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Correction: Halting ErbB-2 isoforms retrograde transport to the nucleus as a new theragnostic approach for triple-negative breast cancer

Cell death & disease, 2023-12, Vol.14 (12), p.833-833, Article 833

2023

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Halting ErbB-2 isoforms retrograde transport to the nucleus as a new theragnostic approach for triple-negative breast cancer

Cell death & disease, 2022-05, Vol.13 (5), p.447-14, Article 447

2022

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Abstract 3633: Exploring a novel crosstalk between hyluronan/CD44 and ErbB-2 pathways in resistance to ErbB-2-targeted therapies in breast cancer

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.3633-3633

2023

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ODP551 Halting ErbB-2 Isoforms Retrograde Transport to the Nucleus as a New Theragnostic Approach for Triple Negative Breast Cancer

Journal of the Endocrine Society, 2022-11, Vol.6 (Supplement_1), p.A872-A872

2022

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Abstract 344: Blockade of retrograde transport in triple negative breast cancer excludes ErbB-2 isoforms from the nucleus and abrogates tumor growth

Cancer research (Chicago, Ill.), 2022-06, Vol.82 (12_Supplement), p.344-344

2022

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ODP571 Blockade of ErbB-2 Nuclear Function Induces the Interferon Signaling Pathway in Breast Cancer Models Resistant to Trastuzumab

Journal of the Endocrine Society, 2022-11, Vol.6 (Supplement_1), p.A878-A878

2022

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Cognitive Flexibility Predicts PTSD Symptoms: Observational and Interventional Studies

Frontiers in psychiatry, 2018-10, Vol.9, p.477-477

2018

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Efficacy and safety of azithromycin versus placebo to treat lower respiratory tract infections associated with low procalcitonin: a randomised, placebo-controlled, double-blind, non-inferiority trial

The Lancet infectious diseases, 2023-04, Vol.23 (4), p.484-495

2023

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Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mapping

Investigative ophthalmology & visual science, 2014-02, Vol.55 (2), p.1149-1160

2014

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A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews

American journal of human genetics, 2011-02, Vol.88 (2), p.207-215

2011

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Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array

Investigative ophthalmology & visual science, 2010-08, Vol.51 (8), p.3884-3892

2010

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Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa

American journal of human genetics, 2010-09, Vol.87 (3), p.382-391

2010

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The impact of neighborhood socioeconomic disparities on injury

International journal of public health, 2018-09, Vol.63 (7), p.855-863

2018

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Eruptive Keloids Associated with Breast Cancer: A Paraneoplastic Phenomenon?

Acta dermato-venereologica, 2011-06, Vol.91 (4), p.480-481

2011

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Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populations

Investigative ophthalmology & visual science, 2013-03, Vol.54 (3), p.2068-2075

2013

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Primary cutaneous mucormycosis at sites of insulin injection

Journal of the American Academy of Dermatology, 2011-05, Vol.64 (5), p.e79-e81

2011

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Novel null mutations in the EYS gene are a frequent cause of autosomal recessive retinitis pigmentosa in the Israeli population

Investigative ophthalmology & visual science, 2010-09, Vol.51 (9), p.4387-4394

2010

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Abstract 798: SeroNet Pooling Project of immunocompromised populations

Cancer research (Chicago, Ill.), 2023-04, Vol.83 (7_Supplement), p.798-798

2023

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Study and Analysis of Various LFSR Architectures

2018 International Conference on Circuits and Systems in Digital Enterprise Technology (ICCSDET), 2018, p.1-6

2018

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AI Based Audio Recognition System For Visually And Audibly Challenged

2020 International Conference on Smart Electronics and Communication (ICOSEC), 2020, p.297-304

2020

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The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patients

Archives of ophthalmology (1960), 2009-03, Vol.127 (3), p.297

2009

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Eruptive keloids associated with breast cancer: a paraneoplastic phenomenon?

Acta dermato-venereologica, 2011, Vol.91 (4), p.480-481

2011

Volltextzugriff (PDF)

Primary cutaneous mucormycosis at sites of insulin injection

Journal of the American Academy of Dermatology, 2011, Vol.64 (5), p.e79-e81

2011

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Hawaii Demonstration Project to Avert Unintended Teenage Pregnancy: 1978-1982. Final Report. Executive Summary

1983

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Correction: Halting ErbB-2 isoforms retrograde transport to the nucleus as a new theragnostic approach for triple-negative breast cancer

Halting ErbB-2 isoforms retrograde transport to the nucleus as a new theragnostic approach for triple-negative breast cancer

Abstract 3633: Exploring a novel crosstalk between hyluronan/CD44 and ErbB-2 pathways in resistance to ErbB-2-targeted therapies in breast cancer

ODP551 Halting ErbB-2 Isoforms Retrograde Transport to the Nucleus as a New Theragnostic Approach for Triple Negative Breast Cancer

Abstract 344: Blockade of retrograde transport in triple negative breast cancer excludes ErbB-2 isoforms from the nucleus and abrogates tumor growth

ODP571 Blockade of ErbB-2 Nuclear Function Induces the Interferon Signaling Pathway in Breast Cancer Models Resistant to Trastuzumab

Cognitive Flexibility Predicts PTSD Symptoms: Observational and Interventional Studies

Efficacy and safety of azithromycin versus placebo to treat lower respiratory tract infections associated with low procalcitonin: a randomised, placebo-controlled, double-blind, non-inferiority trial

Identification of mutations causing inherited retinal degenerations in the israeli and palestinian populations using homozygosity mapping

A Missense Mutation in DHDDS, Encoding Dehydrodolichyl Diphosphate Synthase, Is Associated with Autosomal-Recessive Retinitis Pigmentosa in Ashkenazi Jews

Variable retinal phenotypes caused by mutations in the X-linked photopigment gene array

Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa

The impact of neighborhood socioeconomic disparities on injury

Eruptive Keloids Associated with Breast Cancer: A Paraneoplastic Phenomenon?

Mutations in CRB1 are a relatively common cause of autosomal recessive early-onset retinal degeneration in the Israeli and Palestinian populations

Primary cutaneous mucormycosis at sites of insulin injection

Novel null mutations in the EYS gene are a frequent cause of autosomal recessive retinitis pigmentosa in the Israeli population

Abstract 798: SeroNet Pooling Project of immunocompromised populations

Study and Analysis of Various LFSR Architectures

AI Based Audio Recognition System For Visually And Audibly Challenged

The spectrum of retinal diseases caused by NR2E3 mutations in Israeli and Palestinian patients

Eruptive keloids associated with breast cancer: a paraneoplastic phenomenon?

Primary cutaneous mucormycosis at sites of insulin injection

Hawaii Demonstration Project to Avert Unintended Teenage Pregnancy: 1978-1982. Final Report. Executive Summary

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