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Rationale and preclinical efficacy of a novel anti-EMP2 antibody for the treatment of invasive breast cancer

Molecular cancer therapeutics, 2014-04, Vol.13 (4), p.902-915

2014

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Abstract 1478: Anti-EMP2 IgG1 combined with anti-PD1/PDL1 antibodies synergistically reduce tumor load in animal models of breast cancer

Cancer research (Chicago, Ill.), 2016-07, Vol.76 (14_Supplement), p.1478-1478

2016

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Abstract 654: PG-101 in combination with docetaxel or Herceptin improves breast cancer survival

Cancer research (Chicago, Ill.), 2015-08, Vol.75 (15_Supplement), p.654-654

2015

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Abstract 3965: Epithelial membrane protein-2 is a novel regulator of immune editing in breast cancer

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.3965-3965

2017

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Abstract 240: Therapeutic targeting of EMP2 reduces breast cancer stem cells

Cancer research (Chicago, Ill.), 2013-04, Vol.73 (8_Supplement), p.240-240

2013

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Review of the GAS3 Family of Proteins and their Relevance to Cancer

Critical reviews in oncogenesis, 2015, Vol.20 (5-6), p.435

2015

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Effect of therapeutic targeting of EMP2 on breast and endometrial cancer stem cells

Journal of clinical oncology, 2013-05, Vol.31 (15_suppl), p.3080-3080

2013

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Peroxynitrite upregulates angiogenic factors VEGF-A, BFGF, and HIF-1α in human corneal limbal epithelial cells

Investigative ophthalmology & visual science, 2014-03, Vol.55 (3), p.1637-1646

2014

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Human Embryonic Stem Cell-Derived Mesenchymal Stromal Cells Decrease the Development of Severe Experimental Autoimmune Uveitis in B10.RIII Mice

Ocular immunology and inflammation, 2018-11, Vol.26 (8), p.1228-1236

2018

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Cytoprotective Effect of Lacritin on Human Corneal Epithelial Cells Exposed to Benzalkonium Chloride In Vitro

Current eye research, 2014-06, Vol.39 (6), p.604-610

2014

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Rationale and pre-clinical efficacy of a novel anti-EMP2 antibody for the treatment of invasive breast cancer

Molecular cancer therapeutics, 2014-01, Vol.13 (4), p.902-915

2014

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Nitric oxide reversibly impairs axonal conduction in Guinea pig spinal cord

Journal of neurotrauma, 2006-12, Vol.23 (12), p.1779

2006

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Reactive nitrogen and oxygen species cause reversible axonal conduction deficits in the mammalian spinal cord

Ashki, Negin

2008

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Declining trends in HIV and other sexually transmitted infections among female sex workers in Iran could be attributable to reduced drug injection: a cross-sectional study

Sexually transmitted infections, 2020-02, Vol.96 (1), p.68

2020

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Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia

Hemoglobin, 2015-01, Vol.39 (3), p.201-206

2015

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Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes

Expert review of hematology, 2015-09, Vol.8 (5), p.693-698

2015

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Point mutations which should not be overlooked in Hb H disease

Expert review of hematology, 2016-01, Vol.9 (1), p.107-113

2016

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Characterization of Homozygous Hb Setif (HBA2: c.283G>T) in the Iranian Population

Hemoglobin, 2016-01, Vol.40 (1), p.53-55

2016

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Mutations on the α 2-Globin Gene That May Trigger α + -Thalassemia

Hemoglobin, 2015-11, Vol.39 (6), p.398-402

2015

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Mutations on the α2-Globin Gene That May Trigger α+-Thalassemia

Hemoglobin, 2015, Vol.39 (6), p.398-402

2015

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Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient

Hemoglobin, 2015-06, Vol.39 (3), p.152-155

2015

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A 21 Nucleotide Duplication on the α 1- and α 2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease

Hemoglobin, 2015-06, Vol.39 (3), p.196-200

2015

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Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 Gene

Hemoglobin, 2016-01, Vol.40 (1), p.38-43

2016

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Homozygosity for the AATAAA > AATA- - Polyadenylation Site Mutation on the α2-Globin Gene Causing Transfusion-Dependent Hb H Disease in an Iranian Patient: A Case Report

Hemoglobin, 2015, Vol.39 (5), p.355-358

2015

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A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease

Hemoglobin, 2015, Vol.39 (3), p.196-200

2015

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Rationale and preclinical efficacy of a novel anti-EMP2 antibody for the treatment of invasive breast cancer

Abstract 1478: Anti-EMP2 IgG1 combined with anti-PD1/PDL1 antibodies synergistically reduce tumor load in animal models of breast cancer

Abstract 654: PG-101 in combination with docetaxel or Herceptin improves breast cancer survival

Abstract 3965: Epithelial membrane protein-2 is a novel regulator of immune editing in breast cancer

Abstract 240: Therapeutic targeting of EMP2 reduces breast cancer stem cells

Review of the GAS3 Family of Proteins and their Relevance to Cancer

Effect of therapeutic targeting of EMP2 on breast and endometrial cancer stem cells

Peroxynitrite upregulates angiogenic factors VEGF-A, BFGF, and HIF-1α in human corneal limbal epithelial cells

Human Embryonic Stem Cell-Derived Mesenchymal Stromal Cells Decrease the Development of Severe Experimental Autoimmune Uveitis in B10.RIII Mice

Cytoprotective Effect of Lacritin on Human Corneal Epithelial Cells Exposed to Benzalkonium Chloride In Vitro

Rationale and pre-clinical efficacy of a novel anti-EMP2 antibody for the treatment of invasive breast cancer

Nitric oxide reversibly impairs axonal conduction in Guinea pig spinal cord

Reactive nitrogen and oxygen species cause reversible axonal conduction deficits in the mammalian spinal cord

Declining trends in HIV and other sexually transmitted infections among female sex workers in Iran could be attributable to reduced drug injection: a cross-sectional study

Interaction of an α-Globin Gene Triplication with β-Globin Gene Mutations in Iranian Patients with β-Thalassemia Intermedia

Copy number variations of six and seven α-globin genes in a family with intermedia and major thalassemia phenotypes

Point mutations which should not be overlooked in Hb H disease

Characterization of Homozygous Hb Setif (HBA2: c.283G>T) in the Iranian Population

Mutations on the α 2-Globin Gene That May Trigger α + -Thalassemia

Mutations on the α2-Globin Gene That May Trigger α+-Thalassemia

Hb Dartmouth (HBA2: c.200T>C): An α2-Globin Gene Associated with Hb H Disease in One Homozygous Patient

A 21 Nucleotide Duplication on the α 1- and α 2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease

Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 Gene

Homozygosity for the AATAAA > AATA- - Polyadenylation Site Mutation on the α2-Globin Gene Causing Transfusion-Dependent Hb H Disease in an Iranian Patient: A Case Report

A 21 Nucleotide Duplication on the α1- and α2-Globin Genes Involves a Variety of Hypochromic Microcytic Anemias, From Mild to Hb H Disease

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