Inhibition of cell survival, invasion, tumor growth and histone deacetylase activity by the dietary flavonoid luteolin in human epithelioid cancer cells

Samir Attoub, Ahmed H. Hassan, Barbara Vanhoecke, +11

European Journal of Pharmacology

Tumor BiologyOncogenic AgentMedicineTumor GrowthDietary Flavonoid Luteolin +9

DNA methylation and repressive H3K9 and H3K27 trimethylation in the promoter regions of PD-1, CTLA-4, TIM-3, LAG-3, TIGIT, and PD-L1 genes in human primary breast cancer

Varun Sasidharan Nair, Haytham El Salhat, Rowaida Z. Taha, +3

Clinical Epigenetics

Trafficking defects and loss of ligand binding are the underlying causes of all reported DDR2 missense mutations found in SMED-SL patients

Bassam R. Ali, Huifang Xu, Nadia Akawi, +5

Human Molecular Genetics

Ddr2 Missense MutationsDevelopmental BiologyAutoimmune DiseaseShort LimbsUnited Arab Emirates +13

Characterization of a peptide from skin secretions of male specimens of the frog, Leptodactylus fallax that stimulates aggression in male frogs

Jay D. King, Louise A. Rollins‐Smith, Per F. Nielsen, +2

Peptides

BiologyMale FrogsNatural SciencesEvolutionary BiologyPhysiology +6

Endoplasmic reticulum quality control of LDLR variants associated with familial hypercholesterolemia

Praseetha Kizhakkedath, Anne John, Buthaina K. Al‐Sawafi, +2

FEBS Open Bio

Protein Quality ControlFamilial HypercholesterolemiaSignal TransductionLipid DisorderBiochemistry +12

A Novel Whole Exon Deletion in WWOX Gene Causes Early Epilepsy, Intellectual Disability and Optic Atrophy

Salma Ben‐Salem, Aisha Al‐Shamsi, Anne John, +2

Journal of Molecular Neuroscience

Mendelian DisorderGenetic DisorderGeneticsMolecular GeneticsDisease Gene Identification +4

Endoplasmic Reticulum Quality Control Is Involved in the Mechanism of Endoglin-Mediated Hereditary Haemorrhagic Telangiectasia

Bassam R. Ali, Imen Ben-Rebeh, Anne John, +6

PLoS ONE

GeneticsPathologyHht Type 1Molecular GeneticsDisease Gene Identification +15

Expression of Epstein–Barr virus in Hodgkin lymphoma in a population of United Arab Emirates nationals

Suhail Al‐Salam, Anne John, Sayel Daoud, +2

Leukemia & lymphoma/Leukemia and lymphoma

A novel mutation in DDR2 causing spondylo-meta-epiphyseal dysplasia with short limbs and abnormal calcifications (SMED-SL) results in defective intra-cellular trafficking

Adila Al‐Kindi, Praseetha Kizhakkedath, Huifang Xu, +8

BMC Medical Genetics

Genomic variants in the FTO gene are associated with sporadic amyotrophic lateral sclerosis in Greek patients

Konstantinos Mitropoulos, Eleni Merkouri Papadima, Georgia Xiromerisiou, +29

Human Genomics