Publications by authors named "Zafar Nawaz"

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Caffeine decreases vitamin D receptor protein expression and 1,25(OH)2D3 stimulated alkaline phosphatase activity in human osteoblast cells.
Prema B Rapuri, J C Gallagher, Zafar Nawaz

March 2007

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Understanding the Spectrum of Mild Clinical Outcomes and Novel Findings in Arterial Tortuosity Syndrome Among Qatari Patients: Implications of SLC2A10 Mutation.
Muhammed Riyas K Rahmath, Haytham Ibrahim, Muhammad Faiyaz-Ul-Haque, Zafar Nawaz, Ahmad Zitoun

Biomedicines· January 2025

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Spontaneous Remission in a Patient with Chronic Myeloid Leukemia: A Case Report.
Awni Alshurafa, Yeslem Ekeibed, Susanna Akiki, Muna Alzeyara, Zafar Nawaz

Case Rep Oncol· October 2023

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Ultrastructure abnormalities of collagen and elastin in Arab patients with arterial tortuosity syndrome.
Muhammad Faiyaz-Ul-Haque, Mohammed Mubarak, Atqah AbdulWahab, Ammar C AlRikabi, Abbas H Alsaeed, Zafar Nawaz

J Cutan Pathol· July 2022

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The QChip1 knowledgebase and microarray for precision medicine in Qatar.
Juan L Rodriguez-Flores, Radja Messai-Badji, Amal Robay, Ramzi Temanni, Najeeb Syed, Zafar Nawaz

NPJ Genom Med· January 2022

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P190 in a Patient with Philadelphia Chromosome Positive T-Cell Acute Lymphoblastic Leukemia: A Rare Case Report and Review of Literature.
Samah Kohla, Sarah El Kourashy, Zafar Nawaz, Reda Youssef, Ahmad Al-Sabbagh

Case Rep Oncol· July 2021

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Downregulation of Lymphoid enhancer-binding factor 1 (LEF-1) expression (by immunohistochemistry and/ flow cytometry) in chronic Lymphocytic Leukemia with atypical immunophenotypic and cytologic features.
Dina S Soliman, Einas Al-Kuwari, Kodappully S Siveen, Rajaa Al-Abdulla, Prem Chandra, Zafar Nawaz

Int J Lab Hematol· June 2021

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Outcome associated with EPCAM founder mutation c.499dup in Qatar.
Kamal Hassan, Gulab Sher, Eman Hamid, Khalid Abou Hazima, Hatim Abdelrahman, Zafar Nawaz

Eur J Med Genet· October 2020

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Haploinsufficiency of the FOXA2 associated with a complex clinical phenotype.
Idris Mohammed, Sara Al-Khawaga, David Bohanna, Abdusamea Shabani, Faiyaz Khan, Zafar Nawaz

Mol Genet Genomic Med· June 2020

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Acute Myeloid Leukemia in Qatar (2010-2016): Clinical, Biological, and Prognostic Factors and Treatment Outcomes.
Halima El Omri, Ruba Yasin Taha, Adel Elomri, Nancy Kacem, Hesham Elsabah, Zafar Nawaz

Front Genet· June 2020

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Novel and recurrent germline mutations in the VHL gene in 5 Arab patients with Von Hippel-Lindau disease.
Muhammad Faiyaz-Ul-Haque, Masood Jamil, Muhammad Aslam, Halah Abalkhail, Fouad Al-Dayel, Zafar Nawaz

Cancer Genet· May 2020

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A Rare Case of Systemic Mastocytosis with Associated Hematologic Neoplasm (SM-AHN) Involving Chronic Myeloid Leukemia: A Case Report and Literature Review.
Feryal A Ibrahim, Mohammad A J Abdulla, Dina Soliman, Ahmad Al Sabbagh, Zafar Nawaz

Am J Case Rep· May 2020

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Plasma Cell Myeloma with an Aggressive Clinical Course and Anaplastic Morphology in a 22-Year-Old Patient: A Case Report and Review of Literature.
Hesham Elsabah, Dina S Soliman, Feryal Ibrahim, Ahmad Al-Sabbagh, Mohamed Yassin, Zafar Nawaz

