Shereen Al-Ali

ORCID: 0000-0003-4722-7125
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About
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Research Areas
  • Salivary Gland Disorders and Functions
  • Galectins and Cancer Biology
  • Fibromyalgia and Chronic Fatigue Syndrome Research
  • Cytokine Signaling Pathways and Interactions
  • Systemic Lupus Erythematosus Research
  • Diabetes and associated disorders
  • Asthma and respiratory diseases
  • Genetic Neurodegenerative Diseases
  • IL-33, ST2, and ILC Pathways
  • Adipokines, Inflammation, and Metabolic Diseases
  • Growth Hormone and Insulin-like Growth Factors
  • Heme Oxygenase-1 and Carbon Monoxide
  • Aquaculture Nutrition and Growth
  • Pediatric Hepatobiliary Diseases and Treatments
  • Salivary Gland Tumors Diagnosis and Treatment
  • Biochemical effects in animals
  • Cancer Immunotherapy and Biomarkers
  • Lymphoma Diagnosis and Treatment
  • Psoriasis: Treatment and Pathogenesis
  • MicroRNA in disease regulation
  • Glycosylation and Glycoproteins Research
  • Chemokine receptors and signaling
  • Aquaculture disease management and microbiota
  • Parasitic infections in humans and animals
  • Fibroblast Growth Factor Research

University of Basrah
2015-2025

Newcastle University
2014-2019

University Medical Center Utrecht
2017

Consorci Institut D'Investigacions Biomediques August Pi I Sunyer
2015

King Khaled Eye Specialist Hospital
2015

Oklahoma Medical Research Foundation
2015

University of California, San Francisco
2015

Hospital Clínic de Barcelona
2015

Background Fatigue is a debilitating condition with significant impact on patients' quality of life. frequently reported by patients suffering from primary Sjögren's Syndrome (pSS), chronic autoimmune characterised dryness the eyes and mouth. However, although fatigue common in pSS, it does not manifest all sufferers, providing an excellent model which to explore potential underpinning biological mechanisms. Methods Whole blood samples 133 fully-phenotyped pSS stratified for presence...

10.1371/journal.pone.0143970 article EN cc-by PLoS ONE 2015-12-22

To assess the relationships between systemic IFN type I (IFN-I) and II (IFN-II) activity disease manifestations in primary SS (pSS). RT-PCR of multiple IFN-induced genes followed by principal component analysis whole blood RNA 50 pSS patients was used to identify indicator IFN-I IFN-II activities. Systemic activation levels were analysed two independent European cohorts (n = 86 55, respectively) their with clinical features analysed. Three groups could be stratified according activity:...

10.1093/rheumatology/kex490 article EN Lara D. Veeken 2018-01-03
Jessica Tarn Nadia Howard-Tripp Dennis Lendrem Xavier Mariette Alain Saraux and 95 more Valérie Devauchelle‐Pensec Raphaèle Séror Andrew Skelton Katherine James Peter McMeekin Shereen Al-Ali Katie L. Hackett Clare Lendrem Ben Hargreaves John Casement Sheryl Mitchell Simon J Bowman Elizabeth Price Colin Pease Paul Emery Peter Lanyon John Hunter Monica Gupta Stefano Bombardieri Nurhan Sutcliffe Costantino Pitzalis John McLaren Annie Cooper Marian Regan Ian Giles David Isenberg V. Saravanan David Coady Bhaskar Dasgupta Neil McHugh Steven Young‐Min Robert J. Moots Nagui Gendi Mohammed Akil Bridget Griffiths Svein Joar Auglænd Johnsen Katrine Brække Norheim Roald Omdal Deborah Stocken Colin Everett Catherine Fernandez John D. Isaacs Jacques‐Eric Gottenberg Wan‐Fai Ng Valérie Devauchelle‐Pensec Philippe Dieudé Jean Jacques Dubost Anne-Laure Fauchais Vincent Goëb É. Hachulla C. Larroche Véronique Le Guern Jacques Morel Aleth Perdriger Xavier Puéchal S. Rist Damien Sen Jean Sibilia Olivier Vittecoq Joëlle Bénessiano Sarah Tubiana Karine Inamo Stanie Gaëte Djilali Batouche Domitille Molinari Mickael Randrianandrasana Isabelle Pane Adeline Abbé Gabriel Baron Philippe Ravaud Jacques-Eric Gottenberg Philippe Ravaud Xavier Puéchal Véronique Le Guern Jean Sibilia C. Larroche Alain Saraux Valérie Devauchelle-Pensec Jacques Morel Gilles Hayem P.Y. Hatron Aleth Perdriger Damien Sene Charles Zarnitsky Djilali Batouche Valérie Furlan Joëlle Bénessiano Élodie Perrodeau Raphaèle Séror Xavier Mariette Samuel M. Brown N. Navarro Saaeha Rauz Paul Emery Sue Pavitt

Heterogeneity is a major obstacle to developing effective treatments for patients with primary Sjögren's syndrome. We aimed develop robust method stratification, exploiting heterogeneity in patient-reported symptoms, and relate these differences pathobiology therapeutic response.

