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Investigation of role of CpG methylation in some epithelial mesenchymal transition gene in a chemoresistant ovarian cancer cell line

Scientific reports, 2022-05, Vol.12 (1), p.7494-15, Article 7494

2022

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"In House" assays for the quantification of Annexin V and its autoantibodies in patients with recurrent pregnancy loss and in vitro fertilisation failures

Scientific reports, 2023-12, Vol.13 (1), p.22322-22322, Article 22322

2023

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Induction of G1-phase cell cycle arrest and apoptosis pathway in MDA-MB-231 human breast cancer cells by sulfated polysaccharide extracted from Laurencia papillosa

Cancer cell international, 2016-05, Vol.16 (1), p.39-39, Article 39

2016

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Secretion of Recombinant Human Annexin V in Fusion with the Super Folder GFP for Labelling Phosphatidylserine-Exposing Membranes

The Journal of membrane biology, 2021-04, Vol.254 (2), p.175-187

2021

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Effects of ionizing radiation on the viability and proliferative behavior of the human glioblastoma T98G cell line

BMC research notes, 2018-05, Vol.11 (1), p.330-330, Article 330

2018

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Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia

BMC pediatrics, 2019-02, Vol.19 (1), p.61-61, Article 61

2019

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HLA-DQ2 and -DQ8 genotype frequency in Syrian celiac disease children: HLA-DQ relative risks evaluation

BMC gastroenterology, 2018-05, Vol.18 (1), p.70-70, Article 70

2018

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Characterization of Annexin V Fusion with the Superfolder GFP in Liposomes Binding and Apoptosis Detection

Frontiers in physiology, 2017-05, Vol.8, p.317-317

2017

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Molecular analysis of the AGXT gene in Syrian patients suspected with primary hyperoxaluria type 1

BMC medical genomics, 2021-06, Vol.14 (1), p.146-11, Article 146

2021

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A rare gene variation cap +1 (A>C) (HBB: c. −50A>C) associated with codon 5 (‐CT) (HBB: c.17_18delCT) mutation in Syrian family

Molecular genetics & genomic medicine, 2021-03, Vol.9 (3), p.e1602-n/a

2021

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Exploiting Nanobodies in the Detection and Quantification of Human Growth Hormone via Phage-Sandwich Enzyme-Linked Immunosorbent Assay

Frontiers in endocrinology (Lausanne), 2017-05, Vol.8, p.115-115

2017

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A compound heterozygous −29 A>G and IVS-I-1 G>A mutation of HBB gene leading to β-thalassemia intermedia in a Syrian patient: A case report

Cogent medicine, 2019-01, Vol.6 (1), p.1581448

2019

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First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family

Hemoglobin, 2019-01, Vol.43 (1), p.66-68

2019

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Isolation, Structural characterization, and antiproliferative activity of phycocolloids from the red seaweed Laurencia papillosa on MCF-7 human breast cancer cells

International journal of biological macromolecules, 2018-03, Vol.108, p.916-926

2018

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The Spectrum of α-Thalassemia Mutations in Syrian Patients

Hemoglobin, 2023-11, Vol.47 (6), p.245-248

2023

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Hb Knossos (HBB: c.82G T), [beta]-globin CD 5 (-CT) (HBB: c.17_18delCT) and [delta]-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with [beta]-thalassemia intermedia

BMC pediatrics, 2019-02, Vol.19 (1)

2019

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Hb Knossos mutations in a Syrian patient with [beta]-thalassemia intermedia

BMC pediatrics, 2019-02, Vol.19 (1)

2019

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Compound heterozygosity for Hb C/Hb S (HBB: c.19G>A/HBB: c.20A>T) diseases observed in a Syrian family: a case report

Annals of medicine and surgery, 2023-04, Vol.85 (4), p.1184-1187

2023

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Description of a Rare β-Globin Gene Mutation: -86 (C>G) (HBB: c.-136C>G) Observed in a Syrian Family

Hemoglobin, 2018-05, Vol.42 (3), p.203-205

2018

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Description of a rare β-globin gene mutation, IVS-II-848 (C>A) (HBB: c.316-3C>A) in association with IVS-I-1 (G>A) (HBB: c.92 + 1G>A), observed in a Syrian family: a case report