Am J Case Rep· March 2020

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Sanguinarine Induces Apoptosis in Papillary Thyroid Cancer Cells via Generation of Reactive Oxygen Species.
Abdul Q Khan, Elham A N Mohamed, Ishrat Hakeem, Aneeza Nazeer, Shilpa Kuttikrishnan, Zafar Nawaz

Molecules· March 2020

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Spectrum of the KIT Gene Mutations in Gastrointestinal Stromal Tumors in Arab Patients.
Muhammad Faiyaz-Ul-Haque, Fouad Al-Dayel, Asma Tulba, Halah Abalkhail, Hussa Alhussaini, Zafar Nawaz

Asian Pac J Cancer Prev· October 2018

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Loss of Angelman Syndrome Protein E6AP Disrupts a Novel Antagonistic Estrogen-Retinoic Acid Transcriptional Crosstalk in Neurons.
Jimmy El Hokayem, Edwin Weeber, Zafar Nawaz

Mol Neurobiol· September 2018

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An uncommon case of chronic myeloid leukemia with variant cytogenetic.
Mohamed A Abdullah, Aliaa Amer, Zafar Nawaz, Ali S Abdullah, Ahmad Al-Sabbagh

Acta Biomed· April 2018

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High-Grade B-Cell Neoplasm with Surface Light Chain Restriction and Tdt Coexpression Evolved in a -Rearranged Diffuse Large B-Cell Lymphoma: A Dilemma in Classification.
Dina Sameh Soliman, Ahmad Al-Sabbagh, Feryal Ibrahim, Ruba Y Taha, Zafar Nawaz

Case Rep Hematol· August 2017

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Molecular genetic analysis of consanguineous families with primary microcephaly identified pathogenic variants in the ASPM gene.
Muzammil Ahmad Khan, Christian Windpassinger, Muhammad Zeeshan Ali, Muhammad Zubair, Hadia Gul, Zafar Nawaz

J Genet· June 2017

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Ubiquitination of nuclear receptors.
Jimmy El Hokayem, Celeste Amadei, Jean-Pierre Obeid, Zafar Nawaz

Clin Sci (Lond)· May 2017

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Tumor Necrosis Factor Receptor Associated Factors (TRAFs) 2 and 3 Form a Transcriptional Complex with Phosho-RNA Polymerase II and p65 in CD40 Ligand Activated Neuro2a Cells.
Jimmy El Hokayem, George C Brittain, Zafar Nawaz, John R Bethea

Mol Neurobiol· March 2017

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The Molecular Genetics of Autosomal Recessive Nonsyndromic Intellectual Disability: a Mutational Continuum and Future Recommendations.
Muzammil Ahmad Khan, Saadullah Khan, Christian Windpassinger, Muhammad Badar, Zafar Nawaz

Ann Hum Genet· November 2016

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p53 Restoration in Induction and Maintenance of Senescence: Differential Effects in Premalignant and Malignant Tumor Cells.
Mohamad Harajly, Hasan Zalzali, Zafar Nawaz, Sandra E Ghayad, Farah Ghamloush

Mol Cell Biol· February 2016

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High diagnostic yield of clinical exome sequencing in Middle Eastern patients with Mendelian disorders.
Tarunashree Yavarna, Nader Al-Dewik, Mariam Al-Mureikhi, Rehab Ali, Fatma Al-Mesaifri, Zafar Nawaz

Hum Genet· September 2015

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Nonsense mutation in the WDR73 gene is associated with Galloway-Mowat syndrome.
Tawfeg Ben-Omran, Somayyeh Fahiminiya, Natalie Sorfazlian, Mariam Almuriekhi, Zafar Nawaz

J Med Genet· June 2015

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Loss-of-Function Mutation in APC2 Causes Sotos Syndrome Features.
Mariam Almuriekhi, Takafumi Shintani, Somayyeh Fahiminiya, Akihiro Fujikawa, Kazuya Kuboyama, Zafar Nawaz

Cell Rep· March 2015

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