10.1016/s2665-9913(19)30042-6 article EN cc-by The Lancet Rheumatology 2019-09-25

Asthma is a heterogenic chronic inflammation of the lower respiratory tract. highly prevalent in Basrah city. This study aimed to investigate effect SOCS (SOCS1 & SOCS3) at molecular level on production several cytokines (IL-6, IL-17 and IL-31) asthma. The current included total 80 participants, 54 asthmatic patients 26 heathy controls. levels IL-6, IL-31 were estimated by ELISA while SOCS1 gene polymorphism -1478 CA>del (rs33989964) was detected RFLP-PCR. In addition, SOCS3...

10.35118/apjmbb.2025.033.1.03 article EN Asia-Pacific Journal of Molecular Biology and Biotechnology 2025-01-31

Background. Osteoporosis is a bone disease characterized by low mass and micro-architectural weakening of tissue. It can be influenced, in part, immunological activity. Therapeutically targeting immune factors that promote osteoporosis could protect larger number susceptible individuals, especially postmenopausal women, from this debilitating disease. The aim the present study to evaluate blood levels gene expression for RANKL, RANK, OPG, OSCAR, transcription RORᵧt FOXP3 (as representatives...

10.37897/rmj.2025.1.5 article EN cc-by Romanian Medical Journal 2025-02-24

Chronic Fatigue Syndrome (CFS) is a prevalent debilitating condition that affects approximately 250,000 people in the UK. There growing interest role of mitochondrial function and DNA (mtDNA) variation CFS. It now known fatigue common often severe patients with disease irrespective their age, gender or mtDNA genotype. More recently, it has been suggested some CFS harbour clinically proven mutations. MtDNA sequencing 93 from United Kingdom (UK) South Africa (RSA) was performed using an Ion...

10.1186/s12881-017-0387-6 article EN cc-by BMC Medical Genetics 2017-03-16

10.47278/book.vpph/2021.015 article EN International Journal of Veterinary Science 2021-01-01

Resolving the molecular details of proteome variation in different tissues and organs human body will greatly increase our knowledge biology disease.The Human Protein Atlas (www.proteinatlas.org)project employs an antibody-based proteomics approach to systematically map distribution relative abundance proteins a multitude normal tissues, cancer cells.In this talk, tissue based on integrated omics that involves quantitative transcriptomics at organ level, combined with microarray-based...

10.1111/sji.12291 article EN Scandinavian Journal of Immunology 2015-04-21

Asthma is a well-known illness of the lower respiratory tract. It has many phenotypes including allergic and non-allergic asthma. The mechanism still not entirely understood. aim study to investigate IL-4 response during Blood from asthma patients aged matched healthy controls were collected complete blood count (CBC) was performed on each sample serum level IgE estimated by enzyme linked immunosorbent assay (ELISA). results current showed that majority asthmatic between 51-60 years old with...

10.33545/26646188.2024.v6.i1a.54 article EN International Journal of Clinical Biology and Biochemistry 2024-01-01

Colorectal cancer (CRC) is classified as one of the most prevalent types worldwide, with high morbidity and mortality rates. Patients CRC have been shown to express a detectable cytokine in serum which contributes pathogenesis. Therefore, interleukin 10 (IL-10) level patients was investigated this study. Patients' medical records admitted Rizgary Nanakali hospitals, Erbil, Iraq analyzed study group compared healthy volunteers' control group. Seventy-one samples were collected, thirty-one...

10.9734/jpri/2021/v33i26b31477 article EN Journal of Pharmaceutical Research International 2021-04-27

<h3>Background/Purpose</h3> Micro RNAs (miRNAs) are 18–25 nt non-coding that bind target/complementary sequences within the 3'UTR of RNA molecules steering them towards degradation or translational repression, and play a key role in regulation gene expression. Better understanding expression pattern miRNAs diseases may improve our biological basis disease identify potential biomarkers. The primary Sjögren's syndrome (PSS) PSS-related lymphoma remains poorly understood. aim this project is to...

10.1136/annrheumdis-2015-207259.175 article EN Annals of the Rheumatic Diseases 2015-02-13

Resolving the molecular details of proteome variation in different tissues and organs human body will greatly increase our knowledge biology disease.The Human Protein Atlas (www.proteinatlas.org)project employs an antibody-based proteomics approach to systematically map distribution relative abundance proteins a multitude normal tissues, cancer cells.In this talk, tissue based on integrated omics that involves quantitative transcriptomics at organ level, combined with microarray-based...

10.1111/sji.12290 article EN Scandinavian Journal of Immunology 2015-04-21

<h3>Background</h3> Lymphoma development is a serious complication of Primary Sjögren9s syndrome (pSS). To date, the biological processes that may be involved in pSS-associated lymphoma are not fully understood. <h3>Objectives</h3> The aim our study to use microarray gene expression data from well-defined cohort pSS patients identify relevant lymphoma. <h3>Methods</h3> and healthy controls UK primary registry (UKPSSR) were used this study. All fulfilled AECG criteria. Whole genome whole...

10.1136/annrheumdis-2017-eular.4820 article EN Annals of the Rheumatic Diseases 2017-06-01

<h3>Background</h3> Local and systemic activation of interferons (IFNs) has been demonstrated in primary Sjögren9s syndrome (pSS).[1–4] Type I IFNs are associated with higher disease activity autoantibody levels.[5] Recent findings also show interferon type II (IFNγ) induced gene expression salivary glands pSS patients.[6, 7] Although IFN bind to different receptors they induce partially overlapping patterns. Understanding the relative contribution may deepen our knowledge pathogenesis...

10.1136/annrheumdis-2017-eular.3688 article EN Annals of the Rheumatic Diseases 2017-06-01
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