. Eldar, E. Pras, 2001, Genetic testing.

In vivo administration of BL-3050: highly stable engineered PON1-HDL complexes

Dan S. Tawfik, L. Gaidukov, S. Yacobson, 2009, BMC clinical pharmacology.

Targeted Aptamer-Nanoparticles to Diminish Drug Resistance of Cancer Cells in vitro Study

R. Langer, F. Alexis, P. Basto, 2007 .

HER‐2‐Targeted Nanoparticle–Affibody Bioconjugates for Cancer Therapy

Pamela Basto, Eric Pridgen, Omid C Farokhzad, 2008, ChemMedChem.

Directly Compressed Tablets: A Novel Drug‐Containing Reservoir Combined with Hydrogel‐Forming Microneedle Arrays for Transdermal Drug Delivery

H. McCarthy, Galit Levin, R. Donnelly, 2020, Advanced healthcare materials.

Hydrogel-forming microneedle arrays as a therapeutic option for transdermal esketamine delivery

Maelíosa T. C. McCrudden, H. McCarthy, Galit Levin, 2020, Journal of controlled release : official journal of the Controlled Release Society.

Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

S. Cichon, M. Nöthen, A. Hillmer, 2003, Nature Genetics.

Quantum dot-aptamer conjugates for synchronous cancer imaging, therapy, and sensing of drug delivery based on bi-fluorescence resonance energy transfer.

Robert Langer, Omid C Farokhzad, Liangfang Zhang, 2007, Nano letters.

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.

D. Lancet, O. Man, M. Eldar, 2001, American journal of human genetics.

Transepithelial Transport of Fc-Targeted Nanoparticles by the Neonatal Fc Receptor for Oral Delivery

R. Langer, O. Farokhzad, R. Karnik, 2013, Science Translational Medicine.

Autosomal Recessive Catecholamine- or Exercise-Induced Polymorphic Ventricular Tachycardia: Clinical Features and Assignment of the Disease Gene to Chromosome 1p13-21

D. Kastner, E. Friedman, M. Eldar, 2001, Circulation.

A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish family.

M. Frydman, E. Pras, E. Pras, 2002, American journal of human genetics.

Seborrhoeic keratosis removal in a multicentre phase I/II clinical trial using a novel topical formulation (BL‐5010)

H. Thio, D. Thaçi, E. Levy-Nissenbaum, 2015, The British journal of dermatology.

Clinical manifestations in Israeli cystinuria patients and molecular assessment of carrier rates in Libyan Jewish controls.

Y. Kreiss, E. Pras, E. Levy-Nissenbaum, 2003, The Israel Medical Association journal : IMAJ.

A gene causing autosomal recessive cataract maps to the short arm of chromosome 3.

M. Frydman, E. Pras, H. Garzozi, 2001, The Israel Medical Association journal : IMAJ.

Targeted Nanoparticle-Polypeptide Bioconjugates for Breast Cancer Therapy

F. Gu, R. Langer, O. Farokhzad, 2007 .

Nanoparticle-aptamer bioconjugates for targeted antineoplastic drug delivery

R. Langer, O. Farokhzad, Benjamin A. Teply, 2006 .

A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel.

D. Lancet, M. Eldar, T. Olender, 2001, Cold Spring Harbor symposia on quantitative biology.

Nanotechnology and aptamers: applications in drug delivery.

R. Langer, O. Farokhzad, A. Radovic-Moreno, 2008, Trends in biotechnology.

Engineering of targeted nanoparticles for cancer therapy using internalizing aptamers isolated by cell-uptake selection.

R. Langer, O. Farokhzad, F. Alexis, 2012, ACS nano.

Confirmation of the association between male pattern baldness and the androgen receptor gene.

M. Frydman, E. Pras, M. Bar‐Natan, 2005, European journal of dermatology : EJD.

Ameliorating Active Ulcerative Colitis via an Orally Available Toll-Like Receptor-9 Modifier: A Prospective Open-Label, Multicenter Phase II Trial

H. Soreq, I. Dotan, E. Israeli, 2016, Digestive Diseases and Sciences.