Hemoglobin, 2019-09, Vol.43 (4-5), p.283-285

2019

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Prokaryotic overexpression of TEV–rhGH and characterization of its polyclonal antibody

Gene, 2014-05, Vol.542 (1), p.69-76

2014

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Haplotype Analysis of Three Common β-Thalassemia Mutations in Syrian Patients

Hemoglobin, 2018-11, Vol.42 (5-6), p.302-305

2018

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Geographical distribution of β-globin gene mutations in Syria

Hematology (Luxembourg), 2018-10, Vol.23 (9), p.697-704

2018

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Algal sulfated carrageenan inhibits proliferation of MDA-MB-231 cells via apoptosis regulatory genes

Molecular medicine reports, 2015-03, Vol.11 (3), p.2153-2158

2015

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Effects of γ-radiation on cell growth, cell cycle and promoter methylation of 22 cell cycle genes in the 1321NI astrocytoma cell line

Advances in medical sciences, 2017-09, Vol.62 (2), p.330-337

2017

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Investigation of role of CpG methylation in some epithelial mesenchymal transition gene in a chemoresistant ovarian cancer cell line

"In House" assays for the quantification of Annexin V and its autoantibodies in patients with recurrent pregnancy loss and in vitro fertilisation failures

Induction of G1-phase cell cycle arrest and apoptosis pathway in MDA-MB-231 human breast cancer cells by sulfated polysaccharide extracted from Laurencia papillosa

Secretion of Recombinant Human Annexin V in Fusion with the Super Folder GFP for Labelling Phosphatidylserine-Exposing Membranes

Effects of ionizing radiation on the viability and proliferative behavior of the human glioblastoma T98G cell line

Hb Knossos (HBB: c.82G > T), β-globin CD 5 (-CT) (HBB: c.17_18delCT) and δ-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia

HLA-DQ2 and -DQ8 genotype frequency in Syrian celiac disease children: HLA-DQ relative risks evaluation

Characterization of Annexin V Fusion with the Superfolder GFP in Liposomes Binding and Apoptosis Detection

Molecular analysis of the AGXT gene in Syrian patients suspected with primary hyperoxaluria type 1

A rare gene variation cap +1 (A>C) (HBB: c. −50A>C) associated with codon 5 (‐CT) (HBB: c.17_18delCT) mutation in Syrian family

Exploiting Nanobodies in the Detection and Quantification of Human Growth Hormone via Phage-Sandwich Enzyme-Linked Immunosorbent Assay

A compound heterozygous −29 A>G and IVS-I-1 G>A mutation of HBB gene leading to β-thalassemia intermedia in a Syrian patient: A case report

First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family

Isolation, Structural characterization, and antiproliferative activity of phycocolloids from the red seaweed Laurencia papillosa on MCF-7 human breast cancer cells

The Spectrum of α-Thalassemia Mutations in Syrian Patients

Hb Knossos (HBB: c.82G T), [beta]-globin CD 5 (-CT) (HBB: c.17_18delCT) and [delta]-globin CD 59 (-a) (HBD: c.179delA) mutations in a Syrian patient with [beta]-thalassemia intermedia

Hb Knossos mutations in a Syrian patient with [beta]-thalassemia intermedia

Compound heterozygosity for Hb C/Hb S (HBB: c.19G>A/HBB: c.20A>T) diseases observed in a Syrian family: a case report

Description of a Rare β-Globin Gene Mutation: -86 (C>G) (HBB: c.-136C>G) Observed in a Syrian Family

Description of a rare β-globin gene mutation, IVS-II-848 (C>A) (HBB: c.316-3C>A) in association with IVS-I-1 (G>A) (HBB: c.92 + 1G>A), observed in a Syrian family: a case report

Prokaryotic overexpression of TEV–rhGH and characterization of its polyclonal antibody

Haplotype Analysis of Three Common β-Thalassemia Mutations in Syrian Patients

Geographical distribution of β-globin gene mutations in Syria

Algal sulfated carrageenan inhibits proliferation of MDA-MB-231 cells via apoptosis regulatory genes

Effects of γ-radiation on cell growth, cell cycle and promoter methylation of 22 cell cycle genes in the 1321NI astrocytoma cell line

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