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Cell-cycle regulator E2F1 and microRNA-223 comprise an autoregulatory negative feedback loop in acute myeloid leukemia

Blood, 2010-03, Vol.115 (9), p.1768-1778

2010

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New paradigms of USP53 disease: normal GGT cholestasis, BRIC, cholangiopathy, and responsiveness to rifampicin

Journal of human genetics, 2021-02, Vol.66 (2), p.151-159

2021

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A rare presentation of BCR‐ABL1 and RUNX1‐MECOM rearrangement in a pediatric patient with acute myeloid leukemia

Clinical case reports, 2024-05, Vol.12 (5), p.e8917-n/a

2024

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Favorable outcome of PML‐RARα short isoform and FLT3‐ITD mutation in a patient with several adverse prognostic markers: A case report

Clinical case reports, 2023-07, Vol.11 (7), p.e07637-n/a

2023

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CD44 regulates the apoptotic response and promotes disease development in chronic lymphocytic leukemia

Blood, 2013-05, Vol.121 (20), p.4126-4136

2013

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Use of Array Comparative Genomic Hybridization for the Diagnosis of DiGeorge Syndrome in Saudi Arabian Population

Cytogenetic and genome research, 2018-01, Vol.154 (1), p.20-29

2018

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Atypical presentation of adenosine deaminase 2 deficiency with bi‐allelic ADA2 mutation

Clinical case reports, 2022-03, Vol.10 (3), p.e05408-n/a

2022

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Incidence of Inborn Errors of Metabolism and Endocrine Disorders Among 40965 Newborn Infants at Riyadh Second Health Cluster of the Ministry of Health Saudi Arabia

International journal of neonatal screening, 2024-10, Vol.10 (4), p.72

2024

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Target proteins of C/EBPαp30 in AML: C/EBPαp30 enhances sumoylation of C/EBPαp42 via up-regulation of Ubc9

Blood, 2007-11, Vol.110 (9), p.3301-3309

2007

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Outcome of cerebral venous thrombosis in a critically Ill COVID-19 infected patient: A case report

Journal of infection and public health, 2024-06, Vol.17 (6), p.1152-1153

2024

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Clinical laboratory and radiological findings in COVID-19 patients with variable severity: King Fahad Medical City experience

Journal of infection and public health, 2024-06, Vol.17 (6), p.1152-1152

2024

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Synthesis and Selective Anticancer Activity of Organochalcogen Based Redox Catalysts

Journal of medicinal chemistry, 2010-10, Vol.53 (19), p.6954-6963

2010

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Excessive homozygosity identified by chromosomal microarray at a known GCDH mutation locus correlates with brain MRI abnormalities in an infant with glutaric aciduria

Clinical case reports, 2017-08, Vol.5 (8), p.1303-1308

2017

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A multicenter clinical exome study in unselected cohorts from a consanguineous population of Saudi Arabia demonstrated a high diagnostic yield

Molecular genetics and metabolism, 2017-06, Vol.121 (2), p.91-95

2017

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High expression of matrix metalloproteinases: MMP-2 and MMP-9 predicts poor survival outcome in colorectal carcinoma

Future oncology (London, England), 2016-02, Vol.12 (3), p.323-331

2016

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The evaluation of DiGeorge syndrome gene deletion using molecular cytogenetic techniques

BMC genomics, 2014-04, Vol.15 (S2), p.P30-P30, Article P30

2014

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Downregulation of c-Jun expression and cell cycle regulatory molecules in acute myeloid leukemia cells upon CD44 ligation

Oncogene, 2003-04, Vol.22 (15), p.2296-2308

2003

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Novel de novo heterozygous CACNA1A gene variant in generalised dystonia: a case report

BMJ neurology open, 2024-06, Vol.6 (1), p.e000710

2024

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Targeting the disturbed redox equilibrium in chronic lymphocytic leukemia by novel reactive oxygen species-catalytic 'sensor/effector' compounds

Leukemia & lymphoma, 2011-07, Vol.52 (7), p.1407-1411

2011

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Elevated c-Jun expression in acute myeloid leukemias inhibits C/EBPα DNA binding via leucine zipper domain interaction

Oncogene, 2003-07, Vol.22 (30), p.4760-4764

2003

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Harel-Yoon syndrome: the first case report from Saudi Arabia

Journal of Biochemical and Clinical Genetics, 2020-06, Vol.3 (1), p.22-27

2020

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Glutaric aciduria type 1: a review of phenotypic and genetic characteristics

Journal of Biochemical and Clinical Genetics, 2019-06, Vol.2 (1), p.40-53

2019

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Neurological and extra-neurological clinical spectrum observed in pediatric patients with EMC1 gene variants identified by whole exome sequencing

Journal of Biochemical and Clinical Genetics, 2021-12, Vol.4 (2), p.93-99

2021

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Proteomic analysis of acute promyelocytic leukemia: PML-RARα leads to decreased phosphorylation of OP18 at serine 63

Proteomics (Weinheim), 2006-11, Vol.6 (21), p.5705-5719

2006

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Advancing mass spectrometry-based clinical proteomics in Saudi Arabia. Establishing a Saudi Proteomics Society

Saudi medical journal, 2011-03, Vol.32 (3), p.225

2011

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Cell-cycle regulator E2F1 and microRNA-223 comprise an autoregulatory negative feedback loop in acute myeloid leukemia

New paradigms of USP53 disease: normal GGT cholestasis, BRIC, cholangiopathy, and responsiveness to rifampicin

A rare presentation of BCR‐ABL1 and RUNX1‐MECOM rearrangement in a pediatric patient with acute myeloid leukemia

Favorable outcome of PML‐RARα short isoform and FLT3‐ITD mutation in a patient with several adverse prognostic markers: A case report

CD44 regulates the apoptotic response and promotes disease development in chronic lymphocytic leukemia

Use of Array Comparative Genomic Hybridization for the Diagnosis of DiGeorge Syndrome in Saudi Arabian Population

Atypical presentation of adenosine deaminase 2 deficiency with bi‐allelic ADA2 mutation

Incidence of Inborn Errors of Metabolism and Endocrine Disorders Among 40965 Newborn Infants at Riyadh Second Health Cluster of the Ministry of Health Saudi Arabia

Target proteins of C/EBPαp30 in AML: C/EBPαp30 enhances sumoylation of C/EBPαp42 via up-regulation of Ubc9

Outcome of cerebral venous thrombosis in a critically Ill COVID-19 infected patient: A case report

Clinical laboratory and radiological findings in COVID-19 patients with variable severity: King Fahad Medical City experience

Synthesis and Selective Anticancer Activity of Organochalcogen Based Redox Catalysts

Excessive homozygosity identified by chromosomal microarray at a known GCDH mutation locus correlates with brain MRI abnormalities in an infant with glutaric aciduria

A multicenter clinical exome study in unselected cohorts from a consanguineous population of Saudi Arabia demonstrated a high diagnostic yield

High expression of matrix metalloproteinases: MMP-2 and MMP-9 predicts poor survival outcome in colorectal carcinoma

The evaluation of DiGeorge syndrome gene deletion using molecular cytogenetic techniques

Downregulation of c-Jun expression and cell cycle regulatory molecules in acute myeloid leukemia cells upon CD44 ligation

Novel de novo heterozygous CACNA1A gene variant in generalised dystonia: a case report

Targeting the disturbed redox equilibrium in chronic lymphocytic leukemia by novel reactive oxygen species-catalytic 'sensor/effector' compounds

Elevated c-Jun expression in acute myeloid leukemias inhibits C/EBPα DNA binding via leucine zipper domain interaction

Harel-Yoon syndrome: the first case report from Saudi Arabia

Glutaric aciduria type 1: a review of phenotypic and genetic characteristics

Neurological and extra-neurological clinical spectrum observed in pediatric patients with EMC1 gene variants identified by whole exome sequencing

Proteomic analysis of acute promyelocytic leukemia: PML-RARα leads to decreased phosphorylation of OP18 at serine 63

Advancing mass spectrometry-based clinical proteomics in Saudi Arabia. Establishing a Saudi Proteomics Society

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